Association of CTLA-4 polymorphisms with hematologic malignancy susceptibility: a meta-analysis
Xuefen Yan1, Nana Zhang1, Gang Wang1
1Department of Hematology, the Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, China.
Cytotoxic T-lymphocyte antigen-4 (CTLA-4) 49A/G and 319C/T gene variations are linked to hematologic malignancy risk. This meta-analysis clarifies their association with increased susceptibility to certain blood cancers.
Area of Science:
- Immunogenetics
- Oncology
- Genetic Epidemiology
Background:
- Cytotoxic T-lymphocyte antigen-4 (CTLA-4) gene polymorphisms have been investigated for their role in hematologic malignancy susceptibility.
- Previous studies reported conflicting results, necessitating a comprehensive analysis.
Purpose of the Study:
- To conduct a meta-analysis investigating the association between various CTLA-4 polymorphisms and susceptibility to hematologic malignancies.
- To clarify the inconsistent findings from prior research.
Main Methods:
- A systematic literature search was performed across major databases (Cochrane Library, PubMed, Embase) up to September 20, 2024.
- Pooled odds ratios (OR) and 95% confidence intervals (CI) were calculated to assess the strength of associations.
- Statistical analysis was performed using STATA 12.0.
Main Results:
- The meta-analysis included 13 studies examining CTLA-4 polymorphisms: 49A/G, 60A/G, 318T/C, 1661A/G, and 319C/T.
- CTLA-4 49A/G polymorphism showed a significant association with increased hematologic malignancy risk (OR = 1.77, 95% CI = 1.56-2.02), particularly in non-Hodgkin lymphoma, multiple myeloma, and leukemia.
- CTLA-4 319C/T polymorphism was associated with a decreased risk of chronic lymphocytic leukemia. No significant associations were found for CTLA-4 60A/G, 318T/C, and 1661A/G polymorphisms.
Conclusions:
- CTLA-4 49A/G and 319C/T polymorphisms are significantly associated with hematologic malignancy susceptibility.
- These findings contribute to understanding the genetic factors influencing blood cancer risk.
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