论文标题

用于设置的分层荟萃分析,涉及多个队列的多个结果

A Hierarchical Meta-Analysis for Settings Involving Multiple Outcomes across Multiple Cohorts

论文作者

Hocagil, Tugba Akkaya, Ryan, Louise M., Cook, Richard J., Richardson, Gale A., Day, Nancy L., Coles, Claire D., Olson, Heather Carmichael, Jacobson, Sandra W., Jacobson, Joseph L.

论文摘要

动物模型和流行病学研究的证据将产前酒精暴露(PAE)与多种长期认知和行为缺陷联系起来。但是,科学文献中几乎没有关于与临床上严重不良反应风险增加的PAE水平相关的信息。在1975 - 1993年期间,在美国进行了几项前瞻性纵向队列研究,在怀孕期间获得了有关饮酒的产妇报告,并从童年开始至上曾经评估了后代的认知发展。这些队列中的样本大小没有提供足够的功能来检查与不同水平和模式相关的效果。为了解决这个关键的公共卫生问题,我们开发了一项层次荟萃分析,以综合有关PAE对认知影响的信息,并将数据集成到来自美国六项纵向队列研究的多个终点上的数据。我们的方法涉及估计每个终点的剂量响应系数,然后汇总这些相关剂量反应系数,以获得暴露对认知的估计“全局”影响。在第一阶段,我们使用各个参与者数据来通过拟合使用倾向分数调整潜在混杂变量的回归模型来得出PAE的效果。然后,在每个队列中估计的端点特异性剂量 - 响应系数之间的依赖性依赖性,然后运行,同时运行一些端点上的不完整信息。我们还根据根据完整的多元分析的推论进行比较和讨论推论的推论

Evidence from animal models and epidemiological studies has linked prenatal alcohol exposure (PAE) to a broad range of long-term cognitive and behavioral deficits. However, there is virtually no information in the scientific literature regarding the levels of PAE associated with an increased risk of clinically significant adverse effects. During the period from 1975-1993, several prospective longitudinal cohort studies were conducted in the U.S., in which maternal reports regarding alcohol use were obtained during pregnancy and the cognitive development of the offspring was assessed from early childhood through early adulthood. The sample sizes in these cohorts did not provide sufficient power to examine effects associated with different levels and patterns of PAE. To address this critical public health issue, we have developed a hierarchical meta-analysis to synthesize information regarding the effects of PAE on cognition, integrating data on multiple endpoints from six U.S. longitudinal cohort studies. Our approach involves estimating the dose-response coefficients for each endpoint and then pooling these correlated dose-response coefficients to obtain an estimated `global' effect of exposure on cognition. In the first stage, we use individual participant data to derive estimates of the effects of PAE by fitting regression models that adjust for potential confounding variables using propensity scores. The correlation matrix characterizing the dependence between the endpoint-specific dose-response coefficients estimated within each cohort is then run, while accommodating incomplete information on some endpoints. We also compare and discuss inferences based on the proposed approach to inferences based on a full multivariate analysis

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