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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:用于儿童类固醇耐药综合征的血管紧张素转换酶基因的插入/缺失(I / D)多态性:遗传结合研究和荟萃分析

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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:评估血管紧张素转换酶(ACE)基因插入/缺失(I / D)与儿童类固醇肾病综合征(SRNS)风险的缺陷(I / D)多态性的评估仍存在争议。进行META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了相关研究,并使用Meta分析方法合成了合格的调查。鉴定了七项调查,用于分析ACE I / D基因多态性和儿童SRNS风险之间的关联,其中包括五个中的五个中的亚洲人,其中一个在白种人,其中一个在非洲人。 D等位基因或DD基因型和亚洲人SRNS易感性之间没有明显阳性关联(或= 1.60,p = 0.26;或= 1.90,p = 0.38)和高加索人群(或= 0.92,p = 0.86;或= 0.27,p = 0.22)。然而,在非洲人观察到(或= 4.67,p = 0.003),但不适用于DD基因型(或= 6.00,P = 0.05),观察到具有SRNS易感性的等位基因的关联。有趣的是,II基因型似乎对亚洲和非洲儿童的SRNS发作起阳性作用(或= 0.51,P = 0.02;或= 0.07,P = 0.02),但不适用于高加索人(或= 0.33,P = 0.30)。总之,我们的结果表明D等位基因或DD纯合可能不是用于在亚洲和白种人儿童中发育SRNS的重要遗传分子标记。然而,D等位基因似乎与非洲人的SRNS风险有关,但DD基因型没有。

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