与YKL-40水平升高和早发性房颤风险相关的多态性

Kristoffer M A Henningsen, Morten S Olesen, Golnaz Sajadieh, Stig Haunsoe, Jesper H Svendsen
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引用次数: 12

摘要

背景:房颤(AF)患者血浆中YKL-40水平升高。我们假设影响YKL-40血浆水平的单核苷酸多态性(SNP)与单发房颤的风险相关。研究结果:我们纳入了178例40岁前首次发作的单发房颤的年轻患者,以及875名健康个体的对照组。我们分析了编码YKL-40的几丁质酶3样1 (CHI3L1)基因中的启动子SNP (-131CG) (rs4950928),该基因先前与YKL-40水平升高有关。结论:(-131CG)基因型与房颤风险增加无关,基因性升高的YKL-40水平与房颤无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation.

Background: Plasma levels of YKL-40 are elevated in patients with atrial fibrillation (AF). We hypothesized that a single nucleotide polymorphism (SNP) that affects YKL-40 plasma levels is associated to the risk of lone AF.

Findings: We included 178 young patients with lone AF and the first episode before the age of 40 years, and a control group of 875 healthy individuals. We analyzed a promoter SNP (-131CG) (rs4950928) in the Chitinase 3-like 1 (CHI3L1) gene encoding YKL-40, which had previously been associated with elevated levels of YKL-40.

Conclusions: The (-131CG) genotype was not associated with increased risk of AF. Genetically increased YKL-40 levels were not associated to AF.

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