Researchers complete largest genetic sequencing study of human disease
Posted: May 22, 2013 at 4:49 pm
Public release date: 22-May-2013 [ | E-mail | Share ]
Contact: e.lowry@qmul.ac.uk e.lowry@qmul.ac.uk 020-788-25378 Queen Mary, University of London
Researchers from Queen Mary, University of London have led the largest sequencing study of human disease to date, investigating the genetic basis of six autoimmune diseases.
The exact cause of these diseases autoimmune thyroid disease, coeliac disease, Crohn's disease, psoriasis, multiple sclerosis and type 1 diabetes is unknown, but is believed to be a complex combination of genetic and environmental factors. In each disease only aproportion of the heritability is explained by the identifiedgenetic variants. The techniques used to date, have generally identified common (in the population) variants of weak effect.
In this study, using high-throughput sequencing techniques,a global team of scientistssought to identify new variants, including rare and potentially high risk ones, in 25 previously identified risk genes in a sample of nearly 42,000 individuals (24,892 with autoimmune disease and 17,019 controls).
It has been suggested in the 'rare-variant synthetic genome-wide association hypothesis' that a small number of rare variants in risk genes are likely to be a major cause of the heritability of these conditions.
However, the study published today in the journal Nature, suggests that the genetic risk of these diseasesmore likely involves a complex combination of hundreds of weak-effect variants which are each common in the population.
The authors estimate that rare variants in these risk genes account for only around three per cent of the heritability of these conditions that can be explained by common variants.
David van Heel, Professor of Gastrointestinal Genetics at Barts and The London School of Medicine and Dentistry at Queen Mary and director of the Barts and The London Genome Centre, led the study. He said: "These results suggests that risk for these autoimmune diseases is not due to a few high-risk genetic variations but seems rather due to a random selection frommany common genetic variants which each have a weak effect.
"For each disease there are probably hundreds such variants and the genetic risk is likely to come from inheriting a large number of these variants from both parents. If this is the case then it maynever be possible to accurately predict an individual's genetic risk of these common autoimmune diseases. However, the results do provide important information about the biological basis of these conditions and the pathways involved, which could lead to the identification new drug targets."
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Researchers complete largest genetic sequencing study of human disease
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