2011•Journal of Inherited Metabolic DiseaseRequires access
Effects of enzyme replacement therapy on five patients with advanced late‐onset glycogen storage disease type II: a 2‐year follow‐up study
Yoshihiko Furusawa, Madoka Mori‐Yoshimura, Toshiyuki Yamamoto, Chikako Sakamoto, Mizuki Wakita, Yôko Kobayashi, Yutaka Fukumoto, Yasushi Oya, Tokiko Fukuda, Hideo Sugie, Yukiko Hayashi, Ichizo Nishino, Ikuya Nonaka, Miho Murata
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Abstract
We examined the efficacy of 2-year enzyme replacement therapy (ERT) using recombinant human α-glucosidase (GAA; Myozyme®) in five long-term ventilator-dependent adults and aged patients with advanced, late-onset glycogen storage disease type II (GSDII, also known as Pompe disease). Although all patients had advanced respiratory failure and were ventilator-dependent for more than 6 years, four showed obvious improvements in muscle strength, pulmonary function, and activities of daily living after ERT. Improvement in each parameter was more prominent in the first year than in the second year. Values in the second year were still significantly better than those at study entry and indicate stabilization in the clinical status of all patients. These results suggest that ERT continues to be effective in the second year of treatment even in patients suffering from advanced late-onset GSDII disease with severe respiratory failure.