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Association between habitual coffee consumption and multiple disease outcomes: A Mendelian randomisation phenome-wide association study in the UK Biobank.
Clin Nutr. 2020 11; 39(11):3467-3476.CN

Abstract

BACKGROUND

Coffee is the most commonly consumed beverage in the world after water, however the debate as to whether coffee consumption is beneficial or detrimental to health continues. Current evidence of the link between coffee and health outcomes is predominately observational, thus subject to methodological issues such a confounding and reverse causation.

METHODS

This Mendelian randomisation phenome-wide association study (MR-PheWAS) used information from up to 333,214 participants of White-British ancestry in the UK Biobank to examine the causal association between genetically instrumented habitual coffee consumption and the full range of disease outcomes. We constructed a genetic risk score for habitual coffee consumption and screened for associations with disease outcomes across 1117 case-control series. All signals under false discovery rate controlled threshold (5.8 × 10-4) were followed by Mendelian randomisation (MR) analyses, with replication in independent data sources where possible.

RESULTS

The initial phenome-wide association analysis identified signals for 13 outcomes representing five distinct diseases. The strongest signal was seen for gout (P = 2.3 × 10-12), but there was notable pleiotropy (Pdistortion <0.001) and MR analyses did not support an association with habitual coffee consumption (inverse variance weighted MR OR 0.41, 95% CI 0.08 to 2.25, P = 0.31). Support for a possible causal relationship between habitual coffee consumption was only obtained for four distinct disease outcomes, including an increased odds of osteoarthrosis (OR 1.23, 95% CI 1.11 to 1.35), other arthropathies (OR 1.22, 95% CI 1.12 to 1.33) and overweight (OR 1.28, 95% CI 1.05 to 1.56), and a lower odds of postmenopausal bleeding (OR 0.72, 95% CI 0.63 to 0.82). Evidence for an association between habitual coffee consumption and these four diseases was also supported by phenotypic associations with self-reported coffee consumption.

CONCLUSIONS

This large-scale MR-PheWAS provided little evidence for notable harm or benefit with respect to higher habitual coffee consumption. The only evidence for harm was seen with respect to osteoarthrosis, other arthropathies and obesity.

Authors+Show Affiliations

Australian Centre for Precision Health, University of South Australia Cancer Research Institute, Adelaide, Australia.Australian Centre for Precision Health, University of South Australia Cancer Research Institute, Adelaide, Australia; Department of Pharmacology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.Australian Centre for Precision Health, University of South Australia Cancer Research Institute, Adelaide, Australia.Australian Centre for Precision Health, University of South Australia Cancer Research Institute, Adelaide, Australia; Population, Policy and Practice, UCL Great Ormond Street Institute of Child Health, London, UK; South Australian Health and Medical Research Institute, Adelaide, Australia. Electronic address: elina.hypponen@unisa.edu.au.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

32284183

Citation

Nicolopoulos, Konstance, et al. "Association Between Habitual Coffee Consumption and Multiple Disease Outcomes: a Mendelian Randomisation Phenome-wide Association Study in the UK Biobank." Clinical Nutrition (Edinburgh, Scotland), vol. 39, no. 11, 2020, pp. 3467-3476.
Nicolopoulos K, Mulugeta A, Zhou A, et al. Association between habitual coffee consumption and multiple disease outcomes: A Mendelian randomisation phenome-wide association study in the UK Biobank. Clin Nutr. 2020;39(11):3467-3476.
Nicolopoulos, K., Mulugeta, A., Zhou, A., & Hyppönen, E. (2020). Association between habitual coffee consumption and multiple disease outcomes: A Mendelian randomisation phenome-wide association study in the UK Biobank. Clinical Nutrition (Edinburgh, Scotland), 39(11), 3467-3476. https://doi.org/10.1016/j.clnu.2020.03.009
Nicolopoulos K, et al. Association Between Habitual Coffee Consumption and Multiple Disease Outcomes: a Mendelian Randomisation Phenome-wide Association Study in the UK Biobank. Clin Nutr. 2020;39(11):3467-3476. PubMed PMID: 32284183.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Association between habitual coffee consumption and multiple disease outcomes: A Mendelian randomisation phenome-wide association study in the UK Biobank. AU - Nicolopoulos,Konstance, AU - Mulugeta,Anwar, AU - Zhou,Ang, AU - Hyppönen,Elina, Y1 - 2020/03/13/ PY - 2019/09/08/received PY - 2020/03/03/revised PY - 2020/03/07/accepted PY - 2020/4/15/pubmed PY - 2021/8/20/medline PY - 2020/4/15/entrez KW - Coffee consumption KW - Mendelian randomisation KW - PheWAS KW - UK Biobank SP - 3467 EP - 3476 JF - Clinical nutrition (Edinburgh, Scotland) JO - Clin Nutr VL - 39 IS - 11 N2 - BACKGROUND: Coffee is the most commonly consumed beverage in the world after water, however the debate as to whether coffee consumption is beneficial or detrimental to health continues. Current evidence of the link between coffee and health outcomes is predominately observational, thus subject to methodological issues such a confounding and reverse causation. METHODS: This Mendelian randomisation phenome-wide association study (MR-PheWAS) used information from up to 333,214 participants of White-British ancestry in the UK Biobank to examine the causal association between genetically instrumented habitual coffee consumption and the full range of disease outcomes. We constructed a genetic risk score for habitual coffee consumption and screened for associations with disease outcomes across 1117 case-control series. All signals under false discovery rate controlled threshold (5.8 × 10-4) were followed by Mendelian randomisation (MR) analyses, with replication in independent data sources where possible. RESULTS: The initial phenome-wide association analysis identified signals for 13 outcomes representing five distinct diseases. The strongest signal was seen for gout (P = 2.3 × 10-12), but there was notable pleiotropy (Pdistortion <0.001) and MR analyses did not support an association with habitual coffee consumption (inverse variance weighted MR OR 0.41, 95% CI 0.08 to 2.25, P = 0.31). Support for a possible causal relationship between habitual coffee consumption was only obtained for four distinct disease outcomes, including an increased odds of osteoarthrosis (OR 1.23, 95% CI 1.11 to 1.35), other arthropathies (OR 1.22, 95% CI 1.12 to 1.33) and overweight (OR 1.28, 95% CI 1.05 to 1.56), and a lower odds of postmenopausal bleeding (OR 0.72, 95% CI 0.63 to 0.82). Evidence for an association between habitual coffee consumption and these four diseases was also supported by phenotypic associations with self-reported coffee consumption. CONCLUSIONS: This large-scale MR-PheWAS provided little evidence for notable harm or benefit with respect to higher habitual coffee consumption. The only evidence for harm was seen with respect to osteoarthrosis, other arthropathies and obesity. SN - 1532-1983 UR - https://www.unboundmedicine.com/medline/citation/32284183/Association_between_habitual_coffee_consumption_and_multiple_disease_outcomes:_A_Mendelian_randomisation_phenome_wide_association_study_in_the_UK_Biobank_ DB - PRIME DP - Unbound Medicine ER -