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SNP rs2243828 与髓过氧化物酶水平及中国汉族人群心房颤动风险相关。

SNP rs2243828 in MPO associated with myeloperoxidase level and atrial fibrillation risk in Chinese Han population.

机构信息

Department of Clinical Laboratory, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Geriatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Cell Mol Med. 2020 Sep;24(17):10263-10266. doi: 10.1111/jcmm.15644. Epub 2020 Jul 16.

Abstract

Previous studies shown that myeloperoxidase (MPO) level is higher in patients with atrial fibrillation (AF); however, no genetic evidence between MPO and AF risk in human population was observed. Therefore, the present study was aimed to investigate the association between rs2243828, a variant in promoter region of MPO and the risk of AF in Chinese GeneID population. The results demonstrated that the minor G allele of rs2243828 showed a significant association with AF in two independent population (GeneID-north population with 694 AF cases and 710 controls, adjusted P = 6.25 × 10 with an odds ratio was 0.77, GeneID-central population with 1106 cases and 1501 controls, P = 9.88 × 10 with an odds ratio was 0.75). The results also showed G allele was significantly associated with lower plasma concentration of myeloperoxidase in general population. We also observed a significant difference of odds ratio between subgroups of hypertension and non-hypertension. Therefore, our findings identified variant in MPO associated with risk of AF and it may give strong evidence to link the inflammation with the incidence of AF.

摘要

先前的研究表明,髓过氧化物酶 (MPO) 水平在心房颤动 (AF) 患者中较高;然而,在人类群体中并未观察到 MPO 与 AF 风险之间存在遗传证据。因此,本研究旨在探讨 MPO 启动子区域 rs2243828 变异与中国 GeneID 人群 AF 风险的相关性。结果表明,rs2243828 的次要 G 等位基因与两个独立人群中的 AF 显著相关(GeneID-北部人群中有 694 例 AF 病例和 710 例对照,调整后的 P 值为 6.25×10,优势比为 0.77,GeneID-中部人群中有 1106 例病例和 1501 例对照,P 值为 9.88×10,优势比为 0.75)。结果还表明,G 等位基因与一般人群中髓过氧化物酶的血浆浓度降低显著相关。我们还观察到高血压亚组和非高血压亚组之间的优势比存在显著差异。因此,我们的研究结果确定了与 AF 风险相关的 MPO 变异,这可能为炎症与 AF 发生率之间的关联提供有力证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2203/7520285/3c4732c36aef/JCMM-24-10263-g001.jpg

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