驱动青光眼临床变化的多基因风险评分

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2024-04-10 DOI:10.1146/annurev-genom-121222-105817
Antonia Kolovos, Mark M. Hassall, Owen M. Siggs, Emmanuelle Souzeau, Jamie E. Craig
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引用次数: 0

摘要

青光眼是一种临床异质性疾病,也是导致不可逆失明的全球主要原因。治疗干预可以预防失明,但有赖于早期诊断,而目前的临床风险因素在预测谁会患上危及视力的青光眼方面能力有限。青光眼的高遗传性使其成为遗传风险预测的理想基质,其中大部分风险具有多基因性质。在此,我们总结了青光眼遗传风险的基础、多基因风险预测工具的开发以及遗传风险分层的新机遇。尽管挑战依然存在,但遗传风险分层将大大改善青光眼筛查和管理。
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Polygenic Risk Scores Driving Clinical Change in Glaucoma
Glaucoma is a clinically heterogeneous disease and the world's leading cause of irreversible blindness. Therapeutic intervention can prevent blindness but relies on early diagnosis, and current clinical risk factors are limited in their ability to predict who will develop sight-threatening glaucoma. The high heritability of glaucoma makes it an ideal substrate for genetic risk prediction, with the bulk of risk being polygenic in nature. Here, we summarize the foundations of glaucoma genetic risk, the development of polygenic risk prediction instruments, and emerging opportunities for genetic risk stratification. Although challenges remain, genetic risk stratification will significantly improve glaucoma screening and management.
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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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