Evidence map›Paper›PMID 42274932›Full record

ArticleClinical rheumatology2026

GLP-1-based therapy and ICD-10-documented heart failure or respiratory failure events in non-diabetic adults with rheumatoid arthritis and obesity: a TriNetX federated cohort study.

Giorgos Loizidis, Ross Summer

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Article in Clinical rheumatology, 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

2 authors.

Giorgos LoizidisDivision of Pulmonary, Allergy and Critical Care, Department of Medicine, Sidney Kimmel Medical Collegeat, Thomas Jefferson University , Philadelphia, PA, USA. giorgos.loizidis@jefferson.edu.ORCID http://orcid.org/0000-0003-4113-2221
Ross SummerDivision of Pulmonary, Allergy and Critical Care, Department of Medicine, Sidney Kimmel Medical Collegeat, Thomas Jefferson University , Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-4615-4956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectivesGlucagon-like peptide-1 (GLP-1)-based therapies have emerged as a major advance in cardiometabolic care; however, no prospective outcomes data exist for these agents in non-diabetic adults with rheumatoid arthritis (RA) and obesity. We examined whether GLP-1-based therapy was associated with first post-landmark ICD-10-documented heart failure (HF) or respiratory failure (RF) events.

methodsWe conducted a retrospective cohort study in the TriNetX US Collaborative Network. Adults with RA, body mass index ≥ 30 kg/m

resultsAfter matching, 3483 patients remained per cohort, with all standardized mean differences < 0.10. During days 91-365, the primary endpoint occurred in 23/3176 GLP-1 users (0.7%) and 57/3144 never-users (1.8%) (hazard ratio (HR): 0.48; 95% confidence interval (CI): 0.30-0.78; p = 0.002; absolute risk difference: - 1.1 percentage points). The HF and RF components showed directionally similar associations. Findings were directionally similar at extended follow-up and, where estimable, in the calendar-time-restricted analysis. Bias probes showed no differential utilization.

conclusionsGLP-1-based therapy was associated with substantially lower hazards of first post-landmark ICD-10-documented HF or RF events. These observations, while compelling, are hypothesis-generating and require prospective validation before informing clinical use. Key Points • In a propensity score-matched TriNetX cohort of non-diabetic adults with rheumatoid arthritis and obesity, GLP-1-based therapy was associated with a lower hazard of first post-landmark ICD-10-documented heart failure or respiratory failure events. • In absolute terms, the primary composite occurred in 0.7% of GLP-1 users and 1.8% of never-users during days 91-365, corresponding to approximately one fewer event per 100 patients. • Heart failure and respiratory failure, analyzed separately, showed directionally consistent lower hazards, although event counts were small. • The findings provide preliminary RA-specific evidence for a prospective study, but they should not be used to guide treatment decisions.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidGlucagon-Like Peptide 1Glucagon-Like PeptidesHeart FailureObesityRespiratory InsufficiencyAdultAgedFemaleHumansInternational Classification of DiseasesMaleMiddle AgedRetrospective StudiesSemaglutideAntirheumatic AgentsGlucagon-Like Peptide 1Glucagon-Like PeptidesSemaglutideTirzepatideGLP-1 receptor agonistsHeart failureObesityPharmacoepidemiologyRheumatoid arthritis

Identifiers

PMID42274932

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