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中国汉族人群中与子痫前期相关的白细胞介素27基因多态性

Polymorphisms of the IL27 gene in a Chinese Han population complicated with pre-eclampsia.

作者信息

Liu Bin, Li Yuan, Yao Yuan, Li Hua, Liang Hongda, Xin Miaomiao, Wang Liqin, Zhao Lei, Lin Jizheng, Liu Shiguo

机构信息

Department of Rheumatology, the Affiliated Hospital of Qingdao University, Qingdao, China.

Department of Medical Imageology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Sci Rep. 2016 Mar 14;6:23029. doi: 10.1038/srep23029.

Abstract

IL-27 could inhibit the development of Th17 cells, and the Th17/regulatory T-cell imbalance may reverse maternal tolerance in pre-eclampsia (PE). The aim of this study was to investigate the association between genetic polymorphisms in IL27 with PE. Three SNPs in IL27 (rs153109, rs17855750, and rs181206) were genotyped in a Chinese Han cohort of 1040 PE patients and 1247 normal pregnant women using the TaqMan allelic discrimination real-time PCR method. The CC genotypic distribution of rs153109 was significantly higher among cases than controls (19.1% versus 13.3%, odds ratio [OR]: 1.54, 95% confidence interval [CI]: 1.23-1.93, p < 0.001), and the CT genotype was found to be significantly lower in cases than controls (41.7% versus 49.0%, OR: 0.74, 95% CI: 0.63-0.88, p < 0.001), disputing existing reports indicating the allele frequency of rs153109 is not significantly different between PE patients and controls. Additionally, the CC genotype of rs153109 was significantly more prevalent in PE cases than controls using a recessive model (p < 0.001). The allelic and genotypic frequencies of rs17855750 and rs181206 were not significantly different between two groups. Our results reveal that IL27 polymorphisms may be involved in the development of PE in Chinese Han population.

摘要

白细胞介素-27(IL-27)可抑制辅助性T细胞17(Th17)细胞的发育,而Th17/调节性T细胞失衡可能会逆转子痫前期(PE)患者的母体耐受性。本研究旨在探讨IL27基因多态性与PE之间的关联。采用TaqMan等位基因鉴别实时荧光定量PCR方法,对1040例PE患者和1247例正常孕妇的中国汉族队列进行了IL27三个单核苷酸多态性(SNP,分别为rs153109、rs17855750和rs181206)的基因分型。rs153109的CC基因型分布在病例组中显著高于对照组(19.1%对13.3%,优势比[OR]:1.54,95%置信区间[CI]:1.23 - 1.93,p < 0.001),而CT基因型在病例组中显著低于对照组(41.7%对49.0%,OR:0.74,95% CI:0.63 - 0.88,p < 0.001),这与现有报道称rs153109的等位基因频率在PE患者和对照组之间无显著差异相矛盾。此外,采用隐性模型时,rs153109的CC基因型在PE病例中比对照组更为普遍(p < 0.001)。rs17855750和rs181206的等位基因和基因型频率在两组之间无显著差异。我们的结果表明,IL27基因多态性可能参与了中国汉族人群PE的发生发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d715/4789744/f845b00df52e/srep23029-f1.jpg

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