Pleiotropic Bias and Study Design Considerations in Genetic Association Studies.

Q2 Medicine Medical Journal of the Islamic Republic of Iran Pub Date : 2024-05-07 eCollection Date: 2024-01-01 DOI:10.47176/mjiri.38.51
Sana Eybpoosh, Seyyed Amir Yasin Ahmadi
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Abstract

Background: Case-control studies are efficient designs for investigating gene-disease associations. A discovery of genome-wide association studies (GWAS) is that many genetic variants are associated with multiple health outcomes and diseases, a phenomenon known as pleiotropy. We aimed to discuss about pleiotropic bias in genetic association studies.

Methods: The opinions of the researchers on the basis of the literature were presented as a critical review.

Results: Pleiotropic effect can bias the results of gene-disease association studies if they use individuals with pre-existing diseases as the control group, while the disease in cases and controls have shared genetic markers. The idea supports the conclusion that when the exposure of interest in a case-control study is a genetic marker, the use of controls from diseased cases that share similar genetic markers may increase the risk of pleiotropic effect. However, not manifesting the disease symptoms among controls at the time of recruitment does not guarantee that the individual will not develop the disease of interest in the future. Age-matched disease-free controls may be a better solution in similar situations. Different analytical techniques are also available that can be used to identify pleiotropic effects. Known pleiotropic effects can be searched from various online databases.

Conclusion: Pleiotropic effects may result in bias in genetic association studies. Suggestions consist of selecting healthy yet age-matched controls and considering diseases with independent genetic architecture. Checking the related databases is recommended before designing a study.

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遗传关联研究中的多向偏倚和研究设计考虑因素。
背景:病例对照研究是调查基因-疾病关联的有效设计。全基因组关联研究(GWAS)的一个发现是,许多基因变异与多种健康结果和疾病相关,这种现象被称为 "pleiotropy"。我们旨在讨论基因关联研究中的多效性偏倚:结果:多向效应会使遗传关联研究出现偏差:结果:如果基因疾病关联研究使用已患疾病的个体作为对照组,而病例和对照组的疾病具有共同的遗传标记,则多向效应会使研究结果产生偏差。这一观点支持这样的结论,即当病例对照研究中的相关暴露是一个遗传标记时,使用具有相似遗传标记的病例对照可能会增加多向效应的风险。然而,在招募对照时没有表现出疾病症状并不能保证个人将来不会罹患相关疾病。在类似情况下,年龄匹配的无疾病对照组可能是更好的解决方案。还有不同的分析技术可用于识别多效应。可以从各种在线数据库中搜索已知的多向效应:结论:多向效应可能导致遗传关联研究出现偏差。建议选择健康但年龄匹配的对照组,并考虑具有独立遗传结构的疾病。建议在设计研究前查阅相关数据库。
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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
90
审稿时长
8 weeks
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