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Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort.
- Source :
-
Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2020 Apr 09; Vol. 23, pp. 100581. Date of Electronic Publication: 2020 Apr 09 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- 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.<br />Competing Interests: FR has received speaker fees from: Shering-Plough, Nestlé, MeadJohnson, Ferring, MSD, Johnson & Johnson, Centocor, AbbVie; serves as a board member for: SAC:DEVELOP (Johnson & Johnson), and has been invited to MSD France, Nestlé Nutrition Institute, Nestlé Health Science, Danone, MeadJohnson; TAKEDA, CELLGENE, BIOGENE, ARKOPHARMA. The other authors have no conflicts of interest.<br /> (© 2020 The Authors.)
Details
- Language :
- English
- ISSN :
- 2214-4269
- Volume :
- 23
- Database :
- MEDLINE
- Journal :
- Molecular genetics and metabolism reports
- Publication Type :
- Academic Journal
- Accession number :
- 32300528
- Full Text :
- https://doi.org/10.1016/j.ymgmr.2020.100581