Evidence map›Paper›PMID 37979961›Full record

ArticleAnnals of the rheumatic diseases2024

Long-term mortality in treated-to-target RA and UA: results of the BeSt and IMPROVED cohort.

Sascha Louise Heckert, Johanna Maria Maassen, S le Cessie, Y P M Goekoop-Ruiterman, Melek Güler-Yüksel, Willem Lems, Tom Wj Huizinga, Sytske Anne Bergstra, Cornelia F Allaart

Open access · hybridAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  4. Article
  5. Review
  6. 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

9 authors at 4 institutions in 1 country.

Sascha Louise Heckert *Rheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands s.l.heckert@lumc.nl.ORCID http://orcid.org/0000-0002-3320-905X
Johanna Maria Maassen *Rheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.ORCID http://orcid.org/0000-0002-9591-5398
S le CessieEpidemiology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.
Y P M Goekoop-RuitermanRheumatology, HagaZiekenhuis, Den Haag, Zuid-Holland, The Netherlands.
Melek Güler-YükselRheumatology and Clinical Immunology, Maasstad Hospital, Rotterdam, Zuid-Holland, The Netherlands.ORCID http://orcid.org/0000-0002-6071-0261
Willem LemsRheumatology, Amsterdam UMC Location VUmc, Amsterdam, Noord-Holland, The Netherlands.ORCID http://orcid.org/0000-0002-6885-3953
Tom Wj HuizingaRheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.ORCID http://orcid.org/0000-0001-7033-7520
Sytske Anne BergstraRheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.ORCID http://orcid.org/0000-0002-7136-5248
Cornelia F AllaartRheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.
Leiden University Medical Center · NLAmsterdam UMC Location Vrije Universiteit Amsterdam · NLHaga Hospital · NLMaasstad Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo study long-term (up to 20-year) mortality of two treat-to-target trial cohorts in undifferentiated arthritis (UA) and early rheumatoid arthritis (RA).

methodsThe BeSt (BehandelStrategieën) study (n=508, early RA) was performed between 2000 and 2012. For 10 years, patients were treated-to-target disease activity score (DAS)≤2.4.The Induction therapy with Methotrexate and Prednisone in Rheumatoid Or Very Early arthritic Disease (IMPROVED) study (n=610, early RA/UA) was performed between 2007 and 2015. For 5 years, patients were treated-to-target DAS<1.6.Vital status of BeSt/IMPROVED participants was assessed up to and including 31 December 2021. Standardised mortality ratios (SMRs) were calculated. Stratified analyses for anticitrullinated protein antibody (ACPA) and smoking status were performed. Death causes and the potential effect of disease activity during the trial period on late mortality were assessed.

resultsExcess mortality was found in both BeSt (SMR 1.32, 95% CI 1.14 to 1.53) and IMPROVED (SMR 1.33, 95% CI 1.10 to 1.63) and became manifest after 10 years. Excess mortality was statistically significant in ACPA+ patients who smoked (BeSt: SMR 2.80, 95% CI 2.16 to 3.64; IMPROVED: 2.14, 95% CI 1.33 to 3.45). Mean survival time was 10 (95% CI 5 to 16) months shorter than expected in BeSt and 13 (95% CI 11 to 16) months in IMPROVED. The HR for mortality was 1.34 (95% CI 0.96 to 1.86; BeSt)/1.13 (95% CI 0.67 to 1.91; IMPROVED) per 1 point increase in mean DAS during the trial. The main cause of death was malignancy.

conclusionsAfter long-term treatment-to-target, excess mortality occurred in patients with RA after>10 years since treatment start, with smoking as an important risk factor.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidHumansMethotrexatePrednisoneRisk FactorsAntirheumatic AgentsMethotrexatePrednisoneEpidemiologyOutcome Assessment, Health CareRheumatoid Arthritis

Identifiers

PMID37979961
PMCPMC10850649
OpenAlexW4388792858

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.