Evidence map›Paper›PMID 39399603›Full record

ArticleMedical journal of the Islamic Republic of Iran2024

Pleiotropic Bias and Study Design Considerations in Genetic Association Studies.

Sana Eybpoosh, Seyyed Amir Yasin Ahmadi

Abstract read
In one paragraph

Article in Medical journal of the Islamic Republic of Iran, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Sana EybpooshResearch Centre for emerging and reemerging infectious diseases, Department of Epidemiology and Biostatistics, Pasteur institute of Iran, Tehran, Iran.ORCID https://orcid.org/0000-0002-2304-8352
Seyyed Amir Yasin AhmadiPreventive Medicine and Public Health Research Center, Psychosocial Health Research Institute, Iran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Case-Control StudiesGenetic Association StudiesGenetic EpidemiologyObservational StudyPleiotropyResearch Design

Identifiers

PMID39399603
PMCPMC11469697

What Socratic holds

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