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Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire.
Grünert, Sarah C; Derks, Terry G J; Adrian, Katarina; Al-Thihli, Khalid; Ballhausen, Diana; Bidiuk, Joanna; Bordugo, Andrea; Boyer, Monica; Bratkovic, Drago; Brunner-Krainz, Michaela; Burlina, Alberto; Chakrapani, Anupam; Corpeleijn, Willemijn; Cozens, Alison; Dawson, Charlotte; Dhamko, Helena; Milosevic, Maja Djordjevic; Eiroa, Hernan; Finezilber, Yael; Moura de Souza, Carolina Fischinger; Garcia-Jiménez, Maria Concepción; Gasperini, Serena; Haas, Dorothea; Häberle, Johannes; Halligan, Rebecca; Fung, Law Hiu; Hörbe-Blindt, Alexandra; Horka, Laura Maria; Huemer, Martina; Uçar, Sema Kalkan; Kecman, Bozica; Kilavuz, Sebile; Kriván, Gergely; Lindner, Martin; Lüsebrink, Natalia; Makrilakis, Konstantinos; Mei-Kwun Kwok, Anne; Maier, Esther M; Maiorana, Arianna; McCandless, Shawn E; Mitchell, John James; Mizumoto, Hiroshi; Mundy, Helen; Ochoa, Carlos; Pierce, Kathryn; Fraile, Pilar Quijada; Regier, Debra; Rossi, Alessandro; Santer, René; Schuman, Hester C.
Afiliación
  • Grünert SC; Department of General Pediatrics, Adolescent Medicine and Neonatology, Medical Centre-University of Freiburg, Faculty of Medicine, Freiburg, Germany. Electronic address: sarah.gruenert@uniklinik-freiburg.de.
  • Derks TGJ; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center of Groningen, University of Groningen, Groningen, The Netherlands.
  • Adrian K; Department of Pediatrics, Queen Silvias Childrens Hospital, Sahlgrenska University Hospital, Göteborg, Sweden.
  • Al-Thihli K; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Ballhausen D; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
  • Bidiuk J; Department of Internal Medicine, Hypertension and Vascular Diseases, Medical University of Warsaw, Warsaw, Poland.
  • Bordugo A; Inherited Metabolic Disease Unit, Pediatric Clinic C, Woman and Child Department, Azienda Ospedaliera Università Integrata, Verona, Italy.
  • Boyer M; Division of Metabolic Disorders, CHOC Children's Hospital, Orange, CA.
  • Bratkovic D; Metabolic Clinic, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
  • Brunner-Krainz M; University Children's Hospital Graz, Graz, Austria.
  • Burlina A; Division of Inherited Metabolic Diseases, Department of Diagnostic Services, University Hospital, Padua, Italy.
  • Chakrapani A; Department of Metabolic Medicine, Great Ormond Street Hospital, London, United Kingdom.
  • Corpeleijn W; Department of Pediatrics, Division of Metabolic Disorders, Emma Children's Hospital, Gastroenterology, Endocrinology & Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Cozens A; Royal Hospital for Children and Young People, Edinburgh, United Kingdom.
  • Dawson C; Department of Endocrinology, Diabetes and Metabolism, University Hospitals Birmingham, Birmingham, United Kingdom.
  • Dhamko H; Division of Medical Oncology and Hematology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Milosevic MD; Metabolic and Genetic Department, Mother and Child Health Care Institute of Serbia "Dr Vukan Cupic", Belgrade, Serbia.
  • Eiroa H; Servicio de Errores Congenitos del Metabolismo, Hospital de Pediatria "J.P. Garrahan", Buenos Aires, Argentina.
  • Finezilber Y; Metabolic Diseases Unit and Internal Medicine Department A, Sheba Medical Center, Ramat Gan, Israel.
  • Moura de Souza CF; Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.
  • Garcia-Jiménez MC; Neurometabolic Unit, Pediatric Department, Miguel Servet Universitary Hospital, Zaragoza, Spain.
  • Gasperini S; Metabolic Rare Diseases Unit, Paediatric Department, San Gerardo Hospital, Monza, Italy.
  • Haas D; Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Häberle J; Division of Metabolism and Children`s Research Center, University Children's Hospital Zurich, Zürich, Switzerland.
  • Halligan R; Department of Metabolic Medicine, The Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Fung LH; Department of Pediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Island, Hong Kong.
