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首页> 外文期刊>Renal failure. >Insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme gene in steroid-resistant nephrotic syndrome for children: A genetic association study and meta-analysis
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Insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme gene in steroid-resistant nephrotic syndrome for children: A genetic association study and meta-analysis

机译:儿童类固醇抵抗性肾病综合征中血管紧张素转换酶基因的插入/缺失(I / D)多态性:遗传关联研究和荟萃分析

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An assessment of the association of angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism with steroid-resistant nephrotic syndrome (SRNS) risk in children is still controversial. A meta-analysis was performed to evaluate the relation between ACE gene polymorphisms and SRNS susceptibility. The relevant studies were screened from electronic database and eligible investigations were synthesized using meta-analysis methods. Seven investigations were identified for the analysis of association between ACE I/D gene polymorphism and SRNS risk in children, including five in Asians, one in Caucasians, and one in Africans. There was not a markedly positive association between D allele or DD genotype and SRNS susceptibility in Asians (OR = 1.60, p = 0.26; OR = 1.90, p = 0.38) and for Caucasian population (OR = 0.92, p = 0.86; OR = 0.27, p = 0.22). However, an association of D allele with SRNS susceptibility was observed (OR = 4.67, p = 0.003) in Africans, but not for DD genotype (OR = 6.00, p = 0.05). Interestingly, II genotype seemed to play a positive role against SRNS onset for Asians and African children (OR = 0.51, p = 0.02; OR = 0.07, p = 0.02), but not for Caucasians (OR = 0.33, p = 0.30). In conclusion, our results indicate that D allele or DD homozygous might not be a significant genetic molecular marker for the development of SRNS in Asians and Caucasian children. However, D allele seemed be associated with SRNS risk for Africans but DD genotype did not.
机译:评估儿童血管紧张素转换酶(ACE)基因插入/缺失(I / D)多态性与类固醇抵抗性肾病综合征(SRNS)风险之间的关系仍存在争议。进行荟萃分析以评估ACE基因多态性与SRNS易感性之间的关系。从电子数据库中筛选相关研究,并使用荟萃分析方法对符合条件的研究进行综合。确定了七项调查以分析ACE I / D基因多态性与儿童SRNS风险之间的相关性,其中五项在亚洲人中,一名在白种人中,在非洲人中。在亚洲人(OR = 1.60,p = 0.26; OR = 1.90,p = 0.38)和高加索人(OR = 0.92,p = 0.86; OR =)中,D等位基因或DD基因型与SRNS易感性之间没有明显的正相关。 0.27,p = 0.22)。然而,在非洲人中观察到D等位基因与SRNS易感性相关(OR = 4.67,p = 0.003),而对于DD基因型则没有(OR = 6.00,p = 0.05)。有趣的是,对于亚洲人和非洲儿童来说,II基因型似乎对SRNS发作起积极作用(OR = 0.51,p = 0.02; OR = 0.07,p = 0.02),而对于白种人(SR = 0.33,p = 0.30)则没有。总之,我们的结果表明,D等位基因或DD纯合子可能不是亚洲人和高加索儿童SRNS发育的重要遗传分子标记。但是,D等位基因似乎与非洲人的SRNS风险有关,而DD基因型却没有。

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