Childhood tonsillectomy not tied to obesity or overweight in adulthood: Study

Israel: A recent study published in the prestigious American Journal of Respiratory and Critical Care Medicine revealed that tonsillectomy in children with obstructive sleep apnea (OSA) does not increase the risk of obesity/overweight in adulthood. 

The study, conducted by Ben-Gurion University of the Negev and Soroka University Medical Center, supports tonsillectomy as the primary treatment for obstructive sleep apnea, emphasizing its health benefits and the lack of association with increased obesity risk in adulthood.

A tonsillectomy is surgery for tonsils removal. Tonsils are lumps of tissue on both sides of the back of the throat that protect the body from infections by helping the immune system. Tonsillectomy is one of the most common surgeries kids and teens get.

Obstructive sleep apnea affects 6% of children and is associated with behavioural and learning difficulties. Tonsil surgery is the primary treatment for OSA. However, the medical literature and affected families have raised concerns about post-surgery weight gain and risk for obesity.

A new study by Prof. Aviv Goldbart, Prof. Ariel Tarasiuk, and Dr. Ran Abuhasira at the Faculty of Health Sciences, Ben-Gurion University and Soroka University Medical Center investigated the effects of childhood tonsillectomy on body weight in adulthood.

Their research discovered in 132 children that tonsillectomy (vs. 127 who chose not to perform surgery) did not increase the risk of obesity in adulthood. This long-term study followed children who underwent a whole night sleep study at the Sleep-Wake Disorders Unit of Soroka University Medical Center in 1998, utilizing the databases of Clalit Health Services.

This study supports tonsillectomy as the primary treatment for OSA, emphasizing its health benefits and the lack of association with increased obesity risk in adulthood.

Reference:

Aviv D. Goldbart , Ran Abuhasira , Adi Shiloh , Jacov Even-Tsur , and Ariel Tarasiuk, Childhood Adenotonsillectomy Does Not Increase the Risk of Being Overweight in Adulthood, American Journal of Respiratory and Critical Care Medicine, https://doi.org/10.1164/rccm.202311-2175LE.

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Living near green spaces may boost bone density and lower osteoporosis risk

Living in leafy areas near gardens, parks, and green spaces, may boost bone density and lower the risk of osteoporosis, finds research published online in the Annals of the Rheumatic Diseases.

Lower levels of air pollution in green spaces is a significant contributory factor to the associations found, conclude the researchers.

Osteoporosis weakens bones, making them fragile and prone to fracture. It can lead to chronic pain, diminished mobility, and poorer quality of life. Already a major health issue worldwide, its global prevalence is set to rise with the rapid ageing of the population and changes in lifestyle, note the researchers.

Osteoporosis is caused by genetic, hormonal and environmental factors, and while exposure to green spaces has been linked to lower risks of poor health, it’s not clear if this extends to the risk of osteoporosis, and to what extent genetic susceptibility might be influential.

To explore this further, the researchers analysed data held in the UK Biobank on 391,298 people, average age 56, just over half of whom (53%) were women.

All of them had information recorded on their bone mineral density, and potentially influential factors including ethnicity, annual household income, education level, employment status, residential area, alcohol consumption, physical activity levels, smoking status, and diet.

Their genetic risk of osteoporosis was calculated using a polygenic risk score, and a widely used measure, called a normalized difference vegetation index (NDVI), which is based on satellite imagery, was used to determine the amount of green space in their residential area.

The annual average exposures to the pollutants nitrogen oxide (NO2) and particulate matter PM2.5 were estimated based on residential postcode and data from the ESCAPE project, which is looking at the long-term effects on human health of exposure to air pollution in Europe.

Each participant was monitored until a diagnosis of osteoporosis, death, or 31 March 2021, whichever came first.

During an average monitoring period of 12 years, new cases of osteoporosis arose in 9307 people. They were more likely to be older, female, smokers, and retired. They were also more likely to have lower educational attainment and be more economically disadvantaged.

But a consistent association between the amount of green space and new cases of osteoporosis emerged. The authors estimated the NDVI in steps of about 300 metres of available residential greenness at a range of 300 to 1500 metres. With each such increase of the NDVI they found an increase in bone mineral density and 5% lower risk of developing osteoporosis.

The key moderating factors in the association found between green space and reduction of the risk to develop osteoporosis were lower levels of NO2 and PM2.5

Several studies have shown that exposure to air pollution can produce oxidative stress, inflammation, and disrupt hormones, both of which increase the risk of osteoporosis, note the researchers.

