Sunday, January 19, 2020

Researchers identify new prevention strategy for type 1 diabetes

A protein newly identified as important in type 1 diabetes can delay onset of the disease in diabetic mice, providing a new target for prevention and treatment in people, according to research led by scientists at the U.S. Department of Energy's Pacific Northwest National Laboratory and Indiana University School of Medicine. Because type 1 diabetes is incurable and has serious lifelong health consequences, prevention is a major research goal.

The key to the new study, published online January 9, 2020, in the journal Cell Metabolism, is a technique called mass spectrometry, which can comprehensively detect proteins that are found at extremely low levels in the body, but can have large effects on health.

The multidisciplinary research team of physicians and biochemists used a new strategy to pinpoint proteins in beta cells, a subset of pancreatic islets that increase or decrease in response to immune system attack. Beta cells normally regulate blood sugar levels in the pancreas. In people susceptible to type 1 diabetes (previously called insulin-dependent or juvenile diabetes) these cells are slowly destroyed by the body's own immune system. Here, the researchers focused on how islets respond to inflammation.

The researchers treated human pancreatic islets with substances produced by the body and thought to be involved in the diabetes disease process. They identified a total of 11,324 proteins, with 387 affected by the treatment. Of these 387, they narrowed their focus to one: growth differentiation factor 15 (GDF15).

We wanted to identify proteins that can intervene in the diabetes disease process. We became interested in GDF15 because the protein level was suppressed by 70 percent after treatment. Ernesto Nakayasu, a biomedical scientist at PNNL and co-lead author of the study      

              GDF15 is known for its protective effects in different types of cells in the human body but it had never been studied in islets. When the researchers measured levels of GDF15 in pancreas tissue from people with diabetes, they found the protein was depleted in their malfunctioning islet cells.

But the key piece of evidence emerged when the scientists treated non-obese diabetic mice withGDF15, and it reduced development of diabetes by 53%. Non-obese diabetic mice are a common model for testing type 1 diabetes treatments because they spontaneously develop autoimmune diabetes with many similarities to the human disease. 

"We hypothesized that reduced GDF15 was not a good thing for islet survival, and indeed that was the case," said Raghu Mirmira, a study principal investigator. "This work opens the way for us to consider these sorts of 'islet protective factors' as therapies to prevent or reverse type 1 diabetes." 

Mirmira until recently served as professor of pediatric diabetes and director of the Center for Diabetes and Metabolic Diseases at Indiana University School of Medicine. He is now a professor of medicine in the Section of Endocrinology, Diabetes & Metabolism at the University of Chicago

"This approach differs substantially from current thinking that targets the immune system. While GDF15 may be one new therapy, we identified other proteins that may work in conjunction with GDF15, so this work really represents a treasure-trove of information that can be mined for new therapies," said Mirmira.PNNL's Tom Metz, the co-principal investigator and an expert in mass spectrometry-based proteomics of islets, agreed, adding:

This study illustrates the power of non-reductionist, comprehensive approaches, such as proteomics, for discovering new information in complex systems. The protective role of GDF15 against islet destruction and its ability to delay onset of type 1 diabetes in the mouse model would have been very difficult to discover without performing the initial comprehensive proteomics analysis of stressed human islets.
The researchers are now working on the idea that low levels of GDF15 in islets may somehow be playing a proactive role in instigating the autoimmune attack that ultimately kills them.This thinking is somewhat counterintuitive in the type 1 diabetes field, but it is this kind of out-of-the-box thinking that may lead to therapies we never thought of previously.Raghu Mirmira, a study principal investigator.

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Sunday, August 25, 2019

Scientists identify unique pathway for treating deadly brain cancer in kids

Researchers have discovered a new pathway that can attack and improve survival rate in an incurable type of brain cancer among children.

The study suggested that the pathway disrupts the cellular process that contributes to Diffuse Intrinsic Pontine Gliomas (DIPG).


