Research Unit on Lipids and Atherosclerosis, Universitat Rovira i Virgili, 43201 Reus, Spain.
Vascular Medicine and Metabolism Unit, "Sant Joan de Reus" University Hospital, 43204 Reus, Spain.
Int J Mol Sci. 2024 Nov 7;25(22):11985. doi: 10.3390/ijms252211985.
Growth differentiation factor 15 (GDF15) is a stress-response cytokine related to a wide variety of metabolic diseases. However, the impact of GDF15-specific genetic variants on the abovementioned conditions is poorly known. The aim of this study was to assess the impact of selected GDF15 single-nucleotide polymorphisms (SNPs) on metabolic disturbances and subclinical atherosclerosis. A cross-sectional study involving 153 participants of a metabolic patient-based cohort was performed. Three selected SNPs (rs888663, rs1054564 and rs1059369) in a locus on chromosome 19 including the gene were genotyped by Polymerase Chain Reaction (PCR), and its relationship with the serum GDF15 levels, health status and clinical variables were analyzed. Of the three SNPs analyzed, only rs1054564 showed different distributions between the healthy volunteers and patients suffering lipid alterations and associated disorders. Accordingly, just the rs1054564 variant carriers showed a significant increase in GDF15 serum levels compared to the wild-type carriers. The group of variant carriers showed a higher frequency of individuals with diabetes, compared to the wild-type carrier group, without showing differences in other metabolic conditions. Additionally, the frequency of individuals with atherosclerotic carotid plaque was higher in the rs1054564 variant carriers than in the wild-type carriers. Logistic regression models identified that the presence of the rs1054564 variant carriers increase the likelihood for both diabetes and carotid plaque independently of confounding factors. Overall, the findings of this study identify the rs1054564 variant as a potential indicator for the likelihood of diabetes and subclinical atherosclerosis.
生长分化因子 15(GDF15)是一种与多种代谢疾病相关的应激反应细胞因子。然而,GDF15 特异性遗传变异对上述疾病的影响知之甚少。本研究旨在评估选定的 GDF15 单核苷酸多态性(SNP)对代谢紊乱和亚临床动脉粥样硬化的影响。对代谢患者队列中的 153 名参与者进行了一项横断面研究。在包括基因的 19 号染色体上的一个基因座中选择了三个 SNP(rs888663、rs1054564 和 rs1059369),通过聚合酶链反应(PCR)对其进行了基因分型,并分析了其与血清 GDF15 水平、健康状况和临床变量的关系。在所分析的三个 SNP 中,只有 rs1054564 在脂质改变和相关疾病的健康志愿者和患者之间的分布不同。因此,只有 rs1054564 变异携带者的血清 GDF15 水平与野生型携带者相比显著升高。与野生型携带者相比,变异携带者组的糖尿病患者比例较高,而其他代谢条件没有差异。此外,rs1054564 变异携带者中颈动脉粥样硬化斑块的发生率高于野生型携带者。Logistic 回归模型确定,rs1054564 变异携带者的存在独立于混杂因素增加了糖尿病和颈动脉斑块的可能性。总的来说,这项研究的结果确定了 rs1054564 变异作为糖尿病和亚临床动脉粥样硬化可能性的潜在指标。