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A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26

机译:35个双相情感障碍家系的基因组筛选为染色体15q25-26上的易感基因座提供了重要证据

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摘要

Bipolar affective disorder is a heritable, relatively common, severe mood disorder with lifetime prevalence up to 4%. We report the results of a genome-wide linkage analysis conducted on a cohort of 35 Australian bipolar disorder families which identified evidence of significant linkage on chromosome 15q25-26 and suggestive evidence of linkage on chromosomes 4q, 6q and 13q. Subsequent fine-mapping of the chromosome 15q markers, using allele frequencies calculated from our cohort, gave significant results with a maximum two-point LOD score of 3.38 and multipoint LOD score of 4.58 for marker D15S130. Haplotype analysis based on pedigree-specific, identical-by-descent allele sharing, supported the location of a bipolar susceptibility gene within the Zmax-1 linkage confidence interval of 17 cM, or 6.2 Mb, between markers D15S979 and D15S816. Non-parametric and affecteds-only linkage analysis further verified the linkage signal in this region. A maximum NPL score of 3.38 (P= 0.0008) obtained at 107.16cM (near D15S130), and a maximum two-point LOD score of 2.97 obtained at marker D15S1004 (affecteds only), support the original genome-wide findings on chromosome 15q. These results are consistent with four independent positive linkage studies of mood and psychotic disorders, and raise the possibility that a common gene for susceptibility to bipolar disorder, and other psychiatric disorders may lie in this chromosome 15q25-26 region.
机译:双相情感障碍是一种遗传性,相对常见的严重情绪障碍,终生患病率高达4%。我们报告了对35个澳大利亚双相情感障碍家族进行的全基因组连锁分析的结果,该系列确定了染色体15q25-26上显着连锁的证据以及染色体4q,6q和13q上连锁的暗示性证据。随后使用根据我们的队列计算的等位基因频率对染色体15q标记进行精细映射,得出了显着结果,标记D15S130的最大两点LOD得分为3.38,多点LOD得分为4.58。基于血统特异性,相同的血统等位基因共享的单倍型分析支持双极易感基因在标记D15S979和D15S816之间的Zmax-1连锁置信区间17 cM(或6.2 Mb)内的定位。非参数和仅受影响的连锁分析进一步验证了该区域的连锁信号。在107.16cM(在D15S130附近)获得的最大NPL评分为3.38(P = 0.0008),在标记D15S1004(仅受影响)获得的最大两点LOD评分为2.97,支持了染色体15q上的原始全基因组发现。这些结果与对情绪和精神病的四个独立的正相关研究相一致,并增加了对双相情感障碍和其他精神病易感性的共同基因可能位于该染色体15q25-26区域的可能性。

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