白细胞介素-10 多态性与斯约格伦综合征易感性之间的关系:元分析。

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Young Ho Lee, Gwan Gyu Song
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引用次数: 0

摘要

本研究旨在探讨白细胞介素-10(IL10)多态性与斯尤格林综合征易感性之间的关系。研究人员对 Medline、Embase 和 Web of Science 数据库进行了系统检索,以确定从开始到 2024 年 4 月期间的相关文章。对种族、民族或地理区域没有限制,但只纳入了用英语发表的研究。研究人员进行了一项荟萃分析,以评估 IL10-1082 G/A (rs1800896)、-819 C/T (rs1800871) 和 -592 C/A (rs1800872) 多态性及其单倍型与罹患斯琼综合征风险之间的关联。纳入的研究涉及 998 例斯约格伦综合征患者和 1576 例对照组。有十项研究被纳入了荟萃分析。对IL10-1082 G/A多态性的荟萃分析表明,IL10-1082 G/A多态性与Sjögren综合征无明显关联(几率比[OR] = 1.115,95%置信区间[CI]:0.888-1.401):欧洲人和拉丁美洲人的种族分层结果一致。同样,在任何研究对象中,IL10-819 C/T 多态性都与斯约格伦综合征无关(OR = 0.859,95% CI:0.648-1.138,p = 0.290)。IL10-592 C 等位基因也与斯约格伦综合征无关(OR = 1.131,95% CI:0.776-1.646,p = 0.522)。然而,在所有研究对象中,GCC 携带者状态与斯约格伦综合征有显著关联(OR = 1.496,95% CI:1.200-1.865,p = 0.522)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations Between Interleukin-10 Polymorphisms and Susceptibility to Sjögren's Syndrome: A Meta-Analysis.

This study sought to investigate the association between interleukin-10 (IL10) polymorphisms and susceptibility to Sjögren's syndrome. A systematic search of the Medline, Embase and Web of Science databases was conducted to identify relevant articles from inception to April 2024. No restrictions were placed on race, ethnicity or geographic area, but only studies published in English were included. A meta-analysis was conducted to evaluate the association among the IL10-1082 G/A (rs1800896), -819 C/T (rs1800871) and -592 C/A (rs1800872) polymorphisms, as well as their haplotypes and the risk of developing Sjögren's syndrome. The included studies involved 998 Sjögren's syndrome patients and 1576 controls. Ten studies were included in the meta-analysis. Meta-analysis of the IL10-1082 G/A polymorphism revealed no significant association with Sjögren's syndrome (odds ratio [OR] = 1.115, 95% confidence interval [CI]: 0.888-1.401, p = 0.343), with stratification by ethnicity yielding consistent results for Europeans and Latin Americans. Similarly, the IL10-819 C/T polymorphism was not associated with Sjögren's syndrome in any study subjects (OR = 0.859, 95% CI: 0.648-1.138, p = 0.290). The IL10-592 C allele also exhibited no association with Sjögren's syndrome (OR = 1.131, 95% CI: 0.776-1.646, p = 0.522). However, the GCC carrier status demonstrated a significant association with Sjögren's syndrome across all study subjects (OR = 1.496, 95% CI: 1.200-1.865, p < 0.001), particularly in Europeans (OR = 1.444, 95% CI: 1.085-1.921, p = 0.012) and Latin Americans (OR = 1.324, 95% CI: 1.115-2.366, p = 0.012). A significant protective effect of the homozygous ATA/ATA haplotype on Sjögren's syndrome was found in Europeans (OR = 0.320, 95% CI: 0.121-0.846, p = 0.022). This meta-analysis indicates a significant link between carrying the GCC haplotype of the IL10-1082 G/A, -819 C/T and -592 C/A polymorphisms and an increased susceptibility to Sjögren's syndrome. Conversely, the homozygous ATA/ATA haplotype appears to confer protection against the risk of Sjögren's syndrome, particularly in European populations.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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