通过对巴勒斯坦阿拉伯人群中22号染色体微卫星标记D22S278与双相情感障碍的传递不平衡测试分析,证明了这种联系。

American Journal of Medical Genetics Pub Date : 2000-12-04
M Mujaheed, M Corbex, P Lichtenberg, D F Levinson, J F Deleuze, J Mallet, R P Ebstein
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引用次数: 0

摘要

许多连锁研究表明,精神分裂症易感性位点在22号染色体上,特别是微卫星标记D22S278 (22q12)。除了该地区与精神分裂症相关的一些证据外,还报道了使用该标记与双相情感障碍相关的证据。我们测试了从巴勒斯坦阿拉伯人群中招募的60个双相情感障碍I型三联症患者和79个双相情感障碍I型和双相情感障碍II型三联症患者与D22S278标记的联系。通过双相I型(P = 0.031)和双相I型和双相II型扩展组(P = 0.041)的多等位基因标记扩展传递不平衡测试(ETDT),观察到显著的连锁关系。这些微弱的阳性结果至少与22号染色体的这个区域可能是两种主要精神病的易感性位点的假设相一致,应该考虑进行更深入的研究。点。J. Med. Genet。(Neuropsychiatr。[j] .科学与技术,2000。
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Evidence for linkage by transmission disequilibrium test analysis of a chromosome 22 microsatellite marker D22S278 and bipolar disorder in a Palestinian Arab population.

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. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 96:836-838, 2000.

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