
Health matters newsletter: The whole truth about weight-loss drugs
On 'weight loss' drugs and their impacts, the scorching heat and sleep apnoea, what persists after a Covid-19 infection, AI in healthcare, and more.
Universally, a certain class of drugs have come to be superstars in recent times. The GLP-1 class of drugs, with their capacity for weight loss, though originally conceived and developed for diabetes, has suddenly become the toast of the season, for one reason - their weight loss properties. With celebrities like Elon Musk flaunting their use of these drugs, semaglutide and more recently, tirzepatide, reached homes even before the results of rigorous control trials were ready for publication. While over the months, the trials have indicated good overall results, both for weight loss and blood sugar control, a new field study offers a more realistic estimate of how these GLP-1 receptor agonists work in real time.
A recent study, done in the U.S. indicated that these New 'weight-loss' drugs have lower impact in real life compared to clinical trial results. In a paper published in the journal Obesity, Hamlet Gasoyan et al accessed electronic health record data from a large health system in Ohio and Florida to identify adults with overweight or obesity without type 2 diabetes who started with injectable semaglutide or tirzepatide between 2021 and 2023. The researchers observed that treatment discontinuation and use of lower maintenance dosages might reduce the likelihood of achieving clinically-meaningful weight reduction in patients on these drugs.
This is something that diabetologists in India agreed with, instinctively. In a randomised control trial, there is incentive and constant reminders to take the drugs. In the real world setting, when patients have to pay for their drugs out of their own pocket and without a rigorous reminder, or because of the side effects that they cannot tolerate, a number of people discontinue treatment. And drugs work only as long as they are taken.
Further on this topic, Dr. V. Mohan, Chennai-based diabetologist discusses on The Health Wrap by The Hindu about who are ideal candidates for these drugs, whether a regimen must be followed and deciding the appropriate dosage levels for people on GLP-1 drugs. Zubeda Hamid and I discuss other issues too, including good and bad bacteria, migration and climate change, not to mention a giraffe's cervical structure. Do tune in, to listen.
Having lived out another May, a torrid summer, there is no doubt that a climate crisis is upon us. The WHO says 2024 was the warmest year on record – but the heat is far from over. A new report from the World Meteorological Organization (WMO) warns that global temperatures will likely continue rising, with an 80 per cent chance that at least one year between now and 2029 will be even hotter. Climate emergency is a health crisis 'that is already killing us,' the WHO adds.
Delhi and other parts of northern and central India were severely impacted as temperatures soared beyond bearable. Our stories give you a clear picture: Delhi under 'red alert' as mercury soars beyond 45 degrees C; severe heatwave conditions to persist; Blistering heat continues in north, central India; hills scorch. Meanwhile, we also reported on a study which found that Warmer climate could make sleep apnoea more severe, common. Sleep apnoea, a condition characterised by having trouble breathing properly while sleeping, could become more common and severe in a warmer future, a new study has found. Obstructive Sleep Apnoea (OSA) is a common sleep disorder, estimated to affect about a billion worldwide. The condition occurs when muscles in the throat narrow the airways, impacting breathing and blood oxygen levels during sleep.The findings, published in the journal Nature Communications, show that one's chances of experiencing sleep apnoea could spike by 45 per cent on days with higher temperatures.
Meanwhile, the government is mulling whether to restrict the temperature range on air conditioners. Vasudevan Mukunth, here, explains the Science behind setting the right temperature on the air conditioner.
Last week, a very important document was launched, something we would do well to heed. With the launch of HelpAge India's national report, ahead of World Elder Abuse Awareness Day, which is marked on June 15, on intergenerational dynamics, it is clear that we need to create better bonds with senior citizens and also encourage more digital literacy. For a greying nation, we need to pay more attention to the health and social support needs of the elderly, bringing it back into the DNA of the culture we live in.
We do our periodic dip stick test for COVID-19, profiling various developments in the area, even as the number of cases is going up slowly. Dr. M.S. Seshadri and Dr. T. Jacob John explain what the current Resurgence of COVID 19 means for India. They argue that the recent number of COVID-19 cases, reported as nearly 7,000, reflects the greater volume of testing, not the true magnitude of infection or disease in the population.
More than four years since the COVID-19 pandemic began, the disease remains a global health concern — not because of new surges but because of what persists. Do read about a genetics study that linked a lung gene to known, recorded post-COVID sequelae. Bindu Shajan Perappadan also focuses on the same angle, reminding readers of the the threat of deep vein thrombosis associated with COVID.
