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Pooling Dietary Data Using Questionnaires With Open-ended and Predefined Responses: Implications for Comparing Mean Intake or Estimating Odds Ratios

机译:使用具有不限成员名额和预定义答案的问卷收集饮食数据:比较平均摄入量或估算几率的含义

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摘要

In the current era of diet-gene analyses, large sample sizes are required to uncover the etiology of complex diseases. As such, consortia form and often combine available data. Food frequency questionnaires, which commonly use 2 different types of responses about the frequency of intake (predefined responses and open-ended responses), may be pooled to achieve the desired sample size. The common practice is to categorize open-ended responses into the predefined response categories. A problem arises when the predefined categories are noncontiguous: possible open-ended responses may fall in gaps between the predefined categories. Using simulated data modeled from frequency of intake among 1,664 controls in a lung cancer case-control study at The University of Texas M. D. Anderson Cancer Center (Houston, Texas, 2000–2005), the authors describe the effect of different categories of open-ended responses that fall in between noncontiguous, predefined response sets on estimates of the mean difference in intake and the odds ratios. A significant inflation of false positives appears when comparing mean differences of intake, while the bias in estimating odds ratios may be acceptably small. Therefore, if pooling data cannot be restricted to the same type of response, inferences should focus on odds ratio estimation to minimize bias.
机译:在当前的饮食基因分析时代,需要大量样本才能揭示复杂疾病的病因。这样,联合会形成并经常合并可用数据。可以汇总食物频率问卷,这些问卷通常使用两种不同类型的摄入频率响应(预定义响应和开放式响应),以实现所需的样本量。常见的做法是将开放式响应分类为预定义的响应类别。当预定义类别不连续时会出现问题:可能的开放式响应可能会落在预定义类别之间的间隙中。在德克萨斯大学医学博士安德森癌症中心(德克萨斯州休斯顿,2000–2005年)的一项肺癌病例对照研究中,使用从1,664名对照中的摄入频率建模的模拟数据,作者描述了不同类别的开放性药物的影响响应介于非连续的预定义响应集之间,这些响应集基于摄入量平均差异和优势比的估计值。当比较摄入量的平均差异时,会出现假阳性的明显膨胀,而估计比值比的偏差可能很小。因此,如果不能将合并数据限制为相同类型的响应,则推论应集中在优势比估算上,以最大程度地减少偏差。

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