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北印度儿童社区获得性肺炎中基因多态性的作用:一项病例对照研究。

Role of gene polymorphisms with community acquired pneumonia in North Indian children: a case-control study.

作者信息

Awasthi Nidhi, Awasthi Shally, Pandey Shivani

机构信息

Department of Pediatrics, King George's Medical University Lucknow, UP, India.

Department of Biochemistry, King George's Medical University Lucknow, India.

出版信息

Int J Mol Epidemiol Genet. 2021 Feb 15;12(1):1-8. eCollection 2021.

Abstract

Community-acquired pneumonia (CAP) is a leading cause of death in children under five years of age globally. Currently, the vitamin D receptor () 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 gene polymorphisms 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 gene polymorphisms, 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 (rs2228570 polymorphism, heterozygous genotype (CT) [OR=2.06, 95% CI=1.25-3.39, =0.00] and mutant allele (T) [OR=1.45, 95% CI=1.06-2.00, =0.02] were found to be associated with the risk of CAP. In gene, polymorphism predisposes to CAP in Indian children.

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()基因是一个新出现的调节炎症途径的因素,可能会改变对感染的反应,并可能改变CAP的结局。本研究的目的是调查2至59个月大儿童的基因多态性与CAP之间的关联。在获得家长同意后,将世卫组织定义的CAP住院儿童(2至59个月)纳入病例组。在招募病例组的一周内,从医院免疫诊所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对四个基因多态性进行基因分型。2016年10月至2019年10月,招募了160例病例(女性占34.37%)和160例对照(女性占47.5%)。病例组的平均年龄为26.30±23.10个月,对照组为25.93±15.99个月。在家(rs2228570多态性)中,发现杂合基因型(CT)[OR=2.06,95%CI=1.25-3.39,=0.00]和突变等位基因(T)[OR=1.45,95%CI=1.06-2.00,=0.02]与CAP风险相关。在基因中,多态性使印度儿童易患CAP。

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