Should We Be Concerned About AI Developing Lethal Biological Weapons? Not Now, But Eventually.

AI can be utilized to synthesize the toxin lysine, which is also sourced from castor beans found in many gardens.

American Photo Archives/Alamy

Artificial intelligence holds the potential to revolutionize biology, enhancing the development of advanced drugs, vaccines, and even synthetic organisms that can, for instance, consume waste plastic. Nonetheless, there are concerns about its potential misuse in creating biological weapons that might evade traditional detection methods until it is too late. So, what level of concern is warranted?

“AI advancements are catalyzing breakthroughs in biology and medicine,” states Eric Horvitz, Chief Science Officer at Microsoft. “With these new capabilities comes the responsibility to remain vigilant.”

His research team explored whether AI could be utilized to design proteins that mimic the functions of known hazardous proteins while being distinct enough to avoid detection as dangerous. The specific proteins they attempted to redesign were not disclosed, although some research details were withheld, including toxins such as lysine, infamous for its role in a 1978 assassination, and botulinum, a potent neurotoxin known as Botox.

Creating numerous proteins akin to Botulinum requires a blueprint—the DNA that encodes it. Typically, if biologists need a specific DNA sequence, they order it from specialized companies.

Due to anxieties about bioterrorism, the option to order recipes for biological weapons exists through this method. Some DNA synthesis companies have voluntarily implemented screening processes to detect potentially hazardous orders. Proteins are essentially sequences of amino acids, and the screening examines whether the amino acid sequences correspond to a “sequence of concern,” meaning a biological threat.


However, AI theoretically enables the design of protein versions with altered amino acid sequences that still perform the same functions. Horvitz and his colleagues applied this approach to 72 potentially hazardous proteins and found that existing screening methods frequently overlooked these alternative variations.

This isn’t entirely unexpected. For a variety of reasons, the team did not physically create the redesigned proteins. Additionally, in a previous study conducted earlier this year, they tested a redesigned version of a non-toxic protein and determined that it did not function as intended, as detailed in their findings.

Moreover, while bioterrorist attacks have occurred, the frequency is low, and there’s limited reason to attribute this to a failed voluntary screening system. Numerous methods to circumvent regulations exist without resorting to AI redesign. For example, lysine can be harvested from castor oil plants found in many gardens. This study serves as a cautionary tale that great sophistication is not required to exploit gaps in security—much like in a scene from Mission Impossible, when a vault door remains wide open.

Lastly, apart from government-sponsored actions, historical records show that bioterrorists have rarely leveraged protein-based biological weapons effectively. For instance, the Aum Shinrikyo cult attempted to employ Botulinum for mass harm but ultimately relied on chemical agents. Letters laced with lysin sent to the White House failed to result in any fatalities. Based on casualty statistics, firearms and explosives pose significantly greater risks than biological toxins.

Does this imply we should cease our concerns over AI-generated biological weapons? Not at all. While Horvitz’s research focused strictly on proteins, viruses present a substantial threat. AI is already being leveraged to redesign entire viruses.

Recently, a team from Stanford University unveiled their attempt to redesign a virus that infects bacteria like E. coli. Consistent with findings from the protein redesign efforts, the results were underwhelming with respect to E. coli, but this is merely the beginning.

In discussions regarding AI-created viruses, James Diggans from DNA manufacturer Twist Bioscience, a member of Horvitz’s team, remarked that detecting viruses encoded with DNA is generally easier than finding proteins of concern. “Synthetic screening functions best with abundant data. Therefore, at the genomic level, it proves exceedingly beneficial.”

Nevertheless, not all DNA manufacturers are conducting such screening, and desktop DNA synthesis options are now accessible to the public. There are narratives of developers allegedly refusing to create harmful viruses or attempting to discern malicious intentions, yet individuals have discovered numerous ways to circumvent safeguards against creating bioweapons.

To clarify, history indicates that the threat posed by “wild” viruses is significantly higher than that of bioterrorism. Contrary to assertions from the current U.S. administration, evidence suggests that SARS-CoV-2 emerged as a result of a bat virus crossing over to other wildlife.

Moreover, the act of becoming a bioterrorist could inflict massive damage by merely releasing known viruses such as naturally occurring pathogens. There are substantial gaps in the Bioweapon Control efforts, thus reducing the need to rely on advanced AI techniques.

For all of these reasons, the risk of AI-engineered viruses being deployed is likely minimal at present. However, this risk increases as various technologies continue to improve. The COVID-19 pandemic has illustrated the chaos a new virus can unleash, even when it is not particularly harmful. Thus, there are justified reasons for concern.

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Source: www.newscientist.com

Ozempic: A Potential Key to Reversing Your Biological Age

Growing evidence of Ozempic’s extensive health benefits

David J. Phillip / Associated Press / Alamy Stock Photo

Ozempic, a medication for type 2 diabetes, has been linked to a deceleration in aging, with credible evidence emerging to support this claim.

Drugs like Ozempic and Wegovy, both of which contain semaglutide, have been increasingly recognized for their impact on obesity and are being researched for various conditions, including cardiovascular diseases, addiction, and dementia.

Previously, scientists speculated on their potential to slow biological aging, based primarily on animal studies and observational human data. However, recent clinical trial results offer direct evidence, according to Varun Dwaraka from Trudiagnostic, a diagnostics company based in Lexington, Kentucky.

To evaluate a drug’s impact on biological aging, researchers utilize epigenetic clocks, which highlight patterns of DNA methylation—a chemical modification that influences gene activity. These patterns evolve with age and can be adjusted by lifestyle factors, including diet. Essentially, an individual’s biological age might differ from their chronological age.

Dwaraka and his team examined 108 epigenetic clocks in individuals with HIV-related fat hypertrophy, a condition leading to excess fat accumulation and hastened cellular aging. In a randomized controlled trial, one group received Ozempic weekly for 32 weeks, while the control group received a placebo.


Using blood samples collected pre- and post-trial, the researchers determined the biological ages of 84 participants. “By the study’s conclusion, individuals administered semaglutide were, on average, biologically 3.1 years younger,” states Dwaraka. The placebo group showed no noteworthy changes. “Semaglutide not only decelerates aging but may also reverse it in certain participants,” he adds.

The research revealed that various organs and systems, particularly the heart and kidneys, exhibited slowed biological aging, with the most significant influences noticeable in the inflammatory system and brain.

Dwaraka attributes this phenomenon to semaglutide’s role in fat distribution and metabolic health. Excess fat surrounding organs can release pro-aging molecules that modify the DNA methylation of crucial age-related genes. Semaglutide effectively curtails low-grade inflammation, which is another contributor to epigenetic aging.

While the findings originated from individuals with HIV-associated fat hypertrophy, many of the biological pathways impacted by semaglutide are not unique to HIV. “Thus, similar effects on epigenetic aging may be expected in other populations,” asserts Dwaraka.

It’s not surprising that such drugs can decelerate aging, says Randy Shealy from the University of Michigan School of Medicine, as they alleviate metabolic stress on various cells and diminish inflammation—key drivers of aging throughout different cell types. However, he posits that much of the benefits arise from semaglutide improving overall health rather than direct cellular effects.

It remains to be seen if semaglutide should be taken to maintain biological youth. “It’s premature to widely recommend it as an anti-aging therapy,” Dwaraka cautions. Nonetheless, he believes this study will accelerate ongoing efforts to repurpose existing medications for age-related challenges, expediting approval processes while mitigating the risk of unforeseen side effects. “Semaglutide could become a leading candidate in this arena,” concludes Dwaraka.

