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全基因组连锁扫描结果:支持9号和11号染色体位点增加吸烟风险。

Results of a genomewide linkage scan: support for chromosomes 9 and 11 loci increasing risk for cigarette smoking.

作者信息

Gelernter Joel, Liu Xuexuan, Hesselbrock Victor, Page Grier P, Goddard Andrew, Zhang Heping

机构信息

Department of Psychiatry, Yale University School of Medicine, VA Psychiatry 116A2, 950 Campbell Avenue, West Haven, CT 06516, USA.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):94-101. doi: 10.1002/ajmg.b.30019.

Abstract

UNLABELLED

Cigarette smoking is highly destructive to individuals and society, and is moderately heritable. We completed a genomewide linkage scan to map loci increasing risk for cigarette smoking in a set of families originally identified because they segregate panic disorder (PD). One hundred forty two genotyped individuals in a total of 12 families were studied (214 subjects analyzed, including non-genotyped individuals). Of these individuals, 69 were "affected" with habitual cigarette smoking (i.e., they smoked more than one pack per day for at least a year, or at least 1/2 pack per day for at least 10 years), 49 were "unaffected" (i.e., they smoked less than 1/2 pack per day for less than 1 year), and 24 were scored as "unknown." Nine families from the panic series were excluded from these analyses because they lacked multiple affected individuals with habitual cigarette smoking. In an initial genomewide scan, we genotyped a total of 416 markers (398 autosomal, 18 X-chromosome) with an average spacing of less than 10 cM, spanning the genome. Linkage analysis (pairwise, or single-point, and multi-point) was performed using ALLEGRO. An additional 14 markers were genotyped in a high-density panel to follow-up on an identified region of interest on chromosome 11p. The three highest multi-point Zlr scores (3.43, 3.04, and 3.01; P = 0.0003, P = 0.0012, and P = 0.0013, respectively), which each reflect "suggestive" evidence for linkage, were observed in multi-point linkage analyses using Allegro on chromosomes 11p and 9, near markers D11S4046, D9S283, and D9S1677, respectively. D11S4046 is in a region where linkage to alcohol dependence and linkage disequilibrium to substance dependence have previously been identified. The chromosome 9 region we identified as possibly linked to cigarette smoking in anxiety families, was previously identified as significantly linked to PD in Icelandic pedigrees. We also identified evidence supporting linkage (Zlr score > 2.3, P < 0.01) to regions of chromosomes 14, 16, and X. There was a significant phenotypic association between PD and cigarette smoking (P < 0.001).

CONCLUSIONS

We identified evidence for two loci increasing risk for cigarette smoking that map to chromosomes 9 and 11. There is now evidence supporting linkage or association of chromosome 11 markers with alcohol dependence, illegal drug abuse and dependence, and cigarette smoking. Interestingly, one of our most promising linkage regions, includes a region previously identified as linked to PD.

摘要

未标注

吸烟对个人和社会具有极大的破坏性,且具有中等程度的遗传性。我们完成了一项全基因组连锁扫描,以在一组最初因分离惊恐障碍(PD)而被识别的家庭中绘制增加吸烟风险的基因座。对总共12个家庭中的142名基因分型个体进行了研究(共分析了214名受试者,包括未进行基因分型的个体)。在这些个体中,69名“受影响”于习惯性吸烟(即他们每天吸烟超过一包至少一年,或每天至少半包至少10年),49名“未受影响”(即他们每天吸烟少于半包少于1年),24名得分“未知”。来自惊恐系列的9个家庭被排除在这些分析之外,因为它们缺乏多个患有习惯性吸烟的受影响个体。在最初的全基因组扫描中,我们对总共416个标记(398个常染色体标记,18个X染色体标记)进行了基因分型,平均间距小于10厘摩,覆盖整个基因组。使用ALLEGRO进行连锁分析(成对或单点以及多点分析)。在一个高密度面板中对另外14个标记进行了基因分型,以对在11号染色体p区域识别出的感兴趣区域进行后续研究。在使用Allegro对11号染色体p和9号染色体进行的多点连锁分析中,分别在标记D11S4046、D9S283和D9S1677附近观察到三个最高的多点Zlr分数(分别为3.43、3.04和3.01;P = 0.0003、P = 0.0012和P = 0.0013),每个分数都反映了连锁的“提示性”证据。D11S4046位于一个先前已确定与酒精依赖连锁以及与物质依赖连锁不平衡的区域。我们在焦虑症家庭中确定可能与吸烟连锁的9号染色体区域,先前在冰岛家系中已被确定与PD显著连锁。我们还确定了支持与14号、16号染色体和X染色体区域连锁的证据(Zlr分数> 2.3,P < 0.01)。PD与吸烟之间存在显著的表型关联(P < 0.001)。

结论

我们确定了两个增加吸烟风险的基因座的证据,它们定位于9号和11号染色体。现在有证据支持11号染色体标记与酒精依赖、非法药物滥用和依赖以及吸烟之间的连锁或关联。有趣的是,我们最有希望的连锁区域之一包括一个先前已确定与PD连锁的区域。

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