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[具体基因名称]、[具体基因名称]和[具体基因名称]基因变异与青少年特发性关节炎易感性之间的遗传关联。 (注:原文中基因名称处为缺失状态,需补充完整基因名称才能准确翻译)

Genetic association between the , and gene variants and susceptibility to juvenile idiopathic arthritis.

作者信息

Qian Yufeng, Chen Bingqian, Wang Zhengfei, Peng Yuqin

机构信息

Department of Orthopedics, Changshu Hospital Affiliated to Soochow University, First People's Hospital of Changshu City, Changshu, Jiangsu 215500, P.R. China.

出版信息

Exp Ther Med. 2022 Nov 9;24(6):756. doi: 10.3892/etm.2022.11692. eCollection 2022 Dec.

Abstract

Juvenile idiopathic arthritis (JIA) refers to a group of chronic childhood arthropathies of unknown etiology. In the present study, the genetic association between the variants in genes and susceptibility to JIA was investigated. The distributions of 16 variants in , and genes were analyzed by direct sequencing in 378 patients with JIA and 378 healthy controls. Odds ratios and 95% confidence intervals were used to evaluate the association between the gene variants and JIA. The gene-gene interactions were investigated using multifactor dimensionality reduction. All allelic and dominant models of rs1214414, rs1214418, rs1746853, rs3765598 and rs3811021 were significantly associated with JIA risk (P<0.05). rs10954213 in both allelic and dominant models, as well as the allelic model of rs2004640, was significantly related to JIA risk (P<0.05). In addition, the allelic, recessive and dominant models of rs280500, rs280519, rs2304256 and rs12720270 were significantly related to JIA risk (P<0.05). In addition, three haplotypes (H, H and H ) in gene, three haplotypes (H, H and H) in gene and two haplotypes (H and H) in gene were associated with the risk of JIA (P<0.05). Furthermore, a three-way interaction between rs10954213, rs2004640 and rs1214414 was shown to be associated with JIA risk. In conclusion, rs1214418, rs1746853, rs3765598, rs2004640, rs280500, rs2304256 and a three-way interaction between rs10954213, rs2004640 and rs1214414 may be risk factors for JIA.

摘要

青少年特发性关节炎(JIA)是指一组病因不明的儿童慢性关节病。在本研究中,调查了基因变异与JIA易感性之间的遗传关联。通过直接测序分析了378例JIA患者和378例健康对照中基因、基因和基因中16种变异的分布情况。采用优势比和95%置信区间评估基因变异与JIA之间的关联。使用多因素降维法研究基因-基因相互作用。rs1214414、rs1214418、rs1746853、rs3765598和rs3811021的所有等位基因模型和显性模型均与JIA风险显著相关(P<0.05)。rs10954213的等位基因模型和显性模型以及rs2004640的等位基因模型均与JIA风险显著相关(P<0.05)。此外,rs280500、rs280519、rs2304256和rs12720270的等位基因模型、隐性模型和显性模型均与JIA风险显著相关(P<0.05)。此外,基因中的三种单倍型(H、H和H)、基因中的三种单倍型(H、H和H)以及基因中的两种单倍型(H和H)与JIA风险相关(P<0.05)。此外,rs10954213、rs2004640和rs1214414之间的三方相互作用与JIA风险相关。总之,rs1214418、rs1746853、rs3765598、rs2004640、rs280500、rs2304256以及rs10954213、rs2004640和rs1214414之间的三方相互作用可能是JIA的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5b5/9808742/17b8d42d179a/etm-24-06-11692-g00.jpg

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