Evidence map›Paper›PMID 40691638›Full record

ArticleArthritis research & therapy2025

Mortality in polymyalgia rheumatica: a 38-year prospective population-based cohort study from Southern Norway.

Stig Tengesdal, Øyvind Molberg, Øyvind Holme, Jan Tore Gran, Geirmund Myklebust

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Stig TengesdalDepartment of Research, Sorlandet Hospital, Egsveien 100, Kristiansand, 4615, Norway. stig.tengesdal@sshf.no.ORCID 0000-0003-0994-756X
Øyvind MolbergInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Øyvind HolmeDepartment of Research, Sorlandet Hospital, Egsveien 100, Kristiansand, 4615, Norway.
Jan Tore GranInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Geirmund MyklebustDepartment of Research, Sorlandet Hospital, Egsveien 100, Kristiansand, 4615, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRobust long-term mortality data on patients with polymyalgia rheumatica (PMR) are lacking. The aim of this study was to determine all-cause mortality in isolated PMR using a large, population-based, inception cohort followed prospectively over a 38-year period.

methodsBetween 1987 and 1997, 337 incident cases of PMR and biopsy-proven GCA were included in a prospective, population-based inception cohort in Aust-Agder County, Norway. Diagnosis was ascertained clinically by a rheumatologist, with PMR cases meeting Bird`s criteria. Patients were followed until death or end of study on December 31st, 2024. Each case was matched by gender, age at inclusion, and residency with 15 population comparators drawn from the population registry in Norway. We assessed mortality and survival by standard mortality ratios (SMR) and the Kaplan-Meier method.

resultsA total of 274 patients with isolated PMR (66.1% female, mean age at diagnosis 71.9 years) and 63 patients with GCA (76.2% female, mean age at diagnosis 71.6 years) were included. By the end of the study, 96.4% of all patients were deceased. Mean follow-up time for all patients was 13.7 years, with a maximum of 35.3 years. For cases with isolated PMR, the overall SMR was 0.97 (95% confidence interval [CI] 0.85, 1.09), for men 0.77 (95% CI 0.62, 0.95), and for women 1.11 (95% CI 0.95, 1.28). For GCA, the overall SMR was 1.10 (95% CI 0.85, 1.40), with no gender difference.

conclusionsIn this comprehensive long-term follow-up study with nearly complete data on mortality, isolated PMR was not associated with increased mortality, reinforcing the view that it does not confer a higher mortality risk.

Indexed as

Polymyalgia RheumaticaAgedAged, 80 and overCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedNorwayProspective StudiesRegistriesEpidemiologyGiant cell arteritisMortalityPolymyalgia rheumaticaSurvival

Identifiers

PMID40691638
PMCPMC12278481

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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 OpenQuestion graph.