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Shared genetic architecture of gastroesophageal reflux disease and age related phenotypes
被引:0
|作者:
Wei Liu
[1
]
Yadan Xiao
[2
]
Manting Zeng
[3
]
机构:
[1] Central South University,Department of Gastrointestinal Surgery, Xiangya Hospital
[2] Bin hai wan Central Hospital of Dongguan,Department of Anorectal Surgery
[3] Central South University,Department of Oncology, Xiangya Hospital
[4] Central South University,National Clinical Research Center for Geriatric Disorders, Xiangya Hospital
来源:
关键词:
Gastroesophageal reflux disease;
Aging;
Genome-wide pleiotropic association;
D O I:
10.1038/s41598-025-90943-y
中图分类号:
学科分类号:
摘要:
Increasing age is a risk factor of gastroesophageal reflux disease. This study aims to uncover the shared genetic architecture of gastroesophageal reflux disease (GERD) and age-related phenotypes. Based on publicly available GWAS statistics, this genome-wide pleiotropic association research was performed with multiple genetic approaches sequentially to explore the pleiotropic associations from single-nucleotide polymorphism (SNP) and gene levels, to reveal the underlying shared genetic etiology between GERD and age-related phenotypes. This study featured shared genetic mechanisms between GERD and age-related phenotypes, including frailty index (FI), telomere length (TL), longevity, and parental lifespan (PL). Strong genetic association were observed. A set of pleiotropic loci and genes were identified by PLACO, FUMA, Bayesian colocalization and additional MAGMA analysis. Our research provided strong evidence of genetic correlation between GERD and several age-related phenotypes, especially frailty index (FI) and telomere length (TL), brought novel insight into the shared genetic architecture between GERD and aging.
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