December 21, 2011
Rare Genetic Mutations Linked To Bipolar Disorder
An international team of scientists, led by researchers at the University of California, San Diego School of Medicine, reports that abnormal sequences of DNA known as rare copy number variants, or CNVs, appear to play a significant role in the risk for early onset bipolar disorder.
The findings will be published in the Dec. 22 issue of the journal Neuron.
Principal investigator Jonathan Sebat, PhD, assistant professor of psychiatry and cellular and molecular medicine at UC San Diego's Institute of Genomic Medicine, and colleagues, found that de novo CNVs contribute significant genetic risk in about 5 percent of early onset bipolar disorder, which appears in childhood or early adulthood.
In other words, said the study's first author Dheeraj Malhotra, assistant project scientist in Sebat's lab, "having a de novo mutation increases the chances of having an earlier onset of disease."
The cause or causes of bipolar disorder remain unclear. There is a clear genetic component — the disease runs in families — but previous studies that have focused mainly on common inherited variants have met with limited success in identifying key susceptibility genes.
Malhotra said that — while the findings do not conclusively pinpoint a specific gene or genomic region -- the new findings show "convincing" evidence that rare copy number mutations strongly contribute to the development of early onset bipolar disorder. He added that sequencing of complete genomes or exomes of large number of bipolar families is needed to determine the total genetic contribution of all forms of de novo mutation to risk for bipolar disorder.
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