Body composition and 6 minute walking ability in late-onset pompe disease patients after 9 years of enzyme replacement therapy. (3rd July 2022)
- Record Type:
- Journal Article
- Title:
- Body composition and 6 minute walking ability in late-onset pompe disease patients after 9 years of enzyme replacement therapy. (3rd July 2022)
- Main Title:
- Body composition and 6 minute walking ability in late-onset pompe disease patients after 9 years of enzyme replacement therapy
- Authors:
- Terzis, Gerasimos
Papadimas, Georgios
Krase, Argyro
Kontou, Eleni
Arnaoutis, Ioannis
Papadopoulos, Constantinos - Abstract:
- Abstract: Objective: Pompe disease is a rare autosomal recessive disorder caused by the deficiency of acid α-glycosidase resulting in accumulation of glycogen in the lysosomes. The late-onset form of the disease (LOPD) causes primarily progressive muscle weakness and respiratory insufficiency. Enzyme replacement therapy (ERT) introduced in 2006, showed mild improvement or stabilization of the symptoms although long-term data are limited. Aim of the study was to describe the progression of body composition and walking ability in LOPD patients receiving ERT consistently for 9 years. Methods: Lean body mass, bone mineral density, body fat and 6 min walking distance were assessed in three male and three female LOPD patients (height 165.8 ± 11.2 cm, age 42.3 ± 11.8yrs, body mass 71.1 ± 20.8 kg, at study entry), every three years, for 9 years since ERT initiation (T0, T3, T6, T9). Results: Total body and upper extremities' lean mass remained unchanged ( p < 0.05), but it was decreased for the lower extremities (T3:13.06 ± 3.848 kg vs. T9:11.63 ± 3.49 kg, p < 0.05). Lean body mass was not significantly different after 9 years of ERT compared to before the ERT initiation (T0 to T9). Bone mineral density remained unchanged. Percent body fat increased (T0:39.1 ± 10.3%, vs. T9:43.1 ± 10.4%, p < 0.05). Six minute walking distance tended to increase after 3 years of ERT and decreased gradually thereafter, with no difference between T0-T9. Lean mass of the lower extremities adjustedAbstract: Objective: Pompe disease is a rare autosomal recessive disorder caused by the deficiency of acid α-glycosidase resulting in accumulation of glycogen in the lysosomes. The late-onset form of the disease (LOPD) causes primarily progressive muscle weakness and respiratory insufficiency. Enzyme replacement therapy (ERT) introduced in 2006, showed mild improvement or stabilization of the symptoms although long-term data are limited. Aim of the study was to describe the progression of body composition and walking ability in LOPD patients receiving ERT consistently for 9 years. Methods: Lean body mass, bone mineral density, body fat and 6 min walking distance were assessed in three male and three female LOPD patients (height 165.8 ± 11.2 cm, age 42.3 ± 11.8yrs, body mass 71.1 ± 20.8 kg, at study entry), every three years, for 9 years since ERT initiation (T0, T3, T6, T9). Results: Total body and upper extremities' lean mass remained unchanged ( p < 0.05), but it was decreased for the lower extremities (T3:13.06 ± 3.848 kg vs. T9:11.63 ± 3.49 kg, p < 0.05). Lean body mass was not significantly different after 9 years of ERT compared to before the ERT initiation (T0 to T9). Bone mineral density remained unchanged. Percent body fat increased (T0:39.1 ± 10.3%, vs. T9:43.1 ± 10.4%, p < 0.05). Six minute walking distance tended to increase after 3 years of ERT and decreased gradually thereafter, with no difference between T0-T9. Lean mass of the lower extremities adjusted for body weight was significantly correlated with 6 min walking distance ( r = 0.712, p < 0.05). Conclusion: The current data show that enzyme replacement therapy may preserve lean body mass, bone mineral density and walking capacity in LOPD patients. … (more)
- Is Part Of:
- International journal of neuroscience. Volume 132:Number 7(2022)
- Journal:
- International journal of neuroscience
- Issue:
- Volume 132:Number 7(2022)
- Issue Display:
- Volume 132, Issue 7 (2022)
- Year:
- 2022
- Volume:
- 132
- Issue:
- 7
- Issue Sort Value:
- 2022-0132-0007-0000
- Page Start:
- 699
- Page End:
- 705
- Publication Date:
- 2022-07-03
- Subjects:
- Lysosomal disease -- dual x-ray absorptiometry -- neuromuscular disease -- functional capacity
Nervous system -- Periodicals
612.805 - Journal URLs:
- http://informahealthcare.com/loi/nes ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/00207454.2020.1835902 ↗
- Languages:
- English
- ISSNs:
- 0020-7454
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.386000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22564.xml