Skeletal Muscle Dysfunction and Exercise Intolerance in Children Treated with Haematopoietic Stem Cell Transplant-A Pilot Feasibility Study

Autor: Greg D. Wells, Sarah L. West, Gillian E White, Tammy Rayner, Jessica E. Caterini, Tal Schechter, Paul C. Nathan
Rok vydání: 2019
Předmět:
Male
medicine.medical_specialty
Adolescent
Health
Toxicology and Mutagenesis

muscle metabolism
lcsh:Medicine
Pilot Projects
Exercise intolerance
haematopoietic stem cell transplant
Article
Body Mass Index
03 medical and health sciences
0302 clinical medicine
Internal medicine
medicine
Aerobic exercise
Humans
Adverse effect
Child
Muscle
Skeletal

030304 developmental biology
0303 health sciences
medicine.diagnostic_test
exercise
business.industry
lcsh:R
Public Health
Environmental and Occupational Health

Hematopoietic Stem Cell Transplantation
Skeletal muscle
Magnetic resonance imaging
Magnetic Resonance Imaging
Peripheral
Haematopoiesis
medicine.anatomical_structure
surgical procedures
operative

pediatric
030220 oncology & carcinogenesis
Case-Control Studies
Exercise Test
Feasibility Studies
exercise tolerance
Female
Stem cell
medicine.symptom
business
Zdroj: International Journal of Environmental Research and Public Health
International Journal of Environmental Research and Public Health, Vol 16, Iss 9, p 1608 (2019)
Volume 16
Issue 9
ISSN: 1660-4601
Popis: Haematopoietic stem cell transplant (HSCT) is an intensive therapy for some pediatric hematological illnesses. Survivors are at risk for adverse effects including exercise intolerance. Peripheral tissue dysfunction may contribute to exercise intolerance
therefore, we examined the feasibility of a magnetic resonance spectroscopy (MRS) protocol to evaluate skeletal muscle metabolism in children post-HSCT. We measured demographic characteristics, aerobic exercise capacity (YMCA protocol), and skeletal muscle function in response to exercise (MRS
Siemens 3T MRI) in five children post-allogeneic HSCT and five age/body mass index-matched healthy controls (HCs). The mean age (±
standard deviation) of the HSCT group and HC group were 11 ±
1.2 and 12.8 ±
2.4 years, respectively. Children post-HSCT had a lower peak aerobic exercise capacity compared to HCs (27.8 ±
3.4 vs. 40.3 ±
8.1 mL kg&minus
1 min&minus
1, respectively
p = 0.015). Exercise MRS testing protocols were successfully completed by all HSCT and HC participants
however, MRS-derived skeletal muscle metabolism variables were not different between the two groups. In conclusion, the use of exercise protocols in conjunction with MRS to assess peripheral skeletal muscle metabolism was achievable in children post-HSCT. In the future, larger studies should determine if skeletal muscle function is associated with exercise capacity in children post-HSCT.
Databáze: OpenAIRE