  • Hörbe-Blindt A; Eltern-Kind-Zentrum Prof. Hess, Medical Centre Bremen Mitte, Bremen, Germany.
  • Horka LM; Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
  • Huemer M; Division of Metabolism and Children`s Research Center, University Children's Hospital Zurich, Zürich, Switzerland; Department of Paediatrics, University Children's Hospital Basel and University of Basel, Basel, Switzerland.
  • Uçar SK; Division of Metabolism and Nutrition, Department of Pediatrics, Ege University Children's Hospital, Izmir, Turkey.
  • Kecman B; Metabolic and Genetic Department, Mother and Child Health Care Institute of Serbia "Dr Vukan Cupic", Belgrade, Serbia.
  • Kilavuz S; Division of Pediatric Metabolism, Department of Pediatrics, University of Health Sciences, Van Training and Research Hospital, Van, Turkey.
  • Kriván G; Department for Pediatric Hematology and Hemopoietic Stem Cell Transplantation, Central Hospital of Southern Pest National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
  • Lindner M; Department of Pediatric Neurology, University Children's Hospital Frankfurt, Frankfurt, Germany.
  • Lüsebrink N; Department of Pediatric Neurology, University Children's Hospital Frankfurt, Frankfurt, Germany.
  • Makrilakis K; First Department of Propaedeutic Internal Medicine, National and Kapodistrian University of Athens Medical School, Laiko General Hospital, Athens, Greece.
  • Mei-Kwun Kwok A; Department of Pediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Hong Kong.
  • Maier EM; Section of Inborn Errors of Metabolism, Dr. von Hauner Children's Hospital, University of Munich, Munich, Germany.
  • Maiorana A; Division of Metabolism, Department of Pediatric Subspecialties, Ospedale Pediatrico Bambino Gesù, Istituti di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
  • McCandless SE; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO; Department of Genetics and Metabolism, Children's Hospital Colorado, Aurora, CO.
  • Mitchell JJ; Division of Pediatric Endocrinology, McGill University Health Center, Montreal, Quebec, Canada.
  • Mizumoto H; Department of Pediatrics, Tazuke Kofukai Medical Research Institute, Kitano Hospital, Osaka, Japan.
  • Mundy H; Evelina Children's Hospital, London, United Kingdom.
  • Ochoa C; Department of Pediatrics, Complejo Asistencial de Zamora, Zamora, Spain.
  • Pierce K; York University, Toronto, Ontario, Canada.
  • Fraile PQ; Reference Center for Inherited Metabolic Disorders, Department of Pediatrics, Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Regier D; Genetics and Metabolism, Children's National Hospital, Washington DC.
  • Rossi A; Section of Paediatrics, Department of Translational Medicine, University of Naples "Federico II", Naples, Italy.
  • Santer R; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.
  • Schuman HC; Mediclinic Kloof Hospital, Pretoria, South Africa.
Genet Med ; 24(8): 1781-1788, 2022 08.
Article en En | MEDLINE | ID: mdl-35503103
PURPOSE: This paper aims to report collective information on safety and efficacy of empagliflozin drug repurposing in individuals with glycogen storage disease type Ib (GSD Ib). METHODS: This is an international retrospective questionnaire study on the safety and efficacy of empagliflozin use for management of neutropenia/neutrophil dysfunction in patients with GSD Ib, conducted among the respective health care providers from 24 countries across the globe. RESULTS: Clinical data from 112 individuals with GSD Ib were evaluated, representing a total of 94 treatment years. The median age at start of empagliflozin treatment was 10.5 years (range = 0-38 years). Empagliflozin showed positive effects on all neutrophil dysfunction-related symptoms, including oral and urogenital mucosal lesions, recurrent infections, skin abscesses, inflammatory bowel disease, and anemia. Before initiating empagliflozin, most patients with GSD Ib were on G-CSF (94/112; 84%). At the time of the survey, 49 of 89 (55%) patients previously treated with G-CSF had completely stopped G-CSF, and another 15 (17%) were able to reduce the dose. The most common adverse event during empagliflozin treatment was hypoglycemia, occurring in 18% of individuals. CONCLUSION: Empagliflozin has a favorable effect on neutropenia/neutrophil dysfunction-related symptoms and safety profile in individuals with GSD Ib.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo I / Neutropenia Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Newborn Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo I / Neutropenia Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Newborn Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article