Respiratory involvement in Huntington's disease is not confined to late-stage disease. Measurable reductions in lung volume, cough effectiveness, and respiratory muscle strength can occur well before end-stage, and upper airway changes may be detectable even in pre-symptomatic individuals. Managing this aspect of HD requires targeted attention alongside the broader neurological picture.
Reduced lung function and respiratory muscle strength are not only associated with end-stage disease but occur much earlier, with evidence of some upper airway changes in pre-symptomatic individuals and reduction of cough effectiveness, reduced lung volume, and impaired respiratory strength by mid-disease.
DOI: 10.3389/fneur.2019.00710
Reduced lung function and respiratory muscle strength are not only associated with end stage disease but occur much earlier, with evidence of some upper airway changes in pre-symptomatic individuals and reduction of cough effectiveness, reduced lung volume, and impaired respiratory strength by mid-disease.
Home-based respiratory muscle training program appeared to improve pulmonary function in manifest HD patients but had only a small effect on swallowing function, dyspnea, and exercise capacity (Grade B).
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