Shink E, Morissette J, Sherrington R, Barden N
Neuroscience, CHUL Research Centre and Laval University, CHUQ Pavillon CHUL, Ste-Foy, Québec, Canada.
Mol Psychiatry. 2005 Jun;10(6):545-52. doi: 10.1038/sj.mp.4001601.
Our previous results pointed to a putative gene for susceptibility to bipolar affective disorder located on the chromosomal region 12q23-q24 that segregated in the Saguenay-Lac-St-Jean population of Quebec. We report here results from a second genome-wide scan based on the analysis of 380 polymorphic microsatellite markers. For the purpose of this analysis, an additional 18 families were recruited from the Saguenay-Lac-St-Jean region and pooled to our previous sample to improve its statistical power, giving a total of 394 sampled individuals. This work confirms the presence of a susceptibility locus for affective disorder on chromosome 12q24 with parametric LOD score value of 3.35 at D12S378 when pedigrees were broken into nuclear families and analysed under a recessive segregation model. This result was supported by neighbouring markers and by a LOD score value of 5.05 at D12S378 under model-free analysis. Other regions of lower interest were indicated on chromosomes 2, 5, 7, 9, 10, 17 and 20.
我们之前的研究结果表明,在魁北克的萨格奈-拉克-圣让人群中,一个与双相情感障碍易感性相关的假定基因位于染色体区域12q23-q24。我们在此报告基于对380个多态性微卫星标记分析的第二次全基因组扫描结果。为了此次分析,从萨格奈-拉克-圣让地区额外招募了18个家庭,并与我们之前的样本合并以提高统计效力,最终共有394个采样个体。当系谱被拆分为核心家庭并在隐性遗传模式下进行分析时,这项工作证实了在染色体12q24上存在一个情感障碍易感基因座,在D12S378处的参数化对数优势(LOD)分值为3.35。相邻标记以及在无模型分析下D12S378处5.05的LOD分值支持了这一结果。在染色体2、5、7、9、10、17和20上也指出了其他较低关注度的区域。