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Source: www.newscientist.com

Study Reveals Your Brain’s Biological Age Can Forecast Your Lifespan

Researchers have devised a technique to assess the biological age of the brain, revealing it to be a key indicator of future health and longevity.

A recent study involved an analysis of blood samples from 45,000 adults, with protein levels measured in over 3,000 individuals. Many of these proteins correlate with particular organs, including the brain, enabling the estimation of each organ system’s “biological age.”

If an organ’s protein profile significantly deviated from its expected age (based on birthday count), it was categorized as either “very matured” or “very youthful.”

Among the various organs assessed, the brain emerged as the most significant predictor of health outcomes, according to the research.

“The brain is the gatekeeper of longevity,” stated Professor Tony Wyss-Coray, a senior author of the newly published research in Natural Medicine. “An older brain correlates with a higher mortality rate, while a younger brain suggests a longer life expectancy.”

Participants exhibiting a biologically aged brain were found to be 12 times more likely to receive an Alzheimer’s diagnosis within a decade compared to peers with biologically youthful brains.

Additionally, older brains increased the risk of death from any cause by 182% over a 15-year span, whereas youthful brains were linked to a 40% decrease in mortality.

Wyss-Coray emphasized that evaluating the brain and other organs through the lens of biological age marks the dawn of a new preventive medicine era.

“This represents the future of medicine,” he remarked. “Currently, patients visit doctors only when they experience pain, where doctors address what’s malfunctioning. We are transitioning from illness care to wellness care, aiming to intervene before organ-specific diseases arise.”

The team is in the process of commercializing this test, which is anticipated to be available within the next 2-3 years, starting with major organs like the brain, heart, and immune system.

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Source: www.sciencefocus.com

Nightmares Linked to Accelerated Biological Aging and Increased Mortality Risk

Strategies to Prevent Nightmares, Such as Avoiding Scary Movies

Andrii Lysenko/Getty Images

Experiencing nightmares weekly may accelerate aging and significantly increase the chances of early death.

“Individuals with more frequent nightmares experience faster aging and a higher risk of premature death,” states Abidemi Otaiku from Imperial College London.

In collaboration with his team, Otaiku examined data from over 183,000 adults aged between 26 to 86 who participated in several studies, initially self-reporting their nightmare frequency over a span of 1.5 to 19 years.

The findings revealed that individuals reporting weekly nightmares are over three times more likely to die before reaching 70 compared to those who do not experience nightmares.

Moreover, the researchers noted that the frequency of nightmares is a more potent predictor of preterm birth than factors such as smoking, obesity, poor diet, or inadequate physical activity. Otaiku presented these findings at the European Neurological Society Conference 2025 held in Helsinki, Finland, on June 23rd.

The team additionally assessed participants’ biological ages by measuring telomere lengths, small DNA sequences at the ends of chromosomes that shorten with each cell division; short telomeres linked to premature aging. This segment of the study also included approximately 2,400 children aged 8 to 10, while adults contributed further biological age data using epigenetic clocks.

According to Otaiku, their research established a consistent connection between frequent nightmares and accelerated aging across various ages, genders, and ethnic backgrounds. “Even in childhood, those with frequent nightmares exhibit shorter telomeres, indicating faster cellular aging,” he remarked. In adults, this accelerated biological aging accounts for roughly 40% of their heightened risk of death.

Regarding the reasoning behind this association, Otaiku suggests two main factors. The first is the elevated levels of the stress hormone cortisol triggered by nightmares. These levels are linked to faster cellular aging. “Nightmares elicit a more intense stress response than what is typically experienced upon waking, often rousing us with pounding hearts,” he explained.

The second factor involves sleep disruption, which hinders the body’s overnight cellular repair processes. Poor sleep quality is associated with an increased risk of various health issues, including heart disease.

For those wishing to reduce their occurrence of nightmares, Otaiku suggests straightforward strategies, such as avoiding scary movies and addressing mental health issues like anxiety.

“This is a fascinating finding with a number of biological underpinnings,” said Guy Restiner from the NHS Foundation Trust at Guy and St. Thomas. However, he emphasized that further research is necessary to identify causal relationships, noting that nightmares can be associated with various medical conditions and medications that may impact the findings as individuals age.

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Source: www.newscientist.com

This 80-Million-Year-Old Shark Species Remains a Biological Enigma

Deep within the shadowy oceans, a variety of curious and enigmatic creatures inhabit the depths, such as the frilled shark (Chlamydoselachus anguineus), which has been known for over a century, yet much of its lifestyle remains elusive.

We gain insight into their appearance through the occasional specimens caught in deep-sea fishing nets across the globe.

These sharks typically measure about 2 meters (6.5 feet) in length, with smooth, tube-like brown or gray bodies and dorsal fins positioned lower on their backs, close to the tail of their elongated form.

The most peculiar characteristic is found at the front end. The frilled shark possesses six prominent gill slits, exceeding the number found in most other sharks.

Indeed, there are five other known species in the frilled shark taxonomic order, Hexanchiformes, which include the Sixgill and Seven Gill sharks.

The name “frilled shark” derives from the unique ruffled edges of its gill slits, with the extended tips of the gill filaments visible.

The first pair of gill slits connects beneath the throat, resembling a lacy collar.

Moreover, their mouths are larger, akin to those of lizards, compared to typical sharks. Inside, they feature a series of three-pronged teeth resembling tiny tridents.

Studies of the stomach contents from rare specimens reveal that frilled sharks employ their three-pronged teeth to capture soft-bodied squid.

They are also reported to occasionally consume fish and other shark species. Unlike many sharks, pregnant female frilled sharks do not lay eggs; rather, the eggs hatch internally.

The newborn sharks begin life as embryos, attached to egg yolks, which serve as a nutritional source during their development.

Photos of the frilled shark (Chlamydoselachus anguineus) were taken in collaboration with the University of the Zoological Museum in Hamburg. – Photo credit: Aramie

One mystery that remains unsolved is the duration of their pregnancy. If other deep-sea sharks are indicative, it could take several years before a frilled shark pup emerges into the ocean.

Often mischaracterized as “living fossils,” frilled sharks garnered significant attention in 2022 after a viral video showcased rare footage of live frilled sharks in Japan, prompting news outlets worldwide to clarify misconceptions.

These creatures likely exist for decades.

However, it is indeed true that the oldest known fossils of frilled sharks date back to the late Cretaceous period, approximately 80 million years ago, displaying surprisingly little change through time.

The fossils indicate that the ancestors of frilled sharks exhibited similar deep-sea swimming behaviors.

This suggests that these unusual-looking sharks have been gracefully navigating the oceans with their snake-like bodies for millions of years, and although their young are rarely observed, they continue to thrive today.


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Ancient Enamel Proteins Uncover Biological and Genetic Diversity in Paranthropus robustus

Paranthropus robustus is a well-documented species within the Hominin group that has yet to be associated with genetic evidence. This species thrived in what is now South Africa between 2 million and 1.2 million years ago. In a recent study, paleontologists extracted enamel protein sequences from a dental specimen, believed to be 2 million years old, discovered at the Swartkrans site in South Africa. The results indicate a greater diversity than previously recognized for Paranthropus robustus and support the potential existence of multiple species within the genus.

Paranthropus Boisei. Image credit: ©Roman Yevseyev.

