Scientists pinpoint gene variations linked to higher risk of bipolar disorder

Public release date: 10-Oct-2012
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Contact: Eric Sauter
esauter@scripps.edu
267-337-3859
Scripps Research Institute

JUPITER, FL, October 10, 2012 Scientists from the Florida campus of The Scripps Research Institute (TSRI) have identified small variations in a number of genes that are closely linked to an increased risk of bipolar disorder, a mental illness that affects nearly six million Americans, according to the National Institute of Mental Health.

"Using samples from some 3,400 individuals, we identified several new variants in genes closely associated with bipolar disorder," said Scripps Florida Professor Ron Davis, who led the new study, which was published recently by the journal Translational Psychiatry.

A strong tendency towards bipolar disorder runs in families; children with a parent or sibling who has bipolar disorder are four to six times more likely to develop the illness, according to the National Institute of Mental Health.

While the genetic basis for bipolar disorder is complex and involves multiple genes, it appears to be associated with a biochemical pathway known as cyclic adenosine monophosphate (cAMP) signaling system. The Davis laboratory and others have previously shown that the cAMP signaling plays a critical role in learning and memory processes. The new study focused on this signaling pathway.

"As far as I know, this has not been done beforeto query a single signaling pathway," said Davis. "This is a new approach. The idea is if there are variants in one gene in the pathway that are associated with bipolar disorder, it makes sense there would be variants in other genes of the same signaling pathway also associated with the disorder."

The new study examined variations in 29 genes found in the two common types of bipolar disorderbipolar disorder I (the most common form and the most severe) and bipolar disorder II. Genes from a total of 1,172 individuals with bipolar disorder I; 516 individuals with bipolar disorder II; and 1,728 controls were analyzed.

Several statistically significant associations were noted between bipolar disorder I and variants in the PDE10A gene. Associations were also found between bipolar disorder II and variants in the DISC1 and GNAS genes.

Davis noted that the location of PDE10A gene expression in the striatum, the part of the brain associated with learning and memory, decision making and motivation, makes it especially interesting as a therapeutic target.

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The first author of the study, "Genetic Association of Cyclic AMP Signaling Genes with Bipolar Disorder," is Merry-Lynn McDonald of the Baylor College of Medicine. Other authors include Courtney MacMullen of TSRI, and Dajiang (Jeff) Liu and Suzanne M. Leal of the Baylor College of Medicine. For more information on the study, see http://www.nature.com/tp/journal/v2/n10/full/tp201292a.html.

The study was supported by the National Institutes of Health (grant number MH074791).

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Public release date: 10-Oct-2012
[ | E-mail | Share ]

Contact: Eric Sauter
esauter@scripps.edu
267-337-3859
Scripps Research Institute

JUPITER, FL, October 10, 2012 Scientists from the Florida campus of The Scripps Research Institute (TSRI) have identified small variations in a number of genes that are closely linked to an increased risk of bipolar disorder, a mental illness that affects nearly six million Americans, according to the National Institute of Mental Health.

"Using samples from some 3,400 individuals, we identified several new variants in genes closely associated with bipolar disorder," said Scripps Florida Professor Ron Davis, who led the new study, which was published recently by the journal Translational Psychiatry.

A strong tendency towards bipolar disorder runs in families; children with a parent or sibling who has bipolar disorder are four to six times more likely to develop the illness, according to the National Institute of Mental Health.

While the genetic basis for bipolar disorder is complex and involves multiple genes, it appears to be associated with a biochemical pathway known as cyclic adenosine monophosphate (cAMP) signaling system. The Davis laboratory and others have previously shown that the cAMP signaling plays a critical role in learning and memory processes. The new study focused on this signaling pathway.

"As far as I know, this has not been done beforeto query a single signaling pathway," said Davis. "This is a new approach. The idea is if there are variants in one gene in the pathway that are associated with bipolar disorder, it makes sense there would be variants in other genes of the same signaling pathway also associated with the disorder."

The new study examined variations in 29 genes found in the two common types of bipolar disorderbipolar disorder I (the most common form and the most severe) and bipolar disorder II. Genes from a total of 1,172 individuals with bipolar disorder I; 516 individuals with bipolar disorder II; and 1,728 controls were analyzed.

Several statistically significant associations were noted between bipolar disorder I and variants in the PDE10A gene. Associations were also found between bipolar disorder II and variants in the DISC1 and GNAS genes.

Davis noted that the location of PDE10A gene expression in the striatum, the part of the brain associated with learning and memory, decision making and motivation, makes it especially interesting as a therapeutic target.

###

The first author of the study, "Genetic Association of Cyclic AMP Signaling Genes with Bipolar Disorder," is Merry-Lynn McDonald of the Baylor College of Medicine. Other authors include Courtney MacMullen of TSRI, and Dajiang (Jeff) Liu and Suzanne M. Leal of the Baylor College of Medicine. For more information on the study, see http://www.nature.com/tp/journal/v2/n10/full/tp201292a.html.

The study was supported by the National Institutes of Health (grant number MH074791).

---

[ | E-mail | Share ]

?

AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Source: http://www.eurekalert.org/pub_releases/2012-10/sri-spg101012.php

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