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Tea Intake and Lung Diseases: a Mendelian Randomization Study

Overview
Journal Front Immunol
Date 2024 Feb 20
PMID 38375474
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Abstract

Background: Existing studies on the relationship between tea intake and lung diseases have yielded inconsistent results, leading to an ongoing dispute on this issue. The impact of tea consumption on the respiratory system remained elucidating.

Materials And Methods: We conducted a two-sample Mendelian randomization (MR) study to evaluate the associations between five distinct tea intake phenotypes and 15 different respiratory outcomes using open Genome-wide association study (GWAS) data. The inverse variance weighted (IVW) was used for preliminary screening and a variety of complementary methods were used as sensitivity analysis to validate the robustness of MR estimates. Pathway enrichment analysis was used to explore possible mechanisms.

Results: IVW found evidence for a causal effect of standard tea intake on an increased risk of lung squamous cell cancer (LSCC) (OR = 1.004; 95% CI = 1.001-1.007; P = 0.00299). No heterogeneity or pleiotropy was detected. After adjustment for potential mediators, including smoking, educational attainment, and time spent watching television, the association was still robust in multivariable MR. KEGG and GO enrichment predicted proliferation and activation of B lymphocytes may play a role in this causal relation. No causalities were observed when evaluating the effect of other kinds of tea intake on various pulmonary diseases.

Conclusion: Our MR estimates provide causal evidence of the independent effect of standard tea intake (black tea intake) on LSCC, which may be mediated by B lymphocytes. The results implied that the population preferring black tea intake should be wary of a higher risk of LSCC.

References
1.
Hossain M, Gilbert S, Patel K, Ghosh S, Bhunia A, Kern S . Biological clues to potent DNA-damaging activities in food and flavoring. Food Chem Toxicol. 2013; 55:557-67. PMC: 3608747. DOI: 10.1016/j.fct.2013.01.058. View

2.
Kim T, Jeong G, Yang J, Lee K, Kronbichler A, van der Vliet H . Tea Consumption and Risk of Cancer: An Umbrella Review and Meta-Analysis of Observational Studies. Adv Nutr. 2020; 11(6):1437-1452. PMC: 7666907. DOI: 10.1093/advances/nmaa077. View

3.
Moayedi-Nia S, Pasquet R, Siemiatycki J, Koushik A, Ho V . Occupational Exposures and Lung Cancer Risk-An Analysis of the CARTaGENE Study. J Occup Environ Med. 2022; 64(4):295-304. DOI: 10.1097/JOM.0000000000002481. View

4.
Leong T, Bryant V . B cells in lung cancer-not just a bystander cell: a literature review. Transl Lung Cancer Res. 2021; 10(6):2830-2841. PMC: 8264333. DOI: 10.21037/tlcr-20-788. View

5.
Banat G, Tretyn A, Pullamsetti S, Wilhelm J, Weigert A, Olesch C . Immune and Inflammatory Cell Composition of Human Lung Cancer Stroma. PLoS One. 2015; 10(9):e0139073. PMC: 4587668. DOI: 10.1371/journal.pone.0139073. View