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维生素 D 受体基因多态性(Fok1)、维生素 D 状态与自身免疫性甲状腺炎的关系。

Association between Vitamin D Receptor Gene Polymorphism (Fok 1), Vitamin D Status and Autoimmune Thyroiditis.

机构信息

Dr Manali Sinharay, Associate Professor, Department of Biochemistry, Calcutta National Medical College, Kolkata, West Bengal, India; E-mail:

出版信息

Mymensingh Med J. 2024 Jul;33(3):914-922.

Abstract

Autoimmune thyroiditis gradually destroys the thyroid gland leading to hypothyroidism and may even lead to papillary thyroid carcinoma. Deficiency of Vitamin D has been linked to development of autoimmunity. Single nucleotide polymorphisms of the Vitamin D receptor gene have associated with autoimmune diseases in several studies. In this hospital based non interventional cross-sectional study Vitamin D receptor gene was studied for FokI (rs2228570) polymorphism from purified DNA in forty-eight adult cases and fifty age and sex matched healthy controls. This study was conducted in the department of Biochemistry, Calcutta National Medical College, Kolkata, West Bengal, India from January 2021 to July 2022. Their DNA was isolated using phenol chloroform method and were analysed for the related single nucleotide polymorphism by restriction digestion using appropriate restriction enzymes after amplification by PCR. Differences in allele frequencies between two groups were estimated by chi square and odds ratio test. Any potential association between the vitamin D anti TPO antibody and thyroid hormone status with polymorphic variations were assessed by post hoc ANOVA among the three genotypes. The distribution of FF genotype was significantly higher among the case group (Χ²=10.2788, p=0.006). The odds ratio for the allele F was significantly higher in case group for a range of 1.97 to 5.94 for 95 percent confidence interval (Χ²=13.9678, p=<0.001). The genotype FF group had significantly lowest Vitamin D (p=0.008) and highest Anti TPO ab (p=0.031) compared to Ff and ff genotypes. Thus, significant association was revealed between the VDR gene Fok1(rs2228570) polymorphism and autoimmune thyroiditis with the predominance of FF genotype being a strong susceptibility factor for autoimmune thyroiditis and Vitamin D deficiency in the studied population of Eastern India.

摘要

自身免疫性甲状腺炎逐渐破坏甲状腺,导致甲状腺功能减退症,甚至可能导致甲状腺乳头状癌。维生素 D 缺乏与自身免疫的发展有关。几项研究表明,维生素 D 受体基因的单核苷酸多态性与自身免疫性疾病有关。在这项基于医院的非干预性横断面研究中,从 48 例成年病例和 50 例年龄和性别匹配的健康对照者的纯化 DNA 中研究了维生素 D 受体基因的 FokI(rs2228570)多态性。这项研究是在印度西孟加拉邦加尔各答的加尔各答国家医学院生物化学系进行的,时间是从 2021 年 1 月到 2022 年 7 月。使用苯酚-氯仿法提取他们的 DNA,然后通过聚合酶链反应(PCR)扩增后,使用适当的限制性内切酶进行限制性消化来分析相关的单核苷酸多态性。通过卡方检验和优势比检验估计两组间等位基因频率的差异。在三种基因型之间,通过事后 ANOVA 评估维生素 D 抗 TPO 抗体和甲状腺激素状态与多态性变异之间的任何潜在关联。病例组 FF 基因型的分布明显较高(Χ²=10.2788,p=0.006)。在病例组中,等位基因 F 的优势比显著更高,置信区间为 1.97 至 5.94(Χ²=13.9678,p<0.001)。与 Ff 和 ff 基因型相比,FF 基因型组的维生素 D 显著最低(p=0.008),抗 TPO ab 显著最高(p=0.031)。因此,维生素 D 受体基因 Fok1(rs2228570)多态性与自身免疫性甲状腺炎之间存在显著相关性,FF 基因型的优势是该研究人群中自身免疫性甲状腺炎和维生素 D 缺乏的一个强烈易感因素。

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