Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort. 2020

Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
Reference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.

Glycogenosis type Ib (GSD1B) causes not only hypoglycemia but also infections and "Crohn's disease like" inflammatory bowel disease (IBD) that can significantly impair patient's quality of life. We retrospectively evaluated infectious and digestive complications in 9 French patients (3 girls, 6 boys) diagnosed at 0.8 years on average, with a mean follow-up of 19.1 years. Infections occurred earlier than IBD, at mean ages of 1.7 and 3.8 years, respectively. The number of acute hospitalizations was 0.7/year due to infectious (0.4/year) or digestive symptoms (0.4/year). Clinical presentations allowed separating patients into mild (n = 5) and severe (n = 4) intestinal involvement. Patients in the severe group had more serious digestive symptoms but also earlier neutropenia (median 0.3 vs. 1.5 years, p =0 .046) with a tendency to a lower neutrophil count (NC) during follow-up, and a higher number of acute hospitalizations (median 1.3/year vs. 0.2/year, p =0 .014) due to digestive symptoms (median 0.6/year vs. 0.05/year, p = 0,012) and infections (median 0.8/year vs. 0.2/year, p =0 .014). Treatments included G-CSF and cotrimoxazole (n = 7), 5-aminosalicylic acid (n = 2), and a polymeric solution enriched in the anti-inflammatory cytokine TGF-β (n = 4, "severe" group), and immunomodulatory treatment (n = 1). In conclusion, infections and IBD are rare but severe complications in GSD1B. Neutropenia tended to be more prevalent in the severe IBD group than in the mild IBD group. Dietetic treatment with specific anti-inflammatory solutions seems particularly appropriate in these patients.

UI MeSH Term Description Entries

Related Publications

Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
January 1993, European journal of pediatrics,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
January 1998, Ryoikibetsu shokogun shirizu,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
January 2000, Ryoikibetsu shokogun shirizu,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
June 1983, Archives of pathology & laboratory medicine,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
September 1983, European journal of pediatrics,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
February 1988, Harefuah,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
January 2004, Journal of inherited metabolic disease,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
August 1981, The Journal of pediatrics,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
January 2010, Current opinion in hematology,
Camille Wicker, and Célina Roda, and Ariane Perry, and Jean Baptiste Arnoux, and Anais Brassier, and Martin Castelle, and Aude Servais, and Jean Donadieu, and Juliette Bouchereau, and Bénédicte Pigneur, and Philippe Labrune, and Frank M Ruemmele, and Pascale de Lonlay
August 2000, The Journal of pediatrics,
Copied contents to your clipboard!