People living in the leafiest areas will be exposed to a lower risk because the trees and plants act as natural filters, removing pollutants from the air.

Being physically active was also associated with a lower risk of osteoporosis, possibly because living in areas with green space affords more opportunities to exercise, suggest the researchers.

This is an observational study, and as such, can’t establish cause. The researchers also acknowledge several limitations, including that the NDVI calculation was based on residential addresses so may not have accurately defined the actual amount of green space. And the study participants were generally healthy, so the potential for selection bias can’t be discounted.

But they nevertheless conclude: “The findings from this study present the first evidence indicating that residential greenness is associated with higher bone density and decreased risk of developing osteoporosis.”

They add: “These findings provide valuable insights into the potential of greenness in preventing the onset of osteoporosis and emphasise the significance of urban greening in developing effective prevention strategies.”

Reference:

Tan T, Tang L, Guo X, et alAssociations of residential greenness with bone mineral density and osteoporosis: the modifying effect of genetic susceptibilityAnnals of the Rheumatic Diseases Published Online First: 05 March 2024. doi: 10.1136/ard-2023-224941.

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Semaglutide reduces severity of common liver disease in people with HIV, reveals study

A weekly injection of semaglutide was safe and reduced the amount of fat in the liver by 31% in people with HIV and metabolic dysfunction-associated steatotic liver disease (MASLD), according to a presentation at the 2024 Conference on Retroviruses and Opportunistic Infections (CROI) in Denver. This is the first clinical trial of semaglutide for MASLD in people with HIV. The research was sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, and conducted in the United States and Brazil by ACTG, a global clinical trials network focused on HIV and other infectious diseases. ACTG is funded by NIAID and collaborating NIH institutes. McGovern Medical School at UTHealth Houston also contributed funding for this study.

Previously known as nonalcoholic fatty liver disease, MASLD is characterized by the accumulation of excess fat in the liver that is not caused by alcohol consumption or viral hepatitis. Over time, fat deposits may cause inflammation and cellular damage, and can result in cardiovascular and liver disease. MASLD also is associated with obesity, type 2 diabetes, and other metabolic disorders. It is the most common cause of chronic liver disease in the United States, and a leading reason for liver transplantation. An estimated 30-40% of people with HIV experience MASLD, slightly higher than the average among people without HIV. Semaglutide is an antidiabetic medication approved for use for the treatment of type 2 diabetes and an anti-obesity medication used for long-term weight management.

The Phase 2b pilot study enrolled people with HIV and MASLD aged 18 years and older whose viral load—the amount of HIV in the blood-was suppressed to undetectable levels by antiretroviral therapy (ART). Participants were diverse with respect to ethnicity, race, gender, and age. Of the 49 participants included in the analysis, 40 (82%) were taking ART regimens containing an integrase strand transfer inhibitor, which is a class of antiretroviral drugs shown to be highly effective at suppressing HIV but associated with weight gain in some people.

Participants self-injected semaglutide on a weekly basis at increasing doses until they reached a 1 milligram dose at week four and participated in frequent safety monitoring visits. At 24 weeks, the study team assessed changes in participants’ liver fat content using a type of MRI specifically designed to measure the amount of fat in the liver. Participants experienced an average 31% reduction in liver fat, with 29% of participants experiencing a complete resolution of MASLD, meaning their liver fat decreased to 5% or less of overall liver content. They also experienced weight loss, reduced fasting blood glucose (the amount of sugar in the blood) and reduced fasting triglycerides (a type of fat in the blood), consistent with effects observed in studies of semaglutide in people without HIV.

A separate analysis showed the volume of psoas muscle-a large muscle connecting the torso to the lower body-also decreased with no significant change in physical function. Semaglutide was generally well tolerated with an adverse event profile similar to that observed in people without HIV. The most common adverse events were gastrointestinal and included nausea, diarrhea, vomiting, and abdominal pain. Two participants experienced more significant adverse events possibly related to semaglutide but were able to continue in the study. All participants completed the full 24 weeks of therapy at the originally prescribed dose.

These findings suggest that semaglutide is a safe and effective therapy for MASLD in people with HIV. The study may help inform healthcare decisions by people in consultation with their providers, as part of an approach to healthier aging with HIV over the life span. According to the investigators, additional research is underway to understand whether people with HIV experience any unique immunologic or inflammatory pathway changes while taking semaglutide therapy. 

