Myeloperoxidase and calprotectin; Any role as non-invasive markers for the prediction of ınflammation and fibrosis in non-alcoholic steatohepatitis?


Journal

The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
ISSN: 2148-5607
Titre abrégé: Turk J Gastroenterol
Pays: Turkey
ID NLM: 9515841

Informations de publication

Date de publication:
10 2020
Historique:
entrez: 10 11 2020
pubmed: 11 11 2020
medline: 15 10 2021
Statut: ppublish

Résumé

Specific serum markers reflecting hepatic inflammation and fibrosis are required to tailor the treatment strategies in non-alcoholic steatohepatitis (NASH). We aimed to investigate the roles of myeloperoxidase (MPO) and calprotectin in predicting the hepatic inflammation status and disease severity in NASH. A total of 48 patients with biopsy-proven NASH and 25 healthy volunteers with normal weight were prospectively enrolled. Serum MPO and calprotectin levels were compared between the NASH and control groups. Hepatic MPO and calprotectin expressions were compared in terms of histologic non-alcoholic fatty liver disease activity scores (NAS) (low NAS [≤4] vs. high NAS [>5]) and fibrosis stage (insignificant [F0-1]/significant [F2-4]). Serum MPO and calprotectin levels were not significantly different between the NASH and control groups. In the subgroup analysis, hepatic MPO expression was significantly increased in patients with NASH with significant fibrosis than in those with insignificant fibrosis (F2-4: 7.04±3.61 vs. F0-1: 4.83±2.42, p=0.01). We found no difference between the groups with low and high NAS with regard to serum MPO and calprotectin levels and hepatic MPO and calprotectin expressions. This study demonstrated that hepatic MPO expression can reflect advanced fibrosis in NASH. However, when serum MPO and calprotectin levels were evaluated as potential serum markers, both did not associate with hepatic inflammation status and fibrosis stage in NASH. Therefore, our study results preclude their use as serum markers for hepatic inflammation in NASH.

Sections du résumé

BACKGROUND/AIMS
Specific serum markers reflecting hepatic inflammation and fibrosis are required to tailor the treatment strategies in non-alcoholic steatohepatitis (NASH). We aimed to investigate the roles of myeloperoxidase (MPO) and calprotectin in predicting the hepatic inflammation status and disease severity in NASH.
MATERIALS AND METHODS
A total of 48 patients with biopsy-proven NASH and 25 healthy volunteers with normal weight were prospectively enrolled. Serum MPO and calprotectin levels were compared between the NASH and control groups. Hepatic MPO and calprotectin expressions were compared in terms of histologic non-alcoholic fatty liver disease activity scores (NAS) (low NAS [≤4] vs. high NAS [>5]) and fibrosis stage (insignificant [F0-1]/significant [F2-4]).
RESULTS
Serum MPO and calprotectin levels were not significantly different between the NASH and control groups. In the subgroup analysis, hepatic MPO expression was significantly increased in patients with NASH with significant fibrosis than in those with insignificant fibrosis (F2-4: 7.04±3.61 vs. F0-1: 4.83±2.42, p=0.01). We found no difference between the groups with low and high NAS with regard to serum MPO and calprotectin levels and hepatic MPO and calprotectin expressions.
CONCLUSION
This study demonstrated that hepatic MPO expression can reflect advanced fibrosis in NASH. However, when serum MPO and calprotectin levels were evaluated as potential serum markers, both did not associate with hepatic inflammation status and fibrosis stage in NASH. Therefore, our study results preclude their use as serum markers for hepatic inflammation in NASH.

Identifiants

pubmed: 33169705
doi: 10.5152/tjg.2020.19403
pmc: PMC7659907
doi:

Substances chimiques

Biomarkers 0
Leukocyte L1 Antigen Complex 0
Peroxidase EC 1.11.1.7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

681-687

Références

Am J Pathol. 2009 Oct;175(4):1473-82
pubmed: 19729473
Eur J Biochem. 2000 Jul;267(14):4495-503
pubmed: 10880973
Hepatology. 2005 Jun;41(6):1313-21
pubmed: 15915461
Hepatology. 2007 Nov;46(5):1392-403
pubmed: 17929294
Obesity (Silver Spring). 2009 Nov;17(11):2014-8
pubmed: 19390527
Hepatology. 2008 Aug;48(2):670-8
pubmed: 18666225
Can J Gastroenterol Hepatol. 2015 Apr;29(3):157-63
pubmed: 25855880
Gastroenterology. 2006 Sep;131(3):934-45
pubmed: 16952562
Exp Neurol. 1999 Jan;155(1):31-41
pubmed: 9918702
Obes Surg. 2002 Apr;12(2):230-5
pubmed: 11975218
Intern Emerg Med. 2014 Mar;9(2):123-31
pubmed: 24057419
Postgrad Med. 2017 Jun;129(5):531-537
pubmed: 28425837
JAMA. 2001 Nov 7;286(17):2136-42
pubmed: 11694155
Circulation. 2005 Oct 25;112(17):2735-52
pubmed: 16157765
Am J Pathol. 2001 Dec;159(6):2081-8
pubmed: 11733358
Biol Pharm Bull. 2003 Jun;26(6):753-60
pubmed: 12808281
Am J Clin Pathol. 2007 Nov;128(5):837-47
pubmed: 17951208
J Neuroimmunol. 2009 Nov 30;216(1-2):98-102
pubmed: 19800696
Semin Liver Dis. 2007 Nov;27(4):339-50
pubmed: 17979071
Physiol Res. 2004;53(3):245-53
pubmed: 15209531
Arterioscler Thromb Vasc Biol. 2005 Jun;25(6):1102-11
pubmed: 15790935
J Hepatol. 2002 Jul;37(1):56-62
pubmed: 12076862
J Immunol. 2016 Jan 1;196(1):395-406
pubmed: 26608915

Auteurs

Ercan Bıçakçı (E)

Department of Gastroenterology, Marmara University School of Medicine, İstanbul, Turkey.

Coşkun Özer Demirtaş (CÖ)

Department of Gastroenterology, Marmara University School of Medicine, İstanbul, Turkey.

Çiğdem Çelikel (Ç)

Department of Pathology, Marmara University School of Medicine, İstanbul, Turkey.

Goncagül Haklar (G)

Department of Biochemistry, Marmara University School of Medicine, İstanbul, Turkey.

Deniz Güney Duman (DG)

Department of Gastroenterology, Marmara University School of Medicine, İstanbul, Turkey.

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Classifications MeSH