Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism

Abstract Background Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycaemia in infancy that leads to unfavourable neurological outcome if not treated adequately. In patients with severe diffuse CHI it remains under discussion whether pancreatic surgery should be perform...

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Main Authors: Alena Welters, Thomas Meissner, Jürgen Grulich-Henn, Elke Fröhlich-Reiterer, Katharina Warncke, Klaus Mohnike, Oliver Blankenstein, Ulrike Menzel, Nicolin Datz, Esther Bollow, Reinhard W. Holl
Format: Article
Language:English
Published: BMC 2018-12-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13023-018-0970-8
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spelling doaj-dd74de9e6de743abaa569610acaeea082020-11-25T01:17:05ZengBMCOrphanet Journal of Rare Diseases1750-11722018-12-0113111010.1186/s13023-018-0970-8Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinismAlena Welters0Thomas Meissner1Jürgen Grulich-Henn2Elke Fröhlich-Reiterer3Katharina Warncke4Klaus Mohnike5Oliver Blankenstein6Ulrike Menzel7Nicolin Datz8Esther Bollow9Reinhard W. Holl10Department of General Paediatrics, Neonatology and Paediatric Cardiology, University Children’s Hospital DüsseldorfDepartment of General Paediatrics, Neonatology and Paediatric Cardiology, University Children’s Hospital DüsseldorfCentre for Childhood and Adolescent Medicine (General Paediatrics), University Hospital HeidelbergDepartment of Paediatrics, Medical University of GrazDepartment of Paediatrics, Klinikum rechts der Isar, Technische Universität MünchenDepartment of Paediatrics, Otto von Guericke University MagdeburgCentre for Chronic Sick Children, Institute for Experimental Paediatric Endocrinology, Charité - Universitätsmedizin BerlinDepartment of Paediatric Endocrinology, AKK Altonaer KinderkrankenhausDiabetes Centre for Children and Adolescents, Children’s Hospital AUF DER BULTInstitute of Epidemiology and Medical Biometry, ZIBMT, University of UlmInstitute of Epidemiology and Medical Biometry, ZIBMT, University of UlmAbstract Background Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycaemia in infancy that leads to unfavourable neurological outcome if not treated adequately. In patients with severe diffuse CHI it remains under discussion whether pancreatic surgery should be performed or intensive medical treatment with the acceptance of recurrent episodes of mild hypoglycaemia is justified. Near-total pancreatectomy is associated with high rates of insulin-dependent diabetes mellitus and exocrine pancreatic insufficiency. Little is known about the management and long-term glycaemic control of CHI patients with diabetes after pancreatic surgery. We searched the German/Austrian DPV database and compared the course of 42 CHI patients with diabetes to that of patients with type 1 diabetes mellitus (T1DM). Study groups were compared at diabetes onset and after a follow-up period of 6.1 [3.3–9.7] (median [interquartile range]) years. Results The majority of CHI patients with diabetes were treated with insulin (85.2% [70.9–99.5] at diabetes onset, and 90.5% [81.2–99.7] at follow-up). However, compared to patients with T1DM, significantly more patients in the CHI group with diabetes were treated with conventional insulin therapy (47.8% vs. 24.4%, p = 0.03 at diabetes onset, and 21.1% vs. 6.4% at follow-up, p = 0.003), and only a small number of CHI patients were treated with insulin pumps. Daily insulin dose was significantly lower in CHI patients with diabetes than in patients with T1DM, both at diabetes onset (0.3 [0.2–0.5] vs. 0.6 IE/kg/d [0.4–0.8], p = 0.003) and follow-up (0.8 [0.4–1.0] vs. 0.9 [0.7–1.0] IE/kg/d, p = 0.02), while daily carbohydrate intake was comparable in both groups. Within the first treatment year, HbA1c levels were significantly lower in CHI patients with diabetes (6.2% [5.5–7.9] vs. 7.2% [6.5–8.2], p = 0.003), but increased to a level comparable to that of T1DM patients at follow-up. Interestingly, in CHI patients, the risk of severe hypoglycaemia tends to be higher only at diabetes onset (14.8% vs. 5.8%, p = 0.1). Conclusions In surgically treated CHI patients insulin treatment needs to be intensified in order to achieve good glycaemic control. Our data furthermore emphasize the need for improved medical treatment options for patients with diazoxide- and/or octreotide-unresponsive CHI.http://link.springer.com/article/10.1186/s13023-018-0970-8Congenital hyperinsulinismDiabetesPancreatectomyDPV initiative