We also endeavour to point out areas of hope and positivity, as it is so important in health care. Health is as much about wellness and recovery as it is about disease and pain. There is some hope with reports that Novavax's COVID-flu combo vaccine which showed strong immune response in trial.
In other news, Jacob Koshy reports that SII and DNDi have partnered to expand human trials for dengue treatment. Hopefully, we will have better dengue treatment protocols soon. Again in India, here is a model that could be replicated, as Rajasthan's cash plus model pushes up early breastfeeding rate, dietary diversity among new mothers.
The big minus about treating cancer is the way the treatment causes general toxicity, as it tars even healthy tissue with the same brush. Here, there seems to be a solution to this: In a first, arc therapy beats tricky cancer while sparing nearby tissue.
Afshan Yasmeen reported that Karnataka's MMR was steadily decline; it has reduced to 58 per lakh live births in 2020-22. Great news, indeed.
It was also the week we discussed India's falling fertility rates. As per a UN report, fertility rate drops below replacement level, Purnima Sah wrote. According to the UNFPA, millions of people in India are not able to realise their real fertility goals. Calling this the 'real' crisis, and not overpopulation or underpopulation, the report calls for the pursuit of reproductive agency — a person's ability to make free and informed choices about sex, contraception and starting a family — in a changing world. Replacement-level fertility, commonly defined as 2.1 births per woman, is the rate at which a population size remains constant from one generation to the next.
The recent World Health Assembly has created a turning point for skin health, explained Dr. Monisha Madhumitha. Here's what the WHA's landmark resolution on skin diseases means for the world.
Moving on to a key component of health care, we had articles that discussed the role of AI in the health sector this past week.
While Sayantan Datta asked How safe AI is in healthcare depends on the humans of healthcare, Dr. Aravinda C. took the argument further discussing the promise and pitfalls of evaluating AI tools with mismatched yardsticks. Dr. V. Viju Wilben turned our attention to how technology can help, at a time when most city roads are perennially clogged with traffic jams, to reclaim the Golden Hour, and save lives.
In the tailpiece segment, reverse ageing steals the spotlight. If only it were possible! But Anirban Mukhopadhyay brought hope, with the article. Common molecule offers clue to making old muscles young again. As we age, it gets harder to recover from a fall, injury or even a tough workout because the body's muscle-repair system starts to falter. Muscle stem cells (MuSCs), the in-house repair crew, stop dividing and rebuilding tissue, losing their ability to respond to damage. A study in Cell Stem Cell on June 12 suggested this decline may be reversible. The key isn't some futuristic therapy but a molecule already used in hospitals today -prostaglandin E2.
We had a very healthy, and robust explainers section this week.
Sophie Davies, in The Conversation wrote of Diverticular disease
Sreedevi Jayachandran explained Tourette syndrome and its management
Serena Josephine M.'s story in our 'All You Need to Know About' series was on hernias
Dr. Steve Thomas wrote two fine pieces on the occasion of blood donation day. Do click on the links to read them: Our body's crimson tide: understanding blood disorders and the vital role of blood donation and Our body's crimson tide: the evolving treatment landscape in haematology
Athira Elssa Johnson wrote on The risks of undiagnosed gall bladder stones: doctors call for awareness, timely treatment, how to read the tongue as a measure of health; and filed yet another story in our monthly Nobel winners series: This one on Sir Ronald Ross and his contributions towards malaria control
Dr. Sathyanarayana L.D. elaborated on a little-explored subject, in connection with Brain Tumour Day (June 8) on aphasia, or the loss of language, after brain tumour surgery.
