Friday, May 09, 2025

New Study Shows Effect of Diet Drugs on Fatty Liver Disease

A new clinical trial has found that the weight-loss drug Wegovy significantly improves a serious form of fatty liver disease in nearly two-thirds of patients — a potential breakthrough for millions affected worldwide.

The study, published in the New England Journal of Medicine, focused on metabolic dysfunction-associated steatohepatitis (MASH), an advanced form of what’s now called metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease. MASLD affects roughly a third of U.S. adults, with about 5–7% progressing to MASH — where fat accumulation leads to inflammation and scarring. Left untreated, it can result in cirrhosis, liver failure, or cancer. 
 
Insulin resistance is a key driver of both MASLD and MASH, making individuals with obesity or type 2 diabetes especially vulnerable. Dr. Lior Neuman, a family medicine and obesity specialist, described fatty liver as “one of the most common metabolic complications of excess weight,” and emphasized how often the disease remains silent, even in its advanced stages. Diagnosis typically starts with blood tests showing elevated liver enzymes, followed by imaging like ultrasound. 
 
According to the National Institutes of Health, up to 75% of overweight adults and 90% of those with obesity have MASLD. Of these, roughly 17 million Americans are believed to have MASH. Globally, over 1 billion people may be affected by MASLD, and MASH cases in the U.S. are projected to rise by 56% by 2030. 
 
Dr. Neuman stressed the importance of early detection: “Fat in liver cells can lead to inflammation and scarring. That scarring was once considered permanent — now we know weight loss can reverse it.” He added that while FibroScan is a useful tool for assessing liver fat and fibrosis, it’s not yet publicly available in Israel. 
 
Study Design and Results 
 
The trial, led by Prof. Philip Newsome (King’s College London) and Dr. Arun Sanyal (Virginia Commonwealth University), involved 1,195 people with MASH across 253 sites in 37 countries. Participants had an average age of 56 and an average BMI of 34.6; about half had type 2 diabetes. 
 
Patients received weekly injections of semaglutide — the active compound in Wegovy and Ozempic — or a placebo over a 72-week period, gradually increasing to the standard 2.4 mg weight-loss dose. All participants also received lifestyle counseling. 
 
The results were compelling:
 
62.9% of those on semaglutide showed significant improvement in liver fat and inflammation, compared to 34.3% on placebo. 
 
6.8% had fibrosis improvement, versus 22.4% in the placebo group. 
 
Nearly one-third of semaglutide patients showed both benefits, double the placebo group’s 16.1%. 
 
Most participants had moderate to severe fibrosis (stage 2 or 3) at the study’s start. Prof. Newsome called the outcomes “crucial for patients.”

Semaglutide mimics GLP-1, a natural hormone that reduces appetite and boosts insulin secretion. Patients on the drug lost an average of 10.5% of their body weight, compared to just 2% in the placebo group. While weight loss itself can improve liver function, researchers suspect the drug may also act directly on the disease. “GLP-1 drugs may help reduce inflammation through immune system effects,” said Newsome, though more studies are needed to confirm this. 
 
The treatment was generally well tolerated. Common side effects included nausea, diarrhea, constipation, and vomiting. Only 2.6% of semaglutide users and 3.3% of placebo users dropped out due to side effects. 
 
A Turning Point 
 
Experts view the findings as a significant step forward, though questions remain about long-term results. “This is impressive weight loss — but will patients sustain it?” said Dr. Sobia Laique, a hepatologist at the Cleveland Clinic. “Managing obesity requires a long-term strategy.”
 
Dr. Jeffrey Lazarus of the CUNY School of Public Health called the study “a breakthrough,” noting that the FDA had already approved another drug, resmetirom (Rezdifra), for fatty liver disease and fibrosis in 2023. “We finally have drug options alongside lifestyle changes,” he said, though he emphasized that medications should supplement — not replace — healthy habits. Rezdifra is not yet approved in Israel. 
 
Dr. Susan Spratt, an endocrinologist at Duke University who wasn’t involved in the study, found the semaglutide results “particularly promising,” given how difficult it is to reverse fibrosis. “This is meaningful progress,” she said. 
 
Dr. Neuman agreed: “These findings confirm what we’ve long believed — that losing just 5% or more of your body weight can significantly improve liver health.”
 
Novo Nordisk, the manufacturer of Wegovy, said the FDA has granted the drug “priority review” for treating MASH, with a decision expected within six months. Wegovy was already approved in 2023 to reduce cardiovascular risk in people with obesity. Other GLP-1 drugs like Zepbound (Mounjaro) and Ozempic have also expanded into areas such as sleep apnea and chronic kidney disease. 
 
These results mark another major step in expanding the potential of GLP-1 drugs beyond weight loss and diabetes — giving new hope to millions with serious liver disease.


This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   


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Wednesday, October 13, 2021

Fungal Infection Mimicking Spinal TB Found in 4 Covid-Recovered Patients

The discovery of a new post covid symptom among recovered patients in the last three months has raised serious concerns among the medical fraternity. The new cause of worry seems to be the detection of a fungal infection that has led to severe bone damage to the spinal-discs spaces of a patient.

