30-Second Takeaway
- TNF inhibitors in JIA were linked to markedly lower systemic autoimmune disease risk than IL-6 inhibitors in a large matched cohort.
- Achieving and intensifying urate targets on ULT modestly lowered 5-year MACE risk, especially in high-risk gout patients.
- Low gamma globulin levels in SLE and elevated CCL18 in SSc refined infection and mortality risk stratification.
Week ending January 31, 2026
Recent signals to recalibrate rheumatology practice: biologic selection in JIA, urate targets and SGLT2i in gout, infection and prognostic biomarkers, imaging in RA, and RCT reliability
TNF inhibitors were associated with substantially lower systemic autoimmune disease risk than IL-6 inhibitors in JIA
This TriNetX-based cohort included 2,384 pediatric JIA patients starting TNF or IL-6 inhibitors, matched 1:1 on baseline characteristics. After matching, TNF inhibitor users had fewer systemic autoimmune diseases than IL-6 inhibitor users (17 vs 45 events). TNF inhibition was associated with markedly reduced SAD risk (HR 0.37, 95% CI 0.20–0.63) compared with IL-6 inhibition. Subgroup and sensitivity analyses showed consistent protective associations across age, sex, and concomitant medication strata.
Treat-to-target urate lowering modestly reduced 5-year MACE risk in gout
This emulated target trial followed 109,504 adults with gout newly starting urate-lowering therapy for up to 5 years. Achieving serum urate <6 mg/dL within 12 months was associated with lower MACE risk than not achieving target (weighted HR 0.91, 95% CI 0.89–0.92). Absolute 5-year event-free survival was 1.0% higher with treat-to-target, with larger benefit in patients at high cardiovascular risk. Achieving urate <5 mg/dL yielded greater risk reduction (HR 0.77, 95% CI 0.72–0.81) and higher survival difference.
Incident dermatomyositis showed high steroid burden, heterogeneous immunomodulator use, and substantial complications
This study used US commercial claims and a rheumatology EHR network to describe 2,475 and 1,196 patients with incident dermatomyositis, respectively. Among 998 EHR patients with labs, 35% of those with myositis panels had a positive myositis-specific antibody. Glucocorticoid use was common in both cohorts, usually starting above 20 mg/day with high cumulative exposure. Hydroxychloroquine, methotrexate, and mycophenolate were the most frequently used immunomodulators, but regimens varied widely.
Low gamma globulin independently predicted herpes zoster risk in SLE
Among 224 SLE patients, 13.4% had herpes zoster, with an incidence of 0.81 per 100 patient-years. On univariable analysis, longer steroid and immunosuppressant exposure, biologic use, and lower gamma globulin levels were associated with zoster. In multivariable analysis, only gamma globulin remained independently associated (OR 0.86, 95% CI 0.74–0.98). A gamma globulin threshold of 10.3 g/L best discriminated zoster risk (AUC 0.71, 95% CI 0.59–0.82).
References
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Additional Reads
Optional additional studies from this edition.