Wang S, Sun C E, Walczak C A, Ziegle J S, Kipps B R, Goldin L R, Diehl S R
Molecular Epidemiology and Disease Indicators Branch, NIDR, Bethesda, Maryland 20892, USA.
Nat Genet. 1995 May;10(1):41-6. doi: 10.1038/ng0595-41.
We have performed linkage analysis in 186 multiplex families to search for genes that predispose to schizophrenia. Under a model with partially dominant inheritance, moderately broad disease definition and assuming locus homogeneity, a lod score of 3.2 was obtained for D6S260 on chromosome 6p23. A multipoint lod score of 3.9 (P = 2.3 x 10(-5)) was achieved when the F13A1 and D6S260 loci were analysed, allowing for locus heterogeneity. Adjusted for testing of multiple models, the multipoint lod score of 3.9 under heterogeneity has a genome wide significance of between 5-8%. The nonparametric affected pedigree member test provided results (P = 3 x 10(-4)) also supporting this finding. Our findings provide supportive evidence for a susceptibility locus for schizophrenia on distal chromosome 6p, and support a model of locus heterogeneity.
我们对186个多重家庭进行了连锁分析,以寻找易患精神分裂症的基因。在部分显性遗传模型、适度宽泛的疾病定义并假设基因座同质性的情况下,位于6号染色体6p23的D6S260获得了3.2的对数优势比分。当分析F13A1和D6S260基因座时,考虑到基因座异质性,获得了3.9的多点对数优势比分(P = 2.3 x 10(-5))。针对多个模型的检验进行调整后,异质性下3.9的多点对数优势比分在全基因组中的显著性为5%-8%。非参数受影响家系成员检验也得出了支持这一发现的结果(P = 3 x 10(-4))。我们的研究结果为6号染色体远端存在精神分裂症易感基因座提供了支持性证据,并支持基因座异质性模型。