Advancements in ancient DNA (aDNA) sequencing have provided essential insights into the evolutionary connections among mid- to late Pleistocene hominins. However, our understanding of the earlier Pliocene-Pleistocene species, including Paranthropus robustus, remains limited.

This limitation is primarily due to the poor preservation of aDNA in African hominin fossils older than 20,000 years.

Paranthropus robustus has traditionally been regarded as a singular evolutionary line.

Yet, morphological overlaps between Paranthropus robustus and Australopithecus raise questions about their possible evolutionary links.

Moreover, variations in dental morphology suggest either an undiscovered diversity within Paranthropus robustus or the existence of multiple distinct species.

In this study, researchers from the University of Copenhagen, the University of Cape Town, and Dr. Paresa Madupe employed more durable ancient proteins to explore the variation within this ancient human species.

Four tooth enamel proteins were analyzed using high-resolution mass spectrometry and paleontological techniques, focusing on Paranthropus robustus fossils from the Swartkrans cave.

These specimens, dating from 2.2 to 1.8 million years ago, are among the earliest known hominins.

Molecular analysis of the protein sequences revealed significant variation at the molecular level among Paranthropus robustus individuals, including evidence from both male and female fossils, challenging the reliability of tooth size as a sole indicator of sexual dimorphism and suggesting that this variance cannot be attributed exclusively to sexual differences.

Notably, one individual appears to be genetically distinct from the others, highlighting considerable intraspecies variability within Paranthropus robustus.

The results align with recent morphological evidence, indicating previously unrecognized taxonomic diversity within the genus, including the proposed species Paranthropus capensis.

“Our study illustrates how paleobiological traits can assist in distinguishing sexual dimorphism from other forms of variation in the early Pleistocene human lineage in Africa,” the authors concluded.

The study is published in the journal Science.

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Paresa P. Madupe et al. 2025. Enamel proteins reveal biological and genetic variation in southern Africa Paranthropus robustus. Science 388 (6750): 969-973; doi: 10.1126/science.adt953

Source: www.sci.news

Face: An AI Tool That Reveals Biological Age from a Single Photo

Name: Face.

Year: New.

Exterior: A device designed to estimate your life expectancy.

So, is it going to tell me when I’ll die? No, thank you. Hold on, let me explain.

Not a problem, but that still sounds pretty terrifying. Just give me a moment. It operates similarly to what your doctor does.

Which is what? We will analyze your photos to evaluate your health.

Oh, that doesn’t sound too bad. However, this device can assess you even more accurately. It can also help predict your response to treatments.

Nope, I’m out again. Let me elaborate. Faceage is an AI innovation developed by scientists at Mass General Brigham in Boston. By examining a picture of your face, it can assess your biological age compared to your chronological age.

What does that imply? It means everyone ages differently. For instance, at 50, Paul Rudd had a biological age of 43, while fellow actor Wilford Brimley was biologically 69 at the same age.

Why is this significant? Individuals with older biological ages are less likely to withstand intensive treatments like radiation therapy.

Explain it to me as if I’m clueless. Sure thing. The older your face looks, the worse it is for your health.

Great, just what I needed to hear about my premature grey hairs. Actually, not exactly. Features like gray hair or hair loss can be misleading. This device evaluates factors like skin folding near the mouth and temple hollows for a more accurate health profile.

Wonderful, now I have to obsessively analyze my temple’s condition. No, this is beneficial. With proper usage, such diagnostic tools can enhance countless lives. Although the initial study focused on cancer patients, researchers intend to broaden the tests to others.

I just had plastic surgery. Will Faceage still work for me? As of now, it’s unclear. The developers still need to investigate this.

What about for people of color? Ah, yes. This model was predominantly trained on white faces, so its effectiveness on diverse skin tones is still uncertain.

This sounds a bit concerning. It’s simply a cautionary issue. Let’s consider how quickly AI evolves. Just last year, ChatGPT was lacking but has now transformed industries. We can expect Faceage to improve rapidly, too.

That’s encouraging. Indeed. Before long, it could assess your face and provide a calm, unbiased judgment on your health and longevity.

Is this for real? No, definitely not. At least, not yet.

Say: “Faceage represents a new frontier in medical diagnostics.”

Don’t say: “They claim we’ll perish during the 2028 robot uprising.”

Source: www.theguardian.com

Massive biological study suggests that the once-feared wolf is actually harmless

Giant Biologythe only extinct company in the world has announcement Once extinct rebirth Dire Wolf (Enocion dillus).

At 3 months’ age (born October 1, 2024), the miserable wolves of giant biological sciences, Romulus and Remus. Image credit: Colossal Biosciences.

The miserable wolves were like big cans, and were among the most common extinct carnivorous animals of the late Late Pleistocene megafauna in America.

These animals first appeared in the late Pliocene period 3.5 million to 2.5 million years ago, as a result of the mixing between two ancient Canid strains.

The miserable wolf was 25% heavier than the grey wolf, with a slightly wider head, with light thick fur and strong jaws.

As hypercarnivores, their diet consisted mainly of at least 70% meat from horses and bison.

They were extinct at the end of the recent ice age about 13,000 years ago.

The main hypothesis explaining their extinction is that their body size is larger than gray wolves and coyotes, making them more specialized in hunting large prey and unable to survive the extinction of giant prey.

“Our team collected DNA from 13,000-year-old teeth and 72,000-year-old skulls to create healthy, miserable puppies,” said Ben Lamm, CEO of Colossal Biosciences.

“It was once said that “a sufficiently advanced technology cannot be distinguished from magic.” “

“Today, our team will be unveiling some of the magic they are working on, revealing the broader impact on conservation.”

Three liters of the wicked wolves of giant biological science include two adolescent men (Romulus and Remus) and one female puppy (Khaleesi).

They thrive in more than 2,000 acres of safe ecological reserves, including specialized engagement zones and habit types.

They are continuously monitored through live cameras, security personnel and drone tracking on-site to ensure safety and welfare.

“The disastrous wolves’ disappearance is more than a biological revival,” said Mark Fox, chairman of MHA Nation Tribal.

“Its birth symbolizes awakening. The ancient spirit has returned to the world.”

“The miserable wolves have the echoes of our ancestors, their wisdom, and connections to the wild.”

“Its existence reminds us of our responsibility as custodians of the Earth to protect the delicate balance of not only wolves but life itself.”

“The work of our team…Red wolf (Canis Rufus) From three different genetic founder lines.

These liters include the adolescent female Red Wolf (hope) and three male Red Wolf puppies (flame, cinders, ashes).

“We’ve seen a lot of trouble with the stakes,” said Dr. George Church, a geneticist at Harvard University and co-founder of Colossal Biosciences.

“Another source of ecosystems comes from genes lost after being deelectrically removed from new technologies, such as deep ancient DNA sequencing, polyphyllatic characterization, multiplexed germ cell editing, and cloning.”

“The disastrous wolves are an early example of this, so far, including the maximum number of accurate genome editing in healthy vertebrates: their exponentially growing ability.”

Source: www.sci.news

New research sheds light on the biological characteristics of megalodon

Megatooth shark, Otodus Megalodonthe iconic shark is primarily represented by the enormous teeth of the Neogene fossil record, but the lack of well-preserved skeletal hampers an understanding of various aspects of its biology. In the new study, paleontologists reassessed some of their biological properties using a new approach, based on known vertebral specimens. Otodus Megalodon 165 species of extinction and 10 orders of living sharks. Their results show that Otodus Megalodon Their bodies were thin and could have reached about 24.3 m in length.