Our In Focus podcast discussed the risks of the government's proposed 'mixopathy' move
If you have some extra time on your hands, also read:
C. Maya: Living donor transplants thrive as Kerala turns its face away from deceased donor organ donations
Serena Josephine M.: Many private hospitals in T.N. hit by acute shortage of Hepatitis B vaccine
Indian-origin physician Bobby Mukkamala sworn in as American Medical Association president
Science Quiz: On eye health
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Mint
38 minutes ago
- Mint
Eli Lilly to acquire gene-editing biotech company Verve Therapeutics for $1.3 billion. Here's why
US-based multinational pharmaceutical giant Eli Lilly & Co., on Tuesday, 17 June 2025, announced its plans to acquire gene-editing biotech firm Verve Therapeutics Inc. for $1.3 billion as the big pharma company eyes expansion in experimental medicine for long-term growth, reported the news agency Bloomberg. According to the agency report, Eli Lilly & Co. will pay up to $13.50 per share for the acquisition deal. The breakdown of the deal will be that Eli Lilly & Co. will pay $10.50 per share in cash as well as a non-tradeable contingent value right that entitles the holder to receive as much as $3 extra per share. The transaction is expected to close in the third quarter of the current year, reported the news agency, citing the company. Verve Therapeutics shares skyrocketed 75.12% to $10.99 at the US stock market open at 9:38 a.m. (EDT), compared to $6.27 at the previous market close. However, pharma major Eli Lilly & Co. shares are trading 1.45% lower on Wall Street at $795.84 as of 9:40 a.m. (EDT), compared to $807.58 at the previous stock market close. The US big pharma company Eli Lilly & Co.'s revenues are centred around its iconic weight-loss drug, Zepbound, as the company prepares for the medicine's patent to expire. The news agency reported that the company has been able to target experimental medicines that are still far from the market. In this area, price tags are usually smaller than for therapies that have already undergone multiple patient trials. The long-term return on such early-stage deals can be far larger. In January 2025, Eli Lilly & Co. agreed to pay up to $2.5 billion for a cancer medicine which was being tested by Scorpion Therapeutics Inc., as per the agency report. Further in May, the company announced a plan to buy SiteOne Therapeutics Inc., a biotech firm developing pain medicines, for nearly $1 billion. Eli Lilly & Co. was reportedly in collaboration with Verve Therapeutics on its experimental gene-editing program for reducing lipoprotein, which is a risk factor for plaque buildup in human arteries. This acquisition deal will give Eli Lilly & Co. full control of the program, as the company shows confidence in its gene editing drug, which is a cutting-edge technology in the market, according to the report. However, this technology has struggled to attract investors recently, in part because it's expensive to make and aimed at providing one-time cures for rare diseases that may not be lucrative. Verve is a rare example of a gene editing company targeting a disease that affects a large population and offering better commercial prospects. Its approach, which uses tiny balls of fat to deliver the treatment, is less expensive to make than other gene therapies. Ruth Gimeno, the Vice President for diabetes and metabolic research and development at Eli Lilly & Co., told the news agency that the experimental therapy could be the first to edit genes inside a living body that's targeted to a broad population of patients.


The Print
2 hours ago
- The Print
How Serum Institute, DNDi tie-up for affordable antibody will bolster global fight against dengue
Additionally, a joint project team will be formed to advance clinical trials, with the goal of registering and deploying the dengue monoclonal antibody in India and other dengue-endemic countries, provided the studies confirm its safety and efficacy, they said in a joint statement. The SII and the Drugs for Neglected Diseases initiative (DNDi) entered into a partnership on 13 June, declaring they will develop a workplan to carry out late stage trials and access activities, along with a joint strategy to raise necessary funds and resources for developing the potential drug candidate, formerly known as VIS513 or Dengueshield. New Delhi: Pune-based Serum Institute of India (SII) has joined hands with an international medical research organisation to accelerate the clinical development of an affordable monoclonal antibody for dengue, a vector-borne disease that has emerged as a major public health challenge for countries like India. Dengue is a climate-sensitive, viral infection transmitted to humans through the bite of infected mosquitoes, mainly aedes aegypti that also spreads pathogens which cause zika and chikungunya fever. While many dengue infections are asymptomatic or produce only mild illness, the virus can in several patients cause more severe disease, and even death. It is estimated that one in 20 people who get sick with dengue get severely ill. Despite the alarmingly rising prevalence and severity of the vector-born disease, there is still no specific treatment available for dengue. The collaboration aims at accelerating the development of an effective and affordable monoclonal antibody treatment for dengue caused by any of the four serotypes of dengue virus, in close cooperation with endemic countries, including Thailand, Malaysia, and