Association between the IL1B-511 C>T polymorphism and the risk of hematologic malignancies: data from a meta-analysis

Cancer Biol Ther. 2024 Dec 31;25(1):2382503. doi: 10.1080/15384047.2024.2382503. Epub 2024 Jul 22.

Abstract

The relationship between the IL1B-511C>T (rs16944) polymorphism and the risk of developing hematologic malignancies remains controversial. Thus, we performed a meta-analysis to evaluate the association between IL1B-511C>T polymorphism and the risk of developing hematologic malignancies. A comprehensive search was conducted to identify all eligible studies on IL1B-511C>T polymorphism and hematologic malignancies. Twelve case-control studies, with 2,896 cases and 3,716 controls, were selected for the analysis. The overall data failed to indicate a significant association between IL1B-511C>T polymorphism and the risk of hematologic malignancies (OR:1.06, 95% Confidence Interval [CI]: 0.93-1.22). Moreover, non-significant associations were observed in a stratified analysis according to neoplasm type (multiple myeloma, Hodgkin's lymphoma, and non-Hodgkin's lymphoma), ethnicity (European and Asian), and Hardy-Weinberg equilibrium. In summary, our results suggest that there is no association between the IL1B-511C>T polymorphism and the risk of hematologic malignancies. As such, further large-scale studies are needed to confirm our findings.

Keywords: Interleukin-1; genetic variations; hematologic malignancies; meta-analysis; polymorphism.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Case-Control Studies
  • Genetic Predisposition to Disease*
  • Hematologic Neoplasms* / genetics
  • Humans
  • Interleukin-1beta* / genetics
  • Polymorphism, Single Nucleotide*
  • Risk Factors

Substances

  • Interleukin-1beta

Grants and funding

Financial support was provided in the form of grants from Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM) [Pró-Estado Program - #002/2008, #007/2018 and #005/2019 and POSGRAD Program #002/2023 and #002/2024], Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) [PDPG-CONSOLIDACAO-3-4 Program #88887.707248/2022-00]. FSAH, DSP, and FM-G have fellowships from CAPES and CNPq (Master ’sand PhD students). AGC is a level 2 CNPq research fellow and FAPEAM research fellow [PRODOC Program #003/2022]. The funders had no role in the study design, data collection and analysis, decision to publish, or manuscript preparation.