DIPG is a highly aggressive and inoperable type of tumour that grows in the brain stem and usually strikes children less than 10 years old. Most patients do not survive more than a year after diagnosis.


Earlier studies identified a genetic mutation called PPM1D- which is critical for cell growth and cell stress response-- as a contributor to DIPG. Previous efforts to directly attack the PPM1D mutation, however, proved futile in controlling DIPG.


This study has discovered a vulnerability in the metabolic process for creating NAD,, a metabolite that is necessary for all cell life.


This is really an amazing new way to attack this cancer. We found that the mutated gene PPM1D essentially sets the stage for its own demise, said one the study authors.


Researchers found that mutated PPM1D silences a gene called NAPRT, which is key to the production of the NAD metabolite. With NAPRT unavailable, the cell switches to another protein needed to create NAD called NAMPT. By using a drug that inhibits the production of NAMPT, researchers found they could essentially starve to death those cancer cells with the PPM1D mutation.


Researchers had long thought DIPG was a childhood version of adult brain tumours, and so similar treatments for adult gliomas were tested extensively in children and failed. 


The researchers chose to look at the tumour in terms of its potential vulnerabilities, and  thus began a year-ling molecular journey to understand what role the PPM1D mutation played in altering cancer metabolism.


When epigenetic silencing results were analysed, we were gratified to discover that DIPG cells with the PPM1D mutation had created a vulnerability to a key enzyme for which small molecule inhibitors were already available, said one the study's contributing authors.


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Saturday, May 25, 2019

Bipolar Disorder a Risk Factor for Parkinson’s?

Struggling with bipolar disorder is hard enough, but now a new study suggests these patients are seven times more likely to develop Parkinson's disease.

But U.S. experts cautioned that the absolute risk of developing Parkinson's -- an incurable movement disease -- is still very low for those with the mood disorder.

"I wasn't surprised [by the study's findings], because similar disorders like major depression and anxiety disorder convey a similar increased risk of Parkinson's later in life," said a Dr. "This gives you two reasons to treat bipolar disorder aggressively," he added. 

Also known as manic-depressive illness, bipolar disorder is a mood disorder marked by swings from elated, energized behavior to feelings of sadness and hopelessness. It affects about 2.6% of American adults, according to the researchers.

Parkinson's is a progressive condition causing tremors, rigid muscles and slowed movement, among other symptoms. By 2030, the Parkinson's Foundation projects 1.2 million Americans will be living with the disease.

For the study, researchers  reviewed health records for 56,000 people  who were diagnosed with bipolar disorder between 2001 and 2009. They were compared to 225,000 people with no history of bipolar or Parkinson's. Both groups were tracked until late 2011.

During the study period, 372 people with bipolar disorder -- or 0.7% -- developed Parkinson's. This compared to 222 -- or 0.1% -- of those who didn't have bipolar disorder.

Those with bipolar who developed Parkinson's were nine years younger -- average age 64 -- than others who also developed Parkinson's, the study found.

"When you say there's seven times the risk, it gets scary. But it's still very few [bipolar] patients who get Parkinson's," said a Dr., who reviewed the findings. He's a neurologist specializing in movement disorders and Parkinson's disease. He pointed out that while the study was large, it was limited by including only people in Taiwan.

"We don't know how this would apply more globally or broadly," he said. "I think it's more interesting for physicians to know this and be more aware of the association."

The author said scientists have many theories -- still unproven -- about how bipolar disorder might be connected to the development of Parkinson's. 

"A depressive or manic episode may do something to the brain that renders it more vulnerable" to Parkinson's over time, he said.

And he noted that many medications used to treat bipolar disorder can trigger Parkinson's-like symptoms.

Many experts think Parkinson's is active years or decades before movement problems show up, and mood disorders such as bipolar may actually be an early symptom of Parkinson's, authors said. 

Much more research is still needed, they agreed.

