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Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients

BACKGROUND: In pediatric acute pancreatitis (AP), a family history of pancreatic diseases is prognostic for earlier onset of recurrent AP (ARP) and chronic pancreatitis (CP). No evidence supports the same association in adult-onset pancreatitis. Age-specific reasons for familial aggregation are also...

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Autores principales: Juhász, Márk Félix, Farkas, Nelli, Szentesi, Andrea, Wedrychowicz, Andrzej, Nita, Andreia Florina, Lásztity, Natália, Tészás, Alexandra, Tokodi, István, Vincze, Áron, Eross, Bálint, Izbéki, Ferenc, Czakó, László, Papp, Mária, Hegyi, Péter, Párniczky, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511134/
https://www.ncbi.nlm.nih.gov/pubmed/36172540
http://dx.doi.org/10.3389/fmed.2022.801592
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author Juhász, Márk Félix
Farkas, Nelli
Szentesi, Andrea
Wedrychowicz, Andrzej
Nita, Andreia Florina
Lásztity, Natália
Tészás, Alexandra
Tokodi, István
Vincze, Áron
Eross, Bálint
Izbéki, Ferenc
Czakó, László
Papp, Mária
Hegyi, Péter
Párniczky, Andrea
author_facet Juhász, Márk Félix
Farkas, Nelli
Szentesi, Andrea
Wedrychowicz, Andrzej
Nita, Andreia Florina
Lásztity, Natália
Tészás, Alexandra
Tokodi, István
Vincze, Áron
Eross, Bálint
Izbéki, Ferenc
Czakó, László
Papp, Mária
Hegyi, Péter
Párniczky, Andrea
author_sort Juhász, Márk Félix
collection PubMed
description BACKGROUND: In pediatric acute pancreatitis (AP), a family history of pancreatic diseases is prognostic for earlier onset of recurrent AP (ARP) and chronic pancreatitis (CP). No evidence supports the same association in adult-onset pancreatitis. Age-specific reasons for familial aggregation are also unclear. We aimed to examine the prognostic role of pancreatic family history for ARP/CP and observe possible underlying mechanisms. METHODS: We conducted a secondary analysis of the Hungarian Pancreatic Study Group’s (HPSG) multicenter, international, prospective registry of patients with AP, both children and adults. We compared the positive family history and the negative family history of pancreatic diseases, in different age groups, and analyzed trends of accompanying factors. Chi-square and Fisher exact tests were used. RESULTS: We found a higher rate of ARP/CP in the positive pancreatic family history group (33.7 vs. 25.9%, p = 0.018), peaking at 6–17 years. Idiopathic AP peaked in childhood in the positive family history group (75% 0–5 years) and was consistently 20–35% in the negative group. A higher rate of alcohol consumption/smoking was found in the positive groups at 12–17 years (62.5 vs. 15.8%, p = 0.013) and 18–29 years (90.9 vs. 58.1%, p = 0.049). The prevalence of diabetes and hyperlipidemia steadily rose with age in both groups. CONCLUSION: Positive family history most likely signifies genetic background in early childhood. During adolescence and early adulthood, alcohol consumption and smoking emerge—clinicians should be aware and turn to intervention in such cases. Contrary to current viewpoints, positive pancreatic family history is not a prognostic factor for ARP and CP in adults, so it should not be regarded that way.
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spelling pubmed-95111342022-09-27 Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients Juhász, Márk Félix Farkas, Nelli Szentesi, Andrea Wedrychowicz, Andrzej Nita, Andreia Florina Lásztity, Natália Tészás, Alexandra Tokodi, István Vincze, Áron Eross, Bálint Izbéki, Ferenc Czakó, László Papp, Mária Hegyi, Péter Párniczky, Andrea Front Med (Lausanne) Medicine BACKGROUND: In pediatric acute pancreatitis (AP), a family history of pancreatic diseases is prognostic for earlier onset of recurrent AP (ARP) and chronic pancreatitis (CP). No evidence supports the same association in adult-onset pancreatitis. Age-specific reasons for familial aggregation are also unclear. We aimed to examine the prognostic role of pancreatic family history for ARP/CP and observe possible underlying mechanisms. METHODS: We conducted a secondary analysis of the Hungarian Pancreatic Study Group’s (HPSG) multicenter, international, prospective registry of patients with AP, both children and adults. We compared the positive family history and the negative family history of pancreatic diseases, in different age groups, and analyzed trends of accompanying factors. Chi-square and Fisher exact tests were used. RESULTS: We found a higher rate of ARP/CP in the positive pancreatic family history group (33.7 vs. 25.9%, p = 0.018), peaking at 6–17 years. Idiopathic AP peaked in childhood in the positive family history group (75% 0–5 years) and was consistently 20–35% in the negative group. A higher rate of alcohol consumption/smoking was found in the positive groups at 12–17 years (62.5 vs. 15.8%, p = 0.013) and 18–29 years (90.9 vs. 58.1%, p = 0.049). The prevalence of diabetes and hyperlipidemia steadily rose with age in both groups. CONCLUSION: Positive family history most likely signifies genetic background in early childhood. During adolescence and early adulthood, alcohol consumption and smoking emerge—clinicians should be aware and turn to intervention in such cases. Contrary to current viewpoints, positive pancreatic family history is not a prognostic factor for ARP and CP in adults, so it should not be regarded that way. Frontiers Media S.A. 2022-09-12 /pmc/articles/PMC9511134/ /pubmed/36172540 http://dx.doi.org/10.3389/fmed.2022.801592 Text en Copyright © 2022 Juhász, Farkas, Szentesi, Wedrychowicz, Nita, Lásztity, Tészás, Tokodi, Vincze, Eross, Izbéki, Czakó, Papp, Hegyi and Párniczky. https://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) and the copyright owner(s) 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 Medicine
Juhász, Márk Félix
Farkas, Nelli
Szentesi, Andrea
Wedrychowicz, Andrzej
Nita, Andreia Florina
Lásztity, Natália
Tészás, Alexandra
Tokodi, István
Vincze, Áron
Eross, Bálint
Izbéki, Ferenc
Czakó, László
Papp, Mária
Hegyi, Péter
Párniczky, Andrea
Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title_full Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title_fullStr Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title_full_unstemmed Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title_short Pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: Analysis of an international cohort of 2,335 patients
title_sort pancreatic family history does not predict disease progression but connotes alcohol consumption in adolescents and young adults with acute pancreatitis: analysis of an international cohort of 2,335 patients
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511134/
https://www.ncbi.nlm.nih.gov/pubmed/36172540
http://dx.doi.org/10.3389/fmed.2022.801592
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