Weight Regain: What to Expect After Discontinuing Obesity Medications in Two Years

Weight loss drugs effectiveness

Weight loss medications, including Munjaro (tirzepatide), are effective when taken consistently.

Alan Swart / Alamy

A recent study involving over 9,000 participants revealed that individuals who discontinue weight loss medications often regain the weight lost within two years. This finding underscores the notion that obesity should be viewed as a chronic disease necessitating ongoing treatment.

“These medications are very effective; however, obesity is a chronic, relapsing condition,” explained Susan Jebb, who addressed the press at the University of Oxford. “Similar to hypertension medications, these treatments are likely needed for life.”

It’s evident that weight loss medications can significantly aid individuals in combating obesity, particularly newer GLP-1 medications mimicking gut hormones such as glucagon-like peptide 1—examples include semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro, Zepbound). These drugs not only facilitate weight loss but also positively impact health metrics like blood pressure and cholesterol levels.

Nevertheless, many patients have ceased using GLP-1 medications due to side effects, including nausea, or a lack of availability triggered by heightened demand. “Approximately half of users discontinue these drugs within a year,” remarks Jebb.

While nations like the United States and parts of Europe permit long-term use of GLP-1 medications for weight control, frameworks like the UK’s National Health Service are restricting semaglutide usage for weight management based on cost-effectiveness evaluations over two years.

Previous studies indicate that individuals often regain weight post-semaglutide discontinuation. Yet, it remains unclear if this pattern extends to other weight loss interventions and the swift occurrence of weight gain upon cessation.

To investigate this, Jebb and colleagues reviewed 37 trials, combining data from over 9,000 participants, all classified as overweight or obese and using some form of weight loss medication (including GLP-1) for about 10 months, followed by a monitoring period of roughly 8 months.

From their analysis, the researchers noted that participants lost an average of 8.3 kilograms and experienced improvements in metabolic parameters like blood pressure, cholesterol, and blood glucose levels.

When examining weight patterns during the follow-up phase, the model suggested participants regained the average weight lost within 1.7 years after stopping their medications.

In trials specifically addressing semaglutide and tirzepatide, participants lost an average of 14.7 kilograms, yet it was anticipated they would regain all lost weight within a year and a half. Jebb points out that further insights are required to understand the accelerated weight gain associated with these drugs compared to others.

Additionally, the team discovered that the weight regain rate after ceasing weight loss drugs was about four times steeper than that observed following the termination of a structured behavioral weight loss program, which typically emphasizes healthy eating and increased physical activity.

However, this disparity may be attributed to the greater motivation for weight loss among individuals participating in behavioral programs compared to those relying on medications.

Another factor contributing to this swift weight regain may be the appetite suppression induced by these drugs. Users often report significant increases in hunger and cravings upon discontinuation, possibly leading to rapid weight resurgence, as noted by Taraneh Soleimani from Pennsylvania State University.

Yet, a separate analysis suggested that offering behavioral support during the follow-up phase did not effectively curb weight gain. Soleimani emphasizes that more research is essential to determine optimal strategies for supporting individuals transitioning off weight loss medications.

What Jebb’s research illustrates, according to her, is the critical need to consider obesity as a long-lasting condition. “Weight loss drugs demonstrate effectiveness, and weight regain is prevalent upon cessation,” states Professor Soleimani. “These results confirm obesity as a chronic condition that requires prolonged treatment.”

Topics:

  • obesity/
  • weight loss drugs

Source: www.newscientist.com

2026: The Next Landmark Year for Breakthrough Weight Loss Medications

Travel Pix Pro/Getty Images

Many individuals set New Year’s resolutions to lose weight, particularly following the holiday festivities. Traditionally, this involved adopting a new diet, waking up early for workouts, and other habits that can be challenging to sustain. Consequently, it’s no surprise that numerous people abandon their goals within weeks.

Today, however, an alternative has emerged: weight loss medications. Instead of solely depending on lifestyle changes, individuals can benefit from regular doses of GLP-1 agonists or other therapeutic tablets (as highlighted on page 6). Health professionals still recommend integrating these medications with consistent physical activity for optimal results.

GLP-1 drugs are not only transforming our cyclical health regimens. Restaurants are now crafting menus specifically for Ozempic diners, featuring smaller portion sizes for customers who experience reduced appetite. Additionally, supermarkets have reported declines in sales due to decreased demand from those using these medications. Airlines are also considering the implications, as decreased average passenger weight could lower fuel expenses.

While it’s unclear how much these trends can be attributed to GLP-1 drugs—which are currently used by a minority—and the extent of their impact on brands reacting to this health trend, the statistics surrounding obesity are alarming. Approximately 1 billion individuals globally are affected by obesity, and the adoption of these medications is expected to rise. According to World Health Organization estimates, fewer than 10 percent of people will utilize GLP-1 drugs by 2030, yet this still represents a substantial demographic.


Restaurants are designing menus featuring reduced portions for Ozempic diners.

New advancements in medication are in development (refer to page 7), and the potential impacts could be even more significant. Beyond weight reduction, GLP-1 agonists have shown promise in treating various conditions, from addiction to eye diseases like cataracts.

While there remain numerous uncertainties regarding the long-term consequences, the results of discontinuation, and enhancing accessibility, the future appears bright. As we advance further into the 21st century, weight loss drugs are poised to play a crucial role in shaping health and wellness trends.

Topics:

Source: www.newscientist.com

Monthly Injections May Replace Daily Steroid Medications for Severe Asthma

Severe, poorly controlled asthma might increasingly be managed with monthly injections

Jacob Wackerhausen/Getty Images

Individuals suffering from severe asthma often depend on daily steroid medications, raising their likelihood of diabetes, infections, and bone issues. A new study indicates that monthly antibody injections could serve as a safer alternative.

