American journal of physiology. Endocrinology and metabolism · 2025
Interleukin-6 blockade does not impair exercise-induced glucose uptake and insulin sensitivity in rheumatoid arthritis.
Клиническое исследованиеСтатьяНазвание и аннотация: Перевод в очереди
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Casale Andresa Rossilho, Lemes Ítalo Ribeiro, Smaira Fabiana Infante, Astley Camilla, Oliveira-Junior Gersiel, de Sá Pinto Ana Lúcia, de Medeiros-Ribeiro Ana Cristina, Godoy-Santos Alexandre Leme, Lima Marcos, Carneiro Camila G, Buchpiguel Carlos Alberto, Dantas Wagner Silva, Axelrod Christopher L, Javvadi Pravalika, Ghosh Sujoy, Kirwan John P, Roschel Hamilton, Gualano Bruno
Аннотация
Patients with rheumatoid arthritis (RA) are at increased risk of insulin resistance and cardiovascular disease, and exercise is a key nonpharmacological therapy. We examined whether interleukin-6 (IL-6) inhibition, a common biological treatment for RA, impairs the acute metabolic benefits of exercise, given IL-6's proposed role as a mediator of exercise-induced glucose metabolism. This was a single-center, nonrandomized study involving 20 postmenopausal women with RA [10 on IL-6 inhibitor (IL-6i), 10 on TNF-α inhibitor (TNF-αi)]. Participants underwent a hyperinsulinemic-euglycemic clamp (HEC) and fluorine-18 fluorodeoxyglucose positron emission tomography and magnetic resonance imaging ([18F]FDG PET/MRI) to assess whole body and skeletal muscle glucose uptake. Muscle biopsies were performed before and 240 min after a 30-min moderate-to-vigorous intensity aerobic exercise session to analyze molecular responses, including RNA sequencing (RNA-Seq) and protein expression. Participants had a mean age of 57.8 ± 5.1 yr and a mean body mass index (BMI) of 28.2 ± 4.9 kg/m2. Disease duration averaged 18.0 ± 7.5 yr, and both groups had comparable clinical characteristics. Acute exercise did not elicit significant between-group differences in insulin sensitivity (M value: 4.51 ± 1.34 vs. 4.28 ± 0.87; P value > 0.05) or skeletal muscle glucose uptake, indicating that IL-6 inhibition does not impair the metabolic responses to acute exercise. Comparing post to preexercise, IL-6i participants exhibited increased glucose transporter type 4 (GLUT4) expression (P value = 0.01) and distinct cytokine profiles, including elevated IL-8 (P value = 0.04) and IL-10 (P value = 0.02) levels. RNA-Seq analysis showed comparable pathway enrichment between groups, with upregulation of TNF-α and IL-6-Janus kinase-signal transducer and activator of transcription 3 (JAK-STAT3) signaling. IL-6 inhibition does not blunt the acute metabolic benefits of exercise in RA, supporting its safety as a nonpharmacological intervention. Trial registration: Clinicaltrials.gov (NCT04927546).NEW & NOTEWORTHY A single session of aerobic exercise has a similar effect on insulin sensitivity and muscle glucose uptake in women with RA treated with either IL-6i or TNF-αi. The study supports exercise as a safe and complementary strategy for patients with RA on IL-6i or TNF-αi therapy, reinforcing its inclusion in clinical care and the need for further research on long-term outcomes.