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NEET MDS 2024 not Postponed: Aspirants Approach Supreme Court again

New Delhi: Disappointed with the fact that the NEET-MDS 2024 exam has not been postponed, the aspirants for Master of Dental Surgery (MDS) courses have once again approached the Supreme Court.

Although the exam is scheduled to be conducted on March 18, the aspirants have been demanding the postponement of the same to July 2024. 

Medical Dialogues had earlier reported that the MDS aspirants had approached the Supreme Court previously, seeking postponement of the exam and an extension of the BDS internship completion deadline.

During the hearing of the plea seeking postponement of the NEET MDS 2024 exam, the Union Government had informed the Supreme Court bench that it was looking into the grievances of the candidates regarding the extension of the internship deadline.

Considering this submission, the Apex Court bench had not passed any order on 21st February and had directed the authorities to consider the representations submitted within a period of one week. The Apex Court had clarified that the bench did not express any opinion on the merits of the case and “…it will be open to the union government to take an appropriate view having regard to the entire facts and circumstances.”

However, the NEET MDS 2024 exam did not get rescheduled and yesterday, issuing a notice in this regard, the National Board of Examinations (NBE) confirmed that the exam would be conducted on its scheduled date i.e. on 18th March, 2024. However, based on the directions issued by the Union Health Ministry, NBEMS extended the deadline for completion of BDS internship till 30th June, 2024.

Also Read:Separate counselling for NEET MDS 2024 candidates before NEET PG counselling: Dental Council of India

As per the latest media report by Live Law, expressing concern over the lack of action on the part of the Union Government, the petitioners filed a Miscellaneous Application (MA) seeking restoration of the writ petition which was earlier disposed of by the Court based on the assurance given by the Union Government. The petitioners alleged that the Union Government did not take a final decision within a week of receiving representations from the students.

The counsel for the petitioners mentioned the application before the Chief Justice of India D Y Chandrachud yesterday morning and the CJI asked the counsel to send an email request and stated that a date for listing would be fixed.

In their recent application, the petitioners highlighted that the Union Government has not taken a decision regarding the postponement of the exam despite the looming examination date.

As per the application, the petitioners submitted, “However, despite the order and despite the examination date looming in, the respondents have not taken any decision in this regard till Date.”

“A number of emails and representations were submitted to the respondents both through email and in physical form wherein the dental students have set out their grievances and reiterated their request to postpone the exam and increase the cutoff date. However, the respondents have not acted upon any such representations till date,” the application further mentioned.

Seeking restoration of the plea, the petitioners have urged the Court to issue directions to the Union Government to comply with the order dated 21.02.2024. Further, they also requested the Court to order the rescheduling of NEET-MDS 2024 exams, emphasizing parity with the common counselling for NEET PG and NEET MDS. 

Apart from this, the petitioners also demanded an extension of the eligibility cut-off date in the application, considering the delayed completion of internships by BDS students.

The Prayer of the application, as reported by Live Law, seeks the following :

a) Pass an order allowing the application for restoration of the above-captioned writ petition and direct the respondents to comply with the order dated 21.02.2024 passed by this Hon’ble Court in the present writ petition.

b) Pass an order thereby directing the Respondents to reschedule NEET MDS 2024 in furtherance of the consistent practice and policy to conduct entrance exam and common counselling for NEET PG and NEET MDS, parity.

c) Pass an order thereby directing the Respondents to extend last date of cut-off for eligibility suitably

i) after ascertaining internship completion date from universities offering MDS Course across India;

ii) in accordance with existing policy to conduct entrance exam and common counselling for NEET PG and NEET MDS and/or;

d) pass any other order that is deemed fit and proper in the facts and circumstances of the case.

The application also highlighted the discriminatory nature of fixing the eligibility cut-off March 31, 2024 highlighting that 40% of the 2018 batch BDS interns would not complete their internships by the deadline. The petitioners argued on the overlapping of the UG course curriculum for BDS and MBBS students, both facing delays due to the COVID-19 period. In their plea, the petitioners stressed the need for a uniform approach. They also questioned the discrepancy in the cut-off dates for MBBS and BDS students.

“Roughly 8000 students all across India including Kerala, Orissa, MP, UP, J&K, AP & Rajasthan will be excluded,” the petitioners submitted.

