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维生素D受体基因多态性与原发性高血压伴25-羟基维生素D缺乏的状况

Status of Vitamin D Receptor Gene Polymorphism and 25-Hydroxy Vitamin D Deficiency with Essential Hypertension.

作者信息

Prasad M, Rajarajeswari D, Aruna P, Ramalingam K, Viswakumar R, Fathima Nusrath, Vishwakarma Sandeep Kumar, Khan Aleem Ahmed

机构信息

Department of Biochemistry, Narayana Medical College and Hospital, Chinthareddypalem, Nellore, Andhra Pradesh 524003 India.

Department of Biochemistry, ACSR Government Medical College, Dargamitta, Nellore, Andhra Pradesh 524004 India.

出版信息

Indian J Clin Biochem. 2022 Jul;37(3):335-341. doi: 10.1007/s12291-021-00984-z. Epub 2021 Jun 15.

DOI:10.1007/s12291-021-00984-z
PMID:34149207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8203720/
Abstract

Essential hypertension (EH) is a multifactorial and complex disease with high rate of incidence and associated co-morbidities. Previous studies do not provide unanimous results for the risk of hypertension and association with Fok I genotype frequency and serum vitamin D levels. Hence, this study was undertaken to determine the status of Fok I vitamin D receptor (VDR) gene polymorphism along with vitamin D levels and blood pressure in patients with EH. Four hundred (200 controls and 200 cases of essential hypertension) participants from general Indian population were enrolled in this study. Peripheral blood samples were collected for genotyping Fok I-VDR gene polymorphism using PCR-RFLP method whereas 25-OH vitamin D levels in serum were quantified using high performance liquid chromatography (HPLC). Significantly reduced 25-OH vitamin D levels were observed in patients with EH (24.04 ± 8.62 vs 50.46 ± 15.46) compared to control subjects ( = 0.0001). Homozygous recessive genotype 'ff' frequency was increased by 8.06 fold (CI: 3.71-17.47,  = 0.0001) in patients with EH compared to dominant 'FF' genotype frequency. In conclusion, recessive 'ff' genotype frequency correlates with reduced serum vitamin D levels and results in significantly increased systolic and diastolic blood pressures leading to predisposition of EH.

摘要

原发性高血压(EH)是一种多因素的复杂疾病,发病率高且伴有多种合并症。先前的研究对于高血压风险以及与Fok I基因型频率和血清维生素D水平的关联并未得出一致结果。因此,本研究旨在确定原发性高血压患者中Fok I维生素D受体(VDR)基因多态性状况以及维生素D水平和血压情况。本研究纳入了来自印度普通人群的400名参与者(200名对照者和200例原发性高血压患者)。采集外周血样本,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对Fok I-VDR基因多态性进行基因分型,而血清中25-羟基维生素D水平则采用高效液相色谱法(HPLC)进行定量测定。与对照受试者相比,原发性高血压患者的25-羟基维生素D水平显著降低(24.04±8.62 vs 50.46±15.46,P = 0.0001)。与显性“FF”基因型频率相比,原发性高血压患者中纯合隐性基因型“ff”的频率增加了8.06倍(置信区间:3.71 - 17.47,P = 0.0001)。总之,隐性“ff”基因型频率与血清维生素D水平降低相关,并导致收缩压和舒张压显著升高,从而易患原发性高血压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9e/9300789/6d5cea658835/12291_2021_984_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9e/9300789/5d3f0bfc50be/12291_2021_984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9e/9300789/6d5cea658835/12291_2021_984_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9e/9300789/5d3f0bfc50be/12291_2021_984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9e/9300789/6d5cea658835/12291_2021_984_Fig2_HTML.jpg

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