The presence of this fungal infection came to the fore when a 66-year-old patient was found complaining of mild fever and severe lower back pain a month after recovering from COVID 19. Initially, the patient was treated with muscle relaxants and nonsteroidal anti-inflammatory drugs without relief.

A magnetic resonance imaging or MRI scan then revealed severe infection-led bone damage to the spinal-discs spaces called spondylodiscitis. Medically termed as aspergillus osteomyelitis, the invasive fungal infection was found to be difficult to diagnose as it mimics spinal tuberculosis (TB). Such fungal infection has been detected in mouth cavities of Covid-recovered patients, and, in rare cases, in lungs.

Deliberating on the issue, an infectious diseases expert  told that so far vertebral osteomyelitis caused by aspergillus fungi species has been diagnosed in four patients in three months. Prior to this, vertebral osteomyelitis had not been documented in post-Covid patients in India, he added.

The common thread found in all four was that they had severe Covid and were treated with steroids to get over Covid-linked pneumonia and related complications. The expert contended that long-term use of corticosteroids may increase the risk of opportunistic infections, depending on the underlying disease being treated and what other drugs are being used.

Another rare yet critical fungal infection caused by a group of molds known as mucormycetes called mucormycosis has also been widely reported in recovered patients across India. These molds are present naturally in the environment. However, it affects humans when the body’s immunity system has been weakened and it is vulnerable. It affects the lungs and the sinuses following inhalation of fungal spores from the air. The fungus can also enter the body through open wounds or cuts. This infection is also said to be caused due to the long-term use of corticosteroids.

Earlier, a partial or temporary loss of voice was also detected among many Covid survivors. The experts contended that the condition which is causing hoarseness of voice in some victims due to lung fibrosis or a complete loss of speech for weeks is not directly caused due to the virus but because it is making the victims susceptible to larynx infections which are making them feeling choked.

This condition is said to set in between the first and third weeks of the Covid attack and may last up to 3 months. It has not cased caused a permanent loss of voice in anyone however, it has led to many of those suffering falls into depression.

 

This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   

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Friday, February 21, 2020

Pancreatic cancer 'time machine' reveals tumor development and invasion

Pancreatic cancer has one of the worst survival rates among cancers. Patients can expect as low as a 9% chance to live for at least five years after being diagnosed.

Going back in time to observe how cells with key gene mutations interact and become invasive would help researchers better understand how the cancer starts and identify it sooner.

A pancreatic cancer "time machine" engineered by Purdue University researchers has revealed that the disease is even more unpredictable than previously thought: Cancer cells promote each other's invasiveness when they grow together.

The study, published in the journal Small, is just the beginning of a new discovery about how pancreatic cancer evolves. Since the paper's publication, the researchers also have found drug resistance in cancer cell types originating from two drug-sensitive ones.

The time machine is a hollow tube of collagen that realistically mimics the microanatomy of a pancreatic duct. By injecting cancer cell lines into microfluidic channels within the artificial duct, the researchers can use the system as a model for observing how pancreatic cancer behaves over time.

Typically, it takes 10-20 years for pancreatic cancer to develop in a patient. Even in an animal model, the process is several months long. This pancreatic tumor model condenses cancer development to just two weeks.
We can observe what happens over a long period of time. This helps us to see trends that we wouldn't normally see." Bumsoo Han, Purdue professor of mechanical engineering
Bumsoo Han builds models for studying how cancer cells move in biological systems.

The tumor model speeds up time because researchers can load in cell lines from an animal model or patient without waiting for gene mutation to happen first. The life-like structure of the tumor model allows the researchers to reconstruct the mutation as it would happen in the body.

To go back in time, the researchers just rewind footage taken by imaging equipment from the side of the artificial duct.

For this study, a group led by Stephen Konieczny, a professor of biological sciences at Purdue, developed the pancreatic cell line in a mouse model. Han's team then loaded the cell line through the microfluidic channels of the artificial pancreatic duct. Once inside, the cell lines fill the duct and start growing.

What makes the tumor model so realistic is its shape.

"The curvature of the pancreatic duct affects the behavior of cells. We could culture these cancer cells on a petri dish, but because the dish is flat, we wouldn't see the same behavior," said Han, who is the program leader of the Purdue University Center for Cancer Research and has a courtesy appointment in biomedical engineering.

The researchers saw that after two different cancer cell types merged into the pancreatic tumor model device, these cells became more invasive and sprouted from the duct to form tumors.

Since cancer is technically a group of diseases, and pancreatic cancer involves four major driver mutations, Han's team plans to further explore how each of these mutations interacts with each other. The tumor model also can be used as a prescreening tool to discover new drug targets for better drugs, Han said.

A patent has been issued for the pancreatic tumor model via the Purdue Research Foundation Office of Technology Commercialization.

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