Verma Neha, Awasthi Shally, Pandey Anuj K, Gupta Prashant
Department of Pediatrics, King George's Medical University, Lucknow, Uttar Pradesh, India.
Department of Microbiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Glob Med Genet. 2023 Jun 16;10(2):109-116. doi: 10.1055/s-0043-1770056. eCollection 2023 Jun.
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 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. 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 gene polymorphism. 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 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, < 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 gene was associated with child mortality with CAP cases. In 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.
社区获得性肺炎(CAP)是5岁以下儿童死亡的主要原因。该研究的主要目的是评估2至59个月大儿童的基因多态性与CAP的关联,次要目的是评估基因多态性与住院CAP病例死亡率的关联。 这项病例对照研究在印度北部的一家三级教学机构进行。经家长同意,将2至59个月大的住院儿童纳入病例组,这些儿童符合世界卫生组织定义的CAP。从医院的免疫诊所招募年龄匹配的健康对照。使用聚合酶链反应进行基因分型,以分析基因多态性的串联重复可变数目。 2019年10月至2021年10月,招募了330例病例(123例,女性占37.27%)和330例对照(151例,女性占45.75%)。发现该基因的A2/A2基因型与CAP儿童风险增加相关,调整后的优势比(AOR)为12.24(95%置信区间[CI]5.21-28.7,P<0.001)。还发现A2和A4等位基因与CAP风险相关。发现A1/A2基因型对CAP有保护作用,AOR为0.29(95%CI 0.19-0.45)。该基因的A2/A2基因型和A2等位基因与CAP病例的儿童死亡率相关。 在该基因中,A2/A2基因型和A2等位基因与CAP风险增加相关,而A1/A2被发现对CAP有保护作用。A2/A2基因型和A2与CAP死亡率相关。