Detailed Information

Cited 9 time in webofscience Cited 9 time in scopus
Metadata Downloads

Pancreatic involvement in patients with inborn errors of metabolismopen access

Authors
Hwang, Woo JinLim, Han HyukKim, Yoo-MiChang, Mea YoungKil, Hong RyangKim, Jae YoungSong, Wung JooLevy, Harvey L.Kim, Sook-Za
Issue Date
Jan-2021
Publisher
BMC
Keywords
Pancreatitis; Diabetes mellitus; Inborn errors of metabolism; Methylmalonic aciduria; Propionic acidemia; Newborn screening; Hyperornithinemia; Fatty acid oxidation disorder
Citation
ORPHANET JOURNAL OF RARE DISEASES, v.16, no.1
Indexed
SCIE
SCOPUS
Journal Title
ORPHANET JOURNAL OF RARE DISEASES
Volume
16
Number
1
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/72674
DOI
10.1186/s13023-021-01685-9
ISSN
1750-1172
1750-1172
Abstract
Background Repeated inflammation of the pancreas can cause pancreatitis or diabetes. It is well recognized that the organic acidemias may be complicated by pancreatitis but less recognized are other metabolic disorders in which pancreatitis can occur. This study shows that long-term follow-up of patients with various metabolic disorders in Korea revealed several with episodes of isolated pancreatitis or diabetes concomitantly with pancreatitis. Results and discussion In this study, two patients with methylmalonic aciduria (MMA), two with propionic acidemia (PPA), one with fatty acid oxidation disorder (FAOD), and one with hyperornithinemia, gyrate atrophy, and juvenile onset diabetes mellitus (DM) were clinically followed for up to 10 - 21 years. Two Korean siblings with MMA showed recurrent pancreatitis from the age of 15 and 19, respectively. The frequency of admission due to pancreatitis was up to 11 times. One patient with MMA developed diabetes mellitus at the age of 20. The other patient with MMA developed recurrent pancreatitis at 4 years and diabetes at 8 years of age. One of the patients with PPA presented with diabetic ketoacidosis. The other PPA patient died of cardiac arrest at age 10. The patient with FAOD presented with pancreatitis at 10 years and died at the age of 15 years due to cardiac arrest. A 35-year-old woman with hyperornithinemia/gyrate atrophy was diagnosed with juvenile onset diabetes at the age of 7 years. No pancreatitis occurred during the follow-up period. Conclusions We conclude that various metabolic disorders can trigger acute or chronic pancreatitis. Proper and prompt multidisciplinary management of metabolic derangement is crucial for preventing pancreatic damage. Further clinical and investigational studies are required to elucidate the pathogenesis of pancreatitis and diabetes mellitus in patients with inborn errors in metabolism.
Files in This Item
There are no files associated with this item.
Appears in
Collections
ETC > Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Altmetrics

Total Views & Downloads

BROWSE