Otodus Megalodon It was extinct 3.6 million years ago. Image credit: Alex Boersma/PNAS.

Otodus MegalodonIt is also called Carcharocles MegalodonThis is a giant megatooth shark that lived in the oceans of the world from 23 to 3.6 million years ago.

This creature is usually portrayed as a super-sized monster in popular culture, with a recent example of science fiction films.

Otodus Megalodon A professor, colleagues and colleagues at DePaul University said:

“Several vertebrae, pracoid scales, and tessellated cartilage fragments have also been reported to date.”

“However, the lack of a complete fossil specimen has led to uncertainty regarding the true size of this prehistoric shark.”

In their study, the authors examined incomplete vertebral specimens of Otodus MegalodonIt is composed primarily of trunk vertebrae, 11.1 m from the Miocene of Belgium. It was also a specimen of 165 species of extinction and living Neotheratia sharks.

“Assuming that Otodus Megalodon If there was a body plan that matched the majority of sharks, we determined that their head length and tail length accounted for about 16.6% and 32.6% of the total length, respectively,” they said.

“Because the Belgian specimen is 11.1 m, its head and tail were calculated to be about 1.8 m and 3.6 m in length, respectively, which specifically results in an estimated total length of 16.4 m. Otodus Megalodon Individual. “

“The largest vertebrae in a Belgian specimen is 15.5 cm in diameter, but estimated Otodus Megalodon Vertebrae with a diameter of 23 cm have been reported from Denmark. ”

“If a Danish vertebra represents the largest vertebra in the body, that individual could have measured approximately 24.3 m in length.”

Based on a comparison of their body proportions, they have a body shape Otodus Megalodon It probably looked like a modern lemon shark on the surface (Negaprion Brevillo Stris), has a slender body than the great white sharks of modern times.

They also have huge modern sharks, such as whale sharks.Rhincodon Types) And the shark was exposed (Cetorhinus Maximus), like many other giant aquatic vertebrates like whales, they have slender bodies, as their large stubborn bodies are hydrodynamically inefficient for swimming.

In contrast, dark white sharks that become even more severe as they grow can grow larger, but are not huge (below 7 m) due to hydrodynamic constraints.

“Our new research solidified that idea. Otodus Megalodon “We've been working hard to get the better of our team,” said Phillip Sternes, educator at SeaWorld San Diego.

“What distinguishes our research from all previous papers on body size and shape estimation Otodus Megalodon Jakewood, a doctoral student at Florida Atlantic University, added:

According to the team, it is 24.3 m long. Otodus Megalodon It weighs approximately 94 tons and estimates of cruising speeds of 2.1-3.5 km/h.

“The growth patterns recorded in Belgian vertebral specimens are Otodus Megalodon A newborn about 3.6-3.9 m long was given birth to a newborn, and the embryos were nourished through egg-eating behavior,” the author said.

“A known fossil record with newly inferred additional growth patterns Otodus Megalodon And the white shark lineage supports the idea that the rise of the great white shark likely played a role in the ultimate end mise about five million years ago. Otodus Megalodon For competition. ”

“Many interpretations we have made are still tentative, but they are data-driven and serve as a reasonable reference point for future research into the biology of Otodus MegalodonProfessor Shimada said.

study Published online in the journal Palaeontologia Electronica.

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Shimada Mana et al. 2025. Reassessment of the size, shape, weight, cruising speed and growth parameters of extinct megatooth sharks; Otodus Megalodon (Lamniformes: Otodontidae), and new evolutionary insights into its giants, life history strategies, ecology, and extinction. Palaeontologia Electronica 28(1): A12; doi: 10.26879/1502

Source: www.sci.news

Advancements in Dementia Research: Science can now accurately assess the “biological age” of your brain

If you’re like Khloe Kardashian, who recently turned 40, you may have considered testing your biological age to see if you feel younger than your actual age. But while these tests can tell you a lot about your body’s aging, they often overlook the aging of your brain. Researchers have now developed a new method to determine how quickly your brain is aging, which could help in predicting and preventing dementia. Learn more here.

Unlike your chronological age, which is based on the number of years since you were born, your biological age is determined by how well your body functions and how your cells age. This new method uses MRI scans and artificial intelligence to estimate the biological age of your brain, providing valuable insights for brain health tracking in research labs and clinics.

Traditional methods of measuring biological age, such as DNA methylation, do not work well for the brain due to the blood-brain barrier, which prevents blood cells from crossing into the brain. The new non-invasive method developed at the University of Southern California combines MRI scans and AI to accurately assess brain aging.

Using AI to analyze MRI brain scans, researchers can now predict how quickly the brain is aging and identify areas of the brain that are aging faster. This new model, known as a 3D Convolutional Neural Network, has shown promising results in predicting cognitive decline and Alzheimer’s disease risk based on brain aging rates.

Researchers believe that this innovative approach can revolutionize the field of brain health and provide valuable insights into the impact of genetics, environment, and lifestyle on brain aging. By accurately estimating the risk of Alzheimer’s disease, this method could potentially lead to the development of new prevention strategies and treatments.

Overall, this new method offers a powerful tool for tracking brain aging and predicting cognitive decline, bringing us closer to a future where personalized brain health assessments can help prevent and treat neurodegenerative diseases.

For more information, visit Professor Andrei Ilimia’s profile here.

https://c02.purpledshub.com/uploads/sites/41/2025/02/MRI-scan.mp4
Using AI to analyze MRI brain scans, you can see how quickly your brain is aging.

Source: www.sciencefocus.com

Severe fever can accelerate biological aging in elderly individuals

Woman drinks water during heat waves in French Hierrez

Magali Cohen/Hans Lucas/AFP Getty Images

Extreme fever appears to speed up biological aging in older adults, suggesting that it may increase the risk of age-related diseases.

“This is one of the first large-scale studies linking long-term heat exposure to biological aging in humans,” he says. Eun Young Choi At the University of Southern California. “Elderly people who live in areas with biologically extreme heat in cooler areas.”

Choi and her colleagues analyzed genetic data extracted from blood samples collected by other researchers from 3,600 people in the US in 2006-7. At the time, they were all over 56 years old.

They estimated the biological age of each participant using three so-called epigenetic clocks, including seeing patterns of chemical tags called methyl groups on DNA. These patterns change as we age, and such changes are associated with age-related diseases.

The researchers also looked at daily temperature measurements taken within a few kilometres of where participants lived for six years before blood samples were collected.

They found that every 200 days of six years when participants were exposed to daily maximum temperatures of at least 32.2°C (90°), biological age was on average up to 3.5 months old, and on average up to 3.5 months of age than those in cooler areas. That number depends on which watch was used.

“This refers to heat exposure increasing the rate of biological aging,” he says. Austin Argencheri At Harvard University, where he was not involved in the research.

Previous studies on the Taiwanese and German people have also found a link between extreme heat exposure and biological aging.

However, epigenetic watches do not fully capture the aging process or the risk of people's illnesses, says Argentieri. “More jobs that can link both extreme heat exposure, biological aging from these watches, age-related diseases, mortality and the effects on life expectancy itself will help us drive home what we need to take away from now on.”

Furthermore, the study did not consider access to air conditioners or the duration of time participants spent outdoors, so individual exposure changes to heat exposure, says Argentieri. The team controlled for other factors such as age, gender, race, wealth, ethnicity, smoking status, alcohol consumption, obesity, and physical activity.