When asthma is unmanageable with an inhaler, steroid drugs are commonly used, effectively decreasing airway inflammation and alleviating symptoms alongside the risk of asthma attacks. However, these medications can lead to serious side effects. “We aim to minimize the usage of oral steroids,” says Fan Chun from Imperial College London, who was not part of the research.

Previous studies demonstrated that tezepelumab, a monthly antibody injection, reduces the symptoms of severe asthma more effectively than a placebo. This has led to its approval in several countries, including the UK and the US, over recent years. However, it remained uncertain whether this treatment could lessen or eliminate the reliance on steroid drugs.

To investigate this, David Jackson and his colleagues at Guy’s and St Thomas’ Hospital in London recruited 298 individuals aged 18 to 80 with severe asthma from 11 countries. Participants were already using daily inhalers and steroids and were asked to take tezepelumab for one year. Chung noted that a control group wasn’t necessary since prior trials established that the injection had a significant effect compared to a placebo.

Researchers observed that, under medical supervision, participants’ oral steroid doses gradually decreased throughout the study.

By the end of the year, around half of the participants no longer required steroid medication, while 40% were able to reduce their doses enough to “minimize side effects,” according to Chung. “This outcome is highly successful,” he stated. “The trial confirms that tezepelumab is an effective treatment for patients with severe asthma, decreasing the need for daily medications.”

Side effects, such as worsening asthma symptoms, were reported by 9% of participants. However, it is unclear if these were due to the injection or existed beforehand, Chong explained. Nonetheless, he considers the rate acceptable given the advantages of reducing steroid use.

topic:

Source: www.newscientist.com

ADHD Medications Lower the Risk of Crimes, Substance Abuse, and Accidents

SEI 261892997

ADHD symptoms can be effectively managed through medication and therapy

Alex Di Stasi/Shutterstock

A study involving 150,000 participants in Sweden found that individuals using medications to control their symptoms face a diminished risk of suicidal behavior, criminal charges, substance misuse, accidental injuries, and traffic incidents. Prior research supports this, yet the team behind this latest study claims it’s the most substantial evidence available to date.

“This represents the best methodology, akin to a randomized trial,” states Zheng Chang from the Karolinska Institute in Sweden.

When considering medications for ADHD management, the wider impact of avoiding these treatments might not be fully recognized, according to Samuelle Cortese from the University of Southampton, UK. He suggests parents often become preoccupied with immediate academic challenges but should also consider potential long-term outcomes.

“Neglecting ADHD can be risky,” he emphasizes. “Current evidence indicates that treatment lowers these risks.”

Individuals with ADHD frequently struggle with attention and exhibit impulsivity. Randomized controlled trials indicate that medications are effective in handling immediate symptoms.

Such trials involve randomly assigning individuals to either receive treatment or not, regarded as the gold standard in medical research. However, no randomized studies have yet evaluated the broader effects of ADHD medications, forcing researchers to rely on observational studies, which do not definitively prove that medication leads to noted behavioral changes.

Recently, Chang, Cortese, and their team executed a method known as target trial emulation. They utilized Swedish medical and legal records to compare patients who began ADHD medication promptly after diagnosis with those who delayed.

The results indicated that those using ADHD medications were 25% less likely to face criminal charges or experience substance problems. They also recorded a 16% reduction in traffic accident involvement, a 15% lower risk for suicide attempts, and a 4% decrease in accidental injuries.

“Understanding if medication can influence daily life beyond mere symptom alleviation is invaluable,” stated Adam Guastella during an interview with the UK Science Media Centre at the University of Sydney, Australia. “This knowledge will also assist governments and policymakers in recognizing the potential societal benefits of comprehensive care, including mental health and criminal justice outcomes.”

If you need someone to talk to, please reach out: UK Samaritans: 116123 (samaritans.org); US 988 Suicide & Crisis Lifeline: 988 (988lifeline.org). Find more helplines at bit.ly/suicidehelplines for other regions.

Topic:

Source: www.newscientist.com

Asthma Medications Can Safeguard Against Life-Threatening Allergic Reactions

Stephanie Eisenbarth and Adam Williams prepare peanuts for allergy research in their lab

Northwestern University

Research indicates that common asthma treatments may offer protection against anaphylaxis, a severe allergic reaction. The drug Zileuton, traditionally used for asthma, is now being considered for individuals facing serious food allergies.

Despite the prevalence of food allergies, it can be challenging to foresee the risk of anaphylaxis for an individual. Scientists are investigating why some individuals with positive food allergen tests do not show symptoms, while others have severe, potentially deadly reactions.

“Our aim is to discover methods to help individuals with symptomatic food allergies manage their reactions to allergens,” states Stephanie Eisenbarth from Northwestern University, Illinois.

Eisenbarth and her research team anticipated that mice exposed to peanuts would experience anaphylaxis. They administered a single oral dose of Zileuton to a group of 5-10 mice sensitized to peanut allergens approximately one hour prior to feeding them peanut extract. The control group did not receive any medication. Observations revealed that almost all Zileuton-treated mice showed no symptoms of anaphylaxis, whereas the control group exhibited clear signs of it.

Most dietary proteins are usually broken down, but some can be actively absorbed through the intestines and enter the bloodstream directly. In individuals with severe allergies, these proteins can trigger immune responses, leading to anaphylaxis.

During allergic reactions, the body releases chemicals known as leukotrienes. The researchers found that leukotrienes play a role in the number of intact proteins that penetrate the intestine. They also identified a gene called DPEP1 that is crucial in regulating leukotriene levels.

One significant action of Zileuton is inhibiting the enzyme five lipoxygenase, essential for leukotriene production. Administering this drug to mice lowered leukotriene levels, while DPEP1 also suppressed remaining leukotrienes, preventing allergen absorption and halting anaphylaxis in susceptible mice. A single dose of Zileuton cut the anaphylaxis rate by 95%.

