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Published on: April 17, 2017
Neck flexion weakness predicts respiratory dysfunction in amyotrophic lateral sclerosis.
Nathan Pavey1, Alyssa Tieppo2, Aicee Dawn Calma1
1Brain and Nerve Research Centre, Concord Clinical School, University of Sydney, Concord Hospital, Sydney, Australia.
Neck flexion weakness in amyotrophic lateral sclerosis (ALS) patients is a significant indicator of developing respiratory dysfunction. This simple clinical assessment can predict the need for ventilatory support.
Area of Science:
- Neurology
- Pulmonology
- Biomarkers
Background:
- Neck flexion (NF) weakness is common in amyotrophic lateral sclerosis (ALS), especially in advanced stages.
- The potential of NF weakness as a biomarker for respiratory dysfunction in ALS requires further investigation.
Purpose of the Study:
- To evaluate if neck flexion weakness can serve as a clinical biomarker for the development of respiratory dysfunction in ALS patients.
- To determine the correlation between NF weakness and respiratory function parameters.
Main Methods:
- Prospective recruitment of 62 ALS patients.
- Assessment of neck flexion strength using the Medical Research Council (MRC) score and handheld dynamometry (HHD).
- Evaluation of respiratory function via spirometry, measuring forced vital capacity (FVC) and forced expiratory volume in 1 second (FEV1).
Main Results:
- Neck flexion weakness (MRC ≤4) was observed in 27% of ALS patients.
- Significant reduction in FVC was noted in patients with NF weakness compared to those with normal NF.
- HHD measurements of NF strength strongly correlated with FVC and FEV1, particularly in bulbar-onset ALS.
- NF weakness (MRC ≤4) significantly predicted reduced FVC (≤50% predicted), indicating a need for ventilatory support.
Conclusions:
- Neck flexion weakness, assessed by MRC score and HHD, is a valuable marker for respiratory dysfunction in ALS.
- This clinical assessment can help identify patients at risk of respiratory compromise and the need for ventilatory support.
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