Department of Biochemistry, Armed Forces Medical College, Pune, Maharashtra, India.
Department of Cardiology, Army Institute of Cardio Thoracic Sciences, Pune, Maharashtra, India.
Indian J Med Res. 2023 Aug;158(2):197-200. doi: 10.4103/ijmr.ijmr_3493_21.
BACKGROUND & OBJECTIVES: Despite being a tropical country, vitamin D deficiency is highly prevalent in India with studies indicating 40-99 per cent prevalence. Apart from calcium and phosphate metabolism, vitamin D is involved in cell cycle regulation, cardiovascular, hepatoprotection. The metabolism of vitamin D is regulated by vitamin D tool genes (CYP2R1/CYP27B1/CYP24A1/VDR). The promoter regions of some of these genes have CpG islands, making them prone to methylation induced gene silencing, which may cause a reduction in circulating vitamin D levels. Epigenetic basis of vitamin D deficiency is yet to be studied in India, and hence, this pilot study was aimed to analyze whether methylation levels of CYP2R1 gene were correlated with the levels of 25(OH)D in healthy, adult individuals in Indian population.
In this cross-sectional study, healthy adults of 18-45 yr of age with no history of malabsorption, thyroidectomy, chronic illness or therapeutic vitamin D supplementation were recruited. DNA methylation analysis was carried out by methylation specific quantitative PCR. Serum calcium, phosphate and vitamin D levels were also quantified. Statistical analysis was done by R 4.0.5 software.
A total of 61 apparently healthy adults were analyzed. The serum vitamin D levels did not correlate with CYP2R1 methylation levels in our study population. Significant positive correlation was observed between age and serum vitamin D levels. Significant association of gender was found with CYP2R1 methylation levels.
INTERPRETATION & CONCLUSIONS: This study found no significant correlation between levels of CYP2R1 methylation and circulating 25(OH)D deficiency. Further studies on the Indian population having a larger sample size including entire vitamin D tool genes, among different ethnic groups may be conducted to elucidate molecular etiology of circulating 25(OH)D deficiency. The high prevalence of normal serum calcium and phosphate levels among vitamin D deficient subjects in this study coupled with the strikingly high prevalence of the deficiency at the national level, may suggest the need to revise the cut-off criteria for vitamin D deficiency in the Indian population.
尽管印度是一个热带国家,但维生素 D 缺乏症的发病率很高,有研究表明其发病率为 40-99%。除了钙和磷酸盐代谢,维生素 D 还参与细胞周期调节、心血管和肝保护。维生素 D 的代谢受维生素 D 工具基因(CYP2R1/CYP27B1/CYP24A1/VDR)调节。这些基因的启动子区域存在 CpG 岛,使它们容易受到甲基化诱导的基因沉默的影响,这可能导致循环维生素 D 水平降低。印度尚未研究维生素 D 缺乏的表观遗传基础,因此,这项初步研究旨在分析 CYP2R1 基因的甲基化水平是否与印度人群中健康成年人的 25(OH)D 水平相关。
在这项横断面研究中,招募了年龄在 18-45 岁之间、无吸收不良、甲状腺切除术、慢性疾病或治疗性维生素 D 补充史的健康成年人。通过甲基化特异性定量 PCR 进行 DNA 甲基化分析。还定量检测血清钙、磷和维生素 D 水平。统计分析使用 R 4.0.5 软件进行。
共分析了 61 名看似健康的成年人。在我们的研究人群中,血清维生素 D 水平与 CYP2R1 甲基化水平没有相关性。年龄与血清维生素 D 水平呈显著正相关。性别与 CYP2R1 甲基化水平显著相关。
本研究未发现 CYP2R1 甲基化水平与循环 25(OH)D 缺乏之间存在显著相关性。在印度人群中进行更大样本量的研究,包括整个维生素 D 工具基因,以及不同种族群体之间的研究,可能有助于阐明循环 25(OH)D 缺乏的分子病因。在这项研究中,维生素 D 缺乏的受试者中血清钙和磷水平正常的比例很高,而全国范围内维生素 D 缺乏的比例却很高,这可能表明需要修订印度人群中维生素 D 缺乏的截止标准。