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白细胞介素基因多态性与斑秃:系统评价和荟萃分析。

Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis.

机构信息

Department of Pharmaceutical Sciences, Faculty of Health and Life Sciences, North South University, Dhaka, Bangladesh.

Department of Clinical Pharmacy and Pharmacology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.

出版信息

Medicine (Baltimore). 2024 Feb 23;103(8):e37300. doi: 10.1097/MD.0000000000037300.

Abstract

BACKGROUND

Alopecia areata (AA) is an autoimmune disease which results in non-scarring hair loss on the scalp or any surface with hair. Several genetic polymorphisms of the interleukin genes have been linked with this disease but the results are inconsistent. This systematic review and meta-analysis were done to find the association between rs3118470, rs2275913, rs3212227, and rs10889677 of the IL2RA, IL17A, IL12B, and IL23R genes, respectively, of the interleukin family with alopecia areata.

METHODS

A comprehensive search for relevant research articles was conducted in Pubmed, Google Scholar, and Embase databases. Our search yielded 8 relevant articles with 1940 cases and 1788 controls. The odds ratio with 95% confidence intervals was calculated using fixed effect and random effect models. Heterogeneity was determined using the Q-test and I2 test. Publication bias was determined and funnel plots were used to adjust the odds ratio.

RESULTS

We found a significant risk effect for rs3118470 of the IL2RA gene with alopecia areata in the dominant model (CC + CT vs TT; OR = 1.54, 95% confidence interval = 1.05-2.26, P < .05, I2 = 69.03%) and homozygous model (CC vs TT; OR = 2.00, 95% confidence interval = 1.07-3.71, P < .05, I2 = 72.84%). For the other single nucleotide polymorphisms, we could not find any statistically significant association with the disease.

CONCLUSION

Our analysis showed that mutation of rs3118470 of IL2RA gene possesses a significant risk effect for alopecia areata. Future studies with larger sample sizes and ethnic backgrounds are warranted to confirm our findings.

摘要

背景

斑秃是一种自身免疫性疾病,导致头皮或任何有毛发的部位出现非瘢痕性脱发。白细胞介素基因的几个遗传多态性与这种疾病有关,但结果不一致。本系统评价和荟萃分析旨在探讨白细胞介素家族中的 IL2RA、IL17A、IL12B 和 IL23R 基因的 rs3118470、rs2275913、rs3212227 和 rs10889677 与斑秃之间的关联。

方法

在 Pubmed、Google Scholar 和 Embase 数据库中进行全面检索相关研究文章。我们的搜索共产生了 8 篇相关文章,包括 1940 例病例和 1788 例对照。使用固定效应和随机效应模型计算比值比及其 95%置信区间。使用 Q 检验和 I2 检验确定异质性。确定发表偏倚,并使用漏斗图调整比值比。

结果

我们发现 IL2RA 基因的 rs3118470 与斑秃在显性模型(CC+CT 与 TT;OR=1.54,95%置信区间 1.05-2.26,P<0.05,I2=69.03%)和纯合模型(CC 与 TT;OR=2.00,95%置信区间 1.07-3.71,P<0.05,I2=72.84%)中存在显著的风险效应。对于其他单核苷酸多态性,我们没有发现与疾病有任何统计学上的关联。

结论

我们的分析表明,IL2RA 基因的 rs3118470 突变对斑秃具有显著的风险效应。需要更大样本量和不同种族背景的进一步研究来证实我们的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e0b/10883625/26989d33f721/medi-103-e37300-g001.jpg

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