Effects of Vitamin D Receptor Activation and Dietary Sodium Restriction on Residual Albuminuria in CKD: The ViRTUE-CKD Trial
Reduction of residual albuminuria during single–agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied the individual and combined effects of the vitamin D receptor activator paricalcitol (PARI) and dietary sodium restriction on residual album...
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Published in | Journal of the American Society of Nephrology Vol. 28; no. 4; pp. 1296 - 1305 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society of Nephrology
01.04.2017
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Online Access | Get full text |
ISSN | 1046-6673 1533-3450 |
DOI | 10.1681/ASN.2016040407 |
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Abstract | Reduction of residual albuminuria during single–agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied the individual and combined effects of the vitamin D receptor activator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD. In a multicenter, randomized, placebo (PLAC)–controlled, crossover trial, 45 patients with nondiabetic CKD stages 1–3 and albuminuria >300 mg/24 h despite ramipril at 10 mg/d and BP<140/90 mmHg were treated for four 8-week periods with PARI (2
μ
g/d) or PLAC, each combined with a low-sodium (LS) or regular sodium (RS) diet. We analyzed the treatment effect by linear mixed effect models for repeated measurements. In the intention-to-treat analysis, albuminuria (geometric mean) was 1060 (95% confidence interval, 778 to 1443) mg/24 h during RS + PLAC and 990 (95% confidence interval, 755 to 1299) mg/24 h during RS + PARI (
P
=0.20 versus RS + PLAC). LS + PLAC reduced albuminuria to 717 (95% confidence interval, 512 to 1005) mg/24 h (
P
<0.001 versus RS + PLAC), and LS + PARI reduced albuminuria to 683 (95% confidence interval, 502 to 929) mg/24 h (
P
<0.001 versus RS + PLAC). The reduction by PARI beyond the effect of LS was nonsignificant (
P
=0.60). In the per-protocol analysis restricted to participants with ≥95% compliance with study medication, PARI did provide further albuminuria reduction (
P
=0.04 LS + PARI versus LS + PLAC). Dietary adherence was good as reflected by urinary excretion of 174±64 mmol Na
+
per day in the combined RS groups and 108±61 mmol Na
+
per day in the LS groups (
P
<0.001). In conclusion, moderate dietary sodium restriction substantially reduced residual albuminuria during fixed dose angiotensin–converting enzyme inhibition. The additional effect of PARI was small and nonsignificant. |
---|---|
AbstractList | Reduction of residual albuminuria during single–agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied the individual and combined effects of the vitamin D receptor activator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD. In a multicenter, randomized, placebo (PLAC)–controlled, crossover trial, 45 patients with nondiabetic CKD stages 1–3 and albuminuria >300 mg/24 h despite ramipril at 10 mg/d and BP<140/90 mmHg were treated for four 8-week periods with PARI (2
μ
g/d) or PLAC, each combined with a low-sodium (LS) or regular sodium (RS) diet. We analyzed the treatment effect by linear mixed effect models for repeated measurements. In the intention-to-treat analysis, albuminuria (geometric mean) was 1060 (95% confidence interval, 778 to 1443) mg/24 h during RS + PLAC and 990 (95% confidence interval, 755 to 1299) mg/24 h during RS + PARI (
P
=0.20 versus RS + PLAC). LS + PLAC reduced albuminuria to 717 (95% confidence interval, 512 to 1005) mg/24 h (
P
<0.001 versus RS + PLAC), and LS + PARI reduced albuminuria to 683 (95% confidence interval, 502 to 929) mg/24 h (
P
<0.001 versus RS + PLAC). The reduction by PARI beyond the effect of LS was nonsignificant (
P
=0.60). In the per-protocol analysis restricted to participants with ≥95% compliance with study medication, PARI did provide further albuminuria reduction (
P
=0.04 LS + PARI versus LS + PLAC). Dietary adherence was good as reflected by urinary excretion of 174±64 mmol Na
+
per day in the combined RS groups and 108±61 mmol Na
+
per day in the LS groups (
P
<0.001). In conclusion, moderate dietary sodium restriction substantially reduced residual albuminuria during fixed dose angiotensin–converting enzyme inhibition. The additional effect of PARI was small and nonsignificant. Reduction of residual albuminuria during single-agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied the individual and combined effects of the vitamin D receptor activator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD. In a multicenter, randomized, placebo (PLAC)-controlled, crossover trial, 45 patients with nondiabetic CKD stages 1-3 and albuminuria >300 mg/24 h despite ramipril at 10 mg/d and BP<140/90 mmHg were treated for four 8-week periods with PARI (2 g/d) or PLAC, each combined with a low-sodium (LS) or regular sodium (RS) diet. We analyzed the treatment effect by linear mixed effect models for repeated measurements. In the intention-to-treat analysis, albuminuria (geometric mean) was 1060 (95% confidence interval, 778 to 1443) mg/24 h during RS + PLAC and 990 (95% confidence interval, 755 to 1299) mg/24 h during RS + PARI ( =0.20 versus RS + PLAC). LS + PLAC reduced albuminuria to 717 (95% confidence interval, 512 to 1005) mg/24 h ( <0.001 versus RS + PLAC), and LS + PARI reduced albuminuria to 683 (95% confidence interval, 502 to 929) mg/24 h ( <0.001 versus RS + PLAC). The reduction by PARI beyond the effect of LS was nonsignificant ( =0.60). In the per-protocol analysis restricted to participants with ≥95% compliance with study medication, PARI did provide further albuminuria reduction ( =0.04 LS + PARI versus LS + PLAC). Dietary adherence was good as reflected by urinary excretion of 174±64 mmol Na per day in the combined RS