A meta-analysis of the association between inflammatory cytokine polymorphism and neonatal sepsis
- PMID: 38848433
- PMCID: PMC11161124
- DOI: 10.1371/journal.pone.0301859
A meta-analysis of the association between inflammatory cytokine polymorphism and neonatal sepsis
Abstract
Objective: The purpose of this study is to investigate the relationship between single nucleotide polymorphisms of inflammatory cytokines and neonatal sepsis through meta-analysis.
Methods: We collected research literature on the correlation between inflammatory cytokine polymorphisms and neonatal sepsis published before August 2023 through computer searches of databases such as PubMed, Embase, etc. The Stata 14.0 software was utilized for Meta-analysis. To assess heterogeneity, the chi-squared Q-test and I2 statistics were used. The Egger and Begg tests were conducted to determine the possibility of publication bias.
Results: After reviewing 1129 articles, 29 relevant articles involving 3348 cases and 5183 controls were included in the study. The meta-analysis conducted on IL-1βrs1143643 polymorphism revealed significant findings: the T allele genotype has a lower risk of neonatal sepsis(P = 0.000, OR = 0.224, 95% CI: 0.168-0.299), while the TC and TT genotypes showed an increased risk(TC: P = 0.000,OR = 4.251, 95% CI: 2.226-8.119; TT: P = 0.019,OR = 2.020, 95% CI: 1.122-3.639). Similarly, newborns with the IL-6-174 CC genotype had a significantly higher risk of sepsis(P = 0.000,OR = 1.591, 95% CI: 1.154-2.194), while those with the IL-8-rs4073 TT (P = 0.003,OR = 0.467, 95% CI: 0.280-0.777)and TT + AA(P = 0.003,OR = 0.497, 95% CI: 0.315-0.785) genotypes had a significantly lower risk of sepsis. For the IL-10-1082 gene, newborns with the AA genotype(P = 0.002,OR = 1.702, 95% CI: 1.218-2.377), as well as those with the AA + GA genotype(P = 0.016,OR = 1.731, 95% CI: 1.108-2.705), had a significantly higher risk of sepsis. Lastly, newborns carrying the TNF-α-308 A allele (P = 0.016,OR = 1.257, 95% CI: 1.044-1.513)or the AA genotype(P = 0.009,OR = 1.913, 95% CI: 1.179-3.10) have a significantly increased risk of sepsis. Notwithstanding, additional studies must be included for validation. Applying these cytokines in clinical practice and integrating them into auxiliary examinations facilitates the early detection of susceptible populations for neonatal sepsis, thereby providing a new diagnostic and therapeutic approach for neonatal sepsis.
Copyright: © 2024 Liang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Conflict of interest statement
The authors have declared that no competing interests exist.
Figures



































Similar articles
-
[Association between interleukin-8 rs4073 polymorphisms and susceptibility to neonatal sepsis].Zhongguo Dang Dai Er Ke Za Zhi. 2020 Apr;22(4):323-327. doi: 10.7499/j.issn.1008-8830.1910068. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 32312369 Free PMC article. Chinese.
-
The association between interleukin-8 gene polymorphism and the risk of sepsis in older adults.J Orthop Surg Res. 2024 Nov 28;19(1):804. doi: 10.1186/s13018-024-05296-5. J Orthop Surg Res. 2024. PMID: 39609657 Free PMC article.
-
Investigation of TNF-alpha, TGF-beta 1, IL-10, IL-6, IFN-gamma, MBL, GPIA, and IL1A gene polymorphisms in patients with idiopathic thrombocytopenic purpura.Platelets. 2011;22(8):588-95. doi: 10.3109/09537104.2011.577255. Epub 2011 May 19. Platelets. 2011. PMID: 21591983
-
Interleukin-6 gene-174 G/C promoter polymorphism is not associated with multiple myeloma susceptibility: evidence from meta-analysis: A systematic review and meta-analysis.Medicine (Baltimore). 2021 Feb 12;100(6):e24647. doi: 10.1097/MD.0000000000024647. Medicine (Baltimore). 2021. PMID: 33578591 Free PMC article.
-
Interleukin-23 receptor genetic polymorphisms and ulcerative colitis susceptibility: A meta-analysis.Clin Res Hepatol Gastroenterol. 2015 Sep;39(4):516-25. doi: 10.1016/j.clinre.2014.10.009. Epub 2014 Nov 11. Clin Res Hepatol Gastroenterol. 2015. PMID: 25497273 Review.
Cited by
-
The Role of Cytokine Gene Polymorphisms in Rehabilitation Outcome After Traumatic Brain Injury.Cells. 2025 Jul 10;14(14):1056. doi: 10.3390/cells14141056. Cells. 2025. PMID: 40710309 Free PMC article.
-
Association between tumor necrosis factor-α gene polymorphism and interleukin-6 level with mortality of neonatal sepsis.Narra J. 2024 Dec;4(3):e1234. doi: 10.52225/narra.v4i3.1234. Epub 2024 Oct 31. Narra J. 2024. PMID: 39816047 Free PMC article.
References
-
- The Neonatal Group of the Pediatric Branch of the Chinese Medical Association, The Infection Professional Committee of the Neonatal Pediatric Branch of the Chinese Medical Association. Expert Consensus on Diagnosis and Treatment of Neonatal Septicemia (2019 Edition). Chinese Journal of Pediatrics. 2019; 57 (4): 252–257. - PubMed
-
- Xiao Chen, Jianhua Fu. Research progress in the diagnosis and treatment of neonatal sepsis. Chinese Journal of Neonatology. 2017;32 (3): 236–239.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous