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Multivariate models for human genetic analysis: aggregation coaggregation and tracking of systolic blood pressure and weight.

机译:用于人类遗传分析的多变量模型:聚集共聚集以及跟踪收缩压和体重。

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摘要

A multivariate path model parameterizing the sources of familial aggregation and coaggregation of systolic blood pressure and weight, as well as their tracking across time, is applied to longitudinal data collected in Muscatine, Iowa. Genetic, common household, and individual environmental effects, pleiotropy, and a direct regression effect of blood pressure on weight are parameterized. The sample consisted of 998 individuals distributed in 261 families of whom 601 were measured on four successive occasions. The data were divided with times 1 and 2 forming group 1, and times 3 and 4, group 2. Model fitting and estimation was performed using group 1, followed by testing the model and estimates using the data in group 2. Heritability estimates for systolic blood pressure and weight were .15 and .54, respectively. The genetic correlation between these traits was nonsignificant, but there was a significant direct regression effect. The results indicate that 30% of the full-sib correlation for systolic blood pressure is attributable to the aggregation of weight. In terms of tracking, 59% and 60% of the predicted systolic blood pressure and weight correlations, respectively, were attributable to genetic effects. Testing the model from group 1 in group 2 indicates that the qualitative relationships between blood pressure and weight are stable with time.
机译:将参数化收缩压和体重的家族聚集和共聚集的来源以及它们随时间变化的跟踪的多元路径模型应用于在爱荷华州马斯卡汀收集的纵向数据。参数化遗传,普通家庭和个人的环境影响,多效性以及血压对体重的直接回归影响。该样本由998个个体组成,分布在261个家庭中,其中601个连续四次被测量。将数据分为组1的时间1和2,组2的时间3和4。将模型拟合和估计使用组1进行,然后使用组2中的数据测试模型和估计值。血压和体重分别为.15和.54。这些性状之间的遗传相关性不显着,但存在显着的直接回归效应。结果表明,收缩压的全同胞相关性的30%归因于体重的聚集。在追踪方面,分别有59%和60%的预测收缩压与体重相关性归因于遗传效应。测试第2组第1组的模型表明,血压和体重之间的质量关系随时间稳定。

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