4.3 Article

Dysregulated insulin in pancreatic insufficient cystic fibrosis with post-prandial hypoglycemia

Journal

JOURNAL OF CYSTIC FIBROSIS
Volume 19, Issue 2, Pages 310-315

Publisher

ELSEVIER
DOI: 10.1016/j.jcf.2019.07.006

Keywords

Cystic fibrosis; Hypoglycemia; Glucose tolerance; Insulin secretion; Pancreatic insufficiency

Funding

  1. Cystic Fibrosis Foundation
  2. Public Health Services Research Grants [R01 DK97830, UL1 TR000003, P30 DK19525, K23 DK107937]
  3. Human MetabolismResource of the University of Pennsylvania Institute for Diabetes, Obesity Metabolism

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Background: Post-prandial and oral glucose tolerance test-related hypoglycemia is common in cystic fibrosis (CF); however, the underlying mechanisms are unclear. Methods: To understand the relationship of hypoglycemia with meal-related glucose excursion and insulin secretion, we analyzed plasma glucose, insulin, C-peptide, glucagon and incretins obtained during standardized mixed-meal tolerance tests (Narrr) in non-diabetic adolescents and young adults with pancreatic insufficient CF (PI-CF). Results: Hypoglycemia, defined as glucose <70 mg/dL, occurred in 9/34 subjects at 150 (range:120-210) minutes following initial meal ingestion. Hypoglycemia[+] and hypoglycemia[-] groups did not differ in gender, age, lung function, HbA1c, or BMI. While 11/14 hypoglycemia[-] individuals displayed normal glucose tolerance (NGT), only 2/9 hypoglycemia[+] had NGT. Peak glucose was higher in hypoglycemia[+] vs hypoglycemia[-]. Compared to hypoglycemia[-] NGT, hypoglycemia[+] exhibited lower early-phase insulin secretion (ISR-AUC(0-30)(min)). ISR-AUC(120-180min) was not different in hypoglycemia[+] vs hypoglycemia[-] with abnormal glucose tolerance (AGT); however, glucose-AUC(120-180min) was lower in hypoglycemia[+] vs hypoglycemia[-] AGT. After adjusting for glucose-AUC, hypoglycemia[+] subjects tended to have higher ISR-AUC(120-180min) than hypoglycemia[-] AGT. Glucagon concentration did not differ between groups. Lower GLP-1-AUC(30min) and AUC(180min) and higher GIP-AUC(30min) were present in hypoglycemia[+] individuals. Conclusion: Hypoglycemia is common in PI-CF following muff and is associated with early glucose dysregulation (higher peak glucose), more impaired early-phase insulin secretion (lower ISR-AUC(30min)), and possibly late compensatory hyperinsulinemia. Further study is required to understand whether absence of glucagon difference in the hypoglycemia[+] individuals signals counter-regulatory impairment, to delineate the role of incretins in hypoglycemia, and to determine the relationship of hypoglycemia to emergence of CFRD. (C) 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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