Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study

Abstract Objective The Diabetes Prevention Program (DPP) is the gold standard lifestyle modification program that reduces incident type 2 diabetes mellitus. Patients with prediabetes and patients with non‐alcoholic fatty liver disease (NAFLD) often share metabolic features; we hypothesized that the...

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Main Authors: Melissa Hershman, Karen Torbjornsen, Daniel Pang, Brooke Wyatt, Douglas T. Dieterich, Ponni V. Perumalswami, Andrea D. Branch, Amreen M. Dinani
Format: Article
Language:English
Published: Wiley 2023-06-01
Series:Obesity Science & Practice
Subjects:
Online Access:https://doi.org/10.1002/osp4.637
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author Melissa Hershman
Karen Torbjornsen
Daniel Pang
Brooke Wyatt
Douglas T. Dieterich
Ponni V. Perumalswami
Andrea D. Branch
Amreen M. Dinani
author_facet Melissa Hershman
Karen Torbjornsen
Daniel Pang
Brooke Wyatt
Douglas T. Dieterich
Ponni V. Perumalswami
Andrea D. Branch
Amreen M. Dinani
author_sort Melissa Hershman
collection DOAJ
description Abstract Objective The Diabetes Prevention Program (DPP) is the gold standard lifestyle modification program that reduces incident type 2 diabetes mellitus. Patients with prediabetes and patients with non‐alcoholic fatty liver disease (NAFLD) often share metabolic features; we hypothesized that the DPP could be adapted and used to improve outcomes in patients with NAFLD. Methods NAFLD patients were recruited into a 1 year modified DPP. Demographics, medical comorbidities, and clinical laboratory values were collected at baseline, 6 and 12 months. The primary endpoint was change in weight at 12 months. Secondary endpoints were changes in hepatic steatosis, metabolic comorbidities, and liver enzymes (per‐protocol basis) and retention at 6 and 12 months. Results Fourteen NAFLD patients enrolled; three dropped out before 6 months. From baseline to 12 months, hepatic steatosis (p = 0.03), alanine aminotransferase (p = 0.02), aspartate aminotransferase (p = 0.02), high‐density lipoprotein (p = 0.01) and NAFLD fibrosis score (p < 0.001) improved, but low‐density lipoprotein worsened (p = 0.04). Conclusion Seventy‐nine percent of patients completed the modified DPP. Patients lost weight and had improvements in five out of six indicators of liver injury and lipid metabolism. Clinical Trial Registry Number NCT04988204.
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spelling doaj.art-8d7dfc381c51418a8726558e99503cb62023-06-06T06:00:56ZengWileyObesity Science & Practice2055-22382023-06-019321822510.1002/osp4.637Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot studyMelissa Hershman0Karen Torbjornsen1Daniel Pang2Brooke Wyatt3Douglas T. Dieterich4Ponni V. Perumalswami5Andrea D. Branch6Amreen M. Dinani7Division of Gastroenterology, Oregon Health & Science University Portland Oregon USAIcahn School of Medicine at Mount Sinai New York New York USADepartment of Medicine Icahn School of Medicine at Mount Sinai New York New York USAIcahn School of Medicine at Mount Sinai New York New York USADivision of Liver Diseases Icahn School of Medicine at Mount Sinai New York New York USADivision of Liver Diseases Icahn School of Medicine at Mount Sinai New York New York USADivision of Liver Diseases Icahn School of Medicine at Mount Sinai New York New York USADivision of Liver Diseases Icahn School of Medicine at Mount Sinai New York New York USAAbstract Objective The Diabetes Prevention Program (DPP) is the gold standard lifestyle modification program that reduces incident type 2 diabetes mellitus. Patients with prediabetes and patients with non‐alcoholic fatty liver disease (NAFLD) often share metabolic features; we hypothesized that the DPP could be adapted and used to improve outcomes in patients with NAFLD. Methods NAFLD patients were recruited into a 1 year modified DPP. Demographics, medical comorbidities, and clinical laboratory values were collected at baseline, 6 and 12 months. The primary endpoint was change in weight at 12 months. Secondary endpoints were changes in hepatic steatosis, metabolic comorbidities, and liver enzymes (per‐protocol basis) and retention at 6 and 12 months. Results Fourteen NAFLD patients enrolled; three dropped out before 6 months. From baseline to 12 months, hepatic steatosis (p = 0.03), alanine aminotransferase (p = 0.02), aspartate aminotransferase (p = 0.02), high‐density lipoprotein (p = 0.01) and NAFLD fibrosis score (p < 0.001) improved, but low‐density lipoprotein worsened (p = 0.04). Conclusion Seventy‐nine percent of patients completed the modified DPP. Patients lost weight and had improvements in five out of six indicators of liver injury and lipid metabolism. Clinical Trial Registry Number NCT04988204.https://doi.org/10.1002/osp4.637diabetes prevention programlifestyle interventionnonalcoholic fatty liver diseaseweight loss
spellingShingle Melissa Hershman
Karen Torbjornsen
Daniel Pang
Brooke Wyatt
Douglas T. Dieterich
Ponni V. Perumalswami
Andrea D. Branch
Amreen M. Dinani
Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
Obesity Science & Practice
diabetes prevention program
lifestyle intervention
nonalcoholic fatty liver disease
weight loss
title Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
title_full Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
title_fullStr Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
title_full_unstemmed Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
title_short Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study
title_sort modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease a pilot study
topic diabetes prevention program
lifestyle intervention
nonalcoholic fatty liver disease
weight loss
url https://doi.org/10.1002/osp4.637
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