Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients. Issue 1 (25th November 2019)
- Record Type:
- Journal Article
- Title:
- Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients. Issue 1 (25th November 2019)
- Main Title:
- Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients
- Authors:
- Moravej, Hossein
Altassan, Ruqaiah
Jaeken, Jaak
Enns, Gregory M.
Ellaway, Carolyn
Balasubramaniam, Shanti
De Lonlay, Pascale
Coman, David
Mercimek‐Andrews, Saadet
Witters, Peter
Morava, Eva - Abstract:
- Abstract: Background: Phosphomannomutase 2 deficiency (PMM2‐CDG) is the most common congenital disorder of glycosylation (CDG). Hypoglycemia has been reported in various CDG including PMM2‐CDG. The frequency and etiology of hypoglycemia in PMM2‐CDG are not well studied. Methods: We conducted a systematic review of the literature on genetically and/or biochemically confirmed PMM2‐CDG patients who developed hypoglycemia. Prospective follow‐up information on the patients who received diazoxide therapy was collected and evaluated. Results: A total of 165 peer‐reviewed articles reporting on 933 PMM2‐CDG patients were assessed. Hypoglycemia was specifically mentioned only in 23 of these patients (2.5%). Hyperinsulinism was identified in 10 patients (43% of all hypoglycemic patients). Among these 10 patients, seven were successfully treated with diazoxide. However, most patients remained on therapy longer than a year to stay free of hypoglycemia. Conclusion: Hypoglycemia is a rarely reported finding in patients with PMM2‐CDG. Diazoxide‐responsive hyperinsulinism was found to have a good prognosis on medication in our PMM2‐CDG patients with hypoglycemia. No genotype‐phenotype correlation was observed with respect to hyperinsulinism. A prospective study should be undertaken to explore the hypothesis that hypoglycemia is underdiagnosed in PMM2‐CDG and to evaluate whether hyperinsulinism is always associated with hypoglycemia.
- Is Part Of:
- JIMD reports. Volume 51:Issue 1(2020)
- Journal:
- JIMD reports
- Issue:
- Volume 51:Issue 1(2020)
- Issue Display:
- Volume 51, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 51
- Issue:
- 1
- Issue Sort Value:
- 2020-0051-0001-0000
- Page Start:
- 76
- Page End:
- 81
- Publication Date:
- 2019-11-25
- Subjects:
- CDG -- congenital disorder(s) of glycosylation -- diazoxide -- hyperinsulinism -- hypoglycemia -- phosphomannomutase 2 -- PMM2‐CDG
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- https://onlinelibrary.wiley.com/loi/21928312 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jmd2.12085 ↗
- Languages:
- English
- ISSNs:
- 2192-8304
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 22929.xml