# Association of Biologic/Targeted-Synthetic DMARDs with a Lower Prevalence of Hand Joint Deformity in Rheumatoid Arthritis: A Cross-Sectional Real-World Study

**Authors:** Ying Yang, Jian-Zi Lin, Yao-Wei Zou, Ya-Nan Cao, Tao Wu, Pei-Yu Lin, Ran Shi, Zhi-Ming Ouyang, Kui-Min Yang, Ze-Hong Yang, Jian-Da Ma, Lie Dai

PMC · DOI: 10.3390/medicina62020241 · Medicina · 2026-01-23

## TL;DR

This study found that using biologic or targeted-synthetic DMARDs in rheumatoid arthritis patients is linked to fewer hand joint deformities.

## Contribution

The study provides real-world evidence that b/tsDMARDs reduce hand joint deformity prevalence in RA patients.

## Key findings

- b/tsDMARDs use was associated with a 79% lower prevalence of hand joint deformity after adjusting for confounding factors.
- Patients on b/tsDMARDs had a deformity rate of 27.1%, compared to 61.7% in those on conventional treatments.
- PIP V, PIP III, and PIP IV joints were the most commonly affected by deformities.

## Abstract

Background and Objectives: Hand joint deformity remains a main cause impairing quality of life in rheumatoid arthritis (RA). This study aimed to investigate the association between biologic and targeted-synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) treatment and the prevalence of hand joint deformity in RA patients. Materials and Methods: This cross-sectional analysis included RA patients recruited between 2019 and 2024. Hand joint deformity was defined as the presence of specific deformity in any of 28 hand joints, including the metacarpophalangeal (MCP) joints I-V, proximal interphalangeal (PIP) joints I-V, and distal interphalangeal (DIP) joints II-V. The key exposure was the use of b/tsDMARDs. Multivariable logistic regression was used to assess the association between b/tsDMARDs treatment and hand joint deformity. Results: A total of 1083 RA patients with a mean age of 52.6 ± 12.4 years and a median disease duration of 5 (2,11) years were included. Hand joint deformity was present in 25.4% (275/1083) of patients. The top three deformed joint locations were PIP V (12.9%, 140/1083), PIP III (11.6%, 126/1083), and PIP IV (10.9%, 118/1083). The top three deformity types were ulnar deviation of MCP II-V (8.0%, 87/1083), boutonniere deformity of II-V fingers (6.8%, 74/1083), and swan neck deformity of II-V fingers (6.7%, 73/1083). In total, 17.4% (188/1083) of patients had received b/tsDMARDs. After 1:1 propensity score matching for age, sex, and disease duration, the prevalence of deformity was significantly lower in patients treated with conventional medicine (csDMARDs and/or GCs) add-on b/tsDMARDs compared to those treated with conventional medicine (27.1% vs. 61.7%, p < 0.001). Multivariable logistic regression analysis showed that b/tsDMARDs use was independently associated with a lower prevalence of hand joint deformity after adjusting for confounding factors (OR = 0.211, 95%CI: 0.129–0.345, p < 0.001). Conclusions: The use of b/tsDMARDs was independently associated with a lower prevalence of hand joint deformity in RA.

## Linked entities

- **Diseases:** rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, DIP (interstitial pneumonitis, desquamative, familial) [NCBI Gene 100188011], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PIP (prolactin induced protein) [NCBI Gene 5304] {aka BRST-2, GCDFP-15, GCDFP15, GPIP4}
- **Diseases:** Deformities (MESH:D009140), tender (MESH:D063806), hemiplegia (MESH:D006429), Hand deformities (MESH:D006226), joint destruction (MESH:D008105), subluxation (MESH:D004204), Z-deformity of the thumb (MESH:C536903), functional limitation (MESH:D045745), synovial inflammatory hyperplasia (MESH:D006965), polyarthritis (MESH:D001168), decreased grip strength (MESH:D009123), CDAI (MESH:C566784), RA (MESH:D001172), Deformed joints (MESH:D016916), stiffness (MESH:C566112), nerve or tendon injuries (MESH:D013708), II (MESH:C537730), ACPA (MESH:C536207), synovitis (MESH:D013585), RF (MESH:D001171), RJD (MESH:D007592), bone destruction (MESH:D001847), JE (MESH:D014077), HAQ (OMIM:603663), rheumatic drugs (MESH:D012216), radiographic (MESH:D000089202), structural abnormalities (MESH:C566527), autoimmune disease (MESH:D001327), boutonniere deformity of fingers II (MESH:D005383), systemic lupus erythematosus (MESH:D008180), congenital disorders of fingers (MESH:D009358), hand disability (MESH:D006230), mTSS (MESH:D008947), dermatomyositis (MESH:D003882), cartilage loss (MESH:D002357), systemic sclerosis (MESH:D012595), muscle atrophy (MESH:D009133), inflammation (MESH:D007249), injury to (MESH:D014947), JSN (MESH:D016893), DI (MESH:C564703), morning stiffness (MESH:D048968), physical disability (MESH:D059445), fractures (MESH:D050723), Pain (MESH:D010146), malignancy (MESH:D009369), congenital or (MESH:D008209), hyperextension (MESH:C563315), swan neck (MESH:D006258), Ulnar deviation (MESH:D010262)
- **Chemicals:** ACPA (-), sulfasalazine (MESH:D012460), hydroxychloroquine (MESH:D006886), leflunomide (MESH:D000077339), MTX (MESH:D008727), cyclic citrullinated peptide (MESH:C487763), b (MESH:D001895)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942569/full.md

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Source: https://tomesphere.com/paper/PMC12942569