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Updated: Apr 23, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Paricalcitol and endothelial function in chronic kidney disease trial
Carmine Zoccali1, Giuseppe Curatola2, Vincenzo Panuccio2
1From the Nephrology, Hypertension, and Renal Transplantation Unit, Ospedali Riuniti, Reggio Calabria, Italy (C.Z., V.P., F.M.); CNR-IBIM/IFC Clinical Epidemiology and Pathophysiology of Renal Diseases and Hypertension, Reggio Calabria, Italy (C.Z., G.C., V.P., R.T., P.P., M.V., D.B., S.C., R.P., G.T., F.M.); Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy (L.G.); and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston (R.T.). carmine.zoccali@tin.it.
Insights
Active vitamin D therapy with paricalcitol improved blood vessel function in patients with chronic kidney disease (CKD). This study found paricalcitol enhanced endothelium-dependent vasodilation, suggesting cardiovascular benefits for CKD patients.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Endocrinology
Background:
- Altered vitamin D metabolism is common in chronic kidney disease (CKD).
- Low levels of active 1,25-dihydroxy-vitamin D are a hallmark of CKD.
- No randomized controlled trials have tested active vitamin D's effect on vascular function in CKD patients.
Purpose of the Study:
- To evaluate the effect of paricalcitol, an active form of vitamin D, on vascular function in patients with stage 3-4 CKD.
- To assess paricalcitol's impact on endothelium-dependent and endothelium-independent vasodilation.
- To investigate the relationship between paricalcitol treatment and parathormone levels in CKD patients.
Main Methods:
- A double-blinded randomized controlled trial (PENNY study) involving 88 patients with stage 3-4 CKD and elevated parathormone.
- Patients received either paricalcitol (2 μg/d for 12 weeks) or a placebo.
- Vascular function was assessed by measuring endothelium-dependent and endothelium-independent vasodilation, with flow-mediated dilation as the primary endpoint.
Main Results:
- Paricalcitol significantly reduced parathormone levels compared to placebo.
- Flow-mediated dilation increased by 1.8% in the paricalcitol group versus the placebo group after 12 weeks (P=0.016).
- The improvement in flow-mediated dilation was temporary, disappearing 2 weeks after treatment cessation. No effect on blood pressure or endothelium-independent vasodilation was observed.
Conclusions:
- Paricalcitol improves endothelium-dependent vasodilation in patients with stage 3-4 CKD.
- These findings support the hypothesis that vitamin D may have beneficial cardiovascular effects in CKD patients.
- Further research is warranted to explore the long-term cardiovascular implications of active vitamin D therapy in CKD.
Abstract:
Altered vitamin D metabolism and low levels of the active form of this vitamin, 1,25-dihydroxy-vitamin D, is a hallmark of chronic kidney disease (CKD), but there is still no randomized controlled trial testing the effect of active forms of vitamin D on vascular function in patients with CKD. Paricalcitol and ENdothelial fuNction in chronic kidneY disease (PENNY) is a double-blinded randomized controlled trial (ClinicalTrials.gov, NCT01680198) testing the effect of an active form of vitamin D, paricalcitol (2 μg/d×12 weeks) on endothelium-dependent and endothelium-independent vasodilatation in 88 patients with stage 3 to 4 CKD and parathormone >65 pg/mL (paricalcitol, n=44; placebo, n=44). Paricalcitol treatment reduced parathormone (-75 pg/mL; 95% confidence interval, -90 to -60), whereas parathormone showed a small rise during placebo (21 pg/mL; 95% confidence interval, 5-36). Blood pressure did not change in both study arms. Baseline flow-mediated dilation was identical in patients on paricalcitol (3.6±2.9%) and placebo (3.6±2.9%) groups. After 12 weeks of treatment, flow-mediated dilation rose in the paricalcitol but not in the placebo group, and the between-group difference in flow-mediated dilation changes (the primary end point, 1.8%; 95% confidence interval, 0.3-3.1%) was significant (P=0.016), and the mean proportional change in flow-mediated dilation was 61% higher in paricalcitol-treated patients than in placebo-treated patients. Such an effect was abolished 2 weeks after stopping the treatment. No effect of paricalcitol on endothelium-independent vasodilatation was registered. Paricalcitol improves endothelium-dependent vasodilatation in patients with stage 3 to 4 CKD. Findings in this study support the hypothesis that vitamin D may exert favorable effects on the cardiovascular system in patients with CKD.
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