Association of Interleukin-1 Receptor Antagonist ( IL-1RA ) Gene Polymorphism with Community-Acquired Pneumonia in North Indian Children: A Case-Control Study.

IF 1.2 Q4 GENETICS & HEREDITY
Neha Verma, Shally Awasthi, Anuj K Pandey, Prashant Gupta
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Abstract

Background  Community-acquired pneumonia (CAP) is the leading cause of death in children < 5 years of age. The primary objective of the study was to assess the association of IL-1RA gene polymorphism in children aged 2 to 59 months with CAP and the secondary objective was to assess the association of gene polymorphism with mortality among hospitalized CAP cases. Study Design  This case-control study was conducted in a tertiary teaching institute in Northern India. Hospitalized children aged 2 to 59 months with World Health Organization-defined CAP were included as cases after parental consent. Age-matched healthy controls were recruited from the immunization clinic of the hospital. Genotyping was done using polymerase chain reaction to analyze the variable number of tandem repeats of IL-1RA gene polymorphism. Result  From October 2019 to October 2021, 330 cases (123, 37.27% female), and 330 controls (151, 45.75% female) were recruited. Genotype A2/A2 of the IL-1RA gene was found to be associated with the increased risk for CAP children with adjusted odds ratio (AOR) of 12.24 (95% confidence interval [CI] 5.21-28.7, p  < 0.001). A2 and A4 alleles were also found to be at risk for CAP. A1/A2 genotype was found to be protective for CAP with an AOR of 0.29 (95% CI 0.19-19.0.45). The genotype A2/A2 and A2 allele of IL-1RA gene was associated with child mortality with CAP cases. Conclusion  In IL1RA gene, A2/A2 genotype and A2 allele were associated with increased risk of CAP and A1/A2 were found to be protective for CAP. The genotype A2/A2 and A2 was associated with CAP mortality.

Abstract Image

白介素-1受体拮抗剂(IL-1RA)基因多态性与北印度儿童社区获得性肺炎的关系:一项病例对照研究
背景社区获得性肺炎(CAP)是2 ~ 59月龄CAP患儿IL-1RA基因多态性的主要死亡原因,次要目的是评估基因多态性与住院CAP病例死亡率的关系。研究设计本病例对照研究在印度北部的一所高等教育学院进行。患有世界卫生组织定义的CAP的2至59个月住院儿童经父母同意纳入病例。从该院免疫门诊招募年龄匹配的健康对照。采用聚合酶链反应进行基因分型,分析IL-1RA基因多态性串联重复数的变化。结果2019年10月至2021年10月,共招募病例330例(女性123例,占37.27%),对照组330例(女性151例,占45.75%)。IL-1RA基因A2/A2型与CAP患儿风险增加相关,校正优势比(AOR)为12.24(95%可信区间[CI] 5.21 ~ 28.7), IL-1RA基因与CAP患儿死亡率相关。结论在IL1RA基因中,A2/A2基因型和A2等位基因与CAP风险增加相关,A1/A2基因型对CAP有保护作用,A2/A2基因型和A2基因型与CAP死亡率相关。
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来源期刊
Global Medical Genetics
Global Medical Genetics GENETICS & HEREDITY-
自引率
11.80%
发文量
30
审稿时长
14 weeks
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