Havill L M, Mahaney M C
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas 78227, USA.
BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S54. doi: 10.1186/1471-2156-4-S1-S54.
We used an approach for detecting genotype x environment interactions to detect and characterize genotype x age interaction in longitudinal measures of three well known cardiovascular risk factors: total plasma cholesterol (TC), systolic blood pressure (SBP), and body weight (Wgt). Our objectives were to determine if the same gene or suite of genes influences quantitative variation in each of these phenotypes in the 4th and 6th decades of life, to assess the impact of additive gene effects in these two decades, and to evaluate the stability of pleiotropic relationships among these phenotypes. Using the Framingham Heart Study data, we constructed two cross-sectional samples comprising individuals on whom these phenotypes were measured at ages 30-39 years (Original Cohort: exam 1, Offspring Cohort: exam 2) and at ages 50-59 years (Original Cohort: exam 11, Offspring Cohort: exam 5). We also constructed a longitudinal sample from the cross-sectional sample members for whom measures on these traits were available at both ages (i.e., 4th and 6th decades of life). Patterns of pleiotropy, inferred from genetic correlations between traits, differ between the two age classes. Further, additive genetic variance in SBP during the 4th decade of life is attributable to a different gene or suite of genes than during the 6th. The magnitude of the effect increases for SBP. Variation in TC and Wgt appear to be influenced by the same gene or genes in both decades. The magnitude of the effect is stable for TC, but increases dramatically with age for Wgt.
我们采用了一种检测基因型与环境相互作用的方法,来检测和描述三种著名心血管危险因素(总血浆胆固醇(TC)、收缩压(SBP)和体重(Wgt))纵向测量中的基因型与年龄相互作用。我们的目标是确定在生命的第4个和第6个十年中,同一基因或一组基因是否影响这些表型中每一个的数量变异,评估这两个十年中加性基因效应的影响,并评估这些表型之间多效性关联的稳定性。利用弗雷明汉心脏研究数据,我们构建了两个横断面样本,一个样本包括在30 - 39岁时测量这些表型的个体(原始队列:检查1,子代队列:检查2),另一个样本包括在50 - 59岁时测量这些表型的个体(原始队列:检查11,子代队列:检查5)。我们还从横断面样本成员中构建了一个纵向样本,这些成员在两个年龄(即生命的第4个和第6个十年)都有这些性状的测量数据。从性状之间的遗传相关性推断出的多效性模式在两个年龄组之间有所不同。此外,生命第4个十年期间SBP的加性遗传方差归因于与第6个十年不同的一个基因或一组基因。SBP的效应大小增加。TC和Wgt的变异在两个十年中似乎都受相同的一个或几个基因影响。TC的效应大小是稳定的,但Wgt的效应大小随年龄显著增加。