[Biomarkers of vascular calcifications: what are analytical limits to apply "research-grade" diagnostic kits into daily practice?].

Ann Biol Clin (Paris)

Département de biochimie et d'hormonologie, CHRU de Montpellier, U 1046 Inserm, Université de Montpellier 1, Montpellier, France, Unité de biochimie hormonale et nutritionnelle, Institut de biologie et pathologie, CHU de Grenoble ; Inserm, U1055, Grenoble, France, Service de chimie médicale, CHU Sart Tilman, Université de Liège, Liège, Belgique, Centre hospitalier d'Avignon, Avignon, France, Unité Inserm 1088 : MP3CV « Mécanismes physiopathologiques, causes et conséquences des calcifications vasculaires ». Université de Picardie Jules Verne, Amiens, France, Laboratoire de biochimie, CHU d'Amiens, France, Université Paris Descartes, Faculté de médecine, Inserm U845, Hôpital Necker-Enfants Malades, AP-HP, Paris, France, Centre de recherche clinique, CHU d'Amiens, Amiens, France, Institut de recherche et de formation en dialyse, Montpellier, France.

Published: May 2016

A better knowledge of physiopathologic mechanisms responsible for vascular calcification leads to emerging biological markers of calcifications. The use of these biomarkers in daily practice requires both clinical and analytical validation. This latter point is of particular importance to implement "research-grade" diagnostic kits into daily practice. Data in the literature underline the lack of method standardization and the non-transferability of results. Depending on the method used, important biological associations might be hidden.

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http://dx.doi.org/10.1684/abc.2015.1043DOI Listing

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