ORIGINAL RESEARCH article
Front. Physiol.
Sec. Exercise Physiology
Cardiopulmonary Exercise Testing in Mild Generalized Myasthenia Gravis: An Exploratory Pilot Feasibility Study
Provisionally accepted- 1Charité University Medicine Berlin, Berlin, Germany
- 2Universitat Potsdam, Potsdam, Germany
- 3Charite - Universitatsmedizin Berlin, Berlin, Germany
- 4Hochschule Furtwangen, Furtwangen, Germany
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Introduction: We assessed the feasibility conducted an exploratory pilot feasibility study to assess the safety and feasibility of cardiopulmonary exercise testing (CPET) in patients with mild generalized myasthenia gravis (gMG), aiming to determine whether test termination results from systemic exertion or MG-specific neuromuscular fatigability and to evaluate short-term effects on fatigue. Methods: Nine patients with mild gMG (median age of 58 years, IQR 46.0-66.5) suffering from mild gMG were included in this exploratory feasibility study and underwent a single maximal incremental CPET performed a single CPET testing with a maximum incremental exercise tests on a cycle ergometer with breath-by-breath gas exchange analysis and blood lactate measurements including breath gas analysis and lactate measures. Predefined exertion criteria (EC) included respiratory exchange rate (RER; ≥1.1), ventilatory equivalent for O2 (EQO2; ≥30), attainment of age-related maximum heart rate (ARMHR), peak blood lactate concentration (> 6 mmol·L⁻¹), and Borg Scale for Rated Perceived Exertion (RPE; ≥17). Repetitive nerve stimulation (RNS) was performed before and after CPET to assess neuromuscular fatigability. Fatigue was assessed using the Chalder Fatigue Scale (CFS) at baseline and four weeks after CPET. Results: CPET was completed by all participants without adverse events. All reported symptoms resolved within 30 minutes after exercise termination, and no participant required medical intervention. All participants completed the maximal incremental CPET according to the predefined protocol. Among the predefined EC, 44% of participants achieved an RER ≥1.1, 78% an EQO₂ ≥30, 44% an ARMHR, 67% reached a peak blood lactate concentration > 6 mmol·L⁻¹⁻, and 67% an RPE ≥17. A decremental response in RNS was observed in 78% both before and after CPET. No relevant changes in CFS scores were detected over four weeks. Discussion: CPET appears safe and feasible in mild gMG, with exercise termination primarily driven by systemic exertion rather than MG-specific neuromuscular fatigue. CPET may complement clinical evaluation by enabling supporting individualized training recommendations and the identification of cardiopulmonary limitations. early detection of cardiopulmonary comorbidities.
Keywords: Cardiopulmonary exercise testing, Fatigue, Myasthenia Gravis, Neuromuscular Disease, physical activity
Received: 04 Dec 2025; Accepted: 29 Jan 2026.
Copyright: © 2026 Stascheit, Lauermann, Risch, Mayer, Prof. Dr., Hoffmann, Meisel, Roecker and Cassel. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Frauke Stascheit
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