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ABCB1基因多态性在激素抵抗型肾病综合征中的作用:来自接受激素治疗患者的荟萃分析证据

The role of ABCB1 gene polymorphisms in steroid-resistant nephrotic syndrome: Evidence from a meta-analysis of steroid-receiving patients.

作者信息

Aziz Md Abdul, Islam Mohammad Safiqul

机构信息

Department of Pharmacy, Faculty of Science, Noakhali Science and Technology University, Noakhali, Bangladesh.

Laboratory of Pharmacogenomics and Molecular Biology, Department of Pharmacy, Noakhali Science and Technology University, Noakhali, Bangladesh.

出版信息

J Gene Med. 2022 Jul;24(7):e3436. doi: 10.1002/jgm.3436. Epub 2022 Jun 25.

Abstract

Previous studies in nephrotic syndrome have shown that three common variants in the ABCB1 gene, including rs1128503, rs2032582, and rs1045642, change the expression and activity of ABCB1, which may be responsible for the drug resistance. However, as a result of the inconclusive outcomes of these studies, we performed a meta-analysis to validate the association between ABCB1 polymorphisms and the susceptibility of steroid-resistant nephrotic syndrome (SRNS). The association was evaluated by calculating the odds ratio (OR) and 95% confidence interval. A total of 12 studies containing 1,463 subjects (514 steroid-resistant and 949 steroid-sensitive) were included. Single nucleotide polymorphism rs1128503 showed a significant association with SRNS (p < 0.05) only in the allele model (OR = 1.40) in Africans. A statistically significant association was found for rs2032582 in codominant 2, dominant, recessive, and allele models (OR = 1.85, 1.52, 1.38, and 1.34, respectively). Subgroup analysis revealed that rs2032582 showed a significant correlation with SRNS in codominant 1, 2, dominant, over-dominant, and allele models in Africans (OR = 3.22, 3.52, 3.29, 1.74, and 1.83, respectively). In the case of rs1045642, codominant 1 (OR = 0.72) and recessive models (OR = 1.34) revealed a significant correlation with SRNS. Again, codominant 1 (OR = 0.58), dominant (OR = 0.69), and over-dominant models (OR = 0.62) showed a protective effect in Asians. Haplotype analysis showed that the TGC haplotype is associated with a 1.83, 1.77, and 2.17 times significant correlation in overall, Asian, and African populations, respectively. By contrast, the CGC haplotype showed a 0.69 and 0.57 times lower association in the overall and African populations, respectively. The CTC haplotype also showed a 1.79 times enhanced susceptibility for SRNS in the overall population. Our study suggests that ABCB1 polymorphisms are associated with SRNS development, especially in Africans and Asians.

摘要

先前关于肾病综合征的研究表明,ABCB1基因中的三个常见变异,包括rs1128503、rs2032582和rs1045642,会改变ABCB1的表达和活性,这可能是耐药性的原因。然而,由于这些研究结果尚无定论,我们进行了一项荟萃分析,以验证ABCB1基因多态性与类固醇抵抗性肾病综合征(SRNS)易感性之间的关联。通过计算优势比(OR)和95%置信区间来评估这种关联。总共纳入了12项研究,包含1463名受试者(514名类固醇抵抗者和949名类固醇敏感者)。单核苷酸多态性rs1128503仅在非洲人的等位基因模型中显示与SRNS有显著关联(p < 0.05)(OR = 1.40)。在共显性2、显性、隐性和等位基因模型中,发现rs2032582与SRNS有统计学显著关联(OR分别为1.85、1.52、1.38和1.34)。亚组分析显示,rs2032582在非洲人的共显性1、2、显性、超显性和等位基因模型中与SRNS有显著相关性(OR分别为3.22、3.52、3.29、1.74和1.83)。对于rs1045642,共显性1(OR = 0.72)和隐性模型(OR = 1.34)显示与SRNS有显著相关性。同样,共显性1(OR = 0.58)、显性(OR = 0.69)和超显性模型(OR = 0.62)在亚洲人中显示出保护作用。单倍型分析表明,TGC单倍型在总体、亚洲和非洲人群中分别与SRNS有1.83倍、1.77倍和2.17倍的显著相关性。相比之下,CGC单倍型在总体和非洲人群中的关联分别低0.69倍和0.57倍。CTC单倍型在总体人群中对SRNS的易感性也增强了1.79倍。我们的研究表明,ABCB1基因多态性与SRNS的发生有关,尤其是在非洲人和亚洲人中。

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