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血管紧张素转换酶插入/缺失基因多态性与系统性红斑狼疮/狼疮性肾炎的关系:系统评价和荟萃分析。

Relationship between angiotensin-converting enzyme insertion/deletion gene polymorphism and systemic lupus erythematosus/lupus nephritis: a systematic review and metaanalysis.

机构信息

Department of Pediatrics, The First Affiliated Hospital of GuangXi Medical University, NanNing 530021, China.

出版信息

J Rheumatol. 2012 Apr;39(4):686-93. doi: 10.3899/jrheum.110863. Epub 2012 Feb 15.

Abstract

OBJECTIVE

Results from studies of the association between angiotensin-converting enzyme (ACE) insertion/deletion (I/D) gene polymorphism and systemic lupus erythematosus (SLE)/lupus nephritis (LN) are controversial. We performed this metaanalysis to evaluate the relationship between ACE I/D gene polymorphism and SLE/LN and to explore whether the ACE D allele or DD genotype could become a predictive marker for risk of SLE/LN.

METHODS

Association studies were identified from the databases of PubMed, Embase, Cochrane Library and CBM-disc (China Biological Medicine Database) as of May 1, 2011, and eligible investigations were synthesized using a metaanalysis method. Results were expressed with OR for dichotomous data, and 95% CI were calculated.

RESULTS

Sixteen investigations were identified for the analysis of association between ACE I/D gene polymorphism and SLE, consisting of 1959 patients with SLE and 2078 controls. In the overall populations, there was a marked association between D allele or DD genotype and SLE susceptibility (D: OR 1.29, 95% CI 1.04-1.58, p = 0.02; DD: OR 1.60, 95% CI 1.17-2.19, p = 0.003), and DD homozygous was associated with LN risk (OR 2.78, 95% CI 1.26-6.11, p = 0.01). In the subgroup analysis, DD genotype associated with SLE risk was observed in Asians; no other association was found in Asians, whites, Africans, and Brazilians.

CONCLUSION

D allele and DD homozygous are significant genetic molecular markers to predict SLE susceptibility, and DD genotype is a valuable marker to predict the LN risk. More investigations are required to clarify the association of the D allele or DD homozygous with SLE/LN susceptibility.

摘要

目的

血管紧张素转换酶(ACE)插入/缺失(I/D)基因多态性与系统性红斑狼疮(SLE)/狼疮肾炎(LN)之间关联的研究结果存在争议。我们进行了这项荟萃分析,以评估 ACE I/D 基因多态性与 SLE/LN 的关系,并探讨 ACE D 等位基因或 DD 基因型是否可成为 SLE/LN 风险的预测标志物。

方法

我们从 PubMed、Embase、Cochrane 图书馆和 CBM-disc(中国生物医学数据库)数据库中检索到截至 2011 年 5 月 1 日的关联研究,并使用荟萃分析方法综合了合格的研究。结果以二项数据的 OR 表示,并计算了 95%CI。

结果

共纳入了 16 项 ACE I/D 基因多态性与 SLE 相关性的分析研究,共包括 1959 例 SLE 患者和 2078 例对照。在总体人群中,D 等位基因或 DD 基因型与 SLE 易感性之间存在显著关联(D:OR 1.29,95%CI 1.04-1.58,p = 0.02;DD:OR 1.60,95%CI 1.17-2.19,p = 0.003),DD 纯合子与 LN 风险相关(OR 2.78,95%CI 1.26-6.11,p = 0.01)。在亚组分析中,DD 基因型与亚洲人群的 SLE 发病风险相关;在亚洲、白种人、非洲人和巴西人群中,未发现其他关联。

结论

D 等位基因和 DD 纯合子是预测 SLE 易感性的重要遗传分子标志物,DD 基因型是预测 LN 风险的有价值的标志物。需要进一步的研究来阐明 D 等位基因或 DD 纯合子与 SLE/LN 易感性的关系。

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