Researchers find gene mutation that appears to increase risk of type 2 diabetes

by Barbara Hewitt on May 29, 2014

Researchers in the United States have identified a mutation in a fat storage gene that appears to increase the risk of developing type 2 diabetes and other metabolic disorders.

The team from the University of Maryland School of Medicine discovered the mutation in the hormone sensitive lipase (HSL) gene by studying the DNA of more than 2,700 people in the Old Order Amish community in Pennsylvania.

HSL is a key enzyme involved in breaking down stored fat

The Old Order Amish are regarded as ideal for genetic studies because they are a genetically homogenous population who trace their ancestry back 14 generations to a small group who came to Pennsylvania from Europe in the middle of the eighteenth century.

HSL is a key enzyme involved in breaking down stored fat, known as triglycerides, into fatty acids, thereby releasing energy for use by other cells.

‘We found that Amish people with this mutation have defects in fat storage, increased fat in the liver, high triglycerides, low good cholesterol, insulin resistance and increased risk of developing type 2 diabetes,’ said Coleen Damcott, an assistant professor of medicine in the Division of Endocrinology, Diabetes and Nutrition and member of the Programme for Personalized and Genomic Medicine at the University of Maryland School of Medicine.

In the study 5.1% of the Old Order Amish study participants had at least one copy of the mutation. Four people had two copies of the mutation and consequently produced no HSL enzyme.

Damcott pointed out that the mutation is less common in non-Amish Caucasians of European descent (0.2%), thus the higher prevalence of the mutation in the Amish makes it possible to characterise its full range of effects.

‘Future studies of this gene will allow us to look more closely at the effects of its deficiency on human metabolism to better understand the function of the HSL protein and its impact on fat and glucose metabolism. These studies will also examine the potential of using HSL as a drug target for treating type 2 diabetes and related complications,’ she explained.

She also pointed out that type 2 diabetes is a complex disease whose susceptibility is often determined by interactions between genetics and lifestyle factors, such as over eating and physical inactivity. Susceptibility genes for diabetes may be involved in several different metabolic pathways in the body, including storage and release of fat for energy.

The discovery of this mutation adds to the growing list of insights gained from genomic studies that can be used to develop new treatments and customize existing treatments for type 2 diabetes and related metabolic disorders,’ Damcott added.

 

Co-author Alan Shuldiner, Professor of Medicine, and his colleagues at the University of Maryland School of Medicine have previously identified a number of susceptibility genes for diabetes as well as for obesity, high blood pressure and other complex diseases.

In 2008, they discovered a novel gene mutation among the Old Order Amish population that significantly reduces the level of triglycerides in the blood and appears to help prevent cardiovascular disease. Shuldiner’s team has been conducting genetic research with the Old Order Amish in Pennsylvania since the early 1990s.


The opinions expressed in this article do not necessarily reflect the views of the DiabetesForum.com Community and should not be interpreted as medical advice. Please see your doctor before making any changes to your diabetes management plan.

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