Evidence mapPaperPMID 41909702Full record

ArticleFrontiers in immunology2026

Timing of coffee consumption and insulin resistance: evidence from human and animal studies.

Peiyan Liu, Guixiang Yao, Yixia Wu, Qi Zhou

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Peiyan LiuDepartment of Clinical Nutrition, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Guixiang YaoState Key Laboratory for Innovation and Transformation of Luobing Theory, Key Laboratory of Cardiovascular Remodeling and Function Research of MOE, NHC, CAMS and Shandong Province, Department of Cardiology, Qilu Hospital of Shandong University, Jinan, China.
Yixia WuDepartment of Clinical Nutrition, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Qi ZhouLaboratory of Translational Gastroenterology, Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The role of coffee consumption timing in insulin resistance (IR), a key driver of cardiovascular-metabolic diseases, remains unclear. This study aimed to investigate the association between the timing of coffee consumption and IR in a large population-based study and animal experiments. Methods: This study comprised two phases. First, we performed a secondary data analysis of the US National Health and Nutrition Examination Survey (NHANES), involving a cross-sectional sample of 20,460 adults with complete dietary data. Temporal coffee consumption patterns were identified via two-step clustering and associated with insulin resistance indices using multivariable-adjusted regression models. Subsequently, findings were validated experimentally using mouse models. Results: Two distinct coffee consumption patterns were identified: morning-type (36%) and all-day-type (11%). After multivariable adjustment, only the morning-type pattern was significantly associated with lower IR indices (TyG: β = -0.04; METS-IR: β= -0.59; TG/HDL-C: β= -0.29) and a 17% lower risk of sever IR (OR  =  0.83). Stratified analyses confirmed robustness across coffee intake levels. Notably, coffee consumption timing significantly modified the dose-response relationship between coffee intake amounts and IR indices. Morning-type showed a linear inverse relationship with IR indices, while all-day-type exhibited a J-shaped association. Mediation analysis revealed that inflammatory markers, specifically white blood cell (WBC) count and neutrophil-to-lymphocyte ratio (NLR), partially mediated the beneficial effects of morning coffee consumption on insulin resistance. In mice, morning coffee administration reduced fasting plasma glucose and serum insulin levels, improved glucose tolerance, and lowered proinflammatory cytokines (IL-1β, IL-6, ICAM-1, MCP-1). Conclusion: Drinking coffee in the morning may be more strongly associated with a lower insulin resistance than drinking coffee later in the day.

Indexed as

CoffeeInsulin ResistanceAdultAnimalsBiomarkersBlood GlucoseCross-Sectional StudiesFemaleHumansInsulinMaleMiceMiddle AgedNutrition SurveysTime FactorsBiomarkersBlood GlucoseCoffeeInsulinchrono-nutritioninflammationinsulin resistanceMETS-IRTG/HDL-Ctriglyceride-glucose (TyG) index

Identifiers

PMID41909702
PMCPMC13021422

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.