Statistical methods for building better biomarkers of chronic kidney disease.

Published

Journal Article

The last two decades have witnessed an explosion in research focused on the development and assessment of novel biomarkers for improved prognosis of diseases. As a result, best practice standards guiding biomarker research have undergone extensive development. Currently, there is great interest in the promise of biomarkers to enhance research efforts and clinical practice in the setting of chronic kidney disease, acute kidney injury, and glomerular disease. However, some have questioned whether biomarkers currently add value to the clinical practice of nephrology. The current state of the art pertaining to statistical analyses regarding the use of such measures is critical. In December 2014, the National Institute of Diabetes and Digestive and Kidney Diseases convened a meeting, "Toward Building Better Biomarker Statistical Methodology," with the goals of summarizing the current best practice recommendations and articulating new directions for methodological research. This report summarizes its conclusions and describes areas that need attention. Suggestions are made regarding metrics that should be commonly reported. We outline the methodological issues related to traditional metrics and considerations in prognostic modeling, including discrimination and case mix, calibration, validation, and cost-benefit analysis. We highlight the approach to improved risk communication and the value of graphical displays. Finally, we address some "new frontiers" in prognostic biomarker research, including the competing risk framework, the use of longitudinal biomarkers, and analyses in distributed research networks.

Full Text

Duke Authors

Cited Authors

  • Pencina, MJ; Parikh, CR; Kimmel, PL; Cook, NR; Coresh, J; Feldman, HI; Foulkes, A; Gimotty, PA; Hsu, C-Y; Lemley, K; Song, P; Wilkins, K; Gossett, DR; Xie, Y; Star, RA

Published Date

  • May 20, 2019

Published In

Volume / Issue

  • 38 / 11

Start / End Page

  • 1903 - 1917

PubMed ID

  • 30663113

Pubmed Central ID

  • 30663113

Electronic International Standard Serial Number (EISSN)

  • 1097-0258

Digital Object Identifier (DOI)

  • 10.1002/sim.8091

Language

  • eng

Conference Location

  • England