“Therefore, it is discriminatory for the cutoff date to be pushed back from 31 March 2024 to 15th August 2024 for the 2018 batch of MBBS interns, and not for the BDS students. Counselling for the MBBS students and BDS students after the internship period is over has always been held at the same time,” they demanded.

Meanwhile, recently, the Dental Council of India (DCI) issued a notice and announced that the counselling session will be held separately for NEET MDS 2024 before NEET PG Medical Counselling.

The DCI notice stated, “It is hereby informed to all MDS aspirants that the Govt. of India may conduct the counselling session for NEET-MDS 2024 separately and before NEET PG Medical Counselling.”

Also Read: NEET MDS 2024: No Change in Exam Date, NBE extends BDS Internship Deadline, eligible candidates can apply from tomorrow

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Bengaluru doctor booked for performing 74 illegal abortions in 3 years

Bengaluru: Discovering an illegal abortion racket that has been operating in the city for the last three years, the owner of the private hospital in Nelamangala has been booked for allegedly conducting 74 illegal abortions without the necessary authorization.

As of now, the doctor is on the run. The charges have been labelled against the hospital following allegations of performing illegal abortions since 2021 till date without obtaining a license under the Medical Termination of Pregnancy (MTP) Act in violation of subsection (b) of section 4 of the Medical Abortion Act, 1971.

The racket was uncovered when District Family Welfare Officer Dr S.R. Manjunath visited the hospital for a routine inspection on January 26. The inspection was performed based on the complaints of the locals. 

Also read- Foetus Found In Toilet Of Ludhiana Hospital, FIR Filed

During the inspection, it was found that the hospital did not obtain a license for the 74 illegal abortion procedures in the last three years. Allegedly, it had not maintained records of the procedures performed, which is a gross violation under the Medical Termination of Pregnancy Act, 1971.

As per The Hindu news reports, the inspection team also found that the hospital had failed to keep any records of scanning reports or provide any information regarding procedures to the district authority. 

Moreover, it also emerged that the hospital recorded the abortion details in the operation theatre register instead of maintaining the record in a proper MTP admission register.

According to an Indian Express news report, the hospital was registered under the Karnataka Private Medical Establishments (KPME) however, it failed to keep records of the ultrasound reports in 90 per cent of the case sheets. As a result, the health department seized the Operation Theatre register as part of the ongoing investigation.

In light of these grave findings, the DHO approached the police for the registration of the case on February 20 and also submitted a detailed report to the Health and Family Welfare Department for further action.

Acting on the DHO complaint, the police registered a case and booked the owner of the hospital under 312 (causing miscarriage), 313 (causing miscarriage without woman’s consent), 315 (act done with intent to prevent child being born alive or to cause it to die after birth), and 316 (causing death of quick unborn child by act amounting to culpable homicide) of the Indian Penal Code (IPC).

An investigation is underway to trace the owner of the hospital and gather more evidence regarding the violations. 

Also read- Karnataka Doctor Who Allegedly Performed Around 900 Illegal Abortions Arrested

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Justify bioequivalent data: CDSCO Panel Tells Sun Pharma on Mirabegron Extended-release Tablets

New Delhi: After reviewing the bioequivalence (BE) report of Mirabegron extended-release Tablets 50 mg presented by drug major Sun Pharma, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has opined the firm to justify the product is bioequivalent with the reference product.

This came after the drug major Sun Pharma proposed manufacturing and marketing permission for Mirabegron extended release Tablets 25 mg and 50 mg and presented the BE report of Mirabegron extended-release Tablets 50mg for which permission has been taken from the BA/BE Export Division before the committee.

Mirabegron is a beta-3 adrenergic agonist used to treat overactive bladder and neurogenic detrusor overactivity. Mirabegron has been shown to have a high safety and efficacy profile by large random placebo-controlled clinical trials. Mirabegron is used to treat urgency, urge urinary incontinence, and increased urinary frequency found in the overactive bladder.

Mirabegron is a medication used in the management of overactive bladder. It is in the sympathomimetic class of medications. It received approval from the US Food and Drug Administration (FDA) in June 2012 for treating overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency.

Mirabegron is a potent and selective agonist of beta-3 adrenergic receptors. The activation of beta-3 receptors relaxes detrusor smooth muscle during the storage phase of the urinary bladder fill-void cycle, which increases the bladder’s storage capacity thereby alleviating feelings of urgency and frequency.

