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June 1, 2026Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration0 citations

Sleep disturbances and respiratory dysfunction in amyotrophic lateral sclerosis

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KBKato BracavalJVJoke De VochtFOFouke Ombelet

Key Points

  • To investigate the impact of respiratory dysfunction and site of onset on sleep architecture in people with ALS.
  • Conducted a retrospective observational study analyzing demographic data, lung function tests, and polysomnography measures.
  • Utilized descriptive statistics, correlation analyses, and survival analyses to interpret data.
  • Observed substantial sleep disturbances with increased arousals in the spinal onset group.
  • Found that a preserved FVC (≥ 70%) was associated with improved survival.
  • Demonstrated that FVC is a significant predictor for sleep efficiency.

Abstract

OBJECTIVE: To investigate how respiratory dysfunction and site of onset influences changes in sleep architecture in people with ALS (pwALS). METHODS: We conducted a retrospective observational study, analyzing demographic data, lung function tests, and polysomnography (PSG) measures. Descriptive statistics, correlation analyses, and survival analyses were performed. RESULTS: = 0.0059). Spinal onset, a slower rate of FVC decline in the months preceding PSG and a preserved FVC (≥ 70%) at the time of PSG were associated with improved survival. CONCLUSION: We observed substantial sleep disturbances in our cohort overall with substantially increased arousals in the spinal group. FVC is a significant predictor for sleep efficiency and the decline in FVC is linked to survival.

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Cite This Study

Bracaval et al. (2026) studied this question.

synapsesocial.com/papers/6a1d216202fbce91306376f9https://doi.org/10.1080/21678421.2026.2671162
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