“We can differentiate between mice that respond to food allergens and those that do not. We are now evaluating whether the same asthma medications can limit allergen absorption in the intestines of people with food allergies.”

Jorge Emiliano Gomez Medellin from the University of Chicago suggests that these straightforward tablets might significantly alleviate the consequences of accidental allergen exposure. He added that while Zileuton could potentially inhibit the absorption of food allergens, it won’t alter an individual’s underlying sensitivity over time.

“Nonetheless, Zileuton could be a valuable tool in combating food allergies,” he concludes.

Source: www.newscientist.com

Could Cancer Medications Pave the Way for Alzheimer’s Treatment?

As treatment options for Alzheimer’s disease remain limited, researchers are exploring the repurposing of cancer medications to address cognitive decline.

The incidence of Alzheimer’s is on the rise due to an aging global population, yet no cure currently exists. Efforts to discover new therapies that can halt the progression of the disease instead of merely managing symptoms have often been unsuccessful.

At present, only two medications, Leqembi and Kisunla, have received FDA approval to slow the progression of early Alzheimer’s disease, and the extent of their effectiveness is considered limited.

Several pharmaceutical firms have either shelved or discontinued their Alzheimer’s drug development initiatives after encountering trial failures. Others are investigating the potential of established medications, including popular weight loss drugs in combating the disease.

In this context, researchers at the University of California, San Francisco, conducted extensive screenings of existing drugs that could be repurposed for Alzheimer’s treatment, aiming to shorten the time required for patient access to these drugs. They analyzed a database of over 1,300 different medications, spanning various drug classes such as antipsychotics, antibiotics, antifungals, and chemotherapeutics, and assessed their impact on gene expression.

Their recent study, published in the journal Cell, pinpointed two cancer drugs as the leading candidates to potentially mitigate the risk of Alzheimer’s in patients. When used in combination, these drugs demonstrated the ability to slow or even reverse Alzheimer’s symptoms in mouse models. One of the medications is typically used for breast cancer treatment, while the other targets colon and lung cancers.

Significant alterations in gene expression in the brain are characteristic of Alzheimer’s disease, leading to the increased synthesis of certain proteins and decreased production of others. These disruptions can impair brain functionality and result in symptoms such as memory loss.

According to the researchers, the two drugs, identified from a database of nearly 90, were able to reverse the expression of genes associated with Alzheimer’s in human brain cells. Furthermore, based on electronic medical records, five specific drugs appeared to lower Alzheimer’s risk among actual patients, ultimately leading the authors to select two FDA-approved cancer treatments for animal testing.

“We were not anticipating that cancer medications would emerge as strong contenders,” remarked Marina Sirota, interim director of the UCSF Bakar Computational Health Sciences Institute.

The authors noted that letrozole, a breast cancer treatment, seems to modify gene expression within neurons, while irinotecan, a colon cancer medication, appears to influence gene expression in glial cells that support the nervous system. Alzheimer’s disease leads to nerve cell destruction, excess glial cell proliferation, and brain inflammation.

A 2020 study indicated that breast cancer patients treated with letrozole had a lower incidence of Alzheimer’s disease compared to those who did not receive the drug. Similarly, colorectal cancer survivors who were administered irinotecan exhibited a reduced risk of Alzheimer’s disease, as noted in research from 2021.

After evaluating the drugs in mice, the study authors discovered that the combination of the two medications reversed cognitive decline and enhanced memory in mice displaying traits of Alzheimer’s disease as they aged.

Given that results observed in mice do not always have a direct correlation with human outcomes, researchers aim to conduct clinical trials with Alzheimer’s patients.

“The development of new medications typically incurs costs in the millions, often billions, and can span over a decade. In contrast, repurposed medications may require only two to three years and carry significantly lower costs to reach clinical trial stages,” Sirota explained.

“Currently, we are not producing highly effective treatments that can significantly decelerate cognitive decline,” she added.

The challenge in developing Alzheimer’s treatments lies in the intricate nature of the disease, with its exact causes remaining largely elusive.

At this point, the authors admit that the precise mechanisms by which cancer drugs may be effective against Alzheimer’s are uncertain. One hypothesis suggests that breast cancer medications inhibit estrogen production—a hormone that regulates the expression of numerous genes. Colon cancer drugs might mitigate brain inflammation by preventing glial cell proliferation, yet Huang notes that there could be additional explanations.

Dr. Melanie McReynolds, a biochemistry assistant professor at Penn State University who was not involved in the research, offered another perspective.

She suggested that the study indicates various cancer drugs may prove beneficial in treating Alzheimer’s by modulating glucose metabolism, the process by which cells generate energy. McReynolds emphasized that this process is vital for communication among different brain cells.

“Aging, stress, and illness can disrupt that communication,” she stated.

McReynolds expressed that the drug combinations evaluated in the current research have the potential to reverse metabolic declines.

However, it is crucial to understand how Alzheimer’s patients will respond to these cancer drug combinations. Letrozole can induce hot flashes, while irinotecan is known for causing severe diarrhea. Both treatments may also lead to nausea and vomiting.

“These medications come with significant side effects, so it’s essential to weigh these risks carefully and determine whether such side effects are manageable for individuals with Alzheimer’s,” stated Sirota. “It’s not a straightforward solution.”

Source: www.nbcnews.com

You Can Lose Weight Without Regularly Using Medications Like Ozempic

Ozempic and other GLP-1 medications might not need as frequent dosing as currently prescribed

Associated Press/Alamy

Individuals using GLP-1 medications such as Ozempic can still achieve weight loss despite facing difficulties in obtaining their prescriptions.

Medications like Semaglutide, marketed under the names Ozempic and Wegovy, have transformed obesity treatment, yet the increasing demand has led to significant supply shortages. In the U.S., changes in insurance coverage for these drugs can lead to confusion. For instance, CVS Caremark, which assists insurers in managing their prescription plans, recently discontinued coverage for Eli Lilly’s Zepbound, linked to the GLP-1 drug tilzepatide.