At the recent SEC meeting for Urology held on 20th February 2024, the expert panel reviewed the proposal presented by the drug major Sun Pharma to manufacture and market permission for Mirabegron extended-release Tablets 25 mg and 50 mg.

After detailed deliberation, the committee noted that the firm submitted a 90% Confidence Interval of AUC (0-72) and AUC (0-infinity) was found to be 97.30 to 119.84 and 97.63 to 138.80 respectively against the acceptance limit within 80-125%.

In light of the above, the expert panel suggested that the firm may submit a justification to prove that the product is bioequivalent to the Reference product.

Accordingly, the committee stated that the firm should submit additional data to CDSCO for further review by the committee.

Also Read: Cipla gets CDSCO nod to market novel antibiotic Plazomicin in India, to launch under brand name Zemdri

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Telangana Drug Controller issues alert against drugs by Meg Lifesciences

In a significant move to curb the menace of falsified drugs, the Drugs Control Administration, Telangana, has issued a Spurious Drug Alert and Stop Use Notice for all drugs claiming to be manufactured by ‘Meg Lifesciences’.

Telangana Drug Control Administration has become aware that certain drugs claimed on the label as manufactured by ‘Meg Lifesciences, Khasara No. 47/5, Palli Gaon, Distt. Sirmour, 173 001’ are being circulated in the market after the recent raid conducted by the administration. Stocks worth Rs. 33.35 lakhs seized in the raid claimed to be manufactured by Meg Lifesciences. Cases have been registered against several offenders involved in this spurious drugs racket.

For more information, click on the link below:

Chalk Powder Instead Of Medicines: Telangana Drug Controller Issues Alert Against Drugs By Meg Lifesciences

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Eli Lilly finds bacteria, other impurities in Mounjaro, Zepbound knockoffs

Eli Lilly said on Thursday it has found bacteria and high levels of impurities in products claiming to be compounded versions of tirzepatide, the active ingredient in its popular diabetes drug Mounjaro and weight loss treatment Zepbound.

The U.S. drugmaker has sued several medical spas, weight-loss clinics and compounding pharmacies to stop them from selling products purporting to contain tirzepatide.Compounded drugs are custom-made medicines based on the same ingredients as branded versions, and often cheaper, but also subject to less regulatory scrutiny.
In an open letter, Lilly said some of these products had a different chemical structure as well as a different color than the approved versions of Mounjaro or Zepbound.
“In at least one instance, the product was nothing more than sugar alcohol,” Lilly said.
The company said it does not sell or provide tirzepatide to any compounding pharmacies.
“Lilly rightly notes that compounded drugs are not FDA-approved. But that fact does not mean compounded drugs are unsafe – any more than it means that FDA-approved drugs are always safe,” said Scott Brunner, CEO of the Alliance for Pharmacy Compounding, which represents compounding pharmacists and technicians.
Brunner said it was not clear if the fake drugs were made at a state-licensed pharmacy, which can legally produce compounded drugs when the branded version of a drug is in short supply, in which case they would not be compounded drugs.
Danish rival Novo Nordisk has also taken legal action against those offering products that claim to contain semaglutide, the active ingredient in its popular weight loss drug, Wegovy.
Novo reported in December it had found some samples of compounded semaglutide to be up to 33% impure.
Read also: Eli Lilly gets CDSCO Panel Nod to Import, Market Antidiabetic Drug Tirzepatide solution for injection Single dose vial

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Postpone NEET MDS 2024: FAIMA urges Health Minister

Taking up the issues being faced by the National Eligibility-cum-Entrance Test (NEET) MDS candidates, the doctors under the Federation of All India Medical Association (FAIMA) recently wrote to the Union Health Minister Mansukh Mandaviya and urged to postpone the exam, scheduled to be conducted on 18th March 2024.

Apart from requesting the Health Minister to postpone the exam to July, FAIMA has also urged the authorities to extend the deadline for completion of BDS Internship to August 31, 2024.

For more information click on the link below:

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Ahmedabad Civil Hospital launches Gujarat largest skin bank

The state government in a collaborative effort with the Rotary Club Kankaria has launched Gujarat’s largest government skin bank at Civil Hospital in Ahmedabad on Wednesday.

The Civil Hospital in Ahmedabad on Wednesday launched Gujarat’s largest government skin bank, besides other advanced medical facilities.

For more information click on the link below:

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