Evidence map›Paper›PMID 35731132›Full record

ArticleRheumatology (Oxford, England)2023

Female reproductive status and exogenous sex hormone use in rheumatoid arthritis patients treated with tocilizumab and csDMARDs.

Dala N Daraghmeh, Ashley M Hopkins, Catherine King, Ahmad Y Abuhelwa, Mihir D Wechalekar, Susanna M Proudman, Michael J Sorich, Michael D Wiese

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 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

8 authors.

Dala N DaraghmehHealth and Biomedical Innovation, UniSA: Clinical and Health Sciences, University of South Australia, Adelaide.ORCID 0000-0003-1933-5241
Ashley M HopkinsDiscipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.
Catherine KingHealth and Biomedical Innovation, UniSA: Clinical and Health Sciences, University of South Australia, Adelaide.
Ahmad Y AbuhelwaDiscipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.ORCID 0000-0002-4182-065X
Mihir D WechalekarRheumatology Research Unit, Repatriation General Hospital and Flinders University.
Susanna M ProudmanRoyal Adelaide Hospital and University of Adelaide, Adelaide Medical School, Adelaide, South Australia, Australia.
Michael J SorichDiscipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.
Michael D WieseHealth and Biomedical Innovation, UniSA: Clinical and Health Sciences, University of South Australia, Adelaide.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSex is well known to influence risk, severity and treatment outcomes of RA, although the underlying causes are uncertain. The aim of this research was to examine whether factors influencing female sex hormones (reproductive status and exogenous sex hormone use) are associated with the efficacy of DMARDs.

methodsIndividual participant data were pooled from five phase 3 clinical trials where RA patients were treated with tocilizumab and/or conventional synthetic DMARDs. The primary outcome was the time to first remission according to the Simplified Disease Activity Index. The relationship between menopausal status or use of exogenous sex hormones and the time of first remission was assessed via Cox proportional analysis. Analysed data included sex, baseline menopausal status (premenopausal, perimenopausal, early postmenopausal and postmenopausal), participant age, body mass index, race, number of previous DMARDs and baseline disease activity.

resultsAnalysis included 4474 female patients, of whom 2817 (62.9%) were postmenopausal, 202 (4.5%) were early postmenopausal, 1021 (22.8%) were premenopausal and 414 (9.2%) were perimenopausal. Of these, 221 (7.8%), 13 (6.4%), 255 (25%) and 47 (11.4%), respectively, were taking exogenous sex hormones. In the pooled analysis, perimenopausal status was associated with reduced remission compared with premenopausal status [adjusted HR 0.78 (95% CI 0.61, 0.99)]. Sex hormone use was associated with significantly higher remission [adjusted HR 1.20 (95% CI 1.01, 1.43)].

conclusionPerimenopausal women were less likely to achieve remission compared with premenopausal RA patients. The use of exogenous sex hormones appeared to be associated with more frequent remission in female RA patients, particularly those who were perimenopausal and early postmenopausal, although further research is required to confirm and identify the drivers for this observation and how it interacts with menopausal status.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidGonadal Steroid HormonesAntibodies, Monoclonal, HumanizedFemaleHumansPerimenopausePostmenopauseAntibodies, Monoclonal, HumanizedAntirheumatic AgentsGonadal Steroid HormonestocilizumabcsDMARDsearly post-menopausalexogenous sex hormoneperimenopausalRAremissiontocilizumab

Identifiers

PMID35731132
PMCPMC9891436

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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.