# Assessing respiratory status in myasthenia gravis: limited value of the MG-ADL as a standalone tool compared with spirometry in a Danish cohort

**Authors:** Linda Kahr Andersen, Simone Birnbaum, Malene Missel, Kristine Grøsfjeld Petersen, Cas Mohringer, Eva Deurell, Nanna Witting, John Vissing

PMC · DOI: 10.1007/s00415-026-13757-6 · Journal of Neurology · 2026-03-24

## TL;DR

The study finds that the MG-ADL scale is not reliable for assessing respiratory function in myasthenia gravis patients compared to spirometry.

## Contribution

The study demonstrates that spirometry is more reliable than the MG-ADL for detecting respiratory insufficiency in myasthenia gravis.

## Key findings

- The MG-ADL respiratory item showed poor correlation with spirometry (r = −0.24, p = .048).
- Patients with respiratory insufficiency showed improvement over time, as did the MGC score.
- 30 out of 70 patients reported respiratory symptoms, but none reported severe symptoms.

## Abstract

Patients with generalized Myasthenia Gravis (gMG) may develop respiratory involvement, which can be life-threatening. In clinical practice, the Myasthenia Gravis Activities of Daily Living scale (MG-ADL) is often used to assess patient-reported respiratory impairment, as spirometry can be time-consuming and require specialized equipment and expertise. However, it is unclear whether the MG-ADL is a sufficient screening tool for identifying respiratory insufficiency.

In this cross-sectional study with a longitudinal subgroup, patients completed the MG-ADL, the Myasthenia Gravis Composite scale (MGC), and the Quantitative Myasthenia Gravis score (QMG). As a part of the QMG, spirometry was conducted. All patients had one evaluation, and a subgroup of patients had an additional evaluation after 3 years.

One hundred patients were screened, and 70 were included and tested. Of these, 25 were retested 3 years later. Respiratory symptoms were reported by 30 (43%) of the 70 patients, though none reported severe symptoms. There was a poor correlation (r = − 0.24, p = .048) between the respiratory item of the MG-ADL and spirometry. Patients with respiratory insufficiency showed improvement over time, as did the MGC score.

Our findings indicate limited agreement between patient-reported respiratory symptoms (MG-ADL) and spirometry measures, suggesting that spirometry remains essential for accurate assessment of respiratory function in gMG.

## Linked entities

- **Diseases:** Myasthenia Gravis (MONDO:0009688)

## Full-text entities

- **Diseases:** fatigue of respiratory muscles (MESH:D012133), respiratory (MESH:D012131), fatigue (MESH:D005221), MG (MESH:D009157), dementia (MESH:D003704), autoimmune neuromuscular disease (MESH:D009468), ventilator dependency (MESH:D053717), pulmonary disease (MESH:D008171), dyspnea (MESH:D004417), abnormal neuromuscular transmission (MESH:D020511), weakness (MESH:D018908), facioscapulohumeral muscular dystrophy (MESH:D020391), respiratory symptoms (MESH:D012818), Myasthenia (MESH:D020294)
- **Chemicals:** MGC (-), pyridostigmine (MESH:D011729)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC13013256