Brazil. Despite the… — SerumInstituteIndia (@SerumInstIndia) June 13, 2025 Also Read: India may soon get 1st dengue vaccine, but wait for jab effective against all 4 strains could be longer The latest collaboration The VIS513 is developed by US-based biotechnology company Visterra, a biologic research early-stage clinical development arm of Tokyo-based Otsuka Pharmaceuticals. The VIS513 was later licensed to the SII. The SII has carried out phase 1 and phase 2 trials of the therapy in India, proving its safety and efficacy in a small number of humans. Currently, the pivotal Phase III clinical trial is underway in India, and the collaboration paves way for the expansion of the drug candidate in several other countries where dengue is endemic, the two entities said. Dengue poses a significant threat, with 3.9 billion people at risk and cases more than doubling each year since 2021. The World Health Organization says the actual number of dengue cases globally rose from 5,05,430 cases in 2000 to 5.2 million in 2019. India is among the top 30 countries with the highest burden of dengue, and according to government estimates, among the 20-25 percent of cases where dengue symptoms are clinically apparent, children are at a significantly higher risk of hospitalisation and mortality. This year, the country registered 12,043 dengue cases and six deaths till March, according to the National Centre for Vector Borne Disease Control statistics. Last year, 2,33,519 cases and 297 deaths were reported but experts underline the actual burden of the disease is much higher. 'India reports tens of thousands of dengue cases every year, with outbreaks occurring every two to three years in different states,' said Dr Kavita Singh, the Asia Continental Lead & Director South Asia, DNDi. What is deeply concerning is that dengue is no longer confined to historically endemic regions but is rapidly expanding into newer states, she added. 'Addressing this growing threat demands a multi-pronged approach, including strengthened vector control, surveillance, community awareness and, critically, the development of effective treatments and diagnostics,' Singh also said. A 2024 dengue bulletin by the WHO said that the highest number of dengue cases was recorded in 2023, affecting over 80 countries in all regions of the WHO. In 2023, a combination of ongoing dengue transmission and a significant surge in cases led to a record-breaking 6.5 million infections and over 7,300 deaths globally. New monoclonal antibody offers help Monoclonal antibodies, sometimes also called passive immunisation, are special types of proteins called antibodies which are made in laboratories. Dengue is caused by any of four dengue virus (DENV) serotypes (DENV 1 to 4), each of which can cause minor dengue fever or severe dengue. Dengue can be anything from an infection without symptoms, a mild fever or a severe fever with musculoskeletal pain to haemorrhagic fever (low platelets leading to bleeding) and dengue shock syndrome (severe form of dengue infection that can lead to circulatory collapse). The latter two can be very severe and result in death if not recognised and treated early. And these two conditions usually happen, not in the first but in subsequent infection, when the dengue virus strain is different from the one that caused the earlier infection. According to Dr R.R. Dutta, the head of internal medicine with Paras Health in Gurugram, medical practitioners need to develop customised treatment plans which focus on avoiding severe disease outcomes such as dengue hemorrhagic fever and shock syndrome in patients who experience severe symptoms. Dr Manisha Arora, director, internal medicine with C K Birla Hospital in Delhi, pointed out that unlike bacterial infections, where antibiotics can attack the root cause and cure the disease, dengue, being a viral infection, lacks such a targeted treatment. If we had a specific antiviral for dengue, it would help in directly attacking the virus, thereby reducing the risk of complications and improving patient outcomes, said the clinician. 'Unfortunately, in the absence of such antivirals, doctors are limited to providing only supportive care, such as fluid management, monitoring vital signs, and treating complications as they arise,' Arora stressed. The current treatment regime for severe dengue patients depends heavily on early detection and timely intervention, but it doesn't address the underlying virus. 'The lack of specific antivirals limits our ability to prevent disease progression, especially in severe cases. If an effective antiviral existed, it could potentially reduce hospitalisations, lower the risk of long-term health issues and ultimately save more lives,' Arora also said. The monoclonal antibody candidate by the SII, as per available information, has shown efficacy against all dengue virus serotypes with no serious adverse events. The therapy candidate, designed to be effective against all four DENV serotypes, works by binding to a specific part of DENV called the envelope protein domain III, known for its role in viral entry into host cells and its immunogenicity. The results from a phase 1 clinical trial of the drug involving 40 participants in India—based on follow-ups lasting 85 days—whihc was published in the Lancet last year, showed the drug was found effective and safe in early testing. AV-1, another investigational human monoclonal antibody developed by US-based company AbViro, is also in a similar stage of development and is undergoing safety and efficacy trials across various countries. A dengue vaccine by Japanese pharma giant Takeda, approved by some other countries, is also undergoing trials in India to generate local safety and efficacy data ahead of its regulatory approval in the country. (Edited by Ajeet Tiwari) Also Read: India sees alarming rise in dengue cases even before peak season, steady increase over past 4 years


