Impaired Retinal Vessel Dilation Predicts Mortality in End-Stage Renal Disease

Author:

Günthner Roman1,Hanssen Henner2,Hauser Christine1,Angermann Susanne1,Lorenz Georg1,Kemmner Stephan1,Matschkal Julia1,Braunisch Matthias C.1,Küchle Claudius1,Renders Lutz1,Moog Philipp1,Wassertheurer Siegfried3,Baumann Marcus1,Hammes Hans-Peter4,Mayer Christopher C.3,Haller Bernhard5,Stryeck Sarah6,Madl Tobias67,Carbajo-Lozoya Javier1,Heemann Uwe1,Kotliar Konstantin8,Schmaderer Christoph1

Affiliation:

1. From the Department of Nephrology, Technical University of Munich, School of Medicine, Klinikum rechts der Isar, Germany (R.G., C.H., S.A., G.L., S.K., J.M., M.C.B., C.K., L.R., P.M., M.B., J.C.-L., U.H., C.S.)

2. Department of Sport, Exercise and Health, Preventive Sports Medicine and Systems Physiology, University of Basel, Switzerland (H.H.)

3. Center for Health & Bioresources, AIT Austrian Institute of Technology GmbH, Vienna (S.W., C.C.M.)

4. Medical Faculty Mannheim, Heidelberg University, Germany (H.-P.H.)

5. Institute of Medical Informatics, Statistics and Epidemiology, Technical University of Munich, School of Medicine, Klinikum rechts der Isar, Germany (B.H.)

6. Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Molecular Biology and Biochemistry, Medical University of Graz, Austria (S.S., T.M.)

7. BioTechMed-Graz, Austria (T.M.)

8. Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany (K.K.).

Abstract

Rationale : Patients with end-stage renal disease are characterized by increased cardiovascular and all-cause mortality because of advanced remodeling of the macrovascular and microvascular beds. Objective : The aim of this study was to determine whether retinal microvascular function can predict all-cause and cardiovascular mortality in patients with end-stage renal disease. Methods and Results : In the multicenter prospective observational ISAR study (Risk Stratification in End-Stage Renal Disease), data on dynamic retinal vessel analysis were available in a subcohort of 214 dialysis patients (mean age, 62.6±15.0; 32% women). Microvascular dysfunction was quantified by measuring maximum arteriolar dilation and maximum venular dilation (vMax) of retinal vessels in response to flicker light stimulation. During a mean follow-up of 44 months, 55 patients died, including 25 cardiovascular and 30 noncardiovascular fatal events. vMax emerged as a strong independent predictor for all-cause mortality. In the Kaplan-Meier analysis, individuals within the lowest tertile of vMax showed significantly shorter 3-year survival rates than those within the highest tertile (66.9±5.8% versus 92.4±3.3%). Univariate and multivariate hazard ratios for all-cause mortality per SD increase of vMax were 0.62 (0.47–0.82) and 0.65 (0.47–0.91), respectively. Maximum arteriolar dilation and vMax were able to significantly predict nonfatal and fatal cardiovascular events (hazard ratio, 0.74 [0.57–0.97] and 0.78 [0.61–0.99], respectively). Conclusions : Our results provide the first evidence that impaired retinal venular dilation is a strong and independent predictor of all-cause mortality in hemodialyzed end-stage renal disease patients. Dynamic retinal vessel analysis provides added value for prediction of all-cause mortality and may be a novel diagnostic tool to optimize cardiovascular risk stratification in end-stage renal disease and other high-risk cardiovascular cohorts. Clinical Trial Registration : URL: http://www.clinicaltrials.gov . Unique identifier: NCT01152892.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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