Fakhoury Hana M A, El Shamieh Said, Rifai Amru, Tamim Hani, Fakhoury Rajaa
Department of Biochemistry and Molecular Biology, College of Medicine, Alfaisal University, P.O. Box 50927, Riyadh 11533, Saudi Arabia.
Department of Medical Laboratory Technology, Faculty of Health Sciences, Beirut Arab University, Beirut 11-5020, Lebanon.
J Cardiovasc Dev Dis. 2022 Mar 27;9(4):102. doi: 10.3390/jcdd9040102.
In addition to its role in bone health, vitamin D (VitD) has been implicated in several pathological conditions. Specifically, VitD deficiency has been linked to an increased risk of dyslipidemia. Atherogenic dyslipidemia is characterized by increased low-density lipoprotein-cholesterol (LDL-C) and decreased high-density lipoprotein-cholesterol (HDL-C). In this study, we examined the association of six single nucleotide polymorphisms (SNPs) in VitD-related genes with VitD and lipid levels, in a cohort of 460 Lebanese participants free from chronic diseases. Our results showed no association of the examined SNPs with VitD concentrations. However, the presence of the minor allele in rs10741657G>A of CYP2R1 was associated with increased levels in LDL-C (β = 4.95, p = 0.04)] and decreased levels in HDL-C (β = −1.76, p = 0.007)]. Interestingly, rs10741657G>A interacted with gender to increase LDL-C levels in females (β = 6.73 and p = 0.03) and decrease HDL-C levels in males HDL-C (β = −1.09, p = 0.009). In conclusion, our results suggest that rs10741657 G>A in CYP2R1 is associated with circulating LDL-C and HDL-C levels in a Lebanese cohort. Although this association was gender-specific, where rs10741657G>A was associated with increased LDL in females and decreased HDL in males, the presence of the minor allele A was associated with increased cardiovascular risk in both genders. These findings need to be validated in a larger population. Further investigations are warranted to elucidate the molecular mechanism of VitD polymorphism and dyslipidemia.
除了在骨骼健康方面的作用外,维生素D(VitD)还与多种病理状况有关。具体而言,VitD缺乏与血脂异常风险增加有关。致动脉粥样硬化性血脂异常的特征是低密度脂蛋白胆固醇(LDL-C)升高和高密度脂蛋白胆固醇(HDL-C)降低。在本研究中,我们在460名无慢性疾病的黎巴嫩参与者队列中,研究了VitD相关基因中的六个单核苷酸多态性(SNP)与VitD和血脂水平的关联。我们的结果显示,所检测的SNP与VitD浓度无关联。然而,CYP2R1基因的rs10741657G>A中次要等位基因的存在与LDL-C水平升高(β = 4.95,p = 0.04)和HDL-C水平降低(β = -1.76,p = 0.007)有关。有趣的是,rs10741657G>A与性别相互作用,增加女性的LDL-C水平(β = 6.73,p = 0.03),降低男性的HDL-C水平(β = -1.09,p = 0.009)。总之,我们的结果表明,CYP2R1基因中的rs10741657 G>A与黎巴嫩队列中的循环LDL-C和HDL-C水平有关。尽管这种关联具有性别特异性,即rs10741657G>A与女性LDL升高和男性HDL降低有关,但次要等位基因A的存在与两性心血管风险增加有关。这些发现需要在更大的人群中进行验证。有必要进一步研究以阐明VitD多态性与血脂异常的分子机制。