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首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >Association of HLA-DRB1 and -DQB1 alleles with type 1 (autoimmune) diabetes in African Arabs: systematic review and meta-analysis
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Association of HLA-DRB1 and -DQB1 alleles with type 1 (autoimmune) diabetes in African Arabs: systematic review and meta-analysis

机译:HLA-DRB1和-DQB1等位基因与1型(自身免疫)糖尿病在非洲阿拉伯人:系统评论和荟萃分析

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Several studies confirmed the association of HLA-DRB1 and -DQB1 alleles with altered risk of type 1 diabetes (T1D). However, data from individual studies based on small sample sizes yielded often conflicting findings in African Arabs. This is a systematic review and meta-analysis aimed at comprehensively evaluating this association with T1D, using molecular HLA data. Relevant studies were identified through systemic search of Medline/PubMed, Cochrane, Science Direct, ResearchGate, and EMBASE databases. Statistical analysis was carried out using RevMan, and Comprehensive Meta-analysis programs. Given the heterogeneity of African Arabs, we also performed subgroup analysis according to ethnicity. Analysis of sensitivity, heterogeneity, and publication bias were performed to validate the outcome of the findings. This meta-analysis included 862 T1DM cases, along with 1,390 normoglycemic control, and comprised ten comparisons. Our study indicates that DRB1*03 (OR = 2.86), DRB1*04 (OR = 2.78), and DQB1*02 (OR = 2.29), are positively associated with increased risk of T1DM, while DRB1*07 (OR = 0.48), DRB1*11 (OR = 0.20), DRB1*13 (OR = 0.47), DRB1*15 (OR = 0.30), DQB1*05 (OR = 0.39), and DQB1*06 (OR = 0.27) were negatively associated with T1D, suggesting a protective role against T1D. This meta-analysis was characterized by low heterogeneity, sensitivity, and publication bias, indicating the robustness and reliability of the results. Background: Several studies confirmed the association of HLA-DRB1 and –DQB1 alleles with altered risk of type 1 diabetes (T1D). However, data from individual studies based on small sample sizes yielded often conflicting findings in African Arabs. This is a systematic review and meta-analysis aimed at comprehensively evaluating this association with T1D, using molecular HLA data. Methods: Relevant studies were identified through systemic search of Medline/PubMed, Cochrane, Science Direct, ResearchGate, and EMBASE databases. Statistical analysis was carried out using Revman, and Comprehensive Meta-analysis programs. Given the heterogeneity of African Arabs, we also performed subgroup analysis according to ethnicity. Analysis of sensitivity, heterogeneity, and pub?lication bias were performed to validate the outcome of the findings. This meta-analysis included 862 T1DM cases, along with 1,390 normoglycemic control, and comprised ten comparisons. Results: Our study indicates that DRB1*03 (OR = 2.86), DRB1*04 (OR = 2.78), and DQB1*02 (OR = 2.29), are positively associated with increased risk of T1DM, while DRB1*07 (OR = 0.48), DRB1*11 (OR = 0.20), DRB1*13 (OR = 0.47), DRB1*15 (OR = 0.30), DQB1*05 (OR = 0.39), and DQB1*06 (OR = 0.27) were negatively associated with T1D, suggesting a protective role against T1D. Conclusion: This meta-analysis was characterized by low heterogeneity, sensitivity, and publication bias, indicating the robustness and reliability of the results.
机译:几项研究证实了HLA-DRB1和-DQB1等位基因的关联,具有1型糖尿病(T1D)的风险变化。然而,来自基于小型样本大小的个别研究的数据在非洲阿拉伯人中产生了相互矛盾的调查结果。这是使用分子HLA数据全面评估这种关联的系统审查和荟萃分析。通过Medline / PubMed,Cochrane,Science直接,研究和Embase数据库来确定相关研究。使用Revman进行统计分析和全面的Meta分析计划。鉴于非洲阿拉伯人的异质性,我们还根据种族进行亚组分析。进行敏感性,异质性和出版物偏见的分析以验证调查结果的结果。该META分析包括862个T1DM案例,以及1,390个常规控制,并包含十个比较。我们的研究表明DRB1 * 03(或= 2.86),DRB1 * 04(或= 2.78)和DQB1 * 02(或= 2.29)与T1DM的风险增加呈正相关,而DRB1 * 07(或= 0.48) ,DRB1 * 11(或= 0.20),DRB1 * 13(或= 0.47),DQB1 * 05(OR = 0.39),DQB1 * 05(或= 0.39)和DQB1 * 06(或= 0.27)与T1D,表明对T1D的保护作用。该META分析的特点是低异质性,灵敏度和出版物偏压,表明结果的鲁棒性和可靠性。背景:几项研究证实了HLA-DRB1和-DQB1等位基因的关联,具有1型糖尿病的风险变化(T1D)。然而,来自基于小型样本大小的个别研究的数据在非洲阿拉伯人中产生了相互矛盾的调查结果。这是使用分子HLA数据全面评估这种关联的系统审查和荟萃分析。方法:通过系统性搜索Medline / Pubmed,Cochrane,Science直接,研究和Embase数据库来确定相关研究。使用Revman进行统计分析和全面的Meta分析计划。鉴于非洲阿拉伯人的异质性,我们还根据种族进行亚组分析。敏感性,异质性和酒吧的分析是进行的紊乱偏差以验证调查结果的结果。该META分析包括862个T1DM案例,以及1,390个常规控制,并包含十个比较。结果:我们的研究表明DRB1 * 03(或= 2.86),DRB1 * 04(或= 2.78)和DQB1 * 02(或= 2.29)与T1DM的风险增加呈正相关,而DRB1 * 07(或= 0.48),DRB1 * 11(或= 0.20),DRB1 * 13(或= 0.47),DRB1 * 15(或= 0.30),DQB1 * 05(或= 0.39),DQB1 * 06(或= 0.27)是负面的与T1D相关,表明对T1D的保护作用。结论:该元分析的特点是低异质性,灵敏度和出版物偏差,表明结果的鲁棒性和可靠性。

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