Association of Vitamin D Deficiency and Vitamin D Receptor Gene Polymorphisms with Type 1 Diabetes Risk: A South Indian Familial Study

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Clinical Research in Pediatric Endocrinology Pub Date : 2024-03-11 Epub Date: 2023-08-10 DOI:10.4274/jcrpe.galenos.2023.2022-12-7
Ramasamy Thirunavukkarasu, Ayyappan Chitra, Arthur Asirvatham, Mariakuttikan Jayalakshmi
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引用次数: 0

Abstract

Objective: Vitamin D is a potent immune modulator and is associated with autoimmune diseases, including type 1 diabetes (T1D). The vitamin D levels and its receptor gene polymorphisms together in T1D are not yet investigated in the South Indian population. The present study focused on exploring the significance of vitamin D levels and vitamin D receptor (VDR) gene polymorphisms with the risk of developing T1D in the South Indian population.

Methods: Patients with T1D and unaffected first-degree relatives (FDRs) were included in this study. Genotyping of VDR polymorphisms at four different loci (FokI- F/f, BsmI- B/b, TaqI- T/t, and ApaI- A/a) was assessed through the amplification refractive mutation system-polymerase chain reaction method. Serum vitamin D levels were measured in 98 T1D patients and 75 age- and sex-matched siblings.

Results: A total of 120 patients with T1D and 214 FDRs were included. Vitamin D deficiency (VDD) was observed in a higher proportion of T1D patients than in controls (52% vs. 32%; p<0.03). The frequency of the FokI-FF genotype was significantly higher [odds ratio (OR)=1.66; p<0.03] in T1D patients conferring a susceptible association with the disease. Nevertheless, the increased frequency of heterozygous Ff genotype (OR=0.57; p<0.02) among controls may confer a protective association with T1D. Furthermore, the transmission disequilibrium test revealed over-transmission of ApaI-A (T: U=15/5; p<0.006) and BsmI-B alleles (T: U=17/5; p<0.01) and under-transmission of BsmI-b/ApaI-a/TaqI-T haplotype (T: U=5.4/14.4; p=0.04) from parents to T1D patients.

Conclusion: The present study concludes that VDD is the major contributing risk factor to T1D development in the South Indian population. Furthermore, the FokI-FF genotype, BsmI-B, and ApaI-A alleles were positively associated with T1D. In contrast, the FokI-Ff genotype and BsmI-b/ApaI-a/TaqI-T haplotype were negatively associated with T1D.

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维生素 D 缺乏和维生素 D 受体基因多态性与 1 型糖尿病风险的关系:一项南印度家族研究
目的:维生素 D 是一种有效的免疫调节剂,与自身免疫性疾病(包括 1 型糖尿病)有关。目前尚未在南印度人群中调查维生素 D 水平及其受体基因多态性与 T1D 的关系。本研究主要探讨南印度人群中维生素 D 水平和维生素 D 受体(VDR)基因多态性与 T1D 发病风险的关系:本研究纳入了 T1D 患者和未受影响的一级亲属(FDRs)。通过扩增折射突变系统聚合酶链反应方法,对四个不同位点(FokI- F/f、BsmI- B/b、TaqI- T/t 和 ApaI-A/a)的 VDR 多态性进行基因分型。测量了 98 名 T1D 患者和 75 名年龄和性别匹配的兄弟姐妹的血清维生素 D 水平:结果:共纳入 120 名 T1D 患者和 214 名 FDRs。与对照组相比,T1D 患者中维生素 D 缺乏(VDD)的比例更高(52% 对 32%;p):本研究得出结论,在南印度人群中,维生素 D 缺乏是导致 T1D 发病的主要风险因素。此外,FokI-FF 基因型、BsmI-B 和 ApaI-A 等位基因与 T1D 呈正相关。相反,FokI-Ff 基因型和 BsmI-b/ApaI-a/TaqI-T 单倍型与 T1D 呈负相关。
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来源期刊
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
3.60
自引率
5.30%
发文量
73
审稿时长
20 weeks
期刊介绍: The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.
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