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首页> 外文期刊>Biological psychiatry >Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10.
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Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10.

机译:非洲裔美国人酒精依赖的全基因组连锁扫描:10号染色体上的显着连锁。

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摘要

BACKGROUND: Alcohol dependence (AD) is costly to societies worldwide, moderately heritable, and genetically complex. Risk loci in several populations have been identified with genetic linkage analysis. To date, there has been no published linkage study of AD focused on African Americans (AAs). METHODS: We completed a genomewide linkage scan with approximately 6000 single nucleotide polymorphism markers to map loci increasing risk for DSM-IV AD in a set of 238 small nuclear families ascertained on the basis of multiple individuals affected with cocaine or opioid dependence. Model free linkage analysis was completed with Merlin software. A modified marker set was used to avoid bias due to markers in strong linkage disequilibrium. RESULTS: We identified a genomewide-significant linkage to markers near 117.2 centiMorgans on chromosome 10q23.3-24.1 (logarithm of odds score 3.32; p = 5.0E-05; empirical genomewide p = .033). CONCLUSIONS: These data add to the growing evidence for locations for AD risk loci and provide the first linkage evidence for such a locus in the AA population.
机译:背景:酒精依赖症(AD)对全世界的社会来说都是昂贵的,具有适度的遗传性和遗传复杂性。已经通过遗传连锁分析确定了几个人群中的风险基因座。迄今为止,还没有公开的针对非裔美国人(AA)的AD关联研究。方法:我们用大约6000个单核苷酸多态性标记物完成了全基因组连锁扫描,以绘制在238个小核科家族中,根据多个受可卡因或阿片类药物依赖影响的个体确定的DSM-IV AD风险增加的位点图。使用Merlin软件完成了无模型链接分析。使用改良的标记集来避免由于强连锁不平衡中的标记引起的偏倚。结果:我们确定了全基因组与染色体10q23.3-24.1上117.2厘摩附近标记的显着连锁(对数得分为3.32; p = 5.0E-05;全基因组经验性p = .033)。结论:这些数据增加了AD风险基因座位置的证据,并为AA人群中此类基因座提供了第一个连锁证据。

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