Aller au contenu principal
2025 article

Alcohol consumption and rheumatoid arthritis risk: A prospective cohort study with nonlinear Mendelian randomization analysis

1Citations signalées, ce qui n’est pas une note de qualité
2Institutions déclarées
1Pays d’affiliation déclarés

Rattachement africain : cn. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

BACKGROUND: Previous epidemiological studies have shown a nonlinear relationship between alcohol consumption and rheumatoid arthritis (RA), though these findings may be biased by confounding factors or reverse causation. Additionally, the impact of sex on this association remains inconsistent. Therefore, we aim to investigate whether the causal link between alcohol consumption and RA risk is linear, nonlinear, or both. METHODS: Participants from the UK Biobank who provided detailed alcohol consumption information and complete covariate data were included in this study. Alcohol intake was quantified in units per week. We employed multivariable Cox models with restricted cubic splines for conventional analysis, and both linear and nonlinear Mendelian randomization (MR) analyses to assess causal relationships. RESULTS: Among the 316,717 participants, 3264 incident cases of RA were recorded during an average follow-up of 13.22 years. The Cox regression model suggested that the association between weekly alcohol consumption and RA incidence was an approximate U-shaped relationship, with the lowest risk at 21.95 units/week. Each unit increase in alcohol consumption was significantly associated with a lower risk of RA in women (HR: 0.991; 95% CI: 0.986, 0.996), but not in men (P for interaction <0.001). However, nonlinear MR did not detect a significant nonlinear correlation between alcohol consumption and RA risk, either overall (P for nonlinearity = 0.161) or within sex subgroups. The individual-level linear MR also indicated that genetically predicted alcohol consumption is not associated with RA risk. CONCLUSIONS: The overall and sex-specific associations found in conventional epidemiological analyses were not supported by either linear or nonlinear MR analyses.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.

Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Alcohol consumption and rheumatoid arthritis risk: A prospective cohort study with nonlinear Mendelian randomization analysis
Date Crossref
23/09/2025
Éditeur
Wiley
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

  • Anhui Medical University Department of Epidemiology and Biostatistics pays non établi dans la notice
    Université ou école supérieure
  • Anhui University of Science and Technology pays non établi dans la notice
    Université ou école supérieure
  • Inflammation and Immune Mediated Diseases Laboratory of Anhui Province Hefei Anhui China pays non établi dans la notice
    Structure de recherche
  • School of Public Health Department of Epidemiology and Biostatistics pays non établi dans la notice
    Université ou école supérieure

Department of Epidemiology and Biostatistics — Anhui Medical University, Anhui University of Science and Technology et Inflammation and Immune Mediated Diseases Laboratory of Anhui Province Hefei Anhui China, avec 1 autre affiliation.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Rheumatoid Arthritis Research and TherapiesGenetic Associations and EpidemiologyAlcohol Consumption and Health Effects

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.