Time of India
2 hours ago
- Time of India
Elon Musk passes ketamine test—here's what the drug is and why it raised eyebrows
Credit: X Elon Musk isn't new to controversy, but this time the firestorm came in the form of a drug test. After weeks of speculation following a New York Times report accusing him of heavy ketamine and drug use during his time in the Trump administration as head of the Department of Government Efficiency (DOGE), Musk fired back in his signature style—by posting his urine test results online with just one word: 'Lol. ' The test, taken recently, shows negative results for ketamine and several other substances, directly challenging claims that he regularly used ecstasy, mushrooms, Adderall, and ketamine to the point of suffering bladder damage. Musk doubled down on his denial earlier, calling the NYT article 'lies' and clarified that while he had tried prescription ketamine years ago, it was for mental health purposes and he hadn't taken it since. So what's the big deal about ketamine, and why is a clean test so significant? Understanding ketamine: From surgical anesthetic to controversial antidepressant Ketamine is classified as a Schedule III non-narcotic controlled substance in the United States. It was approved by the Food and Drug Administration (FDA) strictly as a general anesthetic—used alone or in combination with drugs like nitrous oxide. Doctors typically use it in surgical or emergency settings, as a sedative. But ketamine's uses have expanded. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Unfriendliest Countries in the World, Ranked BigGlobalTravel Undo Off-label, doctors are prescribing it for mental health conditions like depression and anxiety, especially in people who don't respond well to traditional medications. While the FDA hasn't formally approved ketamine for these uses, ongoing research shows it can provide rapid relief from symptoms of depression and anxiety—though those effects may be short-lived. A 2023 review emphasized that the effectiveness of ketamine treatment depends on dose and type, with higher doses often leading to better short-term symptom relief. However, a 2022 review on ketamine for anxiety noted that results were mixed, with many people experiencing a return of symptoms within two weeks. How long does Ketamine stay in the body? Ketamine is found in both liquid and powder forms. In medical settings, it's administered as a clear liquid injection. In recreational settings, powdered ketamine—typically off-white—is snorted in lines or mixed into marijuana or tobacco. It's also sometimes added to drinks. As for detection, urine tests are the most common method because they are affordable, easy, and fairly accurate. Here's how long ketamine is detectable: Urine: Up to 3 days after single use; 5–7 days with regular use; up to 30 days in rare chronic-use cases Blood: Around 24 hours Saliva: Up to 72 hours Hair: Up to 90 days A negative urine test, like the one Musk posted, means there's no detectable ketamine or its metabolites in the body above the lab's threshold. This strongly indicates no recent use, especially within the past few days or weeks. Medical uses of ketamine: More than just an anesthetic Besides general anesthesia, ketamine is being explored and used (off-label) for several conditions. Here's a quick look at how and where doctors may prescribe ketamine: Pain treatment (low-dose): For trauma, fractures, abdominal pain, limb injuries, and chronic lower back pain Status epilepticus: In life-threatening seizures that don't respond to other anti-seizure drugs Depression: Especially treatment-resistant depression. Some studies show ketamine can improve mood within hours Anxiety: Though still under research, some evidence shows fast-acting, short-term relief from anxiety symptoms It's worth noting that off-label use means these applications aren't FDA-approved—but doctors may still prescribe ketamine when they believe the benefits outweigh the risks. Risks, side effects, and the darker side of ketamine use Ketamine is generally considered safe when used correctly and under medical supervision. However, it does come with potential side effects, especially when misused or taken recreationally. Common side effects at medical doses include: Drowsiness Double vision Dizziness Confusion Nausea and vomiting Uneasiness or restlessness Less common but serious risks include: Heart and blood vessel instability: Temporary spikes or drops in heart rate and blood pressure Respiratory depression: Risky if overdosed or injected too quickly Emergence reactions: Confusion or agitation during recovery Increased intracranial pressure: Particularly risky for people with brain injuries Liver dysfunction: In some cases, ketamine use has been linked to liver damage Cognitive effects: Some studies suggest thinking and memory deficits, especially in children And because of its dissociative and hallucinogenic effects, ketamine is also misused recreationally and has unfortunately been used in instances of drug-facilitated assault. One step to a healthier you—join Times Health+ Yoga and feel the change