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Association of TLR4 polymorphisms (Asp299Gly and Thr399Ile) with sepsis: a meta-analysis and trial sequence analysis.

Authors :
Mu J
Shen Y
Zhu F
Zhang Q
Source :
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica [APMIS] 2024 Nov; Vol. 132 (11), pp. 869-880. Date of Electronic Publication: 2024 Sep 02.
Publication Year :
2024

Abstract

Several investigations have been carried out to explore the genetic association of TLR4 codon variants, specifically Asp299Gly and Thr399Ile, and susceptibility to sepsis, but the results have been contradictory. The present study aimed to conduct a meta-analysis to draw a definitive conclusion regarding the role of TLR4 genetic variants (Asp299Gly and Thr399Ile) in sepsis. A thorough literature search was conducted using the PubMed, Scopus, and Science Direct databases. The inclusion and exclusion criteria were established to ensure the accuracy of the data. The Comprehensive Meta-Analysis Software v4 was utilized to perform the meta-analysis and related analyses. A total of 13 studies were analyzed, including 2328 sepsis cases and 2495 healthy controls for the TLR4 Asp299Gly variant. Eight studies provided genotype data for the rs4986791 polymorphism. The Asp299Gly variant showed a marginal protective effect in the allele (p = 0.08, odds ratio = 0.71) and dominant (p = 0.09, odds ratio = 0.71) genetic models, although it was not statistically significant. The trial sequential analysis indicated that further case-control studies are necessary to draw definitive conclusions about the TLR4 polymorphisms in sepsis. The TLR4 Asp299Gly variant may have a protective effect against sepsis. However, additional research with larger sample sizes across diverse populations is required to validate this finding.<br /> (© 2024 Scandinavian Societies for Pathology, Medical Microbiology and Immunology.)

Details

Language :
English
ISSN :
1600-0463
Volume :
132
Issue :
11
Database :
MEDLINE
Journal :
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
Publication Type :
Academic Journal
Accession number :
39222487
Full Text :
https://doi.org/10.1111/apm.13463