groups and 108±61 mmol Na per day in the LS groups ( <0.001). In conclusion, moderate dietary sodium restriction substantially reduced residual albuminuria during fixed dose angiotensin-converting enzyme inhibition. The additional effect of PARI was small and nonsignificant. Reduction of residual albuminuria during single-agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied the individual and combined effects of the vitamin D receptor activator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD. In a multicenter, randomized, placebo (PLAC)-controlled, crossover trial, 45 patients with nondiabetic CKD stages 1-3 and albuminuria >300 mg/24 h despite ramipril at 10 mg/d and BP<140/90 mmHg were treated for four 8-week periods with PARI (2 μg/d) or PLAC, each combined with a low-sodium (LS) or regular sodium (RS) diet. We analyzed the treatment effect by linear mixed effect models for repeated measurements. In the intention-to-treat analysis, albuminuria (geometric mean) was 1060 (95% confidence interval, 778 to 1443) mg/24 h during RS + PLAC and 990 (95% confidence interval, 755 to 1299) mg/24 h during RS + PARI (P=0.20 versus RS + PLAC). LS + PLAC reduced albuminuria to 717 (95% confidence interval, 512 to 1005) mg/24 h (P<0.001 versus RS + PLAC), and LS + PARI reduced albuminuria to 683 (95% confidence interval, 502 to 929) mg/24 h (P<0.001 versus RS + PLAC). The reduction by PARI beyond the effect of LS was nonsignificant (P=0.60). In the per-protocol analysis restricted to participants with ≥95% compliance with study medication, PARI did provide further albuminuria reduction (P=0.04 LS + PARI versus LS + PLAC). Dietary adherence was good as reflected by urinary excretion of 174±64 mmol Na+ per day in the combined RS groups and 108±61 mmol Na+ per day in the LS groups (P<0.001). In conclusion, moderate dietary sodium restriction substantially reduced residual albuminuria during fixed dose angiotensin-converting enzyme inhibition. The additional effect of PARI was small and nonsignificant. |
Author | Laverman, Gozewijn D. Hemmelder, Marc H. van Breda, G. Fenna Lambers Heerspink, Hiddo J. Vervloet, Marc G. Keyzer, Charlotte A. Janssen, Wilbert M.T. Bakker, Stephan J.L. Kwakernaak, Arjan J. de Borst, Martin H. de Jong, Maarten A. Navis, Gerjan |
Author_xml | – sequence: 1 givenname: Charlotte A. surname: Keyzer fullname: Keyzer, Charlotte A. organization: Department of Internal Medicine, Division of Nephrology and – sequence: 2 givenname: G. Fenna surname: van Breda fullname: van Breda, G. Fenna organization: Department of Nephrology and Institute for Cardiovascular Research, Vrije University Medical Centre, Amsterdam, The Netherlands – sequence: 3 givenname: Marc G. surname: Vervloet fullname: Vervloet, Marc G. organization: Department of Nephrology and Institute for Cardiovascular Research, Vrije University Medical Centre, Amsterdam, The Netherlands – sequence: 4 givenname: Maarten A. surname: de Jong fullname: de Jong, Maarten A. organization: Department of Internal Medicine, Division of Nephrology and – sequence: 5 givenname: Gozewijn D. surname: Laverman fullname: Laverman, Gozewijn D. organization: Department of Internal Medicine, Division of Nephrology, Zorggroep Twente Hospital, Almelo, The Netherlands – sequence: 6 givenname: Marc H. surname: Hemmelder fullname: Hemmelder, Marc H. organization: Department of Internal Medicine, Division of Nephrology, Medical Centre Leeuwarden, Leeuwarden, The Netherlands; and – sequence: 7 givenname: Wilbert M.T. surname: Janssen fullname: Janssen, Wilbert M.T. organization: Department of Internal Medicine, Division of Nephrology, Martini Hospital Groningen, Groningen, The Netherlands – sequence: 8 givenname: Hiddo J. surname: Lambers Heerspink fullname: Lambers Heerspink, Hiddo J. organization: Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands – sequence: 9 givenname: Arjan J. surname: Kwakernaak fullname: Kwakernaak, Arjan J. organization: Department of Internal Medicine, Division of Nephrology and – sequence: 10 givenname: Stephan J.L. surname: Bakker fullname: Bakker, Stephan J.L. organization: Department of Internal Medicine, Division of Nephrology and – sequence: 11 givenname: Gerjan surname: Navis fullname: Navis, Gerjan organization: Department of Internal Medicine, Division of Nephrology and – sequence: 12 givenname: Martin H. surname: de Borst fullname: de Borst, Martin H. organization: Department of Internal Medicine, Division of Nephrology and |
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Copyright | Copyright © 2017 by the American Society of Nephrology. Copyright © 2017 by the American Society of Nephrology 2017 |
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Keywords | randomized-controlled trial albuminuria chronic kidney disease paricalcitol VDRA dietary sodium restriction |
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Snippet | Reduction of residual albuminuria during single–agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied... Reduction of residual albuminuria during single-agent renin-angiotensin-aldosterone blockade is accompanied by improved cardiorenal outcomes in CKD. We studied... |
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SubjectTerms | Albuminuria - etiology Albuminuria - therapy Clinical Research Combined Modality Therapy Cross-Over Studies Diet, Sodium-Restricted Double-Blind Method Ergocalciferols - therapeutic use Humans Receptors, Calcitriol - physiology Renal Insufficiency, Chronic - complications |
Title | Effects of Vitamin D Receptor Activation and Dietary Sodium Restriction on Residual Albuminuria in CKD: The ViRTUE-CKD Trial |
URI | https://www.ncbi.nlm.nih.gov/pubmed/27856633 https://www.proquest.com/docview/1841801101 https://pubmed.ncbi.nlm.nih.gov/PMC5373450 |
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