MTHFR A1298C多态性和血同型半胱氨酸水平与2型糖尿病患者蛋白尿的关系

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of International Medical Research Pub Date : 2025-07-01 Epub Date: 2025-07-04 DOI:10.1177/03000605251356008
Nga Thi Ngoc Pham, Thao Thai Thanh Le, Hoang Minh Phan, Hang Thi Thu Ho, Ha Hong Nguyen
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Proteinuria was defined as an albumin-to-creatinine ratio ≥30 mg/g.ResultsIn total, 192 patients with a mean age of 63.9 ± 13.1 years were enrolled. Males accounted for 34.9% of the study population. Analysis of A1298C polymorphism revealed genotype distributions of AA, AC, and CC genotypes as 51.6%, 41.1%, and 7.3%, respectively. A significant association was observed between A1298C polymorphism and elevated homocysteine levels, with CC genotype exhibiting a higher prevalence of hyperhomocysteinemia (28.6%) than AA (6.1%) and AC (22.8%) genotypes. Patients carrying AC+CC genotypes had a 2.40-fold higher risk of developing proteinuria (95% confidence interval: 1.30-4.41, p <<i> </i>0.05) than those with AA genotype. Elevated blood homocysteine levels were associated with an 8.98-fold increased risk of proteinuria (95% confidence interval: 2.06-39.11, p <<i> </i>0.05). 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Blood samples were collected for genetic sequencing and homocysteine level testing. Proteinuria was defined as an albumin-to-creatinine ratio ≥30 mg/g.ResultsIn total, 192 patients with a mean age of 63.9 ± 13.1 years were enrolled. Males accounted for 34.9% of the study population. Analysis of A1298C polymorphism revealed genotype distributions of AA, AC, and CC genotypes as 51.6%, 41.1%, and 7.3%, respectively. A significant association was observed between A1298C polymorphism and elevated homocysteine levels, with CC genotype exhibiting a higher prevalence of hyperhomocysteinemia (28.6%) than AA (6.1%) and AC (22.8%) genotypes. Patients carrying AC+CC genotypes had a 2.40-fold higher risk of developing proteinuria (95% confidence interval: 1.30-4.41, p <<i> </i>0.05) than those with AA genotype. Elevated blood homocysteine levels were associated with an 8.98-fold increased risk of proteinuria (95% confidence interval: 2.06-39.11, p <<i> </i>0.05). 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引用次数: 0

摘要

背景:据报道,MTHFR基因的1298c多态性和血同型半胱氨酸水平与2型糖尿病患者蛋白尿的发生有关;然而,数据仍然有限。目的探讨2型糖尿病患者A1298C基因多态性、血同型半胱氨酸水平及其与蛋白尿的关系。材料与方法对2023年8月至2024年8月在芹苴大学药科医院就诊的2型糖尿病患者进行横断面研究。采集血样进行基因测序和同型半胱氨酸水平检测。蛋白尿定义为白蛋白与肌酐比值≥30mg /g。结果共纳入192例患者,平均年龄63.9±13.1岁。男性占研究人群的34.9%。A1298C多态性分析显示,AA、AC和CC基因型的基因型分布分别为51.6%、41.1%和7.3%。A1298C多态性与高同型半胱氨酸水平显著相关,其中CC基因型的高同型半胱氨酸血症患病率(28.6%)高于AA(6.1%)和AC(22.8%)基因型。携带AC+CC基因型的患者发生蛋白尿的风险比携带AA基因型的患者高2.40倍(95%可信区间:1.30-4.41,p 0.05)。血同型半胱氨酸水平升高与蛋白尿风险增加8.98倍相关(95%可信区间:2.06-39.11,p 0.05)。与蛋白尿相关的独立因素包括年龄(优势比= 0.97)、高同型半胱氨酸水平(优势比= 8.79)和AC+CC基因型(优势比= 2.08)。结论a1298c多态性的等位基因频率分别为A的72.1%和C的27.9%,除年龄外,C等位基因的存在和血同型半胱氨酸水平升高是2型糖尿病患者蛋白尿的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of MTHFR A1298C polymorphism and blood homocysteine levels with proteinuria in patients with type 2 diabetes mellitus.

BackgroundA1298C polymorphism of the MTHFR gene and blood homocysteine levels are reported to be associated with the development of proteinuria in patients with type 2 diabetes mellitus; however, data remain limited.ObjectivesTo determine the characteristics of A1298C polymorphism and blood homocysteine levels as well as their association with proteinuria in patients with type 2 diabetes mellitus.Materials and methodsA cross-sectional study with convenient sampling was performed among patients with type 2 diabetes mellitus who visited the Can Tho University of Medicine and Pharmacy Hospital between August 2023 and August 2024. Blood samples were collected for genetic sequencing and homocysteine level testing. Proteinuria was defined as an albumin-to-creatinine ratio ≥30 mg/g.ResultsIn total, 192 patients with a mean age of 63.9 ± 13.1 years were enrolled. Males accounted for 34.9% of the study population. Analysis of A1298C polymorphism revealed genotype distributions of AA, AC, and CC genotypes as 51.6%, 41.1%, and 7.3%, respectively. A significant association was observed between A1298C polymorphism and elevated homocysteine levels, with CC genotype exhibiting a higher prevalence of hyperhomocysteinemia (28.6%) than AA (6.1%) and AC (22.8%) genotypes. Patients carrying AC+CC genotypes had a 2.40-fold higher risk of developing proteinuria (95% confidence interval: 1.30-4.41, p <0.05) than those with AA genotype. Elevated blood homocysteine levels were associated with an 8.98-fold increased risk of proteinuria (95% confidence interval: 2.06-39.11, p <0.05). Independent factors associated with proteinuria included age (odds ratio = 0.97), elevated homocysteine levels (odds ratio = 8.79), and AC+CC genotype (odds ratio = 2.08).ConclusionA1298C polymorphism was characterized by allele frequencies of 72.1% for A and 27.9% for C. In addition to age, the presence of the C allele and elevated blood homocysteine levels were identified as independent risk factors for proteinuria in patients with type 2 diabetes mellitus.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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