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Record W4414457969 · doi:10.70070/fdmnvp18

The Impact of Sleep Disorders on Amyotrophic Lateral Sclerosis: A Systematic Review

2025· article· en· W4414457969 on OpenAlexaboutno aff
Bella Sugih Laksono, Nasyifa Nurul Fitriany, Iklima Fauzi Yazidah, Zam Zanariah, Nadia Amrin

Bibliographic record

VenueThe Indonesian Journal of General Medicine · 2025
Typearticle
Languageen
FieldMedicine
TopicAmyotrophic Lateral Sclerosis Research
Canadian institutionsnot available
Fundersnot available
KeywordsPolysomnographyObservational studySleep (system call)Sleep apneaAmyotrophic lateral sclerosisPittsburgh Sleep Quality IndexObstructive sleep apneaSleep disorderMeta-analysis

Abstract

fetched live from OpenAlex

Introduction: Amyotrophic Lateral Sclerosis (ALS) is increasingly recognized as a multisystem neurodegenerative disorder where sleep disturbances are highly prevalent and clinically significant. This review aims to systematically evaluate the evidence on the impact of various sleep disorders on the pathophysiology, clinical progression, survival, and quality of life in patients with ALS. Methods: A systematic search of PubMed, Google Scholar, Semanthic Scholar, Springer, Wiley Online Library was conducted for observational studies, interventional trials, and meta-analyses published up to September 2024, in accordance with PRISMA guidelines. Studies assessing subjective or objective sleep parameters in ALS patients and their association with clinical outcomes were included. Methodological quality was assessed using the Newcastle-Ottawa Scale for observational studies and the Cochrane Risk of Bias tool for randomized trials. Results: Seventeen studies met the inclusion criteria. The prevalence of poor subjective sleep quality (Pittsburgh Sleep Quality Index > 5) ranged from 50% to 63%. Insomnia, sleep-disordered breathing (SDB), and restless legs syndrome (RLS) were also highly prevalent. Polysomnography (PSG) consistently revealed significant reductions in total sleep time and sleep efficiency, altered sleep architecture with decreased slow-wave and REM sleep, and evidence of nocturnal hypoxemia. Sleep parameters were significantly associated with critical clinical outcomes. Poor sleep quality was linked to a more rapid decline in functional (ALSFRS-R) and respiratory (FVC) status, shorter survival, and reduced quality of life. Specific pathologies, including obstructive sleep apnea (OSA), nocturnal hypoventilation, and periodic limb movements in sleep (PLMS), were independent predictors of mortality. Emerging genetic evidence suggests a potential causal link between OSA and an increased risk of developing ALS. Discussion: The evidence supports a bidirectional model where ALS-related pathophysiology (e.g., respiratory muscle weakness, central neurodegeneration of sleep centers) disrupts sleep, and this sleep disruption, in turn, may accelerate neurodegeneration. Potential mechanisms for the latter include impaired glymphatic clearance of neurotoxic proteins, heightened systemic inflammation, and oxidative stress from intermittent hypoxia. Conclusion: Sleep disorders are an integral and prognostically significant component of ALS, not merely a secondary symptom. Their presence is associated with accelerated disease progression and reduced survival. These findings underscore the critical need for routine sleep assessment, including polysomnography, and proactive management, particularly with non-invasive ventilation (NIV), as a core component of comprehensive ALS care.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.003
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Systematic review · Consensus signal: Systematic review
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.373
Threshold uncertainty score0.446

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0030.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0000.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.022
GPT teacher head0.330
Teacher spread0.308 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSystematic review
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

Explore more

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