Pulse Wave Velocity and Prognosis in End-Stage Kidney Disease

Author:

Tripepi Giovanni1,Agharazii Mohsen2,Pannier Bruno3,D’Arrigo Graziella1,Mallamaci Francesca1,Zoccali Carmine1,London Gerard4

Affiliation:

1. From the Institute of Clinical Physiology (IFC-CNR), Research Unit of Reggio Calabria, Reggio di Calabria, Italy (G.T., G.D’A., F.M., C.Z.)

2. CHU de Québec Research Center, L’Hôtel-Dieu de Québec Hospital, Quebec, Quebec, Canada (M.A.)

3. Centre Hospitalier F.H. Manhes, Fleury Merogis, France (B.P.)

4. and INSERM U970, Hopital Européen Georges Pompidou, Paris, France (G.L.).

Abstract

High pulse wave velocity (PWV) is a hallmark of end-stage kidney disease (ESKD) where it is considered useful for risk stratification. We investigated whether PWV adds meaningful prognostic information to 2 simple, well-validated, clinical risk scores specific to ESKD (the Annualized Rate of Occurrence scores) for predicting all-cause and cardiovascular mortality by applying state-of-the-art prognostic tests including discrimination (Harrell C-index), risk reclassification (integrated discrimination improvement), and calibration. We performed these analyses in the 2 largest ESKD cohorts with available PWV data, the Manhes-Hospital cohort in Paris (n=287 patients) and the Quebec Research Center cohort in Canada (n=246 patients). The Harrell C-index of the 2 clinical risk scores was consistently higher than that by PWV both for all-cause (Manhes cohort, 77.5% versus 73.7%; Quebec cohort, 61.5% versus 58.9%) and cardiovascular mortality (Manhes cohort, 77.9% versus 77.2%; Quebec cohort, 63.8% versus 60.3%). Furthermore, PWV provided a very modest increase in discriminatory power over and above clinical risk scores by Harrell C-index (from 0.5% to 1.8%) and in risk reclassification by Integrated Discrimination Improvement (from 0.9% to 5.1%) and actually worsened models calibration. In patients with ESKD, PWV has a prognostic power for all-cause and cardiovascular mortality inferior to that by simple clinical risk scores and only modestly improves the risk discrimination and reclassification by the same risk scores and worsens models calibration. Clinicians may better rely on available clinical risk scores rather than on PWV for risk stratification in the ESKD population.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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