Evidence map›Paper›PMID 36329101›Full record

ArticleScientific reports2022

Inflammation mediates approximately one quarter of excess relative all-cause mortality in persons with rheumatoid arthritis: the Trøndelag Health Study.

Vibeke Videm, Ingrid Sæther Houge, Marthe Halsan Liff, Mari Hoff

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Vibeke VidemDepartment of Clinical and Molecular Medicine, NTNU-Norwegian University of Science and Technology, Trondheim, Norway. vibeke.videm@ntnu.no.ORCID 0000-0002-1042-3889
Ingrid Sæther HougeDepartment of Clinical and Molecular Medicine, NTNU-Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-2458-208X
Marthe Halsan LiffDepartment of Rheumatology, Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.ORCID 0000-0003-0367-2032
Mari HoffDepartment of Neuromedicine and Movement Science, NTNU-Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-9992-8663
Norwegian University of Science and Technology · NOLevanger Hospital · NO

Funding

Norges Forskningsråd 249944Norges Teknisk-Naturvitenskapelige Universitet 82600805The Liaison Committee for Education, Research and Innovation in Central Norway 2016/29014The Liaison Committee for Education, Research and Innovation in Central Norway 5056/46051000
6 · The paper itself

Abstract

Inflammation may contribute to excess mortality in rheumatoid arthritis (RA) patients. We investigated associations to all-cause mortality of the inflammation markers high-sensitivity C-reactive protein (CRP), lactoferrin (neutrophil activation marker), and neopterin (monocyte activation marker). From the population-based Trøndelag Health Study (3rd wave 2006-2008), 316 RA patients and 43,579 controls were included. Lactoferrin and neopterin were quantified in a nested cohort (n = 283 RA patients, n = 3698 controls). Follow-up was until death found by linkage to the Norwegian Cause of Death Registry or 31.12.2018. All-cause mortality was analyzed using Cox regression and Cox regression-based mediation analysis. Having RA (hazard ratio (HR): 1.25, 95%CI: 1.00, 1.56, p = 0.048), and CRP ≥ 3 mg/L (HR: 1.50, 95%CI: 1.41, 1.60, p < 0.001) were associated with all-cause mortality. The overall excess relative mortality risk of having RA was 38%. CRP ≥ 3 mg/L mediated approximately 1/4 of this risk (p < 0.001). In the nested cohort, CRP ≥ 3 mg/L (HR: 1.51, 95%CI: 1.26, 1.80, p < 0.001) and neopterin (HR: 1.17, 95%CI: 1.01, 1.36, p = 0.031) were associated with all-cause mortality. In conclusion, CRP levels ≥ 3 mg/L mediated approximately a quarter of the 38% excess relative all-cause mortality risk associated with RA. Using definitions of RA remission with emphasis both on joint status and the level of general inflammation may help guide the most efficient treatment regimens.

Indexed as

Arthritis, RheumatoidLactoferrinBiomarkersC-Reactive ProteinHumansInflammationNeopterinProportional Hazards ModelsRisk FactorsBiomarkersC-Reactive ProteinLactoferrinNeopterin

Identifiers

PMID36329101
PMCPMC9633644
OpenAlexW4308482685

What OpenQuestion holds

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Registered trials

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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.