Of all the specific candidate genes shown in one study or another to be associated with bipolar disorder, at this point, none of these findings have been robust enough or tested in large enough samples to definitively implicate them in the genesis of bipolar disorder. Genome-wide association studies Recently, with the advent of genetic chips that can analyze over 500 000 SNPs, and the knowledge-base provided by analysis of the human genome, it, has become possible to construct GWÀ studies in outbred populations. In this approach, a case-control or trio approach (affected subjects, Inhibitors,research,lifescience,medical plus their parents) is utilized, typically requiring thousands

of subjects, and 500 000 or more SNPs arc analyzed in order to determine specific genes or regions associated with a disorder. The approach has recently provided promising results in studies of type II diabetes, cancer, and other medical conditions which can be classified as common and complex diseases, and this has led to Carboplatin supplier efforts in the United States, the United Kingdom, and Inhibitors,research,lifescience,medical elsewhere, to pursue GWA studies on a large scale.100,101 The potential advantage

of whole-genome association studies is that such studies may be able to pick out. associations of genes that do not. have major effect, on a. disease, and (if the sample size is big enough) potentially overcome complications Inhibitors,research,lifescience,medical when disorders are multigcnic. On the other hand, sample sizes needed for analyses may be difficult, to reach without major investments, the cost, of the technology is not. trivial, rare alleles with major effects may be overlooked, stratification issues and multiple testing issues Inhibitors,research,lifescience,medical become even more critical than in linkage studies, selection of individual cases may dilute the study of “genetic” forms of bipolar disorder, and replication will remain a difficult issue, leading some to temper the expectations we might expect from GWA analyses.102 GWA studies in bipolar disorder were initially pursued in the Inhibitors,research,lifescience,medical Costa Rican population, with microsatellitcs placed relatively sparsely across the genome.103-105

Although these studies yielded potentially interesting isothipendyl linkage disequilibrium between bipolar disorder and specific chromosomal regions, the sparseness of the map did not. allow specific genes to be implicated at the screening level. Two recent. GWA studies of bipolar disorder, using dense SNP maps, have been reported thus far. Baum et al106 used a. two-stage strategy, beginning with 461 bipolar cases and 563 controls and following up significant findings in a sample of 772 bipolar cases and 876 controls, and found evidence for novel genes potentially associated with bipolar disorder, including a gene for diacylglycerol kinase, which plays a key role in the lithium sensitive phosphatidyl inositol pathway.