To investigate the impact of this confusion, Kaelen Medeiros and a colleague from a New York firm analyzed data from over 6,000 participants in the U.S. who enrolled in their program for a year between 2021 and 2024.

The program provided access to an app delivering bi-weekly lessons aimed at optimizing lifestyle choices such as nutrition and physical activity. Additionally, participants enjoyed regular one-on-one consultations with a health coach who assisted in applying these lessons. For an extra charge, all participants received GLP-1 medications, like Ozempic, mainly on a weekly basis.

By the program’s conclusion, 73% of participants experienced at least one disruption in GLP-1 access, defined as missing the medication for a minimum of 13 weeks. These participants received, on average, eight months’ supply of GLP-1 over the year-long trial. Participants lost an average of 14% of their body weight, compared to a 17% reduction among those who did not face such disruptions. The findings were shared at the Endocrinology Society’s annual general meeting in San Francisco on July 14th.

A similar rate of weight loss was observed in the program’s second year, regardless of the consistency of GLP-1 supply. “Although this confusion is concerning, it’s encouraging to see significant clinically relevant weight loss achieved despite it,” Medeiros remarks.

“This study is promising,” says Priya Jaisinghani from NYU Langone Health, New York. However, further research is needed to assess how the health coaching and lifestyle lessons provided to participants influenced weight loss, she notes. The researchers didn’t measure the engagement levels of participants in this segment of the program. Medeiros pointed out that variations in adherence might have impacted the outcomes.

Some participants also took metformin, a medication for type 2 diabetes that can aid in weight loss. Nevertheless, metformin is associated with only about a 2% reduction in body weight.

Topics:

  • Medical drugs /
  • Weight loss

Source: www.newscientist.com

Migraine Medications That Alleviate Headaches and Dizziness Symptoms

The debilitating nature of migraines can significantly hinder a person’s daily routine

Alfred Pasieka/Science Photo Library

A medication called Ubrogepant, which is currently prescribed for migraine treatment, has been found to alleviate non-headache symptoms that often precede the onset of migraines. This makes it the first medication known to address these initial signs.

Before migraine headaches decrease in intensity, many individuals experience warning signs such as light sensitivity, sounds, dizziness, and neck stiffness, all of which can significantly disrupt daily activities.

Developers of migraine medications have predominantly concentrated on treating the headaches themselves, with no effective solutions available for alleviating these preliminary symptoms.

However, Ubrogepant demonstrated promising results when administered during the early stages of migraine symptoms, according to Peter Goadsby from King’s College London and his team, who are eager to further explore this potential.

Their study involved 438 participants, aged 18 to 75, all with a history of migraines. Half received a 100 mg dose of the medication upon experiencing suggestive symptoms of an impending migraine. The other half took a placebo during a subsequent episode of prodromal symptoms.

Following the administration of Ubrogepant, participants reported an enhanced ability to focus after 1 hour, decreased sensitivity to light after 2 hours, and reduced fatigue and neck discomfort after 3 hours, compared to their experiences while taking the placebo. They also noted less sensitivity to dizziness and sound when using Ubrogepant.

“Taking Ubrogepant allowed individuals to mitigate these non-pain symptoms even before the headache began,” Goadsby remarked.

This study did not delve into the impact of the medication on aura, another early feature of migraines that includes sensory disturbances like flashing lights or blind spots.

“The potential for intervention in the migraine progression is clinically significant given the often debilitating early symptoms,” remarked Parisa Gazerani from Oslo Metropolitan University, Norway. However, she emphasizes the need for further studies to ensure broad applicability.

“This research indicates that migraine treatments could lessen these preliminary symptoms and may prevent the progression to the main headache phase,” stated Rob Music, head of the Migraine Trust in the UK. “We are eager to see more investigations in this area to lessen the burden of migraines on daily living.”

topic:

Source: www.newscientist.com

Migraine Medications Are Ineffective in Alleviating Dizziness Symptoms

Here’s a rewritten version of your content while keeping the HTML tags intact:

Rizatriptan is frequently recommended for various migraine types

Aleksandr Zubkov/Getty Images

The standard medications prescribed for migraines provide limited relief for the vestibular symptoms, which include dizziness and typical migraine manifestations like headaches and light sensitivity. This is true even for rizatriptan, which is sometimes recommended for such types of migraines.

Research on vestibular migraine treatment has been inconsistent, yielding mixed results across different medications, according to Jeffrey Staab from the Mayo Clinic in Rochester, Minnesota. Some newer medications, like galcanezumab, may reduce the frequency of attacks, but no randomized trials have previously evaluated the effectiveness of migraine medications in alleviating vestibular symptoms during episodes.

To fill this research gap, Staab and his team investigated vestibular migraines. Participants were instructed to take 10 milligrams of rizatriptan or a placebo at the onset of vestibular symptoms, such as balance problems and spinning sensations. Their symptoms were subsequently evaluated on a scale of 0 to 3 at several intervals until the episodes resolved.

One hour after administration—at which point rizatriptan reaches peak concentrations in the bloodstream—it was not more effective than the placebo in relieving symptoms which are often considered to act quickly. Both groups were allowed to use back-up medications after waiting the necessary hour.

After 24 hours, rizatriptan showed a slight improvement in sensitivity to movement, light, and sound, but not in dizziness. Participants also reported marginally higher scores concerning physical well-being—such as energy levels and the ability to carry out daily activities—when compared to those taking the placebo. However, no differences were noted in mental well-being or the acceptance of side effects.

Rizatriptan falls under the triptans class of drugs, typically effective against migraines, but may not alleviate vestibular symptoms, as noted by Staab.

