双变量寿命数据混合模型中死因的遗传分析

A. Wienke, K. Christensen, A. Skytthe, A. Yashin
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引用次数: 34

摘要

提出了多变量生存分析中的混合模型,其中受试者之间的异质性为个体经历事件(即疾病)的风险以及相关的生存时间长度创造了不同的路径。相互竞争的风险之间的依赖关系被包括在内,并呈现为可测试的。该方法是二元相关γ -脆弱性模型的扩展。它被应用于丹麦双胞胎的数据集,其中特定原因的死亡率是已知的。多变量数据的使用解决了单变量寿命竞争风险模型固有的可识别性问题。我们分析了遗传和环境因素对脆弱的影响。使用1470对单卵(MZ)和2730对异卵(DZ)女性双胞胎的样本,我们应用五种遗传模型来分析相关的死亡率数据,特别关注冠心病(CHD)的死亡。采用最佳拟合模型,冠心病死亡遗传风险为0.39(标准误差0.13)。该模型的结果与先前使用受限模型的分析结果进行了比较,其中假设竞争风险的独立性。比较这两种情况,结果表明,由于冠心病导致的虚弱和死亡率的遗传性发生了很大的变化。尽管存在依赖性,但分析证实了个体冠心病死亡风险的重要遗传因素。无论假设依赖性还是独立性,关于冠心病死亡风险分析的最佳模型是假设累加性因素对冠心病易感性的遗传性负责的模型。文章最后讨论了所提出模型的局限性和可能的进一步扩展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic analysis of cause of death in a mixture model of bivariate lifetime data
A mixture model in multivariate survival analysis is presented, whereby heterogeneity among subjects creates divergent paths for the individual’s risk of experiencing an event (i.e., disease), as well as for the associated length of survival. Dependence among competing risks is included and rendered testable. This method is an extension of the bivariate correlated gamma-frailty model. It is applied to a data set on Danish twins, for whom cause-specific mortality is known. The use of multivariate data solves the identifiability problem which is inherent in the competing risk model of univariate lifetimes. We analyse the influence of genetic and environmental factors on frailty. Using a sample of 1470 monozygotic (MZ) and 2730 dizygotic (DZ) female twin pairs, we apply five genetic models to the associated mortality data, focusing particularly on death from coronary heart disease (CHD). Using the best fitting model, the inheritance risk of death from CHD was 0.39 (standard error 0.13). The results from this model are compared with the results from earlier analysis that used the restricted model, where the independence of competing risks was assumed. Comparing both cases, it turns out, that heritability of frailty on mortality due to CHD change substantially. Despite the inclusion of dependence, analysis confirms the significant genetic component to an individual’s risk of mortality from CHD. Whether dependence or independence is assumed, the best model for analysis with regard to CHD mortality risks is a model assuming that additive factors are responsible for heritability in susceptibility to CHD. The paper ends with a discussion of limitations and possible further extensions to the model presented.
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