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印度人群中C反应蛋白的全基因组关联研究重复了常见变异的已知关联。

Genomewide association study for C-reactive protein in Indians replicates known associations of common variants.

作者信息

Prasad Gauri, Giri Anil K, Basu Analabha, Tandon Nikhil, Bharadwaj Dwaipayan

机构信息

Genomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi 110 020, India.

出版信息

J Genet. 2019 Mar;98.

Abstract

Elevated C-reactive protein (CRP) serves as an independent biomarker for acute and chronic inflammation, and is also associated with metabolic diseases. Genomewide loci regulating CRP level in Indian population, a high-risk group for metabolic illness, is unexplored. Therefore, we aimed to discover common polymorphisms associated with plasma CRP level in 4493 Indians of Indo-European origin using genomewide association study. Genomewide strong associations of two known intronic variants in hepatocyte nuclear factor-1 α gene () were identified among Indian subjects. We also detected prior associations of several variants in/near metabolic and inflammatory process genes: , , , , and with modest associations. This study confirms that Indians from Indo-European origin display similar core universal genetic factors for CRP levels.

摘要

C反应蛋白(CRP)水平升高是急性和慢性炎症的独立生物标志物,还与代谢性疾病相关。在代谢疾病高危人群印度人群中,尚未探索调控CRP水平的全基因组位点。因此,我们旨在通过全基因组关联研究,在4493名印欧血统的印度人中发现与血浆CRP水平相关的常见多态性。在印度受试者中,鉴定出肝细胞核因子-1α基因()中两个已知内含子变异的全基因组强关联。我们还检测到代谢和炎症过程基因中/附近的几个变异的先前关联:、、、、和具有适度关联。本研究证实,印欧血统的印度人在CRP水平上表现出相似的核心普遍遗传因素。

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