泯灭随机法在眼科疾病中的应用:综述。

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY Human Genomics Pub Date : 2024-06-17 DOI:10.1186/s40246-024-00637-1
Xiran Zhang, Weichen Yuan, Jun Xu, Fangkun Zhao
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引用次数: 0

摘要

眼部疾病会大大降低患者的生活质量,并给家庭和社会带来经济负担。然而,大多数此类疾病的发病率和发病机制尚不清楚,因此,预防、管理和治疗都具有挑战性。虽然可以通过观察性研究得出暴露因素与疾病之间的联系,但要排除混杂变量和反向因果关系的干扰却很有难度。孟德尔随机法(Mendelian Randomization,MR)是一种将遗传学和流行病学相结合的研究方法,其优势在于可以解决这一问题,因此被广泛应用于眼科疾病的病因学研究中。本文回顾了 MR 在眼科疾病研究中的应用,并提供了相关机制的研究方法和干预策略。
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Application of mendelian randomization in ocular diseases: a review.

Ocular disorders can significantly lower patients' quality of life and impose an economic burden on families and society. However, for the majority of these diseases, their prevalence and mechanisms are yet unknown, making prevention, management, and therapy challenging. Although connections between exposure factors and diseases can be drawn through observational research, it is challenging to rule out the interference of confounding variables and reverse causation. Mendelian Randomization (MR), a method of research that combines genetics and epidemiology, has its advantage to solve this problem and thus has been extensively utilized in the etiological study of ophthalmic diseases. This paper reviews the implementation of MR in the research of ocular diseases and provides approaches for the investigation of related mechanisms as well as the intervention strategies.

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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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