Endothelin-1, Extracellular Volume Overload, and Hemodynamics in Hemodialysis Patients

Author:

Horvit Andrew1,Jeon-Slaughter Haekyung2,Sian Jaspreet3,Roehm Bethany3,Van Buren Peter Noel23ORCID

Affiliation:

1. Department of Internal Medicine, University of Texas Southwestern Medical Center , Dallas, Texas , USA

2. Dallas Veterans Affairs Medical Center , Medical Service, Nephrology Section Dallas, Texas , USA

3. Division of Nephrology, Department of Internal Medicine, University of Texas Southwestern Medical Center , Dallas, Texas , USA

Abstract

Abstract BACKGROUND Extracellular volume (ECV) overload and endothelial cell dysfunction are mortality risk factors in hemodialysis (HD) patients. Endothelin-1 (ET-1), an endothelium-derived vasoconstrictive peptide, is associated with poor outcomes in HD patients. We hypothesized there would be associations between ET-1 and ECV overload in hypertensive HD patients. METHODS We obtained pre-HD ET-1, ECV/weight (bioimpedance spectroscopy), pre-HD hemodynamics, and ambulatory blood pressure (BP) in an HD cohort. Following appropriate transformations, we conducted correlation and linear regression analyses idendifying associations between ET-1, ECV overload, total peripheral resistance index (TPRI), cardiac index (CI), and ambulatory BP. RESULTS Among 66 patients, median ET-1 was 1.93 (1.49–2.56) pg/ml. Median pre-HD ECV/weight, median TPRI, mean CI, and mean systolic ambulatory BP were 0.25 (0.22–0.30) l/kg, 3,161 (2,711–3,642) dynes × s/cm−5/m2, 2.92 (0.6) l/min/m2, and 143 (14) mm Hg, respectively. After reciprocal-transformation, ET-1 correlated with reciprocal-transformed ECV/weight (r = 0.3, P = 0.01), log-transformed TPRI (r = −0.3, P = 0.006), CI (r = 0.3, P = 0.009), and ambulatory BP (r = −0.3, P = 0.02). These associations persisted in linear regression analysis (β = 0.15, P = 0.002; β = −0.8, P = 0.002; β = 0.2, P = 0.002; β = −19, P = 0.03). CONCLUSIONS In hypertensive HD patients, ET-1 associates with ECV overload higher TPRI and ambulatory BP, and lower CI. Further research is necessary to determine if ECV reduction lowers ET-1 or if pharmacologic ET-1 antagonism can improve outcomes in HD patients with refractory ECV overload.

Funder

National Institutes of Health NIDDK

Department of Veterans Affairs

Dedman Family Scholar in Clinical Care

National Center for Advancing Translational Sciences of the National Institutes of Health

Publisher

Oxford University Press (OUP)

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