Furthermore, research should investigate whether results will be translated to younger people or to people living in different countries where people may have different approaches to keeping people cool, says Argentieri.

Identifying the people who are at the lowest risk of aging fastest due to extreme heat could help policymakers develop and deploy measures to protect them, he says.

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Source: www.newscientist.com

Omega-3 Supplements may slow down the process of biological aging

Omega-3 Supplements may be an easy way to slowden aging

EVGENIIA SIANKOVSKAIA/Getty Images

Omega 3 supplements every day, especially when combined with vitamin D and exercise, seems to slow the biological aging of the elderly.

We already knew that “good” fat, which is seen in seeds, nuts, and fish can enhance immunity, heart health, and brain function.

They are also linked to changes “Epigi Nete” markerDNA chemical tags that change the activity of the gene and the behavior of cells. This suggests that Omega 3 reduces pace Biological agingIn many cases, it is defined as a measure of how fast someone has deteriorated, compared to the body of the general group.

To explore this further Heike Bischoff-Ferrari The University of Zurich and her colleagues divided 777 Switzerland, 70 and 91, into eight groups. They also wanted to know how Omega-3 works along with vitamin D supplements and exercise.

“Omega-3 plays on multiple routes of aging, such as anti-inflammatoryness. Similarly, vitamin D and exercise have multiple advantages,” says Bischoff-Ferrari. “Did we think that there are additional advantages if you play in each of these differential routes?”

Some participants had already taken these supplements at the start of the research or doing strength training. According to Bischoff-Ferrari, it was not ethical to stop exercising or stop taking specific supplements, so it was allowed to continue.

In addition to the existing lifestyle habits, each group was told to have a variety of combinations of one grams of Omega-3, placebo tablets, and 2000 international unit vitamin D. Muscle training three times a week.

For example, some people have been asked to take 3 tablets of omega, take vitamin D supplements, and do additional strength training, or have been asked to take vitamin D with strength training. I didn't take Omega 3.

At the start of the research, researchers estimated the biological age of the participants using the “Epi Nete Watch”, which was previously developed by teams and other researchers. These analyzed a DNA marker called methyl group in a blood sample that generally decrease with age and impairs cell function.

Through the same three years later, the scientists have been told to take Omega 3, aging only about three months less than employees who are only given placebo pills. I discovered that there was no. They explained the factors that could affect the results, such as the actual age, gender, weight, and height of the participants.

“This is today's biggest test that suggests that simple supplements contribute to the slowdown of biological aging,” says Bischoff-Ferrari.

Furthermore, those who took Omega-3 with vitamin D and did less tension training compared to those who did not introduce any of these habits as part of the trial. “The effect was somewhat remarkable, and it was almost four months of rejuvenation,” says Bischoff-Ferrari.

These effects may seem small, but it may be important for some people. Richard Siou At King Scarage Rondon. “This is more important for the elderly, because it may be more likely to decrease in age in about three months,” he says.

However, epigenetic watches are not a complete scale of biological aging. “Just because DNA's biomarker indicates that you resemble a young person does not necessarily mean that you are healthy in some way,” says SIOW.

Further research says that it is necessary to evaluate what changes in measures such as cognitive, motor skills, and heart health mean. The Bischoff-Ferrari team analyzes participants' data on these results.

Another restriction of this study was that the participants were relatively healthy and active, and there was almost no lack of vitamin D. Bischoff-Ferrari says that there is a need for a further research in which people who live in other countries without these characteristics and young people in other countries are involved.

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Source: www.newscientist.com

Slow Down Your Biological Age with This One Supplement

When it comes to maintaining health in old age, amidst the plethora of complex supplements advertised by influencers and podcast hosts, the key might just be Omega-3. Recent research suggests that regular consumption of Omega-3 fatty acid capsules can have a significant impact on longevity, potentially slowing the aging process by up to 4 months. Lower aging.

Biological age is a more accurate indicator of your life expectancy than your chronological age. It reflects the rate of DNA changes, which can vary from person to person.

A study published in the journal Nature Aging compared the effects of Omega-3 intake, vitamin D supplementation, and regular exercise on over 700 adults above 70. Participants were divided into three groups, receiving either 1g of Omega-3, 30mg of vitamin D, or engaging in 30 minutes of exercise three times a week, or no treatment at all.

Throughout the study, blood samples were collected and participants’ aging rates were measured using epigenetic “clocks.” The results showed that those taking Omega-3 experienced a biological age reduction of four months. When combined with vitamin D and exercise, the effects were even more pronounced, reducing the risk of various age-related ailments.

Experts, like Dr. Mary Ni Lochlainn, a Geriatrics specialist, are encouraged by these findings. However, some caution that more standardized tests for biological aging are needed to fully understand the impact of such interventions.

Read more:

  • Five tablets that may reverse aging (including those that may already be taken)
  • Are you sick?
  • Five simple ways to instantly find your “biological age”

Source: www.sciencefocus.com

Main Biological Breakthrough: Two Fathers and a Mouse

In a groundbreaking scientific achievement, a mouse with two male parents has successfully reached adulthood.

Researchers utilized embryo stem cell engineering to accomplish this milestone by accurately correcting an important gene involved in reproduction. Double-headed mouse.

This innovative method has allowed scientists to overcome previously insurmountable barriers in reproducing single-identified mammals.

In previous experiments, using two male mice resulted in genetic issues during fertilization, leading to severe congenital defects and early termination of mouse embryo development.

However, the researchers of this new study suspected that these genetic issues were caused by “imprinted” genes, which are inherited from both male and female parents.

“The unique characteristics of imprinted genes have led scientists to believe they are the fundamental barriers to mammal reproduction,” said Research co-author Professor Qi Zhou.

“Even in the artificial creation of a two-cell embryo or double-headed embryo, they were unable to develop properly and stalled at a certain point due to these genes.”

Based on this theory, researchers altered 20 important imprinted genes using various methods before implanting the modified embryos into surrogate mothers.

Their findings revealed that these genetic edits not only allowed for the creation of double-headed mice but also enabled them to survive to adulthood.

“These discoveries offer compelling evidence that imprinted abnormalities are the primary barriers in mammals,” said co-author Professor Guan Zan Ruo from SUN YAT-SEN University.

“This approach greatly advances the manipulation of embryo stem cells and cloned animals, paving the way for progress in regenerative medicine.”

However, researchers noted that only 11.8% of surviving embryos successfully developed to birth, and some did not survive to adulthood due to developmental disorders.

In fact, most of the adult mice displayed abnormal growth and lifespan, and the surviving mice were infertile.

The team is actively working to address these issues by investigating whether altering a specific gene can improve embryo development. They also plan to extend their research to include larger animals like monkeys, though the use of this technology in humans remains uncertain.

Read more:

  • Y chromosome has disappeared. Is this the end of man?
  • Mice display emotions on their faces like humans
  • Male mice transformed into females using previously considered “junk” DNA.

Source: www.sciencefocus.com

Uncover Your True Biological Age with This Straightforward Balance Test

When it comes to balancing on one foot, it may seem like a simple task, but it could actually indicate more than you think. Recent research suggests that struggles with balance could be a sign of accelerated aging in the body.

Scientists at the Mayo Clinic in Minnesota have discovered that the ability to balance on one leg can reveal the rate of aging in the neuromuscular sensory system, particularly in older individuals.

This sensory system, comprised of nerves connecting muscles to the brain and spinal cord, plays a crucial role in facilitating movement. Its decline with age can lead to slower reflexes and movements.


