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Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study
BACKGROUND: The association between coffee and caffeine consumption and the risk of renal cell carcinoma was inconsistent among observational studies, and whether these observed associations were causal remained unclear. Therefore, we performed two-sample Mendelian randomization (MR) study to assess...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441794/ https://www.ncbi.nlm.nih.gov/pubmed/36071939 http://dx.doi.org/10.3389/fnut.2022.898279 |
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author | Li, Bing-Hui Yan, Si-Yu Li, Xu-Hui Huang, Qiao Luo, Li-Sha Wang, Yun-Yun Huang, Jiao Jin, Ying-Hui Wang, Yong-Bo |
author_facet | Li, Bing-Hui Yan, Si-Yu Li, Xu-Hui Huang, Qiao Luo, Li-Sha Wang, Yun-Yun Huang, Jiao Jin, Ying-Hui Wang, Yong-Bo |
author_sort | Li, Bing-Hui |
collection | PubMed |
description | BACKGROUND: The association between coffee and caffeine consumption and the risk of renal cell carcinoma was inconsistent among observational studies, and whether these observed associations were causal remained unclear. Therefore, we performed two-sample Mendelian randomization (MR) study to assess the causal nature of the association. MATERIALS AND METHODS: In this study, 12 and two independent single nucleotide polymorphisms (SNPs) related to coffee and caffeine consumption at a genome-wide significance level of p < 5 × 10(–8) were used as instrumental variables (IVs), respectively. Summary-level data for renal cell carcinoma were taken from the FinnGen consortium with up to 174,977 individuals, and the International Agency for Research on Cancer (IARC) with 13,230 individuals. We used inverse-variance weighted (IVW) as the main method, followed by the weighted median method, the MR-Egger regression method, and the MR robust adjusted profile score method. Outlier and pleiotropic variants were assessed by the MR Pleiotropy RESidual Sum and Outlier test and MR-Egger regression. We used meta-analysis methods in fixed-effects to combine the estimates from the two sources. RESULTS: The genetically predicted coffee consumption was not associated with the risk of renal cell carcinoma in the FinnGen consortium, and the relationship was consistent in the IARC consortium. The pooled odds ratio (OR) per 50% increase of coffee consumption was 0.752 [95% confidence interval (CI), 0.512–1.105; p = 0.147]. In addition, complementary analyses that separated the coffee-related SNPs according to their relationship with blood levels of caffeine metabolites (higher, lower, or unrelated) found no relationship with renal cell carcinoma. The results were consistent after excluding eight SNPs due to potential risk factors at genome-wide significance (p < 5 × 10(–8)). Moreover, genetically predicted per 80-mg increase in caffeine consumption was not associated with the risk of renal cell carcinoma (pooled OR = 0.872, 95% CI: 0.676–1.125, p = 0.292). CONCLUSION: Our MR study provided no convincing evidence for a causal effect between coffee and caffeine consumption and the risk of renal cell carcinoma. The associations for renal cell carcinoma need to be verified in well-powered studies. |
format | Online Article Text |
id | pubmed-9441794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94417942022-09-06 Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study Li, Bing-Hui Yan, Si-Yu Li, Xu-Hui Huang, Qiao Luo, Li-Sha Wang, Yun-Yun Huang, Jiao Jin, Ying-Hui Wang, Yong-Bo Front Nutr Nutrition BACKGROUND: The association between coffee and caffeine consumption and the risk of renal cell carcinoma was inconsistent among observational studies, and whether these observed associations were causal remained unclear. Therefore, we performed two-sample Mendelian randomization (MR) study to assess the causal nature of the association. MATERIALS AND METHODS: In this study, 12 and two independent single nucleotide polymorphisms (SNPs) related to coffee and caffeine consumption at a genome-wide significance level of p < 5 × 10(–8) were used as instrumental variables (IVs), respectively. Summary-level data for renal cell carcinoma were taken from the FinnGen consortium with up to 174,977 individuals, and the International Agency for Research on Cancer (IARC) with 13,230 individuals. We used inverse-variance weighted (IVW) as the main method, followed by the weighted median method, the MR-Egger regression method, and the MR robust adjusted profile score method. Outlier and pleiotropic variants were assessed by the MR Pleiotropy RESidual Sum and Outlier test and MR-Egger regression. We used meta-analysis methods in fixed-effects to combine the estimates from the two sources. RESULTS: The genetically predicted coffee consumption was not associated with the risk of renal cell carcinoma in the FinnGen consortium, and the relationship was consistent in the IARC consortium. The pooled odds ratio (OR) per 50% increase of coffee consumption was 0.752 [95% confidence interval (CI), 0.512–1.105; p = 0.147]. In addition, complementary analyses that separated the coffee-related SNPs according to their relationship with blood levels of caffeine metabolites (higher, lower, or unrelated) found no relationship with renal cell carcinoma. The results were consistent after excluding eight SNPs due to potential risk factors at genome-wide significance (p < 5 × 10(–8)). Moreover, genetically predicted per 80-mg increase in caffeine consumption was not associated with the risk of renal cell carcinoma (pooled OR = 0.872, 95% CI: 0.676–1.125, p = 0.292). CONCLUSION: Our MR study provided no convincing evidence for a causal effect between coffee and caffeine consumption and the risk of renal cell carcinoma. The associations for renal cell carcinoma need to be verified in well-powered studies. Frontiers Media S.A. 2022-08-22 /pmc/articles/PMC9441794/ /pubmed/36071939 http://dx.doi.org/10.3389/fnut.2022.898279 Text en Copyright © 2022 Li, Yan, Li, Huang, Luo, Wang, Huang, Jin and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Li, Bing-Hui Yan, Si-Yu Li, Xu-Hui Huang, Qiao Luo, Li-Sha Wang, Yun-Yun Huang, Jiao Jin, Ying-Hui Wang, Yong-Bo Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title | Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title_full | Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title_fullStr | Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title_full_unstemmed | Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title_short | Coffee and caffeine consumption and risk of renal cell carcinoma: A Mendelian randomization study |
title_sort | coffee and caffeine consumption and risk of renal cell carcinoma: a mendelian randomization study |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441794/ https://www.ncbi.nlm.nih.gov/pubmed/36071939 http://dx.doi.org/10.3389/fnut.2022.898279 |
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