2026/02/01 by Francesca Lanfranconi, L. Peli, L. Pollastri +16 · 1 voice
Medicine · #Glycogen Storage Diseases and Myoclonus #Lysosomal Storage Disorders Research #Parkinson's Disease and Spinal Disorders
paper · doi:10.14814/phy2.70771
openalex publication_date 2026/02/01 · openalex created_date 2026/02/24 · openalex updated_date 2026/07/23
Abstract People with glycogen storage disease type III (GSDIII‐p) have a remarkably reduced exercise tolerance. Aim of this study was to analyze the oxygen transport‐utilization chain strategies adopted by GSDIII‐p during exercise. Nine GSDIII‐p (39.4 ± 10.0 year, 33% female) and 11 healthy controls (CTRL), age and gender matched, underwent an incremental cardiopulmonary exhaustion test (CPET) to assess peak heart rate (HR), blood lactate [La]p and vastus lateralis O 2 fractional extraction (ΔHHb/isch) using near‐infrared spectroscopy. Patterns of breathing (PBr) were assessed accordingly by analyzing pulmonary O 2 uptake (V̇O 2 ), tidal volume (Vt), respiratory frequency (Rf), end‐tidal CO 2 (PETCO 2 ) and alveolar ventilation (V̇A). GSDIII‐p exhibited significantly ( p < 0.05) lower peak values of V̇O 2 , pulmonary ventilation (V̇E) [La] and ΔHHb/isch compared to CTRL (1.7 ± 0.7 vs. 3.2 ± 1.1 L/min, 50.5 ± 19.8 vs. 113.6 ± 40.4 L/min, 1.8 ± 0.7 vs. 7.6 ± 3.0 mmol/L and 39.1% ± 9.9% vs. 74.8% ± 36.6%, respectively). The range of peak V̇O 2 values for GSDIII‐p, compared to the predicted values for age and sex, was between 79% and 35%. Both GSDIII‐p and CTRL were arbitrarily divided into 4 groups according to individual V̇E values. GSDIII‐p with exercise intolerance relied on increased Rf with inadequate Vt adaptation to maintain V̇E and reduce PETCO 2 , with low V̇A values and low to moderate workloads tolerance. Reduced exercise tolerance in GSDIII‐p is related to respiratory and skeletal muscle inefficiencies. GSDIII‐p strong heterogeneity evaluated throught CPET provides insights into clinical management.