4.7 Article

Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophy

Journal

JOURNAL OF NEUROLOGY
Volume 269, Issue 7, Pages 3682-3689

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-022-10990-7

Keywords

Facioscapulohumeral muscular dystrophy; Respiratory function; Spirometry; Long-term follow-up

Funding

  1. charitable foundation Prinses Beatrix Spierfonds [W.OR12-22, W.OR18-07]

Ask authors/readers for more resources

The study aimed to evaluate the change in respiratory function in patients with facioscapulohumeral muscular dystrophy (FSHD) over a period of 5 years. The results showed that the respiratory function remained stable in most patients, but a subgroup of patients experienced a significant deterioration. These patients had more severe muscle weakness, spinal and thorax deformities, and a relatively fast decline in axial muscle function over the follow-up period.
Objective To evaluate the 5-year change in respiratory function in patients with facioscapulohumeral muscular dystrophy (FSHD). Methods Genetically confirmed patients with FSHD aged >= 18 years were examined twice over five years. Forced vital capacity (FVC) and forced expiratory volume in 1 s (FEV1) were measured using hand-held spirometry with a face mask. Several clinical outcome measures were correlated to respiratory function. Results Ninety-two patients were included (57% male, age 18-75 years). At baseline, the spirometry outcomes of 41 patients showed a restrictive ventilatory pattern (FVC < 80% and FEV1/FVC >= 70% of predicted) and of 48 patients at follow-up. The mean FVC decreased from baseline to follow-up from 79.0 to 76.7% predicted (p = 0.021). This decrease was driven by a subgroup of 15 patients who had a deterioration of FVC of > 10% predicted. The subgroup of 15 patients was more severely affected at baseline (p = 0.002 for FSHD clinical score and 0.007 for Ricci score). They developed more frequently spinal and thorax deformities (p < 0.001 for kyphoscoliosis and 0.012 for pectus excavatum) and had a larger decline in axial muscle function (p = 0.020). Only weak correlations were found between the change in FVC% predicted and the change in clinical scores between baseline and follow-up. Interpretation Respiratory function remained stable in most patients with FSHD, but a subgroup of patients showed a pronounced deterioration. They showed more severe muscle weakness including the leg muscles at baseline (Ricci score >= 6), had spinal and thorax deformities and a relatively fast decline in axial muscle function at follow-up.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available