Christiane Mayrhofer Grocoske de Lima, Rafaela Cirillo de Melo, Nathalia Marçallo Peixoto Souza, Paula Rothbarth Silva, Dayane Ferreira Aguiar, Luana Mota Ferreira, Waldemar Volanski, Geraldo Picheth, Fabiane Gomes de Moraes Rego, Marcel Henrique Marcondes Sari
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This scoping review investigated the association between <i>VEGF</i> gene and <i>VEGF</i> receptors single-nucleotide polymorphisms (SNPs) and susceptibility to T2DM and vascular complications. <b>Methods</b>: A thorough systematic review was performed utilizing scientific databases (PubMed, Web of Science, and Scopus) in March 2025. From an initial pool of 796 records, 59 relevant articles were selected for inclusion in the analysis. <b>Results:</b> The most frequently studied SNPs were rs2010963 (31/59), rs699947 (16/59), rs3025039 (15/59), rs833061 (11/59), rs1570360 (7/59) in the <i>VEGFA</i> gene and rs2071559(6/59) in <i>VEGFR2</i>. The studies include a diverse range of ethnic groups, including Asian, European and Middle Eastern populations. The main complications associated with these SNPs were microvascular conditions such as diabetic retinopathy (DR) (49/59), diabetic neuropathy (DPN) (6/59), diabetic nephropathy (DNP) (2/59), and as well as macrovascular complications including diabetic foot ulcers (DFU) (10/59). The results revealed that these polymorphisms, particularly rs3025039 and rs2010963, were more consistently associated with microvascular complications such as DR rather than with T2DM itself. The C allele of rs2010963 was associated with increased risk of DR in Indian populations, while no such association was observed in European. 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引用次数: 0
摘要
背景/目的:2型糖尿病(T2DM)是一种与遗传和环境因素相关的慢性多因素代谢性疾病。血管内皮生长因子(VEGF)在血管生成和血管稳态中起着至关重要的作用,VEGF信号通路的遗传多态性与T2DM的发生、进展和并发症有关。本综述调查了VEGF基因和VEGF受体单核苷酸多态性(snp)与2型糖尿病和血管并发症易感性之间的关系。方法:于2025年3月利用科学数据库(PubMed、Web of Science和Scopus)进行全面的系统评价。从最初的796条记录中,选择59篇相关文章纳入分析。结果:研究频率最高的snp为VEGFA基因中的rs2010963(31/59)、rs699947(16/59)、rs3025039(15/59)、rs833061(11/59)、rs1570360(7/59)和VEGFR2基因中的rs2071559(6/59)。这些研究涵盖了不同的种族群体,包括亚洲、欧洲和中东人口。与这些snp相关的主要并发症是微血管疾病,如糖尿病视网膜病变(DR)(49/59)、糖尿病神经病变(DPN)(6/59)、糖尿病肾病(DNP)(2/59),以及大血管并发症,包括糖尿病足溃疡(DFU)(10/59)。结果显示,这些多态性,特别是rs3025039和rs2010963,更一致地与微血管并发症(如DR)相关,而不是与T2DM本身相关。rs2010963的C等位基因与印度人群DR风险增加相关,而在欧洲人群中未观察到这种关联。同样,rs3025039的T等位基因在中国人群中对DPN具有保护作用,但在印度的一项研究中,它与更高的DR风险相关,这表明相同的等位基因可能根据种族背景和临床表型发挥不同的作用。结论:VEGF信号通路遗传多态性显示出作为糖尿病并发症,尤其是微血管结局的生物标志物的潜力。这一发现提示了2型糖尿病并发症差异的遗传基础。未来的研究应调查不同种族群体的相关snp,以更好地了解与该疾病及其血管并发症相关的遗传风险。
Polymorphisms in VEGF Signaling Pathway Genes and Their Potential Impact on Type 2 Diabetes Mellitus and Associated Complications: A Scoping Review.
Background/Objectives: Type 2 diabetes mellitus (T2DM) is a chronic and multifactorial metabolic disorder associated with genetic and environmental factors. Vascular endothelial growth factor (VEGF) plays a crucial role in angiogenesis and vascular homeostasis, and genetic polymorphisms in the VEGF signaling pathway have been linked to the T2DM development, progression, and complications. This scoping review investigated the association between VEGF gene and VEGF receptors single-nucleotide polymorphisms (SNPs) and susceptibility to T2DM and vascular complications. Methods: A thorough systematic review was performed utilizing scientific databases (PubMed, Web of Science, and Scopus) in March 2025. From an initial pool of 796 records, 59 relevant articles were selected for inclusion in the analysis. Results: The most frequently studied SNPs were rs2010963 (31/59), rs699947 (16/59), rs3025039 (15/59), rs833061 (11/59), rs1570360 (7/59) in the VEGFA gene and rs2071559(6/59) in VEGFR2. The studies include a diverse range of ethnic groups, including Asian, European and Middle Eastern populations. The main complications associated with these SNPs were microvascular conditions such as diabetic retinopathy (DR) (49/59), diabetic neuropathy (DPN) (6/59), diabetic nephropathy (DNP) (2/59), and as well as macrovascular complications including diabetic foot ulcers (DFU) (10/59). The results revealed that these polymorphisms, particularly rs3025039 and rs2010963, were more consistently associated with microvascular complications such as DR rather than with T2DM itself. The C allele of rs2010963 was associated with increased risk of DR in Indian populations, while no such association was observed in European. Similarly, the T allele of rs3025039 conferred protection against DPN in a Chinese population but was associated with higher DR risk in an Indian study, suggesting that the same allele may play distinct roles depending on ethnic background and clinical phenotype. Conclusions: VEGF signaling pathway genetic polymorphisms demonstrate potential as biomarkers for diabetic complications, especially microvascular outcomes. The findings suggest a genetic basis for differences in complications of T2DM. Future studies should investigate relevant SNPs across diverse ethnic groups to better understand genetic risks associated with the disease and its vascular complications.
BiomedicinesBiochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍:
Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.