Shawdesh desk:

During a recent study an international team of scientists shed light on how genes can contribute to type-2 diabetes. The findings of the study were published in the journal, ‘Nature Genetics’. “Our findings matter because we’re moving toward using genetic scores to weigh up a person’s risk of diabetes,” said co-author Cassandra Spracklen, assistant professor of biostatistics and epidemiology at the UMass Amherst School of Public Health and Health Sciences.

The meta-analysis by the DIAMANTE (DIabetes Meta-ANalysis of Trans-Ethnic association studies) Consortium of 122 different genome-wide association studies (GWAS) was co-led by Andrew Morris, professor of statistical genetics at The University of Manchester, and University of Oxford professors Mark McCarthy and Anubha Mahajan.

“The global prevalence of type 2 diabetes, a life-changing disease, has quadrupled over the last 30 years, affecting approximately 392 million people in 2015,” Morris said.

The research is a major step toward the ultimate goal of identifying novel genes and understanding the biology of the disease, which has the potential to help scientists develop new treatments.

It is also an important milestone in the development of “genetic risk scores” to identify individuals who are more predisposed to develop type 2 diabetes, regardless of their population background.

The meta-analysis compared the DNA of almost 181,000 people with type 2 diabetes against 1.16 million people who didn’t have the disease. Searching across the entire human genome for sets of genetic markers called single nucleotide polymorphisms, or SNPs, genome-wide association studies look for genetic differences between people with and without a disease.

The technique allows scientists to zero in on parts of the genome involved in disease risk, which helps pinpoint the genes that cause the disease.

However, the largest genome-wide association studies of type 2 diabetes historically have involved the DNA of people of European descent, which has limited progress in understanding the disease in other population groups.

To address this bias, scientists from the DIAMANTE Consortium assembled the world’s most diverse collection of genetic information on the disease, with almost 50 per cent of individuals from East Asian, African, South Asian and Hispanic population groups.

The meta-analysis compared the DNA of almost 181,000 people with type 2 diabetes against 1.16 million people who didn’t have the disease. Searching across the entire human genome for sets of genetic markers called single nucleotide polymorphisms, or SNPs, genome-wide association studies look for genetic differences between people with and without a disease.

The technique allows scientists to zero in on parts of the genome involved in disease risk, which helps pinpoint the genes that cause the disease.

However, the largest genome-wide association studies of type 2 diabetes historically have involved the DNA of people of European descent, which has limited progress in understanding the disease in other population groups.

To address this bias, scientists from the DIAMANTE Consortium assembled the world’s most diverse collection of genetic information on the disease, with almost 50 per cent of individuals from East Asian, African, South Asian and Hispanic population groups.

Mahajan added, “We have now identified 117 genes that are likely to cause Type 2 diabetes, 40 of which have not been reported before. That is why we feel this constitutes a major step forward in understanding the biology of this disease.”

Source: ANI