Cargando…

Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort

BACKGROUND AND AIMS: A method for assessment of liver fibrosis and cirrhosis without the need for a liver biopsy is desirable. Microfibrillar-associated protein 4 (MFAP4) is a suggested biomarker for identification of high-risk patients with severe fibrosis stages. This study aimed to examine associ...

Descripción completa

Detalles Bibliográficos
Autores principales: Sækmose, Susanne Gjørup, Mössner, Belinda, Christensen, Peer Brehm, Lindvig, Kristoffer, Schlosser, Anders, Holst, René, Barington, Torben, Holmskov, Uffe, Sorensen, Grith Lykke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604125/
https://www.ncbi.nlm.nih.gov/pubmed/26460565
http://dx.doi.org/10.1371/journal.pone.0140418
_version_ 1782395008939196416
author Sækmose, Susanne Gjørup
Mössner, Belinda
Christensen, Peer Brehm
Lindvig, Kristoffer
Schlosser, Anders
Holst, René
Barington, Torben
Holmskov, Uffe
Sorensen, Grith Lykke
author_facet Sækmose, Susanne Gjørup
Mössner, Belinda
Christensen, Peer Brehm
Lindvig, Kristoffer
Schlosser, Anders
Holst, René
Barington, Torben
Holmskov, Uffe
Sorensen, Grith Lykke
author_sort Sækmose, Susanne Gjørup
collection PubMed
description BACKGROUND AND AIMS: A method for assessment of liver fibrosis and cirrhosis without the need for a liver biopsy is desirable. Microfibrillar-associated protein 4 (MFAP4) is a suggested biomarker for identification of high-risk patients with severe fibrosis stages. This study aimed to examine associations between plasma MFAP4 (pMFAP4) and transient elastography or chronic hepatitis C virus infection in drug users and in a mixed patient cohort with increased risk of liver disease. Moreover, the study aimed to identify comorbidities that significantly influence pMFAP4. METHODS: pMFAP4 was measured in samples from 351 drug users attending treatment centres and from 248 acutely hospitalized medical patients with mixed diagnoses. Linear and logistic multivariate regression analyses were performed and nonparametric receiver operating characteristic-curves for cirrhosis were used to estimate cut-off points for pMFAP4. Univariate and subgroup analyses were performed using non-parametric methods. RESULTS: pMFAP4 increased significantly with liver fibrosis score. pMFAP4 was significantly associated with chronic viral infection in the drug users and with transient elastography in both cohorts. In the mixed patient cohort, pMFAP4 was significantly increased among patients with a previous diagnosis of liver disease or congestive heart failure compared to patients with other diagnoses. CONCLUSIONS: pMFAP4 has the potential to be used as an outreach-screening tool for liver fibrosis in drug users and in mixed medical patients. pMFAP4 level is positively associated with transient elastography, but additional studies are warranted to validate the possible use of pMFAP4 in larger cohorts and in combination with transient elastography.
format Online
Article
Text
id pubmed-4604125
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46041252015-10-20 Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort Sækmose, Susanne Gjørup Mössner, Belinda Christensen, Peer Brehm Lindvig, Kristoffer Schlosser, Anders Holst, René Barington, Torben Holmskov, Uffe Sorensen, Grith Lykke PLoS One Research Article BACKGROUND AND AIMS: A method for assessment of liver fibrosis and cirrhosis without the need for a liver biopsy is desirable. Microfibrillar-associated protein 4 (MFAP4) is a suggested biomarker for identification of high-risk patients with severe fibrosis stages. This study aimed to examine associations between plasma MFAP4 (pMFAP4) and transient elastography or chronic hepatitis C virus infection in drug users and in a mixed patient cohort with increased risk of liver disease. Moreover, the study aimed to identify comorbidities that significantly influence pMFAP4. METHODS: pMFAP4 was measured in samples from 351 drug users attending treatment centres and from 248 acutely hospitalized medical patients with mixed diagnoses. Linear and logistic multivariate regression analyses were performed and nonparametric receiver operating characteristic-curves for cirrhosis were used to estimate cut-off points for pMFAP4. Univariate and subgroup analyses were performed using non-parametric methods. RESULTS: pMFAP4 increased significantly with liver fibrosis score. pMFAP4 was significantly associated with chronic viral infection in the drug users and with transient elastography in both cohorts. In the mixed patient cohort, pMFAP4 was significantly increased among patients with a previous diagnosis of liver disease or congestive heart failure compared to patients with other diagnoses. CONCLUSIONS: pMFAP4 has the potential to be used as an outreach-screening tool for liver fibrosis in drug users and in mixed medical patients. pMFAP4 level is positively associated with transient elastography, but additional studies are warranted to validate the possible use of pMFAP4 in larger cohorts and in combination with transient elastography. Public Library of Science 2015-10-13 /pmc/articles/PMC4604125/ /pubmed/26460565 http://dx.doi.org/10.1371/journal.pone.0140418 Text en © 2015 Sækmose et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sækmose, Susanne Gjørup
Mössner, Belinda
Christensen, Peer Brehm
Lindvig, Kristoffer
Schlosser, Anders
Holst, René
Barington, Torben
Holmskov, Uffe
Sorensen, Grith Lykke
Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title_full Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title_fullStr Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title_full_unstemmed Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title_short Microfibrillar-Associated Protein 4: A Potential Biomarker for Screening for Liver Fibrosis in a Mixed Patient Cohort
title_sort microfibrillar-associated protein 4: a potential biomarker for screening for liver fibrosis in a mixed patient cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604125/
https://www.ncbi.nlm.nih.gov/pubmed/26460565
http://dx.doi.org/10.1371/journal.pone.0140418
work_keys_str_mv AT sækmosesusannegjørup microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT mossnerbelinda microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT christensenpeerbrehm microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT lindvigkristoffer microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT schlosseranders microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT holstrene microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT baringtontorben microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT holmskovuffe microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort
AT sorensengrithlykke microfibrillarassociatedprotein4apotentialbiomarkerforscreeningforliverfibrosisinamixedpatientcohort