High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD

Overconsumption of carbohydrates and lipids are well known to cause nonalcoholic fatty liver disease (NAFLD), while the role of nutritional protein intake is less clear. In Western diet, meat and other animal products are the main protein source, with varying concentrations of specific amino acids....

Full description

Bibliographic Details
Main Authors: Sonja Lang, Anna Martin, Fedja Farowski, Hilmar Wisplinghoff, Maria J.G.T. Vehreschild, Jinyuan Liu, Marcin Krawczyk, Angela Nowag, Anne Kretzschmar, Jens Herweg, Bernd Schnabl, Xin M. Tu, Frank Lammert, Tobias Goeser, Frank Tacke, Kathrin Heinzer, Philipp Kasper, Hans‐Michael Steffen, Münevver Demir
Format: Article
Language:English
Published: Wolters Kluwer Health/LWW 2020-05-01
Series:Hepatology Communications
Online Access:https://doi.org/10.1002/hep4.1509
_version_ 1797936933571133440
author Sonja Lang
Anna Martin
Fedja Farowski
Hilmar Wisplinghoff
Maria J.G.T. Vehreschild
Jinyuan Liu
Marcin Krawczyk
Angela Nowag
Anne Kretzschmar
Jens Herweg
Bernd Schnabl
Xin M. Tu
Frank Lammert
Tobias Goeser
Frank Tacke
Kathrin Heinzer
Philipp Kasper
Hans‐Michael Steffen
Münevver Demir
author_facet Sonja Lang
Anna Martin
Fedja Farowski
Hilmar Wisplinghoff
Maria J.G.T. Vehreschild
Jinyuan Liu
Marcin Krawczyk
Angela Nowag
Anne Kretzschmar
Jens Herweg
Bernd Schnabl
Xin M. Tu
Frank Lammert
Tobias Goeser
Frank Tacke
Kathrin Heinzer
Philipp Kasper
Hans‐Michael Steffen
Münevver Demir
author_sort Sonja Lang
collection DOAJ
description Overconsumption of carbohydrates and lipids are well known to cause nonalcoholic fatty liver disease (NAFLD), while the role of nutritional protein intake is less clear. In Western diet, meat and other animal products are the main protein source, with varying concentrations of specific amino acids. Whether the amount or composition of protein intake is associated with a higher risk for disease severity has not yet been examined. In this study, we investigated associations of dietary components with histological disease activity by analyzing detailed 14‐day food records in a cohort of 61 patients with biopsy‐proven NAFLD. Furthermore, we used 16S ribosomal RNA gene sequencing to detect associations with different abundances of the gut microbiota with dietary patterns. Patients with definite nonalcoholic steatohepatitis (NAFLD activity score of 5‐8 on liver biopsy) had a significantly higher daily relative intake of protein compared with patients with a NAFLD activity score of 0‐4 (18.0% vs. 15.8% of daily protein‐based calories, P = 0.018). After adjustment for several potentially confounding factors, a higher protein intake (≥17.3% of daily protein‐based calories) remained associated with definite nonalcoholic steatohepatitis, with an odds ratio of 5.09 (95% confidence interval 1.22‐21.25, P = 0.026). This association was driven primarily by serine, glycine, arginine, proline, phenylalanine, and methionine. A higher protein intake correlated with a lower Bacteroides abundance and an altered abundance of several other bacterial taxa. Conclusion: A high protein intake was independently associated with more active and severe histological disease activity in patients with NAFLD. Further studies are needed to investigate the potential harmful role of dietary amino acids on NAFLD, with special attention to meat as their major source.
first_indexed 2024-04-10T18:36:57Z
format Article
id doaj.art-f7b838653ae0472fb8e62f4afbe99923
institution Directory Open Access Journal
issn 2471-254X
language English
last_indexed 2024-04-10T18:36:57Z
publishDate 2020-05-01
publisher Wolters Kluwer Health/LWW
record_format Article
series Hepatology Communications
spelling doaj.art-f7b838653ae0472fb8e62f4afbe999232023-02-02T01:02:54ZengWolters Kluwer Health/LWWHepatology Communications2471-254X2020-05-014568169510.1002/hep4.1509High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLDSonja Lang0Anna Martin1Fedja Farowski2Hilmar Wisplinghoff3Maria J.G.T. Vehreschild4Jinyuan Liu5Marcin Krawczyk6Angela Nowag7Anne Kretzschmar8Jens Herweg9Bernd Schnabl10Xin M. Tu11Frank Lammert12Tobias Goeser13Frank Tacke14Kathrin Heinzer15Philipp Kasper16Hans‐Michael Steffen17Münevver Demir18Department of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Internal Medicine Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyWisplinghoff Laboratories Cologne GermanyDepartment of Internal Medicine Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDivision of Biostatistics and Bioinformatics Department of Family Medicine and Public Health University of California San Diego San Diego CADepartment of Medicine Saarland University Medical Center Homburg GermanyWisplinghoff Laboratories Cologne GermanyWisplinghoff Laboratories Cologne GermanyWisplinghoff