Cell-free DNA: Preanalytical variables.

Clin Chim Acta

Centre for Human Metabonomics, Biochemistry Division, North-West University, Potchefstroom 2520, South Africa.

Published: October 2015

AI Article Synopsis

  • Since its discovery in blood, the focus of cell-free DNA (cfDNA) research has largely been on its diagnostic and prognostic application for solid tumors, but practical use in clinical settings is still far off.
  • Key challenges preventing clinical adoption include limited understanding of cfDNA's origin and function, inadequate molecular characterization, and lack of standardized analytical methods.
  • The review emphasizes that while single measurements of cfDNA may not be very informative, tracking changes in cfDNA levels over time is important and calls for process optimization and standardization to improve the reliability of quantitative assessments.

Article Abstract

Since the discovery of cell-free DNA (cfDNA) in human blood, most studies have focused on diagnostic and prognostic uses of these markers for solid tumors. Except for some prenatal tests and BEAMing, cfDNA analysis has not yet been translated to clinical practice and routine application appears distant. This can be attributed to overlapping factors: (i) a lack of knowledge regarding the origin and function of cfDNA, (ii) insufficient molecular characterization, and (iii) the absence of an analytical consensus. In this review, we address the latter determinant and focus specifically on quantitative analysis of cfDNA. While the literature reports limited value for a single quantitative assessment, cfDNA kinetic assessment will be an essential component to qualitative characterization. In order to establish quantitative analysis for accurate kinetic assessments, process optimization and standardization are crucial. This report elucidates the most confounding variables of each preanalytic step that must be considered for optimal analysis.

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Source
http://dx.doi.org/10.1016/j.cca.2015.08.028DOI Listing

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