Genetics and Bipolar Disorder
The Link Between Genetics and Bipolar Disorder
There is a growing pool of researchers and scientists focusing on genetics and bipolar disorder. There is increasing evidence for a genetic component in the causation of bipolar disorder.
One way that genetics and bipolar disease are researched is to perform twin studies and gene linkage studies.
In specific terms, the monozygotic concordance rate for the disorder is seventy percent. That means that if someone has bipolar disorder, their identical twin has a seventy percent likelihood of having the disorder as well. Recent studies have shown a lower rate, of around 40 percent, and these types of twin studies are ongoing.
Genetics and bipolar disorder are studied through gene research as well. In 2003, for example, a group of American and Canadian researchers published a paper that used gene linkage techniques to identify a mutation in the GRK3 gene as a possible cause of as many as ten percent of bipolar disorder cases. Discovering the link in this gene is significant in pushing forward understanding of bipolar disorder in general.
The identified gene is associated with a kinase enzyme called G protein receptor kinase 3, which appears to be involved in dopamine metabolism. This is important because it may provide a possible means of creating new drugs to treat bipolar disorder.
In addition, genetics and bipolar disorder were also studied in a 2007 gene linkage study. This study, by an international team coordinated by the National Institute of Mental Health, identified a number of genes likely to also be involved in bipolar disorder, suggesting that the disorder may be related to multiple genes.
Generally speaking, the link between genetics and bipolar disorder has not been completely established, but it is clear that there has been progress in the research. There are many promising studies that look to link genes and the disorder, so that treatment can be more targeted and diagnosis can be more conclusive.