Publication:
Serum proteomics for biomarker discovery in nonalcoholic fatty liver disease

dc.contributor.authorYILMAZ, YUSUF
dc.contributor.authorsYilmaz, Yusuf
dc.date.accessioned2022-03-10T15:25:09Z
dc.date.accessioned2026-01-11T17:57:22Z
dc.date.available2022-03-10T15:25:09Z
dc.date.issued2012
dc.description.abstractProteomic platforms have gained increasing attention in the clinical spectrum of nonalcoholic fatty liver disease (NAFLD). This approach allows for the unbiased discovery of circulating biochemical markers, i.e., it is not limited to known molecules of presumed importance. This manuscript provides an overview of proteomic serum biomarker discovery in NAFLD. Hemoglobin is currently the most widely replicated proteomic circulating biomarker of NAFLD; it was identified as a biomarker of fatty liver in two distinct proteomic studies and subsequently validated using distinct analytical methods by independent research groups in large replication cohorts. Given the increasing availability of numerous serum samples and the refinement of the technological platforms available to scrutinize the blood proteome, large collaborative studies between academia and industry are warmly encouraged to identify novel, unbiased circulating biomarkers of NAFLD. (C) 2012 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.cca.2012.04.019
dc.identifier.issn0009-8981
dc.identifier.pubmed22546610
dc.identifier.urihttps://hdl.handle.net/11424/220130
dc.identifier.wosWOS:000305370300005
dc.language.isoeng
dc.publisherELSEVIER SCIENCE BV
dc.relation.ispartofCLINICA CHIMICA ACTA
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectNonalcoholic fatty liver disease
dc.subjectProteomics
dc.subjectSerum
dc.subjectBiomarkers
dc.subjectHemoglobin
dc.subjectMASS-SPECTROMETRY
dc.subjectMETABOLIC SYNDROME
dc.subjectNONINVASIVE DIAGNOSIS
dc.subjectCLINICAL PROTEOMICS
dc.subjectSTEATOHEPATITIS
dc.subjectCHALLENGES
dc.subjectPATHOPHYSIOLOGY
dc.subjectBIOINFORMATICS
dc.subjectEPIDEMIOLOGY
dc.subjectHEMOGLOBIN
dc.titleSerum proteomics for biomarker discovery in nonalcoholic fatty liver disease
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage1193
oaire.citation.issue15-16
oaire.citation.startPage1190
oaire.citation.titleCLINICA CHIMICA ACTA
oaire.citation.volume413

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