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Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis
Type 3C Diabetes, or diseases of the exocrine pancreas has been reported to occur in approximately 30% of adult patient with pancreatitis. The incidence of glucose abnormalities or risk factors that may predict the development of abnormal glucose in the pediatric pancreatitis population is not known...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209152/ https://www.ncbi.nlm.nih.gov/pubmed/30379828 http://dx.doi.org/10.1371/journal.pone.0204979 |
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author | Abu-El-Haija, Maisam Hornung, Lindsey Denson, Lee A. Husami, Ammar Lin, Tom K. Matlock, Kristal Nathan, Jaimie D. Palermo, Joseph J. Thompson, Tyler Valencia, C. Alexander Wang, Xinjian Woo, Jessica Zhang, Keijan Elder, Deborah |
author_facet | Abu-El-Haija, Maisam Hornung, Lindsey Denson, Lee A. Husami, Ammar Lin, Tom K. Matlock, Kristal Nathan, Jaimie D. Palermo, Joseph J. Thompson, Tyler Valencia, C. Alexander Wang, Xinjian Woo, Jessica Zhang, Keijan Elder, Deborah |
author_sort | Abu-El-Haija, Maisam |
collection | PubMed |
description | Type 3C Diabetes, or diseases of the exocrine pancreas has been reported to occur in approximately 30% of adult patient with pancreatitis. The incidence of glucose abnormalities or risk factors that may predict the development of abnormal glucose in the pediatric pancreatitis population is not known. We performed a retrospective chart review from 1998–2016 for patients who carry the diagnosis of acute pancreatitis (AP), acute recurrent pancreatitis (ARP), and chronic pancreatitis (CP). We extracted glucose values, HbA1c%, and data from oral glucose tolerance and mixed meal testing with timing in relation to pancreatic exacerbations. Patient characteristic data such as age, gender, body proportions, family history of pancreatitis, exocrine function and genetic mutations were also assessed. Abnormal glucose was based on definitions put forth by the American Diabetes Society for pre-diabetes and diabetes. Fifty-two patients had AP and met criteria. Of those, 15 (29%) had glucose testing on or after the first attack, 21 (40%) were tested on or after the second attack (in ARP patients) and 16 (31%) were tested after a diagnosis of CP. Of the patients tested for glucose abnormalities, 25% (13/52) had abnormal glucose testing (testing indicating pre-DM or DM as defined by ADA guidelines. A significantly higher proportion of the abnormal glucose testing was seen in patients (85%, 11/13) with a BMI at or greater than the 85(th) percentile compared to the normal glucose patients (28%, 11/39) (p = 0.0007). A significantly higher proportion of the abnormal glucose patients (77%, 10/13) had SAP during the prior AP episode to testing compared to the 10% (4/39) of the normal glucose patients (p<0.0001). Older age at DM testing was associated with a higher prevalence of abnormal glucose testing (p = 0.04). In our patient population, a higher proportion of glucose abnormalities were after the second episode of pancreatitis, however 62% (8/13) with abnormalities was their first time tested. We identified obesity and having severe acute pancreatitis (SAP) during the prior AP episode to testing could be associated with abnormal glucose. We propose that systematic screening for abnormal glucose after the first episode of acute pancreatitis in order to better establish the timing of diabetes progression. |
format | Online Article Text |
id | pubmed-6209152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62091522018-11-19 Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis Abu-El-Haija, Maisam Hornung, Lindsey Denson, Lee A. Husami, Ammar Lin, Tom K. Matlock, Kristal Nathan, Jaimie D. Palermo, Joseph J. Thompson, Tyler Valencia, C. Alexander Wang, Xinjian Woo, Jessica Zhang, Keijan Elder, Deborah PLoS One Research Article Type 3C Diabetes, or diseases of the exocrine pancreas has been reported to occur in approximately 30% of adult patient with pancreatitis. The incidence of glucose abnormalities or risk factors that may predict the development of abnormal glucose in the pediatric pancreatitis population is not known. We performed a retrospective chart review from 1998–2016 for patients who carry the diagnosis of acute pancreatitis (AP), acute recurrent pancreatitis (ARP), and chronic pancreatitis (CP). We extracted glucose values, HbA1c%, and data from oral glucose tolerance and mixed meal testing with timing in relation to pancreatic exacerbations. Patient characteristic data such as age, gender, body proportions, family history of pancreatitis, exocrine function and genetic mutations were also assessed. Abnormal glucose was based on definitions put forth by the American Diabetes Society for pre-diabetes and diabetes. Fifty-two patients had AP and met criteria. Of those, 15 (29%) had glucose testing on or after the first attack, 21 (40%) were tested on or after the second attack (in ARP patients) and 16 (31%) were tested after a diagnosis of CP. Of the patients tested for glucose abnormalities, 25% (13/52) had abnormal glucose testing (testing indicating pre-DM or DM as defined by ADA guidelines. A significantly higher proportion of the abnormal glucose testing was seen in patients (85%, 11/13) with a BMI at or greater than the 85(th) percentile compared to the normal glucose patients (28%, 11/39) (p = 0.0007). A significantly higher proportion of the abnormal glucose patients (77%, 10/13) had SAP during the prior AP episode to testing compared to the 10% (4/39) of the normal glucose patients (p<0.0001). Older age at DM testing was associated with a higher prevalence of abnormal glucose testing (p = 0.04). In our patient population, a higher proportion of glucose abnormalities were after the second episode of pancreatitis, however 62% (8/13) with abnormalities was their first time tested. We identified obesity and having severe acute pancreatitis (SAP) during the prior AP episode to testing could be associated with abnormal glucose. We propose that systematic screening for abnormal glucose after the first episode of acute pancreatitis in order to better establish the timing of diabetes progression. Public Library of Science 2018-10-31 /pmc/articles/PMC6209152/ /pubmed/30379828 http://dx.doi.org/10.1371/journal.pone.0204979 Text en © 2018 Abu-El-Haija et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Abu-El-Haija, Maisam Hornung, Lindsey Denson, Lee A. Husami, Ammar Lin, Tom K. Matlock, Kristal Nathan, Jaimie D. Palermo, Joseph J. Thompson, Tyler Valencia, C. Alexander Wang, Xinjian Woo, Jessica Zhang, Keijan Elder, Deborah Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title | Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title_full | Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title_fullStr | Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title_full_unstemmed | Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title_short | Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
title_sort | prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209152/ https://www.ncbi.nlm.nih.gov/pubmed/30379828 http://dx.doi.org/10.1371/journal.pone.0204979 |
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