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“Balancing on one leg involves various physiological components like leg strength, postural stability muscles, neuromuscular coordination, and sensory information, all of which tend to decrease with age,” explained Professor David Proctor, an aging and exercise expert at Pennsylvania State University in the US. This information was reported by BBC Science Focus.

Preventing or slowing down the decline in strength and balance as we age can significantly impact one’s ability to stay functionally independent in the long term.

The study involved 40 participants aged between 50 and 80, who were assessed on their ability to balance on one leg. Despite similar height, weight, and activity levels, age was the only differing factor among the participants.

Each participant performed four 30-second balances with eyes closed and eyes open for both legs. The researchers recorded the duration of balance maintained within each 30-second interval to evaluate the impact of age on balance.

The results indicated a direct correlation between age and trembling, with a 6.3% increase in tremors with eyes open and a 10.5% increase with eyes closed for every decade of age. Additionally, the time spent balancing decreased by 2.2 seconds per decade on the non-dominant leg and 1.7 seconds on the dominant leg.

This suggests that balance duration is a valid marker of aging and a potential indicator of fall risk in older adults.

Although balancing for 30 seconds may not require significant muscle strength, it heavily relies on good neuromuscular control, which diminishes with age, leading to increased sway and reduced balancing time.

Fortunately, research highlights the benefits of balance and aerobic exercises like swimming, running, and cycling in preventing age-related decline in balance and muscle control.

About our experts

Dr. David Proctor, a professor at Pennsylvania State University, USA, specializes in kinesiology, physiology, and medicine. His research has been featured in various scientific journals.

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Source: www.sciencefocus.com

New study claims that this diet can reverse biological age in just eight weeks

Increasing plant-based food consumption is known to benefit both health and the environment, yet only a few individuals fully commit to a vegan diet.

However, a recent study suggests that following a vegan diet for just eight weeks could potentially reverse one’s biological age. Researchers discovered that participants who adhered to a vegan diet showed a reduction in their estimated biological age, as indicated by DNA methylation, an epigenetic marker.

Dr. Lucia Aronica, along with other co-authors from BBC Science Focus, explains, “DNA methylation and other epigenetic modifications regulate gene activity and expression.” These modifications change in specific ways as we age, allowing scientists to track and understand the aging process.

The study, as detailed in BMC Medicine, involved 21 adult identical twin pairs, where one twin followed a vegan diet while the other maintained an omnivorous diet for eight weeks. Blood samples were taken before and after the study to measure DNA methylation levels and assess the effects of each diet.

Results demonstrated that only the vegan group showed a slowing of the epigenetic aging clock, with some participants appearing almost one year younger by certain measures. A vegan diet was associated with reduced estimated ages of various organ systems, such as the heart, hormones, liver, and inflammatory and metabolic systems.

The average reduction in biological age for the vegan group was a remarkable 0.63 years. However, researchers caution that these findings should be interpreted carefully due to other factors like weight loss, as participants in the vegan group lost an average of 2 kilograms more than those in the omnivorous group.

Despite the promising outcomes, further research is necessary to understand the long-term effects of a vegan diet on aging and to differentiate between the effects of dietary composition and weight loss.

Experts like Dr. Hou Lifang suggest that additional studies are needed to validate these results, emphasizing the need for caution when drawing broad conclusions. While the study provides valuable insights, more research is required to fully comprehend the impact of a vegan diet on aging.

About our experts

Lucia Aronica focuses on epigenetics and gene-environment interactions in health outcomes. She is currently leading epigenetic analysis in the largest low-carb vs. low-fat diet study for weight loss. Aronica teaches nutritional genomics at Stanford University.

Varun Dwaraka is a bioinformatics researcher specializing in aging, epigenetics, and genetics. He has co-authored various publications on DNA methylation, tissue regeneration, and the epigenetic clock.

Hou Li-Fan, MD, MS, PhD, is a Professor of Preventive Medicine, integrating epidemiology with molecular technologies in disease studies focused on molecular markers and disease prevention.

Source: www.sciencefocus.com

The Impact of Alcohol on Biological Age: A Closer Look

It is widely known that excessive alcohol consumption is detrimental to health, a fact that has been established by scientific research over many years.

Despite this, there is still much to learn about the effects of alcohol on the body and whether consuming small amounts of certain types of alcohol may have potential benefits.

New research is shedding light on how alcohol impacts the body and accelerates the aging process, particularly at a cellular level that determines biological age.

Unlike chronological age, which simply counts the number of years someone has lived, biological age assesses cellular function and disease risk. Two key indicators of biological age, telomere length, and epigenetic age, provide evidence of the harmful effects of alcohol consumption on the body.


Drinking alcohol increases the risk of DNA damage

Telomeres are essential components of our genetic structure, protecting chromosomes from damage during cell replication. Over time, telomeres naturally shorten as cells divide. Shortened telomeres are associated with age-related diseases such as Alzheimer’s, cancer, and heart disease.

Research conducted by Anya Topiwala and her team at Oxford University in 2022 found that excessive alcohol consumption leads to a reduction in telomere length, accelerating the biological aging process.

Observational studies have shown that consuming 29 or more units of alcohol per week can result in a 1-2 year change in telomere length compared to drinking less than six units per week. Individuals with alcohol use disorders were found to have even shorter telomeres.

The exact mechanism by which alcohol shortens telomeres is not fully understood, but it is believed to be related to oxidative stress caused by alcohol consumption.

Certain types of alcohol are bad for you

Epigenetic age, which assesses DNA methylation linked to aging using multiple biomarkers, indicates the impact of lifestyle choices on biological age. Studies have shown that cumulative alcohol exposure increases biological age, with liquor drinkers being at a higher risk of premature aging compared to beer or wine drinkers.

Further research is being conducted to better understand the connection between alcohol consumption and biological aging, as the specific reasons behind these effects are not fully clear.

Can biological age be reversed?

While biological aging is theoretically reversible, the practical methods to achieve this reversal are not yet established. Scientists believe that by addressing environmental factors and lifestyle choices that impact DNA function, it may be possible to slow down the aging process.

Quitting or reducing alcohol consumption has been shown to slow down biological aging. Both studies emphasize that moderate drinking does not have any protective effects and that increased alcohol consumption accelerates the aging process.

About our experts

Anya Topiwala: A psychiatrist at Oxford University, Topiwala’s research focuses on the impact of alcohol consumption on brain health using large datasets and advanced imaging techniques.

Hou Li-Fan: A Professor of Preventive Medicine at Northwestern University, Dr. Hou’s research integrates epidemiological methods with molecular technologies to identify molecular markers and understand their role in disease prevention.


Source: www.sciencefocus.com

Research suggests that biological amino acids could potentially endure in the near-surface ice of Europa and Enceladus

Europa and Enceladus are important targets for the search for evidence of extraterrestrial life in the solar system. However, the surfaces and shallow subsurfaces of these airless icy moons are constantly exposed to ionizing radiation that can degrade chemical biosignatures. Therefore, sampling the icy surfaces in future life-searching missions to Europa and Enceladus requires a clear understanding of the required ice depths where intact organic biomolecules may exist. A team of scientists from NASA and Pennsylvania State University conducted experiments exposing individual biological and abiotic amino acids in the ice to gamma radiation to simulate conditions on these icy worlds.

Europa's surface stands out in this newly reprocessed color image. The image scale is 1.6 km per pixel. Europa's north side is on the right. Image courtesy of NASA / JPL-Caltech / SETI Institute.

