Pulse Brain · Growing Health Evidence Index
Tier 1 — Meta-analysis / systematic reviewPeer-reviewed

Coffee and tea consumption in relation with non-alcoholic fatty liver and metabolic syndrome: A systematic review and meta-analysis of observational studies

Stefano Marventano, Federico Salomone, Justyna Godos, Francesca Romana Pluchinotta, Daniele Del Rio, Antonio Mistretta, Giuseppe Grosso

Clinical Nutrition · 2016

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Summary

This systematic review and meta-analysis synthesises observational evidence on coffee and tea consumption in relation to metabolic disorders. Coffee intake was associated with reduced likelihood of metabolic syndrome (RR 0.87, 95% CI 0.79–0.96), as was tea consumption (RR 0.83, 95% CI 0.73–0.95). Evidence on coffee consumption in NAFLD patients suggested potential protective effects on fibrosis severity, though heterogeneity in study design precluded formal pooling of these analyses.

Regional applicability

The findings are based on international observational studies and are broadly applicable to United Kingdom populations, though the review does not assess UK-specific cohorts. Transferability depends on dietary patterns and healthcare contexts being reasonably similar; the protective associations observed may vary with coffee and tea preparation methods and consumption patterns in different regions.

Key measures

Risk ratios (RRs) and 95% confidence intervals for MetS; fibrosis scores in NAFLD patients; individual components of metabolic syndrome

Outcomes reported

The study examined associations between coffee and tea consumption and prevalence of non-alcoholic fatty liver disease (NAFLD) and metabolic syndrome (MetS) across observational studies. Pooled analyses estimated risk ratios for MetS according to higher versus lower consumption levels of both beverages.

Theme
Nutrition & health
Subject
Dietary patterns & chronic disease
Study type
Meta-analysis
Study design
Systematic review and meta-analysis
Source type
Peer-reviewed study
Status
Published
Geography
International
System type
Human clinical
DOI
10.1016/j.clnu.2016.03.012
Catalogue ID
SNmuw727oq-clb2a8

Topic tags

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