From "clinical proteomics" to "clinical chemistry proteomics": considerations using quantitative mass-spectrometry as a model approach.

Abstract:

:Clinical Proteomics biomarker discovery programs lead to the selection of putative new biomarkers of human pathologies. Following an initial discovery phase, validation of these candidates in larger populations is a major task that recently started relying upon the use of mass spectrometry approaches, especially in cases where classical immune-detection methods were lacking. Thanks to highly sensitive spectrometers, adapted measurement methods like selective reaction monitoring (SRM) and various pre-fractionation methods, the quantitative detection of protein/peptide biomarkers in low concentrations is now feasible from complex biological fluids. This possibility leads to the use of similar methodologies in clinical biology laboratories, within a new proteomic field that we shall name "Clinical Chemistry Proteomics" (CCP). Such evolution of Clinical Proteomics adds important constraints with regards to the in vitro diagnostic (IVD) application. As measured values of analytes will be used to diagnose, follow-up and adapt patient treatment on a routine basis; medical utility, robustness, reference materials and clinical feasibility are among the new issues of CCP to consider.

journal_name

Clin Chem Lab Med

authors

Lehmann S,Poinot P,Tiers L,Junot C,Becher F,Hirtz C

doi

10.1515/CCLM.2011.744

subject

Has Abstract

pub_date

2011-10-08 00:00:00

pages

235-42

issue

2

eissn

1434-6621

issn

1437-4331

pii

/j/cclm.2012.50.issue-2/cclm.2011.744/cclm.2011.74

journal_volume

50

pub_type

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