“Based on our experiments, a 'safe' sampling depth for amino acids on Europa is about 20 centimetres (8 inches) at high latitudes in the trailing hemisphere (the hemisphere opposite the direction Europa moves around Jupiter), in an area where the surface has not been significantly disturbed by meteorite impacts,” said Dr. Alexander Pavlov, a research scientist at NASA's Goddard Space Flight Center.

“Detecting amino acids on Enceladus does not require subsurface sampling; these molecules survive radiolysis (breakdown by radiation) anywhere on Enceladus' surface, within a few millimeters (tenths of an inch) of the surface.”

Dr. Pavlov and his colleagues used amino acids in their radiolysis experiments as representative examples of biomolecules on icy moons.

Amino acids are produced by both living organisms and non-living processes.

But if certain types of amino acids were found on Europa or Enceladus, they could be a sign of life, as they may be used by life on Earth as building blocks of proteins.

Proteins are essential for life because they are used to create structures and to produce enzymes that speed up or control chemical reactions.

Amino acids and other compounds found underground in the ocean could be transported to the surface by geyser activity or the slow churning motion of the ice shell.

To assess the survival of amino acids on these planets, the researchers mixed amino acid samples with ice cooled to minus 196 degrees Celsius (minus 321 degrees Fahrenheit) in sealed, airless vials and exposed them to various doses of gamma rays (a type of high-energy light).

Because the ocean may harbor microorganisms, the researchers also tested the viability of amino acids contained in dead bacteria in the ice.

Finally, the researchers tested samples of amino acids in the ice mixed with silicate dust to see if meteorites or interior materials could be mixing with the surface ice.

This experiment provided vital data for determining the rate at which amino acids break down (called the radiolysis constant).

Using these, the scientists used the age and radiation environment of the icy surfaces of Europa and Enceladus to calculate drilling depths and where 10% of amino acids would survive radiolysis.

While experiments have been done before to test for the survival of amino acids in ice, this is the first to use low doses of radiation that don't completely break down the amino acids – changing or breaking them down would be insufficient to determine whether they were a sign of life.

This is also the first experiment to use Europa/Enceladus conditions to assess the survival of these compounds in microbes, and the first to test the survival of amino acids mixed with dust.

Scientists have found that amino acids break down faster when mixed with dust, but more slowly when they come from microorganisms.

“The slow rate of breakdown of amino acids in biological samples under surface conditions like those on Europa and Enceladus strengthens the case for future life detection measurements from lander missions to Europa and Enceladus,” Dr Pavlov said.

“Our results indicate that the decomposition rates of potential organic biomolecules are higher in the silica-rich regions of both Europa and Enceladus than in pure ice. Future missions to Europa and Enceladus should therefore be careful when sampling the silica-rich regions of these icy moons.”

“A possible explanation for why amino acids survive longer in bacteria is the way that ionizing radiation alters molecules, either directly by breaking chemical bonds or indirectly by creating nearby reactive compounds that alter or break down the target molecule.”

“It's possible that the bacterial cellular material protected the amino acids from reactive compounds produced by the radiation.”

Team paper Published in the journal Astrobiology.

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Alexander A. Pavlov others2024. Effects of radiolysis on biological and abiotic amino acids in shallow subsurface ice on Europa and Enceladus. Astrobiology 24(7); doi: 10.1089/ast.2023.0120

This article has been edited based on the original NASA release.

Source: www.sci.news

Does biological sex impact cancer susceptibility?

Cancer is the leading cause of death in humans, accounting for almost 13% of deaths worldwide. Global Health Observatory by the World Health Organization. Biological males (or those assigned male at birth) account for 56% of cancer-related deaths, while biological females (or those assigned female at birth) account for only 44%.

The researchers showed that these differences between biological sexes are not limited to mortality rates, but are also evident in cancer development, progression, and treatment. For example, in the United States, women have a higher risk of developing breast and thyroid cancers, while men are more likely to develop prostate, colon, and stomach cancers.

Doctors also found that women tend to have colorectal cancer more often on the right side of the body, while men tend to have colorectal cancer more often on the left side of the body. Doctors want to know how biological sex affects different aspects of cancer so they can develop treatments tailored to a patient’s gender.

A team of scientists from Adityunchanagiri Pharmaceutical University in Karnataka state, India recently reviewed research on the role of biological sex in cancer. They explained that because every cell in the human body is controlled by DNA, gender can influence cancer growth at the genetic, molecular, and hormonal levels. Every patient’s biological sex changes the types of hormones and enzymes they produce, as well as the way their bodies respond to and metabolize carcinogens.

Researchers have previously found that men and women have different immune responses to cancer and chemotherapy. Women tend to have stronger immune systems that respond more strongly to cancer than men. The researchers suggested that this discrepancy may explain why fewer women die from cancer.

They also looked at data from doctors treating cancer patients and showed that similar treatments for male and female patients with the same cancer diagnosis resulted in different levels of side effects. For example, female cancer patients experience higher levels of drug-induced toxicity, infection, nausea, and vomiting during treatment than male cancer patients. They found that some anti-cancer treatments can even cause women to develop diabetes.

The researchers concluded that cancer behaves differently in male and female patients. However, despite differences in immune responses and side effects, physicians are still unable to customize immunotherapy treatments for different patients based on their biological sex. They suggested that the typical “one size fits all” approach to cancer treatment could be better tailored to specific cancer patients.

They recommended that drug companies test how new drugs affect male and female cancer patients during clinical trials before the drugs are approved. They suggested that drug companies could use this data to better estimate how much medication male and female patients should take, or for how long. They proposed that treatments tailored to each patient’s biological sex could help doctors treat patients in a more efficient manner with minimal side effects.


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Source: sciworthy.com

Study claims new diet that mimics fasting could reverse biological age

A new study led by the University of South Carolina Leonard Davis School of Gerontology suggests that fasting-mimetic dieting (FMD) cycles can significantly reduce disease risk factors and decrease human biological age. FMD was developed by Professor Walter Longo and his team, involving a five-day diet high in unsaturated fats and low in overall calories, protein, and carbohydrates. The diet mimics the effects of water-only fasting while providing necessary nutrients and making fasting more manageable for individuals.

During the five-day fasting period, participants were allowed to consume specified amounts of plant-based soups, energy bars, energy drinks, chip snacks, and tea and given supplements to ensure they didn’t miss out on important vitamins, minerals, and essential fatty acids.

Previous studies have shown the various health benefits of FMD, including promoting stem cell regeneration, reducing chemotherapy side effects, and decreasing signs of dementia in mice. The recent study focuses on the effects of FMD on human immune system aging, insulin resistance, liver fat, and biological age.

The research team analyzed two groups of men and women aged 18-70 who received three to four cycles of FMD per month. The results showed reductions in diabetes risk factors, reduced fat in the abdomen and liver, and rejuvenation of the immune system. Data analysis also demonstrated that FMD participants lost an average of 2.5 years in biological age.

Professor Longo hopes these findings will encourage more doctors to recommend FMD cycles to patients with elevated risk factors for disease and to the general public interested in improving their health and vitality. He suggested that healthy people between the ages of 20 and 70 should consider trying FMD two or three times a year, cautioning that there may be concerns when used in combination with certain diabetes medications.

About our experts:

Walter Longo is the Edna M. Jones Professor of Gerontology and Biological Sciences and Director of the Longevity Institute at the University of Southern California Leonard Davis School of Gerontology in Los Angeles.