Laboratories Cologne GermanyDepartment of Medicine University of California San Diego La Jolla CADivision of Biostatistics and Bioinformatics Department of Family Medicine and Public Health University of California San Diego San Diego CADepartment of Medicine Saarland University Medical Center Homburg GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Hepatology and Gastroenterology Charité University Medicine Campus Virchow ClinicBerlin GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyDepartment of Gastroenterology and Hepatology Faculty of Medicine University of Cologne University Hospital Cologne Cologne GermanyOverconsumption of carbohydrates and lipids are well known to cause nonalcoholic fatty liver disease (NAFLD), while the role of nutritional protein intake is less clear. In Western diet, meat and other animal products are the main protein source, with varying concentrations of specific amino acids. Whether the amount or composition of protein intake is associated with a higher risk for disease severity has not yet been examined. In this study, we investigated associations of dietary components with histological disease activity by analyzing detailed 14‐day food records in a cohort of 61 patients with biopsy‐proven NAFLD. Furthermore, we used 16S ribosomal RNA gene sequencing to detect associations with different abundances of the gut microbiota with dietary patterns. Patients with definite nonalcoholic steatohepatitis (NAFLD activity score of 5‐8 on liver biopsy) had a significantly higher daily relative intake of protein compared with patients with a NAFLD activity score of 0‐4 (18.0% vs. 15.8% of daily protein‐based calories, P = 0.018). After adjustment for several potentially confounding factors, a higher protein intake (≥17.3% of daily protein‐based calories) remained associated with definite nonalcoholic steatohepatitis, with an odds ratio of 5.09 (95% confidence interval 1.22‐21.25, P = 0.026). This association was driven primarily by serine, glycine, arginine, proline, phenylalanine, and methionine. A higher protein intake correlated with a lower Bacteroides abundance and an altered abundance of several other bacterial taxa. Conclusion: A high protein intake was independently associated with more active and severe histological disease activity in patients with NAFLD. Further studies are needed to investigate the potential harmful role of dietary amino acids on NAFLD, with special attention to meat as their major source.https://doi.org/10.1002/hep4.1509
spellingShingle Sonja Lang
Anna Martin
Fedja Farowski
Hilmar Wisplinghoff
Maria J.G.T. Vehreschild
Jinyuan Liu
Marcin Krawczyk
Angela Nowag
Anne Kretzschmar
Jens Herweg
Bernd Schnabl
Xin M. Tu
Frank Lammert
Tobias Goeser
Frank Tacke
Kathrin Heinzer
Philipp Kasper
Hans‐Michael Steffen
Münevver Demir
High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
Hepatology Communications
title High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
title_full High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
title_fullStr High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
title_full_unstemmed High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
title_short High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD
title_sort high protein intake is associated with histological disease activity in patients with nafld
url https://doi.org/10.1002/hep4.1509
work_keys_str_mv AT sonjalang highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT annamartin highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT fedjafarowski highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT hilmarwisplinghoff highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT mariajgtvehreschild highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT jinyuanliu highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT marcinkrawczyk highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT angelanowag highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT annekretzschmar highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT jensherweg highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT berndschnabl highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT xinmtu highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT franklammert highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT tobiasgoeser highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT franktacke highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT kathrinheinzer highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT philippkasper highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT hansmichaelsteffen highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld
AT munevverdemir highproteinintakeisassociatedwithhistologicaldiseaseactivityinpatientswithnafld