From 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.).
Hypertension. 2014 Nov;64(5):1005-11. doi: 10.1161/HYPERTENSIONAHA.114.03748. Epub 2014 Aug 4.
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.
维生素 D 代谢改变和活性形式维生素 D(1,25-二羟维生素 D)水平降低是慢性肾脏病(CKD)的标志,但目前仍没有随机对照试验测试活性形式的维生素 D 对 CKD 患者血管功能的影响。甲状旁腺素和慢性肾脏病中的内皮功能(PENNY)是一项双盲随机对照试验(ClinicalTrials.gov,NCT01680198),旨在测试活性形式的维生素 D,帕立骨化醇(2 μg/d×12 周)对 88 例 3 至 4 期 CKD 和甲状旁腺素 >65 pg/mL(帕立骨化醇组 44 例,安慰剂组 44 例)患者的内皮依赖性和非内皮依赖性血管舒张的影响。帕立骨化醇治疗可降低甲状旁腺素(-75 pg/mL;95%置信区间,-90 至-60),而安慰剂组甲状旁腺素略有升高(21 pg/mL;95%置信区间,5-36)。在两个研究组中,血压均未发生变化。帕立骨化醇组(3.6±2.9%)和安慰剂组(3.6±2.9%)的基线血流介导的扩张率相同。治疗 12 周后,帕立骨化醇组的血流介导的扩张增加,而安慰剂组没有增加,组间血流介导的扩张变化差异(主要终点,1.8%;95%置信区间,0.3-3.1%)具有显著性(P=0.016),帕立骨化醇治疗患者的血流介导的扩张平均比例变化比安慰剂治疗患者高 61%。这种作用在停止治疗后 2 周即消失。帕立骨化醇对内皮非依赖性血管舒张没有影响。帕立骨化醇可改善 3 至 4 期 CKD 患者的内皮依赖性血管舒张。本研究结果支持维生素 D 可能对 CKD 患者的心血管系统产生有利影响的假说。