Evidence for linkage by transmission disequilibrium test analysis of a chromosome 22 microsatellite marker D22S278 and bipolar disorder in a Palestinian Arab population.
Author: Mujaheed M, Corbex M, Lichtenberg P, Levinson DF, Deleuze JF, Mallet J, Ebstein RP.
Source:
American journal of medical genetics, 96(6), 836-838.
A number of linkage studies suggest a schizophrenia susceptibility locus on
chromosome 22, particularly with microsatellite marker D22S278 (22q12). In
addition to some evidence for linkage to schizophrenia in this region, linkage to
bipolar disorder using this marker has also been reported. We tested a group of
60 Bipolar I triads and an expanded group of 79 Bipolar I and Bipolar II triads
recruited from a Palestinian Arab population for linkage with the D22S278 marker.
Significant linkage was observed using the extended transmission disequilibrium
test for multiallelic markers (ETDT) for both Bipolar I (P = 0.031) and the
expanded group of Bipolar I and Bipolar II (P = 0.041). These weakly positive
results are at least consistent with the hypothesis that this region of
chromosome 22 might harbor a susceptibility locus for both major psychoses and
should be considered for more intensive study