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Association between FCGR2A rs1801274 and MUC5B rs35705950 variations and pneumonia susceptibility
Xueshu Shi1, Yue Ma2, Haiyan Li3
1Nursing Division, The second affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, 300150, P.R. China.
Background:
Herein, we collected currently published data to comprehensively evaluate the impact of the FCGR2A (Fc fragment of IgG receptor IIa) rs1801274 and MUC5B (mucin 5B, oligomeric mucus/gel-forming) rs35705950 variations on susceptibility to pneumonia diseases.
Methods:
We retrieved case-control studies from three online databases and applied the statistical approach of meta-analysis for a series of pooling analyses.
Results:
A total of fourteen case-control studies were included for FCGR2A rs1801274; while thirty-one case-control studies were included for MUC5B rs35705950. No significant difference between pneumonia cases and controls for FCGR2A rs1801274 was found. However, MUC5B rs35705950 was significantly associated with pneumonia susceptibility in the whole population under the genetic models of allelic T vs. G [OR (odds ratio) =3.78], carrier T vs. G (OR = 3.31), TT vs. GG (OR = 13.66), GT vs. GG (OR = 4.78), GT + TT vs. GG (OR = 5.05), and TT vs. GG + GT (OR = 6.47) (all P < 0.001, Bonferroni-adjusted P < 0.006; false discovery rate-adjusted P < 0.0010). Furthermore, we observed a similar positive result for subgroup analyses of "Caucasian", "Asian", "population-based control", and "idiopathic pulmonary fibrosis".
Conclusions:
MUC5B rs35705950, but not FCGR2A rs1801274, increases susceptibility to clinical pneumonia, especially to idiopathic pulmonary fibrosis, in both the Caucasian and Asian populations.
Insights
Genetic variations in MUC5B rs35705950 significantly increase pneumonia susceptibility, particularly idiopathic pulmonary fibrosis. FCGR2A rs1801274 showed no association with pneumonia risk in this meta-analysis.
Area of Science:
- Genetics
- Pulmonology
- Epidemiology
Background:
- Pneumonia susceptibility is influenced by genetic factors.
- The roles of FCGR2A rs1801274 and MUC5B rs35705950 in pneumonia risk require comprehensive evaluation.
- Published data on these genetic variations and pneumonia are fragmented.
Purpose of the Study:
- To conduct a meta-analysis evaluating the impact of FCGR2A (Fc fragment of IgG receptor IIa) rs1801274 and MUC5B (mucin 5B, oligomeric mucus/gel-forming) rs35705950 variations on pneumonia susceptibility.
- To pool data from existing case-control studies for robust statistical analysis.
- To clarify the association between these specific genetic markers and the risk of developing pneumonia.
Main Methods:
- Systematic retrieval of case-control studies from multiple online databases.
- Application of meta-analysis techniques for pooling and analyzing genetic association data.
- Inclusion of fourteen studies for FCGR2A rs1801274 and thirty-one studies for MUC5B rs35705950.
Main Results:
- No significant association was found between FCGR2A rs1801274 and pneumonia susceptibility.
- MUC5B rs35705950 demonstrated a significant association with increased pneumonia susceptibility across various genetic models (allelic, carrier, homozygous, heterozygous).
- Subgroup analyses confirmed the positive association for MUC5B rs35705950 in Caucasian and Asian populations, and for idiopathic pulmonary fibrosis.
Conclusions:
- The MUC5B rs35705950 polymorphism is a significant risk factor for pneumonia, especially idiopathic pulmonary fibrosis.
- FCGR2A rs1801274 does not appear to influence susceptibility to clinical pneumonia.
- These findings highlight the importance of MUC5B rs35705950 in respiratory disease pathogenesis across diverse populations.
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