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Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism

BACKGROUND: Congenital hyperinsulinism (CHI) is a rare but severe disorder of hypoglycemia in children, often complicated by brain injury. In CHI, the long-term prevention of hypoglycemia is dependent on reliable enteral intake of glucose. However, feeding problems (FPs) often impede oral glucose de...

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Autores principales: Banerjee, Indraneel, Forsythe, Lynette, Skae, Mars, Avatapalle, Hima Bindu, Rigby, Lindsey, Bowden, Louise E., Craigie, Ross, Padidela, Raja, Ehtisham, Sarah, Patel, Leena, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747152/
https://www.ncbi.nlm.nih.gov/pubmed/26903946
http://dx.doi.org/10.3389/fendo.2016.00008
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author Banerjee, Indraneel
Forsythe, Lynette
Skae, Mars
Avatapalle, Hima Bindu
Rigby, Lindsey
Bowden, Louise E.
Craigie, Ross
Padidela, Raja
Ehtisham, Sarah
Patel, Leena
Cosgrove, Karen E.
Dunne, Mark J.
Clayton, Peter E.
author_facet Banerjee, Indraneel
Forsythe, Lynette
Skae, Mars
Avatapalle, Hima Bindu
Rigby, Lindsey
Bowden, Louise E.
Craigie, Ross
Padidela, Raja
Ehtisham, Sarah
Patel, Leena
Cosgrove, Karen E.
Dunne, Mark J.
Clayton, Peter E.
author_sort Banerjee, Indraneel
collection PubMed
description BACKGROUND: Congenital hyperinsulinism (CHI) is a rare but severe disorder of hypoglycemia in children, often complicated by brain injury. In CHI, the long-term prevention of hypoglycemia is dependent on reliable enteral intake of glucose. However, feeding problems (FPs) often impede oral glucose delivery, thereby complicating the management of hypoglycemia. FPs have not been systematically characterized in follow-up in a cohort with CHI. AIMS: We aimed to determine the prevalence, types, and persistence of FPs in a cohort of children with CHI and investigate potential causal factors. METHODS: FPs were defined as difficulty with sucking, swallowing, vomiting, and food refusal (or a combination) in an observational study in 83 children in a specialized CHI treatment center. The prevalence of FPs at diagnosis, 6, and 12 months after diagnosis were noted. Genetic mutation status and markers of severity of CHI were tested for association with FPs. RESULTS: A third of children with CHI had FPs (n = 28), of whom 93% required antireflux medication and 75% required nasogastric and gastrostomy tube feeding. Sucking and swallowing problems were present at diagnosis but absent later. Vomiting was present in 54% at 6 months, while food refusal was present in 68% at 6 months and 52% at 12 months. The age at commencing and stopping nasogastric tube feeding did not correlate with FPs frequency at 6 and 12 months. Children with FPs had severe hypoglycemia at diagnosis and required glucagon infusion more often [odds ratio (OR) (95% confidence intervals) (95% CI) 28.13 (2.6–300.1), p = 0.006] to normalize glucose levels. FPs were more frequent in those with diffuse CHI undergoing subtotal pancreatectomy [n (%) = 10 (35%) vs. 0 (0%), p < 0.001], in contrast to those with spontaneous resolution [6 (22%) vs. 32 (58%), p = 0.002]. Those undergoing focal lesionectomy also had reduced FPs at 6 months after diagnosis [OR (95% CI) 0.01 (0.0–0.2), R(2) = 0.42, p = 0.004]. These observations suggest that persistence of hyperinsulinism was associated with FPs. CONCLUSION: FPs occur in a significant proportion of children with CHI. Severe hyperinsulinism, rather than nasogastric tube feeding or medications, is the main factor associated with FPs.
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spelling pubmed-47471522016-02-22 Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism Banerjee, Indraneel Forsythe, Lynette Skae, Mars Avatapalle, Hima Bindu Rigby, Lindsey Bowden, Louise E. Craigie, Ross Padidela, Raja Ehtisham, Sarah Patel, Leena Cosgrove, Karen E. Dunne, Mark J. Clayton, Peter E. Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Congenital hyperinsulinism (CHI) is a rare but severe disorder of hypoglycemia in children, often complicated by brain injury. In CHI, the long-term prevention of hypoglycemia is dependent on reliable enteral intake of glucose. However, feeding problems (FPs) often impede oral glucose delivery, thereby complicating the management of hypoglycemia. FPs have not been systematically characterized in follow-up in a cohort with CHI. AIMS: We aimed to determine the prevalence, types, and persistence of FPs in a cohort of children with CHI and investigate potential causal factors. METHODS: FPs were defined as difficulty with sucking, swallowing, vomiting, and food refusal (or a combination) in an observational study in 83 children in a specialized CHI treatment center. The prevalence of FPs at diagnosis, 6, and 12 months after diagnosis were noted. Genetic mutation status and markers of severity of CHI were tested for association with FPs. RESULTS: A third of children with CHI had FPs (n = 28), of whom 93% required antireflux medication and 75% required nasogastric and gastrostomy tube feeding. Sucking and swallowing problems were present at diagnosis but absent later. Vomiting was present in 54% at 6 months, while food refusal was present in 68% at 6 months and 52% at 12 months. The age at commencing and stopping nasogastric tube feeding did not correlate with FPs frequency at 6 and 12 months. Children with FPs had severe hypoglycemia at diagnosis and required glucagon infusion more often [odds ratio (OR) (95% confidence intervals) (95% CI) 28.13 (2.6–300.1), p = 0.006] to normalize glucose levels. FPs were more frequent in those with diffuse CHI undergoing subtotal pancreatectomy [n (%) = 10 (35%) vs. 0 (0%), p < 0.001], in contrast to those with spontaneous resolution [6 (22%) vs. 32 (58%), p = 0.002]. Those undergoing focal lesionectomy also had reduced FPs at 6 months after diagnosis [OR (95% CI) 0.01 (0.0–0.2), R(2) = 0.42, p = 0.004]. These observations suggest that persistence of hyperinsulinism was associated with FPs. CONCLUSION: FPs occur in a significant proportion of children with CHI. Severe hyperinsulinism, rather than nasogastric tube feeding or medications, is the main factor associated with FPs. Frontiers Media S.A. 2016-02-09 /pmc/articles/PMC4747152/ /pubmed/26903946 http://dx.doi.org/10.3389/fendo.2016.00008 Text en Copyright © 2016 Banerjee, Forsythe, Skae, Avatapalle, Rigby, Bowden, Craigie, Padidela, Ehtisham, Patel, Cosgrove, Dunne and Clayton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Banerjee, Indraneel
Forsythe, Lynette
Skae, Mars
Avatapalle, Hima Bindu
Rigby, Lindsey
Bowden, Louise E.
Craigie, Ross
Padidela, Raja
Ehtisham, Sarah
Patel, Leena
Cosgrove, Karen E.
Dunne, Mark J.
Clayton, Peter E.
Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title_full Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title_fullStr Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title_full_unstemmed Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title_short Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism
title_sort feeding problems are persistent in children with severe congenital hyperinsulinism
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747152/
https://www.ncbi.nlm.nih.gov/pubmed/26903946
http://dx.doi.org/10.3389/fendo.2016.00008
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