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Abstract Number: 1735

High-Intensity Interval Training Outperforms Moderate Exercise in Aerobic Capacity for Recent-Onset Idiopathic Inflammatory Myopathies: A Randomized Controlled Trial

Kristofer Andreasson1, Cecilia Leijding1, Maryam Dastmalchi2, Antonella Notarnicola3, Stefano Gastaldello1, Heléne Sandlund2, Daniel Andersson4, Ingrid Lundberg5 and Helene Alexanderson2, 1Karolinska Institutet, Stockholm, Sweden, 2Karolinska University hospital, Stockholm, Sweden, 3Karolinska University Hospital and Karolinska Institutet, Stockholm, Stockholms Lan, Sweden, 4Karolinska Institutet, Solna, Sweden, 5Karolinska Universitetssjukhuset, Karolinska Institutet, Stockholm, Sweden

Meeting: ACR Convergence 2024

Keywords: exercise, Mitochondrial Dysfunction, Muscle Biology, Myositis, Randomized Trial

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Session Information

Date: Sunday, November 17, 2024

Title: Abstracts: Muscle Biology, Myositis & Myopathies – Basic & Clinical Science I

Session Type: Abstract Session

Session Time: 3:00PM-4:30PM

Background/Purpose: Exercise is a recognized adjunctive therapy for patients with idiopathic inflammatory myopathies (IIM), enhancing physical capacity and reducing inflammation. Hitherto, moderate-to-intensive exercise has been investigated in established, low-active IIM, hence, effects of intensive exercise in recent-onset, active IIM is less known. This study aimed to evaluate tolerance and efficacy of High-Intensity Interval Training (HIIT) compared to clinical standard moderate-intensity home-based training (CON) in patients with recent onset IIM.

Methods: Between 2017-2023, patients with adult IIM (≤ 12 months of diagnosis), fulfilling EULAR/ACR classification criteria for myositis, excluding IBM, aged < 70 years, and capable of performing HIIT were recruited. Patients deemed unfit for participation (e.g., severe lung-involvement or active myocarditis) were excluded. Participants underwent pre- and post-intervention investigations to assess disease activity using the International Myositis Assessment Clinical Studies (IMACS) disease core set. This included the physician’s global activity (PhGA), patient’s global assessment (PtGA), HAQ, muscle enzymes, Manual Muscle Test 80 (MMT8), and extra-muscular global assessment. Additionally, exercise effects were measured by maximal exercise tests on a stationary bike, including measure of peak oxygen uptake (peakVO2), peak power, and time-to-exhaustion (TTE). Limb muscle biopsies were performed at diagnosis and post-intervention. HIIT included supervised 30-45-second stationary bike intervals (≥ 85% of maximal heart rate), thrice weekly. The controls followed a home-based exercise regimen (< 70% of maximal heart rate) with five sessions weekly. Intensity and resistance were tailored to individual limitations and heart rate was monitored during exercise. To study muscle adaptations to aerobic capacity muscle biopsies were analyzed for expression of key mitochondrial proteins by Western Blot.

Results: Twenty-three patients, with a median disease duration of 5 months, were randomized into HIIT (n=12) or CON (n=11, 8 finishing). There were non-significant differences in sex, age, and type of IIM between the groups (Table 1). Patients in the HIIT protocol demonstrated a significant improvement in exercise capacity with higher peakVO2 (16.2 % vs 1.8 %), peak power (18.4 % vs 8.2 %), and TTE (23.1 % vs 11.5 %) compared to CON (Table 2). In the HIIT group, an increase in muscle mitochondria protein expression was recorded after training compared to before (p< 0.05) (Figure 1). No significant changes were seen among the blood biomarkers for adverse reactions (CK, ASAT, ALAT and LD) or for PtGA and extra-muscular global assessment. However, CON improved significantly in MMT8 and PhGA (Table 2).

Conclusion: Supervised HIIT was safe and provided superior enhancement of exercise capacity compared to CON. Furthermore HIIT, but not CON, led to increased expression mitochondrial proteins showing adaptation in aerobic metabolism within the myositis muscle that links to aerobic capacity and clinical improvement. This study offers novel insights into using intensive exercise for recent onset IIM, suggesting potential changes in future exercise recommendations.

Supporting image 1

All data presented in median and interquartile range, except disease duration which is (min-max); HIIT, high-intensity interval training; CON, control; F, female; M, male; PM, polymyositis; DM, dermatomyositis; ASSD, antisynthetase syndrome; DMARDs, disease modifying anti-rheumatic drugs; mg, milligram; MMT8, manual muscle test 80; VAS, visual analog scale; HAQ, health assessment questionnaire; CK, creatine phosphokinase; µkat/L, microkatals per liter; LD, lactate dehydrogenase; ASAT, aspartate transaminase; ALAT, alanine transaminase. Normative values male/female: CK 0.8-6.7/0.6_3.5, LD <3.5/<3.5, ASAT <0.76/<0.61, ALAT <1.1/<0.76. Superscript numbers indicate n of missing data.

Supporting image 2

All data presented in median (interquartile range); HIIT, high-intensity interval training; CON, control; 95 % CI, change is presented in 95 % confidence interval; VO2, peak oxygen uptake; L/min, liters per minute; mL/kg/min, milliliters per kilogram per minute; W, watts; time to exhaustion, time from start to finish; MMT8, manual muscle test 80; VAS, visual analog scale; mm, millimeters; HAQ, health assessment questionnaire. Significant results marked in bold.

Supporting image 3

Figure 1. Increased performance after HIIT is accompanied with increased protein expression in the mitochondrial electron transport chain, citrate synthetase (CS) and VDAC1 in skeletal muscle. Protein quantification for the mitochondria electron transport chain complexes I-V (A-E), citrate synthetase (F), and VDAC1 (G) of skeletal muscle lysates from the High Intensity Interval Training (HIIT) group (n= 7) and the control (CON) group (n=6), before (PRE) and after (POST) (paired) exercises. Band intensity expressed in arbitrary units (A.U.) were determined by ImageJ and normalized to myosin as internal loading control. Representative blots and the specific antibodies to the quantified proteins: I-V (A-E) anti-OxPhos, anti-citrate synthetase (F), and anti-VDAC1 (G) are indicated below the graphs. Paired t-test was performed PRE vs POST within the groups, * p<0.05.


Disclosures: K. Andreasson: None; C. Leijding: None; M. Dastmalchi: None; A. Notarnicola: Boehringer-Ingelheim, 1, 6; S. Gastaldello: None; H. Sandlund: None; D. Andersson: None; I. Lundberg: Argenx, 1, Astra Zeneca, 1, Boehringer Ingelheim, 6, Bristol Myers Squibb, 1, Chugai, 1, Galapagos, 1, Janssen, 1, 6, Novartis, 11, Pfizer, 1, Roche, 11; H. Alexanderson: None.

To cite this abstract in AMA style:

Andreasson K, Leijding C, Dastmalchi M, Notarnicola A, Gastaldello S, Sandlund H, Andersson D, Lundberg I, Alexanderson H. High-Intensity Interval Training Outperforms Moderate Exercise in Aerobic Capacity for Recent-Onset Idiopathic Inflammatory Myopathies: A Randomized Controlled Trial [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/high-intensity-interval-training-outperforms-moderate-exercise-in-aerobic-capacity-for-recent-onset-idiopathic-inflammatory-myopathies-a-randomized-controlled-trial/. Accessed .
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