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最大吸烟量表型的遗传分析。

Genetic analysis of maximum cigarette-use phenotypes.

作者信息

Saccone Nancy L, Neuman Rosalind J, Saccone Scott F, Rice John P

机构信息

Department of Genetics, Washington University School of Medicine, St, Louis, Missouri, USA.

出版信息

BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S105. doi: 10.1186/1471-2156-4-S1-S105.

Abstract

BACKGROUND

Using the Framingham Heart Study data set provided for Genetic Analysis Workshop 13, we defined the cigarette-use phenotype M for smokers to be the maximum number of cigarettes-per-day (MAXCIG) reported over the longitudinal course of the study. Adjustments were made for the significant covariates of gender and year of birth, and sib-pair based linkage analysis was performed.

RESULTS

The primary analyses, in which individuals with MAXCIG = 0 were considered to have missing phenotype, resulted in modest linkage evidence, with LOD scores over 1 on chromosomes 5, 9, 13, 14, and 22.

CONCLUSIONS

While the results reported here do not indicate definitive evidence for linkage to specific chromosomal regions, future studies may find it useful to include direct assessments of maximum and quantitative cigarette use. In defining and analyzing quantitative or "maximum use" phenotypes, the choice of how to handle individuals with MAXCIG = 0, or alternatively, individuals who are substance-naive, is a crucial one for genetic studies of nicotine and other substance use. In this study, the linkage results vary greatly depending on whether or not these "unexposed" individuals are included in the analyses.

摘要

背景

利用为遗传分析研讨会13提供的弗明汉心脏研究数据集,我们将吸烟者的吸烟使用表型M定义为研究纵向过程中报告的每日最大吸烟量(MAXCIG)。对性别和出生年份这些显著协变量进行了调整,并进行了基于同胞对的连锁分析。

结果

主要分析中,将MAXCIG = 0的个体视为表型缺失,结果显示连锁证据较弱,在5号、9号、13号、14号和22号染色体上的LOD得分超过1。

结论

虽然此处报告的结果并未表明与特定染色体区域连锁的确切证据,但未来的研究可能会发现,纳入对最大吸烟量和定量吸烟使用的直接评估是有用的。在定义和分析定量或“最大使用量”表型时,对于尼古丁和其他物质使用的遗传研究而言,如何处理MAXCIG = 0的个体或从未接触过物质的个体是一个关键问题。在本研究中,连锁结果根据这些“未接触者”是否纳入分析而有很大差异。

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Genetic analysis of maximum cigarette-use phenotypes.最大吸烟量表型的遗传分析。
BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S105. doi: 10.1186/1471-2156-4-S1-S105.

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