The study’s findings indicate that the brain pathways linked to vestibular migraines (the vestibular system, which is considered “primitive” from an evolutionary standpoint) may lack sensitivity to triptans for reasons that are yet to be explored. According to Peter Goadsby from King’s College London, vestibular migraines should not be treated as distinct conditions from other migraine types; rather, their symptoms represent a “slight variation” of migraine pathology that necessitates targeted treatment approaches.

“I think it’s important to communicate with fellow clinicians about these symptoms,” Goadsby states. “For instance, if you are treating someone with a vestibular migraine using a triptan, be prepared for it to potentially be ineffective. It’s crucial to recognize that this doesn’t imply the patient is difficult or unreasonable.”

Topics:

This retains the original HTML structure while rephrasing the content for clarity and flow.

Source: www.newscientist.com

Reasons Patients Must Transition to Second-Line Obesity Medications

Soon, tens of thousands of Americans will be compelled to transition from well-known obesity medications to alternatives that are likely to yield less effective weight loss, thanks to decisions made by Health’s insurance providers.

This situation exemplifies the consequences of a clandestine agreement between a pharmaceutical company and an intermediary known as a pharmacy benefits manager (PBM), appointed by employers to manage prescription coverage for their workforce. While employers benefit from lower medication costs, employees find themselves restricted from accessing competitive healthcare options. This type of insurance denial has become increasingly prevalent in the last decade.

Caremark, part of CVS Health and one of the largest PBMs, has opted to eliminate coverage for Zepbound, despite research indicating its weight loss efficacy surpasses that of Wegovy.

These findings, which were first announced in December, were confirmed in an article published in the New England Journal of Medicine on Sunday. The study encompassed a significant clinical trial evaluating these drugs, funded by Eli Lilly, the producer of Zepbound. Previous research not funded by Eli Lilly reached similar conclusions.

Ellen Davis, a 63-year-old resident of Huntington, Massachusetts, is one of those affected by Caremark’s decision. “It’s as if the rug has been pulled out from under me,” she expressed.

After using Zepbound for a year, she lost 85 pounds and experienced significant health improvements, having retired after a 34-year tenure at Verizon.

In a letter addressed to Verizon, she stated, “This forces patients to transition to less effective medications without any justification for medical care.”

Verizon did not respond to inquiries.

Following Caremark’s announcement, word spread rapidly online. A physician’s assistant at a weight loss clinic in New Hampshire started a Change.org petition to urge the company to reconsider. As of Sunday afternoon, it had garnered over 2,700 signatures. Caremark is set to cease Zepbound coverage in July.

Doctors assert that both Wegovy, from Novo Nordisk, and Zepbound are effective medications; however, they prefer Zepbound for most patients. This shift greatly limits their ability to tailor obesity medication prescriptions to individual needs.

It remains unclear if the omission of Zepbound will enhance Caremark’s profit margins.

Executives from Novo Nordisk claim they are not attempting to obstruct Zepbound’s availability. They maintain that patients and healthcare providers should have the autonomy to select their preferred medications.

David Whitrap, a spokesperson for Caremark, stated that the firm’s objective was to reduce drug costs. He noted that the agreement would lower obesity drug prices for Caremark’s employer clients by 10-15% compared to the previous year.

“CVS Caremark has aimed to let PBMs competitors often put forth their best efforts. Our choice is to encourage competition among clinically similar products while providing the lowest net costs to our clients,” Whitrap commented.

When queried about studies highlighting Zepbound’s advantages, Whitrap indicated that both medications are highly effective, and that clinical trial outcomes frequently diverge from real-world results.

The actual pricing that employers pay for medications is usually confidential. The Health Transformation Alliance, a consortium of major employers, reports that the average monthly cost for a large employer falls between $550 and $650.

Without insurance, patients might spend approximately $500 monthly on their medications. Many recently lost cheaper alternatives when regulators halted the sale of generic versions that cost below $200 monthly.

Countless employers do not cover either Zepbound or Wegovy due to their high cost. Medicare excludes most drugs for obese patients, and the Trump administration recently declined to support the Biden administration’s proposal to expand coverage.

Caremark, along with two other PBMs, dominates 80% of the prescription market. Other players, like Cigna’s Express Scripts and UnitedHealth’s Optum Rx, have not implemented similar restrictions on weight loss medications.

Since 2012, major PBMs have increasingly employed strategies that disrupt patient care and complicate treatment plans. Medications have been abruptly removed from the PBM’s official list of covered drugs.

According to a drugmaker-funded analysis, the number of medications excluded from at least one PBM list surged from 50 in 2014 to 548 in 2022. This count reflects instances where patients were compelled to switch to entirely different drugs, not merely to a standard version or alternative replica.

Limitations fluctuate frequently, leaving patients uncertain about the reasons behind them. One PBM might cover a specific drug while another does not, but competing managers may do the reverse.

Exclusions are generally purported not to harm patients; in certain instances, they may even be beneficial if patients are nudged toward more effective medications.

However, some exclusions have prompted significant concern among patients and healthcare providers.

In 2022, Caremark compelled patients to switch from one widely utilized blood-thinning elixir to Xarelto, leading to anecdotal reports that patients experienced complications during their treatment change. A group of physicians criticized this move, and the company restored coverage for the elixir six months later.

Individuals with autoimmune diseases, such as arthritis, often face similar mandatory drug switches. Asthma patients are also experiencing transitions to alternate inhalers.

“We’ve witnessed numerous situations,” remarked Dr. Robin Cohen, an asthma specialist at Boston Medical Center.

Representatives on behalf of employers indicate that patients affiliated with Caremark have already reached out via calls and emails, inquiring about the potential impact on their prescriptions. While they may remain on the PBM’s drug list, they have not played an active role in shaping it.

Caremark’s changes are applicable only to specific private insurance beneficiaries whose employers selected the most prevalent drug list managed by PBMs. This movement excludes patients receiving a version of diabetes medication.

