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一种新型的 CD209 多态性与台湾的类风湿关节炎患者相关。

A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan.

机构信息

Center for Lipid Biosciences, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.

Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.

出版信息

J Clin Lab Anal. 2021 May;35(5):e23751. doi: 10.1002/jcla.23751. Epub 2021 Apr 1.

Abstract

Single nucleotide polymorphisms (SNPs) in the promoter region of CD209 (cluster of differentiation 209) may influence expression levels, and higher expression of CD209 on immune cells correlate with severity of cartilage destruction in patients with rheumatoid arthritis (RA). Due to the lack of a comprehensive study, this study aimed to investigate the CD209 promoter variants and haplotypes in a Taiwanese population and the association with RA development. Deoxyribonucleic acid (DNA) of peripheral blood mononuclear cells from 126 RA patients and 124 healthy controls was purified, and the CD209 gene promoter was amplified by polymerase chain reaction and analyzed by Sanger sequencing. Results showed that a novel variant -96C>A polymorphism in CD209 promoter was identified in the Taiwanese population, and the frequency was significantly higher in RA patients than in controls (11.51% vs. 2.42%, P < .0001). The odds ratio (OR) for the development of RA was 5.88 (95% CI 2.35-14.74, P < .0001). Other known variants were also evaluated; for instance, -1180 T/T (rs7359874) was increased in RA patients, and the OR for the development of RA was 3.26, 95% CI 0.85-12.52, P = .07). Besides, the haplotype frequencies were calculated; -1180A-939C-871 T-336 T-139 T-96A and -1180 T-939 T-871C-336 T-139C-96A were increased in RA patients (P = .004 and 0.05, respectively). In summary, CD209-96A variant could be an important factor for the development of RA in the Taiwanese population.

摘要

单核苷酸多态性(SNPs)在 CD209(分化群 209)启动子区域可能影响表达水平,免疫细胞上 CD209 的高表达与类风湿关节炎(RA)患者软骨破坏的严重程度相关。由于缺乏全面的研究,本研究旨在探讨台湾人群中 CD209 启动子变异体和单倍型与 RA 发病的关系。从 126 例 RA 患者和 124 例健康对照者的外周血单核细胞中提取脱氧核糖核酸(DNA),通过聚合酶链反应扩增 CD209 基因启动子,并进行 Sanger 测序分析。结果显示,在台湾人群中发现了 CD209 启动子的一种新的-96C>A 多态性,RA 患者的频率明显高于对照组(11.51%比 2.42%,P<0.0001)。RA 发病的优势比(OR)为 5.88(95%可信区间 2.35-14.74,P<0.0001)。还评估了其他已知的变体;例如,-1180T/T(rs7359874)在 RA 患者中增加,RA 发病的 OR 为 3.26,95%可信区间 0.85-12.52,P=0.07)。此外,还计算了单倍型频率;-1180A-939C-871T-336T-139T-96A 和-1180T-939T-871C-336T-139C-96A 在 RA 患者中增加(P=0.004 和 0.05)。总之,CD209-96A 变异可能是台湾人群 RA 发病的一个重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/197f/8128313/4704b488a9d1/JCLA-35-e23751-g002.jpg

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