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白细胞介素1受体拮抗剂基因可变数目串联重复序列多态性与骨关节炎风险关联的Meta分析。

Meta-analysis of the association of IL1-RN variable number of tandem repeats polymorphism with osteoarthritis risk.

作者信息

Xu Bo, Shi Xiao-Qing, Xing Run-Lin, Xiao Yan-Cheng, Wu Peng, Wang Pei-Min

机构信息

The Affiliated Hospital of Nanjing University of TCM, Jiangsu Province Hospital of TCM, Nanjing, PR China.

出版信息

Acta Orthop Traumatol Turc. 2019 Nov;53(6):497-501. doi: 10.1016/j.aott.2019.07.004. Epub 2019 Aug 21.

Abstract

OBJECTIVE

The aim of this meta-analysis was to clarify the role of Interleukin-1 receptor antagonist gene (IL1-RN) Variable Number of Tandem Repeats (VNTR) polymorphism on the risk of OA by means of meta-analysis.

METHODS

Eligible articles were retrieved from PubMed, Web of science and Google scholar with a total of 1187 OA cases and 2659 controls. The strength of the association between the IL1-RN VNTR polymorphism and the risk of OA was assessed by odds ratios (ORs) with the corresponding 95% confidence interval (CI) for each study.

RESULTS

The meta-analysis of seven published studies retrieved from the literature search showed a significantly increased OA risk in the recessive model analysis (22 vs 2L + LL: P = 0.18, I = 32.8, OR(95% CI) = 1.50(1.12, 2.02), P = 0.007), the additive model analysis (22 vs LL: P = 0.08, I = 46.8, OR(95% CI) = 1.56(1.15, 2.12), P = 0.004) and in the allele contrast model (2 vs L: P = 0.02, I = 58.8, OR(95% CI) = 1.20(1.05, 1.36), P = 0.007). By subgroup analysis, the IL1-RN VNTR polymorphism was found to be significantly associated with OA susceptibility in Caucasian and Hospital based case-control study (HCC) groups.

CONCLUSION

This meta-analysis showed that IL1-RN VNTR polymorphism may increase the susceptibility to OA. More studies with detailed information are needed to validate our conclusion.

LEVEL OF EVIDENCE

Level III, diagnostic study.

摘要

目的

本荟萃分析旨在通过荟萃分析阐明白细胞介素-1受体拮抗剂基因(IL1-RN)串联重复序列可变数目(VNTR)多态性在骨关节炎(OA)风险中的作用。

方法

从PubMed、科学网和谷歌学术中检索符合条件的文章,共纳入1187例OA病例和2659例对照。通过比值比(OR)及各研究对应的95%置信区间(CI)评估IL1-RN VNTR多态性与OA风险之间关联的强度。

结果

从文献检索中获取的七项已发表研究的荟萃分析显示,在隐性模型分析(22 vs 2L + LL:P = 0.18,I = 32.8,OR(95% CI) = 1.50(1.12, 2.02),P = 0.007)、加性模型分析(22 vs LL:P = 0.08,I = 46.8,OR(95% CI) = 1.56(1.15, 2.12),P = 0.004)以及等位基因对比模型(2 vs L:P = 0.02,I = 58.8,OR(95% CI) = 1.20(1.05, 1.36),P = 0.007)中,OA风险显著增加。通过亚组分析,发现IL1-RN VNTR多态性与白种人群以及基于医院的病例对照研究(HCC)组中的OA易感性显著相关。

结论

本荟萃分析表明,IL1-RN VNTR多态性可能增加OA易感性。需要更多具有详细信息的研究来验证我们的结论。

证据水平

III级,诊断性研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66a8/6939037/fe06e2851ba8/gr1.jpg

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