Patients can consider switching to Wegovy or three other weight loss alternatives.

Whitrap noted that Caremark provides a “case-by-case medical exception process for individuals who may require alternatives,” including patients who have previously utilized Wegovy and saw insufficient weight loss.

However, many individuals may not meet the criteria for the exemption. In a conversation, one patient expressed a desire for Zepbound specifically and was not interested in switching.

“I selected Zepbound in consultation with my physician,” stated Carl Hoode, 49, from Saugus, Massachusetts.

Some patients are contemplating using their own funds to continue Zepbound. For 28-year-old Victoria Bello of Syracuse, New York, the medication has provided significant health improvements, and she fears losing access to it.

“I wasn’t prepared for such a sudden change,” she remarked. “I’m concerned for my health and the potential setback in my progress.”

A study funded by Eli Lilly conducted direct comparisons of medications across 750 clinical trials over a span of 16 months.

Participants receiving high doses of Zepbound shed an average of 50 pounds, whereas those on Wegovy lost around 33 pounds. Though both medications are administered via injection and share side effects such as nausea, vomiting, diarrhea, and constipation, the frequency of these effects was generally comparable between the two drugs. A small proportion of patients in both groups discontinued medication due to side effects.

Both drugs function similarly but have critical differences. Wegovy mimics only a single appetite-regulating hormone, while Zepbound influences two. Researchers believe that engaging more hormones leads to greater weight loss.

Dr. Jason Brett, an executive at Novo Nordisk, indicated in a recent interview that the quantity of weight lost is just one aspect of obesity treatment. Both medications are associated with improved heart health, though only Novo Nordisk has obtained regulatory approval to market the drug with that claim.

Medical professionals contend that both options must remain accessible, as Wegovy may outshine Zepbound in terms of weight loss efficacy or having milder side effects.

Healthcare providers advocate for the availability of both medications due to the diverse responses patients exhibit when using either Wegovy or Zepbound.

Supporters of Caremark argue that their decision to restrict Zepbound is merely fulfilling their responsibilities.

Benefits managers engage with pharmaceutical companies to negotiate payments known as rebates, which ultimately reduce employers’ costs for prescription drugs. These negotiations can yield substantial fees for the biggest market players. Caremark stood to gain significant revenue from weight loss medications without needing to exclude Zepbound.

The weight loss pill market is thriving, with both Novo Nordisk and Eli Lilly vying for market share.

Caremark engaged both drug manufacturers regarding rebate amounts associated with making their products available. However, neither Novo Nordisk nor Eli Lilly disclosed specific amounts provided. Novo Nordisk maintains that it did not advocate for or pay to inhibit Zepbound’s availability, emphasizing that the exclusion was solely Caremark’s decision.

“We believe that patients and physicians should determine what’s in the best interest of the patient,” stated Lars Flugaard Jorgensen, CEO of Novo Nordisk. He elaborated to Wall Street analysts this month.

Elizabeth DeGalier, 56, of Rochester, Minnesota, shared that Zepbound had a transformative impact on her life, expressing her frustration over Caremark’s choice. “It appears they overlooked scientific evidence,” she remarked. “They were primarily motivated by financial considerations.”

She added, “I am apprehensive about the future. I rely on several other expensive medications. Will they also be discontinued?”

Source: www.nytimes.com

Medications Similar to Wegovy Show Effectiveness in Treating Fatty Liver Disease

Fatty liver disease can lead to cirrhosis and cancer

3dmedisphere/shutterstoc k

Currently, common medications used for treating obesity and diabetes are showing promise in combating life-threatening liver diseases.

Semaglutide, marketed under names like Ozempic and Wegovi, mimics the hormone GLP-1, which aids in weight loss and regulates blood sugar levels, helps suppress appetite, and promotes insulin secretion. Researchers have now found that this drug therapy can halt or even reverse a condition known as metabolic dysfunction-associated steatohepatitis (MASH).

“This could offer a groundbreaking way to manage this condition,” says Philip Newsom from King’s College London. “It’s incredibly promising for patients.”

MASH, formerly known as NASH, is a severe version of non-alcoholic fatty liver disease marked by inflammation, fibrosis (scar tissue formation), and excessive liver fat accumulation, occasionally leading to cirrhosis and cancer. MASH is commonly linked to obesity and often coexists with type 2 diabetes.

A study conducted in 2020 involving 320 participants revealed that daily semaglutide injections led to a reduction in liver fat and inflammation in 59% of those with MASH. However, a more recent investigation involving 71 patients found no benefits from the weekly dosage.

For a broader perspective, Newsom and Arun Sanyal from Virginia Commonwealth University initiated a larger trial involving 1,195 MASH patients across 253 clinical sites in 37 countries. Participants averaged 56 years old with a body mass index of 34.6, and about 50% had type 2 diabetes.

The physician prescribed each participant a weekly semaglutide injection for four and a half years, gradually increasing the dose to 2.4 milligrams over the first four months, mirroring those used in Wegovy based on prior test findings. Participants also received lifestyle counseling to encourage a healthier diet and exercise.

While the full study is ongoing, results from biopsies taken 72 weeks later revealed that among the first 800 patients, including 266 receiving a placebo, 62.9% of those on semaglutide showed significant reductions in liver fat and inflammation, compared to 34.3% in the placebo group. Improvements in fibrosis were observed in 36.8% of the treatment group versus only 22.4% for the placebo group. About one-third of all treated patients and 16.1% of placebo patients experienced these benefits.

Weight loss alone could explain some of these improvements, as patients in the treatment cohort lost an average of 10.5% of their body weight, while those on the placebo lost only 2%. Although further research is needed to fully uncover the mechanisms behind the treatment, it may also directly target the processes driving the disease.

“It’s not yet established, but part of the efficacy of GLP-1-like drugs might be due to their effects on immune cells and reduction of inflammation,” notes Newsom.

