Clinical risk factors for sarcopenia in acute and chronic pancreatitis

Abstract Background Sarcopenia is common in chronic pancreatitis (CP) and has been associated with unfavorable outcomes; however, it is not well studied in acute pancreatitis (AP). Aims To evaluate risk factors for sarcopenia among individuals with AP or CP. Methods A cross sectional analysis was pe...

Full description

Saved in:
Bibliographic Details
Main Authors: Mitchell L. Ramsey, Andrew Lu, Kristyn Gumpper-Fedus, Stacey Culp, David Bradley, Darwin L. Conwell, Zobeida Cruz-Monserrate, J. Royce Groce, Samuel Han, Somashekar G. Krishna, Peter Lee, Thomas Mace, Georgios I. Papachristou, Kristen M. Roberts, Zarine K. Shah, Phil A. Hart
Format: Article
Language:English
Published: BMC 2025-02-01
Series:BMC Gastroenterology
Subjects:
Online Access:https://doi.org/10.1186/s12876-025-03609-4
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1823862177876934656
author Mitchell L. Ramsey
Andrew Lu
Kristyn Gumpper-Fedus
Stacey Culp
David Bradley
Darwin L. Conwell
Zobeida Cruz-Monserrate
J. Royce Groce
Samuel Han
Somashekar G. Krishna
Peter Lee
Thomas Mace
Georgios I. Papachristou
Kristen M. Roberts
Zarine K. Shah
Phil A. Hart
author_facet Mitchell L. Ramsey
Andrew Lu
Kristyn Gumpper-Fedus
Stacey Culp
David Bradley
Darwin L. Conwell
Zobeida Cruz-Monserrate
J. Royce Groce
Samuel Han
Somashekar G. Krishna
Peter Lee
Thomas Mace
Georgios I. Papachristou
Kristen M. Roberts
Zarine K. Shah
Phil A. Hart
author_sort Mitchell L. Ramsey
collection DOAJ
description Abstract Background Sarcopenia is common in chronic pancreatitis (CP) and has been associated with unfavorable outcomes; however, it is not well studied in acute pancreatitis (AP). Aims To evaluate risk factors for sarcopenia among individuals with AP or CP. Methods A cross sectional analysis was performed among subjects with AP or CP seen in a tertiary care Pancreas Clinic. TeraRecon software was used to calculate the cross-sectional area of skeletal muscle, visceral fat, and subcutaneous fat at the level of the L3 vertebrae. Sarcopenia was classified using sex-specific skeletal muscle index. Univariate and multivariate logistic regressions were performed to assess differences between groups and associations with sarcopenia. Results A total of 49 subjects with AP and 54 subjects with CP were included. Sarcopenia was more frequently observed in CP compared to AP (83.3% vs. 46.9%, p < 0.001). The multivariate logistic regression demonstrated CP, male sex, increased age, and decreased subcutaneous fat were independently associated with sarcopenia. Conclusion Sarcopenia is observed in both CP and AP. In addition to traditional risk factors (including male sex, older age, and decreased subcutaneous fat), CP is independently associated with sarcopenia. Further investigations are necessary to gain deeper insights into sarcopenia pathogenesis, which could inform potential intervention strategies.
format Article
id doaj-art-67b497654bbe4b7185e2ef9c2428a7fd
institution Kabale University
issn 1471-230X
language English
publishDate 2025-02-01
publisher BMC
record_format Article
series BMC Gastroenterology
spelling doaj-art-67b497654bbe4b7185e2ef9c2428a7fd2025-02-09T12:39:36ZengBMCBMC Gastroenterology1471-230X2025-02-012511910.1186/s12876-025-03609-4Clinical risk factors for sarcopenia in acute and chronic pancreatitisMitchell L. Ramsey0Andrew Lu1Kristyn Gumpper-Fedus2Stacey Culp3David Bradley4Darwin L. Conwell5Zobeida Cruz-Monserrate6J. Royce Groce7Samuel Han8Somashekar G. Krishna9Peter Lee10Thomas Mace11Georgios I. Papachristou12Kristen M. Roberts13Zarine K. Shah14Phil A. Hart15Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDepartment of Radiology, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDepartment of Biomedical Informatics, The Ohio State University College of MedicineDepartment of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Penn State Health Milton S. Hershey Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterDepartment of Radiology, The Ohio State University Wexner Medical CenterDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical CenterAbstract Background Sarcopenia is common in chronic pancreatitis (CP) and has been associated with unfavorable outcomes; however, it is not well studied in acute pancreatitis (AP). Aims To evaluate risk factors for sarcopenia among individuals with AP or CP. Methods A cross sectional analysis was performed among subjects with AP or CP seen in a tertiary care Pancreas Clinic. TeraRecon software was used to calculate the cross-sectional area of skeletal muscle, visceral fat, and subcutaneous fat at the level of the L3 vertebrae. Sarcopenia was classified using sex-specific skeletal muscle index. Univariate and multivariate logistic regressions were performed to assess differences between groups and associations with sarcopenia. Results A total of 49 subjects with AP and 54 subjects with CP were included. Sarcopenia was more frequently observed in CP compared to AP (83.3% vs. 46.9%, p < 0.001). The multivariate logistic regression demonstrated CP, male sex, increased age, and decreased subcutaneous fat were independently associated with sarcopenia. Conclusion Sarcopenia is observed in both CP and AP. In addition to traditional risk factors (including male sex, older age, and decreased subcutaneous fat), CP is independently associated with sarcopenia. Further investigations are necessary to gain deeper insights into sarcopenia pathogenesis, which could inform potential intervention strategies.https://doi.org/10.1186/s12876-025-03609-4SarcopeniaSubcutaneous fatVisceral fatSkeletal muscleBody composition
spellingShingle Mitchell L. Ramsey
Andrew Lu
Kristyn Gumpper-Fedus
Stacey Culp
David Bradley
Darwin L. Conwell
Zobeida Cruz-Monserrate
J. Royce Groce
Samuel Han
Somashekar G. Krishna
Peter Lee
Thomas Mace
Georgios I. Papachristou
Kristen M. Roberts
Zarine K. Shah
Phil A. Hart
Clinical risk factors for sarcopenia in acute and chronic pancreatitis
BMC Gastroenterology
Sarcopenia
Subcutaneous fat
Visceral fat
Skeletal muscle
Body composition
title Clinical risk factors for sarcopenia in acute and chronic pancreatitis
title_full Clinical risk factors for sarcopenia in acute and chronic pancreatitis
title_fullStr Clinical risk factors for sarcopenia in acute and chronic pancreatitis
title_full_unstemmed Clinical risk factors for sarcopenia in acute and chronic pancreatitis
title_short Clinical risk factors for sarcopenia in acute and chronic pancreatitis
title_sort clinical risk factors for sarcopenia in acute and chronic pancreatitis
topic Sarcopenia
Subcutaneous fat
Visceral fat
Skeletal muscle
Body composition
url https://doi.org/10.1186/s12876-025-03609-4
work_keys_str_mv AT mitchelllramsey clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT andrewlu clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT kristyngumpperfedus clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT staceyculp clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT davidbradley clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT darwinlconwell clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT zobeidacruzmonserrate clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT jroycegroce clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT samuelhan clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT somashekargkrishna clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT peterlee clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT thomasmace clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT georgiosipapachristou clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT kristenmroberts clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT zarinekshah clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis
AT philahart clinicalriskfactorsforsarcopeniainacuteandchronicpancreatitis