Source: www.sciencefocus.com

Researchers can now estimate your biological age based on a snapshot of your body

It is now possible to measure a person’s biological age, which refers to the wear and tear of the body’s cells, as opposed to the chronological age based on the number of years lived. Chinese scientists have developed a new method to predict biological age using artificial intelligence to analyze 3D images of the face, tongue, and retina.

This approach provides a way to estimate biological age more accurately than previous methods that primarily relied on DNA or blood tests and brain scans. By combining images of the face, tongue, and retina, scientists have created a model that can accurately predict biological age. This allows for easier, more accessible, and less invasive methods to estimate a person’s biological age compared to traditional tests.

Research from China’s Macau University of Science and Technology and Shanghai Jiao Tong University involved testing this model on healthy individuals and those with chronic diseases. The results showed that the biological age of individuals with chronic diseases was significantly higher than their chronological age compared to healthy individuals, indicating the potential impact of chronic diseases on aging.

Furthermore, this new method could also be used to assess the effectiveness of anti-aging treatments, such as diet, exercise, and longevity drugs. Dr. Andrew Steele, a longevity expert, highlighted the potential for using photos to evaluate the efficacy of anti-aging strategies and speed up clinical trials in the future.

About our experts

Dr. Andrew Steele is a scientist, author, and presenter, known for his work in the field of aging. He is the author of Ageless: The new science of growing older without getting older. After earning his doctorate in physics, Steele transitioned into biology, using computers to decipher human DNA at the Francis Crick Institute in London.

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Source: www.sciencefocus.com

Active Matter Theory sheds new light on longstanding biological enigmas

November 22, 2023A team of scientists has developed a new algorithm to solve theoretical equations for active materials, deepening our understanding of living materials. This research is of vital importance in biology and computational science, paving the way for new discoveries in cell morphology and the creation of artificial biological machines. Advanced open-source supercomputer algorithms predict the patterns and dynamics of living matter and enable exploration of its behavior across space and time. Biological materials are made up of individual components, such as tiny motors that convert fuel into motion. This process creates a pattern of movement, guiding the shape of the material itself through a consistent flow driven by constant energy consumption. Such permanently driven substances are called “active substances.”

How cells and tissues work can be explained by active matter theory, a scientific framework for understanding the shape, flow, and form of living matter. Active matter theory consists of many difficult mathematical equations. Scientists from Dresden’s Max Planck Institute for Molecular Cell Biology and Genetics (MPI-CBG), the Dresden Center for Systems Biology (CSBD), and the Dresden University of Technology have developed an algorithm implemented in open-source supercomputer code. For the first time, you can solve active matter theory equations in realistic scenarios. These solutions bring him a big step closer to solving his century-old mystery of how cells and tissues acquire their shape, and to designing artificial biological machines. 3D simulation of active substances in a dividing cell-like geometry. Credit: Singh et al. Physics of Fluids (2023) / MPI-CBG

Biological processes and behaviors are often highly complex. Physical theory provides a precise and quantitative framework for understanding physical theories. Active matter theory provides a framework for understanding and explaining the behavior of active substances, which are materials made up of individual components that can convert chemical fuels (“food”) into mechanical forces. The development of this theory was led by several Dresden scientists, including Frank Uricher, director of the Max Planck Institute for Complex Systems Physics, and Stefan Grill, director of MPI-CBG. These physical principles allow us to mathematically describe and predict the dynamics of active organisms. However, these equations are very complex and difficult to solve. Therefore, scientists need the power of supercomputers to understand and analyze living matter. There are various ways to predict the behavior of active materials, including by focusing on small individual particles, by studying active materials at the molecular level, and by studying active fluids on a larger scale. These studies help scientists understand how active substances behave at different scales in space and time. Scientist in the research group of Dresden University of Technology Ivo Sbalzarini Professor at the Dresden Center for Systems Biology (CSBD), research group leader at the Max Planck Institute molecular cell The Dean of the Department of Biology and Genetics (MPI-CBG) and Computer Science at the Technical University of Dresden has now developed a computer algorithm to solve the active substance equation. Their research was published in the journal fluid physics and it appeared on the cover. They present an algorithm that is capable of solving complex equations for active materials in three-dimensional and complex-shaped spaces.

“Our approach can handle a variety of shapes in three dimensions over time,” says research mathematician Abhinav Singh, one of the study’s first authors. He continued, “Even when the data points are not regularly distributed, our algorithm employs a novel numerical approach that works seamlessly for complex biologically realistic scenarios, and the theoretical equations Using our approach, we can finally understand the long-term behavior of active materials in both mobile and non-mobile scenarios in order to predict dynamic scenarios. Additionally, theory and simulation can be used to program biological materials and create engines at the nanoscale to extract useful work.” The other first author, Philipp Suhrcke, holds a master’s degree in computational modeling and simulation from the Technical University of Dresden. “Thanks to our research, scientists can predict, for example, the shape of tissues and when biological materials will become unstable or dysregulated, leading to growth and disease. This has far-reaching implications for our understanding of mechanisms.”

The scientists implemented the software using the open source library OpenFPM. This means that others can use it freely. OpenFPM was developed by his Sbalzarini group to democratize large-scale scientific and technical computing. The authors first developed a custom computer language that allows computational scientists to write code for a supercomputer by specifying mathematical formulas that let the computer do the work of writing the correct program code. As a result, you no longer have to start from scratch every time you write code, effectively reducing code development time in scientific research from months or years to days or weeks, greatly increasing productivity.

Because the study of three-dimensional active materials has significant computational demands, using OpenFPM the new code is scalable on shared and distributed memory multiprocessor parallel supercomputers. This application is designed to run on powerful supercomputers, but can also be run on regular office computers to study 2D materials. Ivo Sbalzarini, the study’s lead researcher, summarizes: All this has been integrated into a tool for understanding her three-dimensional behavior of living matter. Our code, which is open source, scalable, and able to handle complex scenarios, opens new avenues in active materials modeling. This could ultimately lead to an understanding of how cells and tissues acquire their shape, addressing fundamental questions in morphogenesis that have puzzled scientists for centuries. There is a gender. But it may also be useful for designing artificial biological machines with minimal components.

References: “Numerical solver for three-dimensional active fluid dynamics and its application to active turbulence” by Abhinav Singh, Philipp H. Suhrcke, Pietro Incardina, and Ivo F. Sbalzarini, October 30, 2023. fluid physics. DOI: 10.1063/5.0169546 This research was funded by the Federal Ministry of Education and Research (Bundesministerium f€ur Bildung und Forschung, BMBF), the Federal Center for Scalable Data Analysis and Artificial Intelligence, ScaDS.AI, and Dresden/Leipzig. The computer code supporting the results of this study is publicly available in the 3Dactive-hydynamics github repository at: https://github.com/mosaic-group/3Dactive-hydrodynamic sThe open source framework OpenFPM is available at: https://github.com/mosaic-group/openfpm_pdataRelated publications for embedded computer languages https://doi.org/10.1016/j.cpc.2019.03.007https://doi.org/10.1140/epje/s10189-021-00121-x (function (d, s, id) {var js, fjs = d.getElementsByTagName (s) [0]; if (d.getElementById (id)) return; js = d.createElement (s); js.id = id; js.src = “https://connect.facebook.net/en_US/sdk.js#xfbml=1&version=v2.6”; fjs.parentNode.insertBefore (js, fjs); } (document, ‘script’, ‘facebook-jssdk’));

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