collection DOAJ
language English
format Article
sources DOAJ
author Alena Welters
Thomas Meissner
Jürgen Grulich-Henn
Elke Fröhlich-Reiterer
Katharina Warncke
Klaus Mohnike
Oliver Blankenstein
Ulrike Menzel
Nicolin Datz
Esther Bollow
Reinhard W. Holl
spellingShingle Alena Welters
Thomas Meissner
Jürgen Grulich-Henn
Elke Fröhlich-Reiterer
Katharina Warncke
Klaus Mohnike
Oliver Blankenstein
Ulrike Menzel
Nicolin Datz
Esther Bollow
Reinhard W. Holl
Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
Orphanet Journal of Rare Diseases
Congenital hyperinsulinism
Diabetes
Pancreatectomy
DPV initiative
author_facet Alena Welters
Thomas Meissner
Jürgen Grulich-Henn
Elke Fröhlich-Reiterer
Katharina Warncke
Klaus Mohnike
Oliver Blankenstein
Ulrike Menzel
Nicolin Datz
Esther Bollow
Reinhard W. Holl
author_sort Alena Welters
title Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
title_short Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
title_full Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
title_fullStr Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
title_full_unstemmed Characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
title_sort characterization of diabetes following pancreatic surgery in patients with congenital hyperinsulinism
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2018-12-01
description Abstract Background Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycaemia in infancy that leads to unfavourable neurological outcome if not treated adequately. In patients with severe diffuse CHI it remains under discussion whether pancreatic surgery should be performed or intensive medical treatment with the acceptance of recurrent episodes of mild hypoglycaemia is justified. Near-total pancreatectomy is associated with high rates of insulin-dependent diabetes mellitus and exocrine pancreatic insufficiency. Little is known about the management and long-term glycaemic control of CHI patients with diabetes after pancreatic surgery. We searched the German/Austrian DPV database and compared the course of 42 CHI patients with diabetes to that of patients with type 1 diabetes mellitus (T1DM). Study groups were compared at diabetes onset and after a follow-up period of 6.1 [3.3–9.7] (median [interquartile range]) years. Results The majority of CHI patients with diabetes were treated with insulin (85.2% [70.9–99.5] at diabetes onset, and 90.5% [81.2–99.7] at follow-up). However, compared to patients with T1DM, significantly more patients in the CHI group with diabetes were treated with conventional insulin therapy (47.8% vs. 24.4%, p = 0.03 at diabetes onset, and 21.1% vs. 6.4% at follow-up, p = 0.003), and only a small number of CHI patients were treated with insulin pumps. Daily insulin dose was significantly lower in CHI patients with diabetes than in patients with T1DM, both at diabetes onset (0.3 [0.2–0.5] vs. 0.6 IE/kg/d [0.4–0.8], p = 0.003) and follow-up (0.8 [0.4–1.0] vs. 0.9 [0.7–1.0] IE/kg/d, p = 0.02), while daily carbohydrate intake was comparable in both groups. Within the first treatment year, HbA1c levels were significantly lower in CHI patients with diabetes (6.2% [5.5–7.9] vs. 7.2% [6.5–8.2], p = 0.003), but increased to a level comparable to that of T1DM patients at follow-up. Interestingly, in CHI patients, the risk of severe hypoglycaemia tends to be higher only at diabetes onset (14.8% vs. 5.8%, p = 0.1). Conclusions In surgically treated CHI patients insulin treatment needs to be intensified in order to achieve good glycaemic control. Our data furthermore emphasize the need for improved medical treatment options for patients with diazoxide- and/or octreotide-unresponsive CHI.
topic Congenital hyperinsulinism
Diabetes
Pancreatectomy
DPV initiative
url http://link.springer.com/article/10.1186/s13023-018-0970-8
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