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Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations.
Rossi, Alessandro; Hoogeveen, Irene J; Bastek, Vanessa B; de Boer, Foekje; Montanari, Chiara; Meyer, Uta; Maiorana, Arianna; Bordugo, Andrea; Dianin, Alice; Campana, Carmen; Rigoldi, Miriam; Kishnani, Priya S; Pendyal, Surekha; Strisciuglio, Pietro; Gasperini, Serena; Parenti, Giancarlo; Parini, Rossella; Paci, Sabrina; Melis, Daniela; Derks, Terry G J.
Afiliación
  • Rossi A; Department of Translational Medicine, Section of Pediatrics, University of Naples "Federico II", Naples, Italy.
  • Hoogeveen IJ; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Bastek VB; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • de Boer F; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Montanari C; Department of Pediatrics, San Paolo Hospital, ASST Santi Paolo e Carlo, University of Milan, Milan, Italy.
  • Meyer U; Department of Pediatrics, Hannover Medical School, Hannover, Germany.
  • Maiorana A; Division of Metabolic Diseases, Department of Pediatric Specialties, Bambino Gesù Children's Hospital, Rome, Italy.
  • Bordugo A; Inherited Metabolic Diseases Unit, Department of Paediatrics, Regional Centre for Newborn Screening, Diagnosis and Treatment of Inherited Metabolic Diseases and Congenital Endocrine Diseases, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
  • Dianin A; Inherited Metabolic Diseases Unit, Department of Paediatrics, Regional Centre for Newborn Screening, Diagnosis and Treatment of Inherited Metabolic Diseases and Congenital Endocrine Diseases, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
  • Campana C; Division of Metabolic Diseases, Department of Pediatric Specialties, Bambino Gesù Children's Hospital, Rome, Italy.
  • Rigoldi M; Rare Diseases Center, ASST Monza, San Gerardo Hospital, Monza, Italy.
  • Kishnani PS; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
  • Pendyal S; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
  • Strisciuglio P; Department of Translational Medicine, Section of Pediatrics, University of Naples "Federico II", Naples, Italy.
  • Gasperini S; Rare Metabolic Diseases Pediatric Center, Pediatric Clinic, Fondazione MBBM, San Gerardo Hospital, Monza, Italy.
  • Parenti G; Department of Translational Medicine, Section of Pediatrics, University of Naples "Federico II", Naples, Italy.
  • Parini R; Rare Metabolic Diseases Pediatric Center, Pediatric Clinic, Fondazione MBBM, San Gerardo Hospital, Monza, Italy.
  • Paci S; Department of Pediatrics, San Paolo Hospital, ASST Santi Paolo e Carlo, University of Milan, Milan, Italy.
  • Melis D; Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", Section of Pediatrics, University of Salerno, Baronissi (SA), Italy.
  • Derks TGJ; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
J Inherit Metab Dis ; 43(4): 770-777, 2020 07.
Article en En | MEDLINE | ID: mdl-32064649
ABSTRACT
A potential role of dietary lipids in the management of hepatic glycogen storage diseases (GSDs) has been proposed, but no consensus on management guidelines exists. The aim of this study was to describe current experiences with dietary lipid manipulations in hepatic GSD patients. An international study was set up to identify published and unpublished cases describing hepatic GSD patients with a dietary lipid manipulation. A literature search was performed according to the Cochrane Collaboration methodology through PubMed and EMBASE (up to December 2018). All delegates who attended the dietetics session at the IGSD2017, Groningen were invited to share unpublished cases. Due to multiple biases, only data on GSDIII were presented. A total of 28 cases with GSDIII and a dietary lipid manipulation were identified. Main indications were cardiomyopathy and/or myopathy. A high fat diet was the most common dietary lipid manipulation. A decline in creatine kinase concentrations (n = 19, P < .001) and a decrease in cardiac hypertrophy in paediatric GSDIIIa patients (n = 7, P < .01) were observed after the introduction with a high fat diet. This study presents an international cohort of GSDIII patients with different dietary lipid manipulations. High fat diet may be beneficial in paediatric GSDIIIa patients with cardiac hypertrophy, but careful long-term monitoring for potential complications is warranted, such as growth restriction, liver inflammation, and hepatocellular carcinoma development.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Grasas de la Dieta / Enfermedad del Almacenamiento de Glucógeno Tipo III / Cardiomiopatías Tipo de estudio: Systematic_reviews Límite: Child / Humans Idioma: En Revista: J Inherit Metab Dis Año: 2020 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Grasas de la Dieta / Enfermedad del Almacenamiento de Glucógeno Tipo III / Cardiomiopatías Tipo de estudio: Systematic_reviews Límite: Child / Humans Idioma: En Revista: J Inherit Metab Dis Año: 2020 Tipo del documento: Article País de afiliación: Italia