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Can we further enrich autosomal dominant polycystic kidney disease clinical trials for rapidly progressive patients? Application of the PROPKD score in the TEMPO trial

Authors :
Peter C. Harris
John Ouyang
Yannick Le Meur
Arlene B. Chapman
Christina M. Heyer
Sarah R. Senum
Ron T. Gansevoort
Ronald D. Perrone
Frank S. Czerwiec
Maria V. Irazabal
Jaime D. Blais
Vicente E. Torres
Olivier Devuyst
Emilie Cornec-Le Gall
CHRU - Service de néphrologie, dialyse et transplantation rénale
Centre Hospitalier Régional Universitaire de Brest (CHRU Brest)
Mayo Clinic [Rochester]
Otsuka PDC, Rockville, MD, USA
Otsuka PDC
Institute of Nephrology, University of Zurich, Switzerland
Department of Nephrology
University Medical Center, University of Groningen
Tufts University School of Medicine [Boston]
Section of Nephrology University of Chicago
University of Chicago
Division of Nephrology and Hypertension
Mayo Clinic
Lymphocyte B et Auto-immunité (LBAI)
Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Brestois Santé Agro Matière (IBSAM)
Université de Brest (UBO)
Université de Brest (UBO)-Institut Brestois Santé Agro Matière (IBSAM)
Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)
University of Zurich
Cornec-Le Gall, Emilie
Cardiovascular Centre (CVC)
Groningen Kidney Center (GKC)
Source :
Nephrology Dialysis Transplantation, Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2017, ⟨10.1093/ndt/gfx188⟩, Nephrology, Dialysis, Transplantation, 33(4), 645-652. Oxford University Press
Publication Year :
2017
Publisher :
HAL CCSD, 2017.

Abstract

Background: The PROPKD score has been proposed to stratify the risk of progression to end-stage renal disease in autosomal dominant polycystic kidney disease (ADPKD) subjects. We aimed to assess its prognostic value in a genotyped subgroup of subjects from the Tolvaptan Phase 3 Efficacy and Safety Study in Autosomal Dominant Polycystic Kidney Disease (TEMPO3/4) trial.Methods: In the post hoc analysis, PKD1 and PKD2 were screened in 770 subjects and the PROPKD score was calculated in mutation-positive subjects (male: 1 point; hypertension Results: The PROPKD score was calculated in 749 subjects (LR = 132, IR = 344 and HR = 273); age was inversely related to risk (LR = 43.6 years, IR = 39.5 years, HR = 36.2 years; P Conclusion: This study confirms the prognostic value of the PROPKD score and suggests that it could reduce costs and enhance endpoint sensitivity by enriching future study populations for rapidly progressing ADPKD subjects.

Details

Language :
English
ISSN :
09310509 and 14602385
Database :
OpenAIRE
Journal :
Nephrology Dialysis Transplantation, Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2017, ⟨10.1093/ndt/gfx188⟩, Nephrology, Dialysis, Transplantation, 33(4), 645-652. Oxford University Press
Accession number :
edsair.doi.dedup.....b102eeee18327f402889b58c648eb06d