Topic:

Source: www.newscientist.com

Trump refuses Medicare proposals to include Wegovy and other medications for obesity

The Trump administration rejected the Biden plan on Friday, which proposed Medicare and Medicaid covering obesity drugs and increasing access to millions of people.

The Biden administration’s proposal aimed to circumvent the ban on Medicare paying for weight loss drugs by claiming they would treat diseases related to obesity.

Expanding drug coverage would cost the federal government billions of dollars, with an estimated cost of around $35 billion over a decade according to the Congressional Budget Office Estimates.

The decision was part of a larger set of regulations contained in a 438-page document aimed at updating Medicare benefits and private insurance plans used by about half of Medicare beneficiaries.

Catherine Howden, a spokesperson for the Centers for Medicare and Medicaid Services, stated that the agency did not believe it was appropriate at the time to approve the Biden plan.

Medicare currently covers a limited set of weight loss medications for individuals with specific health conditions, such as diabetes and heart problems.

The Biden plan aimed to extend coverage to obese patients without these specific diseases, with an estimated 3.4 million people potentially benefiting from the policy.

Popular weight loss pills like Wegovy by Eli Lilly and other related products are now available at reduced prices to patients paying out of pocket.

Eli Lilly and Novo Nordisk offer discounts for their products to patients paying out of pocket instead of through insurance, significantly reducing the cost for individuals.

Health Secretary Robert F. Kennedy Jr. criticized weight loss pills, advocating for a diet of healthy foods instead.

Clinical trials have shown benefits of weight loss drugs beyond just weight loss, including preventing heart attacks and strokes.

Supporters of expanded drug coverage argue that the long-term health benefits will outweigh the costs, potentially reducing overall medical expenses. However, the realization of such savings remains uncertain.

States’ Medicaid programs now have the option to decide whether to cover obesity drugs or not, with some already opting to provide coverage. If the Biden policy had been implemented, all states would have been required to provide coverage.

The exact cost of obesity drugs for Medicare and Medicaid patients is undisclosed, but it is estimated to be several hundred dollars per patient per month.

Many employers and private health insurance plans do not cover weight loss drugs, leading some to discontinue coverage due to high costs.

Patients without insurance often rely on cheaper generic versions of drugs created through compounding, costing less than $200 a month. However, regulators are phasing out this option due to improved supply of branded products.

Congressional Republicans have shown some interest in urging Medicare to cover weight loss drugs, although this is not a current priority. Negotiations with Novo Nordisk for lower drug prices under a 2022 law have been initiated, with reduced prices scheduled to start in 2027 for eligible individuals.

Source: www.nytimes.com

GLP-1 medications like Ozempic and Wegovy lower susceptibility to 42 illnesses

Semaglutide and other GLP-1 agonists are injected

Yulia Burmystrova/Getty Images

Drugs like Ozempic and Wigovy, called GLP-1 agonists, offer more benefits than risks when taken for their approved uses, according to a comprehensive analysis of their effects on 175 conditions. However, the same may not be true for people who are taking the drug for other purposes.

“In this new area of ​​GLP-1, we wanted to really map the benefits and risks for all the conditions that we thought were relevant,” he says. Jiyad Al Ali at Washington University in St. Louis, Missouri.

These drugs are best known for helping control type 2 diabetes and treating obesity. They mimic the hormone GLP-1 in the body, which lowers blood sugar levels and keeps you feeling full for longer.

Dozens of studies suggest that GLP-1 agonists may also reduce the risk of many other conditions, from heart disease to dementia to substance use disorders. These studies have involved hundreds or thousands of people and have focused on one or a few symptoms at a time, but now that millions of people are using the drug, they are much more This means that less frequent effects can be investigated, Al Ali said.

To get a more comprehensive picture, he and his colleagues examined the health records of more than 200,000 diabetic patients who took GLP-1 agonists over a four-year period in addition to standard treatment. They also looked at 1.2 million people with diabetes who received only standard treatment over the same time period and assessed both groups' risk of developing 175 different health conditions.

The research team found that people who took GLP-1 agonists had a lower risk of 42 diseases. For example, the risk of heart attack was reduced by 9% and the risk of dementia was reduced by 8%. The probability that this group would suffer from suicidal ideation or substance use disorders such as alcohol or opioid addiction was also approximately decreased by 1/10. .

However, there were also downsides for people taking GLP-1 drugs. They were more likely to experience known side effects, such as nausea and vomiting, as well as previously undescribed side effects. These include a 15% higher risk of kidney stones and more than double the risk of pancreatic inflammation or drug-induced pancreatitis. In total, 19 conditions were at increased risk, but taking GLP-1 drugs had no significant effect on risk levels for most of the conditions evaluated, including bronchitis, rheumatoid arthritis, and obsessive-compulsive disorder. Ta.

The fact that these drugs affect such a wide range of symptoms remains surprising, but it is unclear exactly why they have this effect. “They're reducing obesity, which is the root of all disease. If you treat obesity, the heart, kidneys, brain, and everywhere else will benefit later,” Al-Aly said. They also reduce inflammation, which commonly damages organs, and appear to target parts of the brain associated with addiction, he says.

One problem with this analysis is that the research team did not report the actual number of people affected by each condition, making the results difficult to interpret. Daniel Drucker from the University of Toronto and has worked with obesity drug companies. Reducing the risk of common conditions such as heart attacks and dementia is probably worth taking seriously, but the association with rare conditions like pancreatitis is so small that the risk is low for most people. He says it's unlikely. Al-Aly said the research team plans to publish specific numbers of cases in future studies.

Overall, this study provides reassurance that the benefits of GLP-1 agonists outweigh the risks, at least for patients with type 2 diabetes and obesity. “There are no red flags with this group,” he says. stefan trapp He is a professor at University College London and has worked with obesity drug companies.

