Evidence map›Paper›PMID 41884268›Full record

ArticleFrontiers in physiology2026

Cardiopulmonary exercise testing in mild generalized myasthenia gravis: an exploratory pilot feasibility study.

Frauke Stascheit, Maximilian Lauermann, Lucie Risch, Frank Mayer, Sarah Hoffmann, Andreas Meisel, Kai Roecker, Michael Cassel

Abstract read
In one paragraph

Article in Frontiers in physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Frauke StascheitCharité - Universitätsmedizin Berlin, Department of Neurology with Experimental Neurology, Berlin, Germany.
Maximilian LauermannUniversity Outpatient Clinic for Sports Medicine and Sports Orthopedics, University of Potsdam, Potsdam, Germany.
Lucie RischUniversity Outpatient Clinic for Sports Medicine and Sports Orthopedics, University of Potsdam, Potsdam, Germany.
Frank MayerUniversity Outpatient Clinic for Sports Medicine and Sports Orthopedics, University of Potsdam, Potsdam, Germany.
Sarah HoffmannCharité - Universitätsmedizin Berlin, Department of Neurology with Experimental Neurology, Berlin, Germany.
Andreas MeiselCharité - Universitätsmedizin Berlin, Department of Neurology with Experimental Neurology, Berlin, Germany.
Kai RoeckerInstitute for Applied Health Promotion and Exercise Medicine (IfAG), Furtwangen University, Furtwangen, Germany.
Michael CasselUniversity Outpatient Clinic for Sports Medicine and Sports Orthopedics, University of Potsdam, Potsdam, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: We 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) were included in this exploratory feasibility study and underwent a single maximal incremental CPET on a cycle ergometer with breath-by-breath gas exchange analysis and blood lactate measurements. Predefined exertion criteria (EC) included respiratory exchange rate (RER; ≥1.1), ventilatory equivalent for O Results: CPET was completed by all participants without adverse events. All reported symptoms resolved within 30 min 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 EQO 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 supporting individualized training recommendations and the identification of cardiopulmonary limitations.

Indexed as

cardiopulmonary exercise testingfatiguemyasthenia gravisneuromuscular diseasephysical activity

Identifiers

PMID41884268
PMCPMC13008673

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.