Evidence map›Paper›PMID 41168624›Full record

ArticleClinical rheumatology2026

Biological/targeted synthetic disease-modifying antirheumatic drugs improve not only muscle mass but also phase angle in patients with rheumatoid arthritis.

Masahiro Tada, Yoshinari Matsumoto, Tatsuya Koike, Kenji Mamoto, Tomoyuki Nakamura, Shohei Anno, Takahiro Iida, Hitoshi Goto, Masanori Matsuura

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Longitudinal Course of Muscle Status in Patients With Rheumatoid Arthritis.International journal of rheumatic diseases · 2026
    Article
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.

Masahiro TadaDepartment of Orthopaedic Surgery, Osaka City General Hospital, 2-13-22 Miyakojima-Hondori, Miyakojima-Ku, Osaka, 534-0021, Japan. m-tada@omu.ac.jp.ORCID http://orcid.org/0000-0003-3161-3929
Yoshinari MatsumotoDepartment of Nutrition, Graduate School of Human Life and Ecology, Osaka Metropolitan University, 3-7-30 Habikino, Habikino-Shi, Osaka, 583-8555, Japan.
Tatsuya KoikeDepartment of Orthopaedic Surgery, Koryokai Hospital, 4-15-6 Hiranohonmachi, Hirano-Ku, Osaka, 547-0044, Japan.
Kenji MamotoDepartment of Orthopaedic Surgery, Osaka Metropolitan University Medical School, 1-4-3 Asahimachi, Abeno-Ku, Osaka, 545-8585, Japan.
Tomoyuki NakamuraDepartment of Internal Medicine, Osaka City General Hospital, 2-13-22 Miyakojima-Hondori, Miyakojima-Ku, Osaka, 534-0021, Japan.
Shohei AnnoDepartment of Orthopaedic Surgery, Yodogawa Christian Hospital, 1-7-50 Kunijima, Higashiyodogawa-Ku, Osaka, 533-0024, Japan.
Takahiro IidaDepartment of Orthopaedic Surgery, Koryokai Hospital, 4-15-6 Hiranohonmachi, Hirano-Ku, Osaka, 547-0044, Japan.
Hitoshi GotoDepartment of Internal Medicine, Osaka City General Hospital, 2-13-22 Miyakojima-Hondori, Miyakojima-Ku, Osaka, 534-0021, Japan.
Masanori MatsuuraDepartment of Orthopaedic Surgery, Osaka City General Hospital, 2-13-22 Miyakojima-Hondori, Miyakojima-Ku, Osaka, 534-0021, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study investigated whether treatment with biological/targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD) affects muscle mass and phase angle in patients with rheumatoid arthritis (RA). Additionally, whether these improvements were a direct effect of the b/tsDMARD treatment, an indirect effect mediated by improved disease activity and glucocorticoid reduction, or both was clarified.

methodsData from 104 weeks of a prospective study comparing b/tsDMARD (n = 76) and conventional synthetic disease-modifying antirheumatic drug (csDMARD) treatments (n = 71) on body composition in RA patients were used. The phase angle measured using bioelectrical impedance analysis was used to evaluate muscle quality. Changes in body composition, including phase angle, were compared between the groups. We also examined the results using the mode of action. Parallel mediation analysis was used to investigate the effects of the b/tsDMARD treatment.

resultsBaseline median age and disease duration were 69.0 and 4.5 years, respectively. Changes (Δ) in muscle mass and phase angle were significantly higher in the b/tsDMARD group than the csDMARD group (0.4 kg vs. - 0.3 kg: p < 0.001 and 0.02° vs. - 0.06°: p = 0.047, respectively). There were no significant differences in the change in muscle mass or phase angle when examined using the mode of action. On parallel mediation analysis, the b/tsDMARD usage showed a significant direct effect on Δmuscle mass and Δphase angle (p = 0.012 and p = 0.047, respectively). Indirect effects via ΔDAS28-ESR (p = 0.510 and p = 0.695, respectively) and Δglucocorticoid dosage (p = 0.816 and p = 0.552, respectively) were not statistically significant.

conclusionsTreatment with b/tsDMARD improved muscle mass and phase angle by blocking inflammatory cytokines and JAK-STAT signaling. Key Points • This study is the first to report that b/tsDMARD treatment is effective not only for increasing muscle mass but also for improving phase angle. • These effects appear to be primarily direct, rather than mediated through disease activity improvement or glucocorticoid reduction. • There were no significant differences in muscle mass gain or phase angle improvement when examined using the mode of action.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidBiological ProductsBody CompositionMuscle, SkeletalAgedFemaleHumansMaleMiddle AgedProspective StudiesTreatment OutcomeAntirheumatic AgentsBiological ProductsAntirheumatic agentsBody compositionProspective studyRheumatoid arthritisSarcopenia

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.