VDR基因多态性在北印度儿童社区获得性肺炎中的作用:一项病例对照研究

International journal of molecular epidemiology and genetics Pub Date : 2021-02-15 eCollection Date: 2021-01-01
Nidhi Awasthi, Shally Awasthi, Shivani Pandey
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引用次数: 0

摘要

社区获得性肺炎(CAP)是全球五岁以下儿童死亡的主要原因。目前,维生素D受体(VDR)基因是一个新兴的调节炎症途径的因子,可能会改变对感染的反应,并可能改变CAP的结果。本研究的目的是研究2-59个月儿童VDR基因多态性ApaI, FokI, TaqI, BsmI与CAP的关系。经父母同意,患有世卫组织定义的CAP的住院儿童(2-59个月)被纳入病例。招募病例后一周内从医院免疫门诊招募年龄匹配的健康对照。排除临床诊断为囊性纤维化和先天性心脏病的儿童。采用PCR-RFLP方法对4个VDR基因多态性ApaI、FokI、TaqI、BsmI进行分型。2016年10月至2019年10月,共招募160例(女性占34.37%)和160例对照组(女性占47.5%)。患者平均年龄26.30±23.10个月,对照组25.93±15.99个月。在FokI (rs2228570)多态性中,杂合子基因型(CT) [OR=2.06, 95% CI=1.25 ~ 3.39, P=0.00]和突变等位基因(T) [OR=1.45, 95% CI=1.06 ~ 2.00, P=0.02]与CAP风险相关。在VDR基因中,FokI多态性易患印度儿童CAP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of VDR gene polymorphisms with community acquired pneumonia in North Indian children: a case-control study.

Community-acquired pneumonia (CAP) is a leading cause of death in children under five years of age globally. Currently, the vitamin D receptor (VDR) gene is an emerging factor that regulates inflammatory pathways that may alter the response to infections and possibly modify the outcome of CAP. The objective of this study was to investigate the association of VDR gene polymorphisms ApaI, FokI, TaqI, BsmI with CAP in children aged 2-59 months. Hospitalized children aged (2-59 months) with WHO-defined CAP were included as cases after parental consent. Age-matched healthy controls were recruited from the immunization clinic of the hospital within one week of the recruitment of the case. Children with a clinical diagnosis of cystic fibrosis and congenital heart disease were excluded. Four VDR gene polymorphisms, ApaI, FokI, TaqI, BsmI were genotyped by using PCR-RFLP. From Oct-2016 to Oct-2019, 160 cases (34.37% females) and 160 controls (47.5% females) were recruited. Mean age of the cases was 26.30±23.10 months and controls 25.93±15.99 months. In FokI (rs2228570 polymorphism, heterozygous genotype (CT) [OR=2.06, 95% CI=1.25-3.39, P=0.00] and mutant allele (T) [OR=1.45, 95% CI=1.06-2.00, P=0.02] were found to be associated with the risk of CAP. In VDR gene, FokI polymorphism predisposes to CAP in Indian children.

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