糖尿病肾病和2型糖尿病患者COL4A1基因的基因型分析:一项比较遗传学研究

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Neha Shukla, Shivani Kumari, Poornima Verma, Atar Singh Kushwah, Monisha Banarjee, S N Sankhwar, Aneesh Srivastava, M S Ansari, Naveen Kumar Gautam
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引用次数: 0

摘要

糖尿病肾病(DN)是由微量白蛋白尿、肾小球病变和肾纤维化导致终末期肾脏疾病所确定的。DN的病理生理是多因素的,是基因与环境相互作用的结果。临床研究表明,基因突变影响DN涉及的多种途径,包括细胞外基质(ECM)。在慢性高血糖期间,4型胶原介导的ECM过度产生,导致肾纤维化和DN的发展。本研究分析了研究人群中糖尿病和DN患者的COL4A1基因变异rs605143 (G/A)。我们对386名研究对象进行了基因分型,其中包括120名2型糖尿病(T2DM)患者,120名DN和146名健康对照。所有研究对象采用市售试剂盒进行生化分析,采用聚合酶链反应-限制性片段长度多态性进行基因型分析,并通过Sanger测序进行确认。采用SPSS和GraphPad进行统计分析。人类临床病理参数显示T2DM与DN有显著相关性。与对照组相比,COL4A1基因变异rs605143 (G/A) AA型与T2DM和DN有显著相关性,风险分别为5.87倍和8.01倍。与健康对照相比,突变等位基因A与T2DM和DN独立相关,风险分别为2.29倍和2.81倍。本研究结果提示COL4A1基因变异rs605143 (G/A)可独立作为T2DM和DN的预测生物标志物。然而,该基因变异需要在大样本中进行分析,以探索T2DM和DN之间的共同遗传关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotypic Analysis of COL4A1 Gene in Diabetic Nephropathy and Type 2 Diabetes Mellitus Patients: A Comparative Genetic Study.

Diabetic nephropathy (DN) is specified by microalbuminuria, glomerular lesions, and renal fibrosis leading to end-stage renal disease. The pathophysiology of DN is multifactorial as a result of gene-environment interaction. Clinical studies suggested that gene mutations affect various pathways involved in DN, including extracellular matrix (ECM). During chronic hyperglycemia, collagen type-4-mediated ECM overproduction occurs, leading to renal fibrosis and DN development. In this study, COL4A1 gene variant rs605143 (G/A) was analyzed in diabetes and DN patients from the study population. We genotyped 386 study subjects, comprising 120 type 2 diabetes mellitus (T2DM) patients, 120 DN, and 146 healthy controls. All study subjects were analyzed for biochemical assays by commercially available kits and genotypic analysis by polymerase chain reaction-restriction fragment length polymorphism and confirmed by Sanger sequencing. Statistical analyses were done using SPSS and GraphPad. Anthroclinicopathological parameters showed a significant association between T2DM and DN. Genotype AA of COL4A1 gene variant rs605143 (G/A) showed a significant association with T2DM and DN compared with controls with 5.87- and 8.01-folds risk, respectively. Mutant allele A also significantly associated with T2DM and DN independently compared with healthy controls with 2.29- and 2.81-time risk in the study population. This study's findings suggested that COL4A1 gene variant rs605143 (G/A) can be used as predictive biomarkers for T2DM and DN independently. However, this gene variant needs to be analyzed in a large sample to explore the shared genetic association between T2DM and DN.

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来源期刊
DNA and cell biology
DNA and cell biology 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
93
审稿时长
1.5 months
期刊介绍: DNA and Cell Biology delivers authoritative, peer-reviewed research on all aspects of molecular and cellular biology, with a unique focus on combining mechanistic and clinical studies to drive the field forward. DNA and Cell Biology coverage includes: Gene Structure, Function, and Regulation Gene regulation Molecular mechanisms of cell activation Mechanisms of transcriptional, translational, or epigenetic control of gene expression Molecular Medicine Molecular pathogenesis Genetic approaches to cancer and autoimmune diseases Translational studies in cell and molecular biology Cellular Organelles Autophagy Apoptosis P bodies Peroxisosomes Protein Biosynthesis and Degradation Regulation of protein synthesis Post-translational modifications Control of degradation Cell-Autonomous Inflammation and Host Cell Response to Infection Responses to cytokines and other physiological mediators Evasive pathways of pathogens.
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