Author:
Lachmann Mark J.,Salgin Burak,Kummer Sebastian,Welters Alena,Döing Carsten,Zenker Martin,Wieland Ilse,Mayatepek Ertan,Meissner Thomas
Abstract
AbstractDuring conservative treatment, congenital hyperinsulinism (CHI) can resolve spontaneously. This study describes the hormonal and metabolic profiles in three patients withAn age-adapted fasting and oral glucose tolerance test (OGTT) were performed.All patients (aged 6–9 years) tolerated age-adapted fasting durations (20, respectively 24 h), without reaching glucose concentrations ≤2.5 mmol/L, nor developing hypoglycemia-related symptoms. Nevertheless, insulin concentrations from all patients exceeded the 90th reference percentile at the end of the fasting test (range: 4.2–15.8 mU/L). During the OGTT, one patient (patient 2; BMI: 23.4 kg/mThe insulin concentration profiles in CHI patients in apparent clinical remission range from almost complete normalization to persistent, yet attenuated, hypersecretion. The hyperglycemia, detected during the OGTT, must be further monitored.
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Reference48 articles.
1. Hyperinsulinism caused by paternal - specific inheritance of a recessive mutation in the sulfonylurea - receptor gene;Glaser;Diabetes,1999
2. CA in infants children;Stanley;Clin Am,1997
3. Congenital hyperinsulinism current trends in diagnosis and therapy;Arnoux;Orphanet J Rare Dis,2011
4. Recent advances in hyperinsulinism and the pathogenesis of diabetes mellitus;Bruining;Curr Opin Pediatr,1990
5. Novel de novo mutation in sulfonylurea receptor presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence;Abdulhadi;Diabetes,2008
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献