我们是否可以将生物标志物与自我报告相结合来加强营养流行病学研究的分析?

Laurence S Freedman, Victor Kipnis, Arthur Schatzkin, Natasa Tasevska, Nancy Potischman
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引用次数: 98

摘要

在营养队列研究中确定饮食与疾病的关系受到自我报告摄入量测量误差的困扰。作者建议使用已知的与饮食摄入相关的生物标志物,以加强对饮食疾病假设的分析。作者考虑将自我报告的摄入量和生物标志物水平结合使用主成分,Howe的方法,或在双变量模型中对效果进行联合统计检验。他们将这些方法的统计能力与传统的自我报告摄入量或生物标志物水平的单变量分析进行了比较。他们使用计算机模拟不同的疾病风险模型,输入参数基于叶黄素摄入量与年龄相关性黄斑变性之间关系的文献数据。结果表明,如果饮食对疾病的影响完全通过生物标志物水平介导,那么生物标志物的单变量分析是最有效的方法。然而,组合方法,特别是主成分和Howe的方法,在这种情况下并不差很多,如果中介只是部分或不存在,则与单变量生物标志物分析一样好,甚至更好。在某些情况下,样本量要求减少到自我报告摄入量的传统分析所需样本量的20-50%。作者得出结论:(1)在队列中除了常规的饮食数据外,还包括生物标志物数据可以大大加强对饮食-疾病关系的调查,(2)当生物标志物的调节程度未知时,使用主成分或Howe的方法似乎是一个很好的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Can we use biomarkers in combination with self-reports to strengthen the analysis of nutritional epidemiologic studies?

Can we use biomarkers in combination with self-reports to strengthen the analysis of nutritional epidemiologic studies?

Identifying diet-disease relationships in nutritional cohort studies is plagued by the measurement error in self-reported intakes. The authors propose using biomarkers known to be correlated with dietary intake, so as to strengthen analyses of diet-disease hypotheses. The authors consider combining self-reported intakes and biomarker levels using principal components, Howe's method, or a joint statistical test of effects in a bivariate model. They compared the statistical power of these methods with that of conventional univariate analyses of self-reported intake or of biomarker level. They used computer simulation of different disease risk models, with input parameters based on data from the literature on the relationship between lutein intake and age-related macular degeneration. The results showed that if the dietary effect on disease was fully mediated through the biomarker level, then the univariate analysis of the biomarker was the most powerful approach. However, combination methods, particularly principal components and Howe's method, were not greatly inferior in this situation, and were as good as, or better than, univariate biomarker analysis if mediation was only partial or non-existent. In some circumstances sample size requirements were reduced to 20-50% of those required for conventional analyses of self-reported intake. The authors conclude that (i) including biomarker data in addition to the usual dietary data in a cohort could greatly strengthen the investigation of diet-disease relationships, and (ii) when the extent of mediation through the biomarker is unknown, use of principal components or Howe's method appears a good strategy.

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