Impaired retinal vessel dilation predicts mortality in end-stage renal disease

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-cau...

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Hauptverfasser: Günthner, Roman (VerfasserIn) , Hanssen, Henner (VerfasserIn) , Hauser, Christine (VerfasserIn) , Angermann, Susanne (VerfasserIn) , Lorenz, Georg (VerfasserIn) , Kemmner, Stephan (VerfasserIn) , Matschkal, Julia (VerfasserIn) , Braunisch, Matthias C. (VerfasserIn) , Küchle, Claudius (VerfasserIn) , Renders, Lutz (VerfasserIn) , Moog, Philipp (VerfasserIn) , Wassertheurer, Siegfried (VerfasserIn) , Baumann, Marcus (VerfasserIn) , Hammes, Hans-Peter (VerfasserIn) , Mayer, Christopher C. (VerfasserIn) , Haller, Bernhard (VerfasserIn) , Stryeck, Sarah (VerfasserIn) , Madl, Tobias (VerfasserIn) , Carbajo-Lozoya, Javier (VerfasserIn) , Heemann, Uwe (VerfasserIn) , Kotliar, Konstantin (VerfasserIn) , Schmaderer, Christoph (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1 Apr 2019
In: Circulation research
Year: 2019, Jahrgang: 124, Heft: 12, Pages: 1796-1807
ISSN:1524-4571
DOI:10.1161/CIRCRESAHA.118.314318
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1161/CIRCRESAHA.118.314318
Verlag, lizenzpflichtig, Volltext: https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.118.314318
Volltext
Verfasserangaben:Günthner Roman, Hanssen Henner, Hauser Christine, Angermann Susanne, Lorenz Georg, Kemmner Stephan, Matschkal Julia, Braunisch Matthias C., Küchle Claudius, Renders Lutz, Moog Philipp, Wassertheurer Siegfried, Baumann Marcus, Hammes Hans-Peter, Mayer Christopher C., Haller Bernhard, Stryeck Sarah, Madl Tobias, Carbajo-Lozoya Javier, Heemann Uwe, Kotliar Konstantin, Schmaderer Christoph
Beschreibung
Zusammenfassung: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.
Beschreibung:Gesehen am 06.04.2020
Beschreibung:Online Resource
ISSN:1524-4571
DOI:10.1161/CIRCRESAHA.118.314318