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Association of IL-6-572 polymorphism with sepsis: An updated meta-analysis.
Hou, Fang; Gao, Jing; Zhang, Li; Liu, Chang.
Afiliação
  • Hou F; Department of Intensive Care Unit, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, China.
  • Gao J; Department of Nursing, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, China. Electronic address: xydyfy_gaojing@126.com.
  • Zhang L; Department of Nursing, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, China.
  • Liu C; First Affiliated Hospital of Xinjiang Medical University, Xinjiang, China.
Cytokine ; 179: 156597, 2024 07.
Article em En | MEDLINE | ID: mdl-38643631
ABSTRACT

OBJECTIVES:

To analyze the relationship between IL and 6 572C/G polymorphism with sepsis.

METHODS:

Searching 8 databases the Cochrane Library, China National Knowledge Infrastructure (CNKI), China Biology Medicine (CBM), Chongqing VIP, Embase, PubMed, WanFang Data, and Web of Science from inception to October 1, 2023. Meta-analysis was performed by using Review Manager 5.4 and STATA 15.0.

RESULTS:

9 studies were included, 1 study was excluded from the previous meta-analysis, and 6 studies were added. Sensitivity analysis suggested that the results were relatively robust. The P values of Egger test indicated that no conspicuous publication bias was found.

CONCLUSION:

According to the meta-analysis results of existing studies, the IL-6 572C/G GG genotype and G allele are risk factors for sepsis, this result changes the previous conclusion that the IL-6 572 polymorphism is not related to sepsis. However, the results still need to be conservatively treated due to the sample size was not large enough.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interleucina-6 / Sepse / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interleucina-6 / Sepse / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article