"We definitely need to look more at a global population," he said. "The researchers here did follow patients for 10 years, but it needs to be extended longer to see how many of these patients convert to Parkinson's down the road."

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Wednesday, December 12, 2018

Coffee compounds could fight Parkinson's and dementia

Researchers have found a compound in coffee that may team up with caffeine to fight Parkinson’s disease and Lewy body dementia—two progressive and currently incurable diseases associated with brain degeneration.

While caffeine has traditionally been credited as coffee’s special protective agent, coffee beans contain more than a thousand other compounds that are less well known.

The study, suggests these two compounds combined may become a therapeutic option to slow brain degeneration. 

Lead author said prior research has shown that drinking coffee may reduce the risk of developing Parkinson’s disease. 

Parkinson’s disease is a brain disorder that can lead to shaking, stiffness and difficulty with walking, balance and coordination. Nearly one million people in the United States are living with Parkinson’s disease. Lewy body dementia, one of the most common forms of dementia, affects more than one million people in the United States. It causes problems with thinking, behavior, mood, and movement.

The study focused on a fatty acid derivative of the neurotransmitter serotonin, called EHT (Eicosanoyl-5-hydroxytryptamide), found in the bean’s waxy coating. The team found that EHT protects the brains of mice against abnormal protein accumulation associated with Parkinson’s disease and Lewy body dementia.

The team studied whether EHT and caffeine could work together for even greater brain protection. They gave mice small doses of caffeine or EHT separately as well as together. Each compound alone was not effective, but when given together they boosted the activity of a catalyst that helps prevent the accumulation of harmful proteins in the brain. This suggests the combination of EHT and caffeine may be able to slow or stop the progression of these diseases. Current treatments address only the symptoms of Parkinson’s disease but do not protect against brain degeneration.

The researcher said further research is needed to determine the proper amounts and ratio of EHT and caffeine required for the protective effect in people. “EHT is a compound found in various types of coffee but the amount varies. It is important that the appropriate amount and ratio be determined so people don’t over-caffeinate themselves, as that can have negative health consequences,” she said.

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Friday, June 09, 2017

A new blood test can predict the onset & track progression of Huntington's disease

In a first, a blood test that can predict the onset and track progression of Huntington's disease has been developed.

The finding may help identify new treatments for the genetic brain disorder, which is fatal and currently incurable.

Huntington's disease is an inherited condition in which nerve cells in the brain break down over time.

The study showed that measuring the levels of neurofilament -- a protein released from damaged brain cells -- may help predict the onset of the disease as well as its progression.

"This is the first time a potential blood biomarker has been identified to track Huntington's disease so strongly," said Edward Wild from the University College London.

The results showed that the patients who were carriers of the genetic mutation of the disease had neurofilament concentrations that were 2.6 times that of the control participants.

Further, the level rose throughout the disease course from premanifest to stage 2 disease, the researchers said.

"Neurofilament has the potential to serve as a speedometer in Huntington's disease, since a single blood test reflects how quickly the brain is changing," Wild added.

For the study, published in the journal Lancet Neurology, the team measured neurofilament levels in blood samples from 366 volunteers who were followed for three years.

In the group who had no symptoms at the start of the study, the level of neurofilament predicted subsequent disease onset, as volunteers with high neurofilament levels in the blood at the start were more likely to develop symptoms in the following three years.

Scientists are presently in the process of testing a new generation of so-called 'gene silencing' drugs that may put brakes on the disease.

"Measuring neurofilament levels could help us figure out whether those brakes are working," Wild noted.

  this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   
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In a first, a blood test that can predict the onset and track progression of Huntington's disease has been developed.

The finding may help identify new treatments for the genetic brain disorder, which is fatal and currently incurable.

Huntington's disease is an inherited condition in which nerve cells in the brain break down over time.

The study showed that measuring the levels of neurofilament -- a protein released from damaged brain cells -- may help pre ..

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