Non-osteogenic muscle hypertrophy in children with McArdle disease

Introduction McArdle disease is an inborn disorder of muscle glycogen metabolism that produces exercise intolerance, and has been recently associated with low values of lean mass (LM) and bone mineral content (BMC) and density (BMD) in affected adults. Here we aimed to study whether this bone health...

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Detalles Bibliográficos
Autores: Rodríguez Gómez, Irene, Santalla Hernández, Alfredo, Díez Bermejo, Jorge, Munguía Izquierdo, Diego, Alegre Durán, Luis María
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/19657
Acceso en línea:http://hdl.handle.net/10578/19657
Access Level:acceso abierto
Palabra clave:Non-osteogenic muscle hypertrophy
Hipertrofia muscular no osteogénica
McArdle disease
Enfermedad de McArdle
Children
Niños
Descripción
Sumario:Introduction McArdle disease is an inborn disorder of muscle glycogen metabolism that produces exercise intolerance, and has been recently associated with low values of lean mass (LM) and bone mineral content (BMC) and density (BMD) in affected adults. Here we aimed to study whether this bone health problem begins in childhood. Methods Forty children and adolescents were evaluated: 10 McArdle disease and 30 control children (mean age of both groups, 13 ± 2y). Body composition was evaluated by dual-energy X-ray absorptiometry and creatine kinase (CK) levels were determined in the patients as an estimate of muscle damage. Results Legs bone mass was significantly lower in patients than in controls (−36% for BMC and −22% for BMD). Moreover, patients had significantly higher LM values in the legs than controls, whereas no difference was found for fat mass. CK levels were positively associated withLM in McArdle patients. A correlation was found between LM and BMD variables in the control group but not in McArdle patients. Conclusion We have identified a ‘non-osteogenic muscle hypertrophy’ in children with McArdle disease. This phenomenon warrants special attention since low osteogenesis at an early age predicts a high risk for osteoporosis later in life.