However, the situation may be different for people who do not have these conditions, such as people who are not obese and buy drugs to lose weight. “I don't know if the benefits outweigh the risks,” Drucker said.

topic:

Source: www.newscientist.com

Rapamycin could potentially enhance the safety of epilepsy medications in pregnant women

Sodium valproate is an effective drug for epilepsy, but its consumption is not recommended during pregnancy

Miljan Zivković/Shutterstock

The drug rapamycin may prevent the epilepsy drug sodium valproate from causing developmental problems during pregnancy.

Sodium valproate is used to treat epilepsy, bipolar disorder, and sometimes migraines. Although effective, it is not recommended during pregnancy as it can cause birth defects such as spina bifida and lifelong learning disabilities.

Giovanni Pietrogrande Researchers from the University of Queensland in Australia wanted to understand why sodium valproate could have such an effect. So they used stem cells to create mini-spinal cords called organoids in the lab. These mimic the spine of a fetus during early pregnancy.

When organoids were exposed to sodium valproate, their cells changed in ways that may be associated with risk of congenital disease.

The researchers looked for reasons for this and found that activity in one of the cell's signaling pathways, called mTOR, indicates that cells are aging. This is a process in which cells stop growing but do not die, but instead continue to release chemicals that can cause inflammation.

Rapamycin, which was initially developed as an immunosuppressant but has some promise for anti-aging effects, also targets the mTOR pathway.

In another experiment, researchers exposed a new set of spinal cord organoids to a combination of sodium valproate and rapamycin and found that no aging occurred. They then replicated this test in zebrafish larvae and found that the cells similarly did not undergo senescence and showed no signs of the changes that occur when exposed to sodium valproate alone.

Rather than doctors discontinuing sodium valproate if an epileptic patient is pregnant or may become pregnant, someday doctors may be able to prevent the negative effects of sodium valproate by combining it with rapamycin. Pietro Grande says. Human studies are needed to make this recommendation.

Frank Vajda The University of Melbourne says sodium valproate is “a critically important drug and the single most effective treatment for generalized seizures, where abnormal electrical activity begins in both halves of the brain at the same time.”

“I think this is a very important paper that could lead to a return to the level of importance that this drug had before its side effects were discovered,” he says.

topic:

Source: www.newscientist.com

New GLP-1 medications offer potential for weight loss and improved health

Exciting developments are on the horizon in the world of obesity medications.

Pharmaceutical companies are racing to create new drugs, building on the success of existing medications like Novo Nordisk’s Ozempic and Wegovi, as well as Eli Lilly’s Maunjaro and Zepbound.

In addition to targeting diabetes and weight loss, some experimental drugs show promise in improving liver and heart function while reducing common side effects such as muscle loss seen with current treatments. Data on 27 GLP-1 drugs in development will be presented at the 2024 American Diabetes Association meeting in Orlando, Florida.

According to Marlon Pragnell, PhD, the ADA’s vice president of research and science, the pipeline now includes a variety of drug candidates in different stages of development, creating an exciting landscape of innovation.

While most of the data currently available comes from animal studies or early human trials, some drugs may be available in the United States over the counter within a few years, with FDA approval likely further down the line.

As the field of GLP-1 drugs continues to expand, there is hope for more affordable medications with fewer side effects to become available, offering new possibilities for patients.

Exploring Different Hormones for Weight Loss

GLP-1 drugs function by slowing down the digestive process and promoting a sense of fullness. In addition to GLP-1, emerging weight-loss drugs are examining the impact of another hormone called glucagon, which can mimic the effects of exercise.

One such drug, Pemvidutide from Maryland-based Altimmune, combines glucagon with GLP-1 to potentially enhance weight loss effects.

Results from a Phase 2 trial involving obese or overweight adults showed promising weight loss outcomes, paving the way for further research into the drug’s potential benefits.

Altimmune’s Chief Medical Officer, Dr. Scott Harris, highlighted the drug’s ability not only to aid in weight loss but also to provide additional health benefits for liver and heart function while preserving lean body mass.

Altimmune plans to move forward with Phase 3 trials and aims to introduce the drug in the U.S. by 2028.

Competition and Cost Considerations

Having a variety of weight-loss drugs available can help address shortages and potentially drive down costs over time. The high prices of current medications like Wegobee and Zepbound in the U.S. can pose financial challenges for many patients.

Different patients may respond differently to various treatments, as highlighted by Dr. Fatima Cody Stanford of Harvard Medical School. Having a range of options is crucial to tailor treatments to individual needs.

Stay Informed with the Latest News on Weight Loss Drugs

New developments in the pharmaceutical world present opportunities for improved treatment outcomes and potentially life-changing solutions for patients struggling with obesity.

For individuals like Danielle Griffin, who have not seen the desired results from current medications, the prospect of innovative drugs offers hope and excitement for the future.

Advancements in Metabolic Health

Companies like Eli Lilly are exploring new combinations of hormones to enhance the efficacy of weight-loss drugs. Retatortide, a new injectable medication from Lilly, shows promising results in weight loss and blood sugar control.

Additional studies on drugs like Mazduchid highlight the potential for improved metabolic status and weight loss outcomes, paving the way for new treatment options in the near future.

These ongoing developments underscore the dynamic landscape of obesity treatment, offering hope for a new generation of medications that could revolutionize the field and improve outcomes for patients.

The Future of Obesity Treatment

As research and development in the field of obesity medications continue to advance, there is optimism for more effective, affordable, and patient-friendly treatments to become available in the coming years.

With the potential for improved metabolic health, weight loss outcomes, and reduced side effects, the next wave of obesity treatments holds great promise for individuals struggling with obesity-related health issues.

The ongoing innovation in this field signifies a new era of possibilities in obesity treatment, offering hope for a healthier future for many individuals.

Source: www.nbcnews.com