Paricalcitol and Extended-Release Calcifediol for Treatment of Secondary Hyperparathyroidism in Non-Dialysis Chronic Kidney Disease: Results From a Network Meta-Analysis

Author:

Franchi Matteo1ORCID,Gunnarsson Joel2ORCID,Gonzales-Parra Emilio3,Ferreira Anibal4,Ström Oskar25,Corrao Giovanni1ORCID

Affiliation:

1. Department of Statistics and Quantitative Methods, Bicocca University Milan , 20126 Milan , Italy

2. Quantify Research , 112 21 Stockholm , Sweden

3. Nephrology and Hypertension Clinic, Fundación Jiménez Díaz , 28040 Madrid , Spain

4. NOVA Medical School, Faculty of Medical Sciences, Nova University of Lisbon , 1169-056 Lisbon , Portugal

5. Department of Medicine, Huddinge, Karolinska Institutet , 141 57 Stockholm , Sweden

Abstract

Abstract Context Secondary hyperparathyroidism (SHPT) is a complication of chronic kidney disease (CKD) affecting mineral and bone metabolism and characterized by excessive parathyroid hormone (PTH) production and parathyroid hyperplasia. Objective The objective of this analysis was to compare the efficacy and adverse effects of extended-release calcifediol (ERC) and paricalcitol (PCT) by assessing their effect on the biomarkers PTH, calcium, and phosphate in patients with non-dialysis CKD (ND-CKD). Methods A systematic literature research was performed in PubMed to identify randomized control trials (RCTs). Quality assessment was done with the GRADE method. The effects of ERC vs PCT were compared using random effects in a frequentist setting. Results Nine RCTs comprising 1426 patients were included in the analyses. The analyses were performed on 2 overlapping networks, due to nonreporting of outcomes in some of the included studies. No head-to-head trials were identified. No statistically significant differences in PTH reduction were found between PCT and ERC. Treatment with PCT showed statistically significant increases in calcium compared with ERC (0.2 mg/dL increase; 95% CI, −0.37 to −0.05 mg/dL). No differences in effects on phosphate were observed. Conclusion This network meta-analysis showed that ERC is comparable in lowering PTH levels vs PCT. ERC displayed avoidance of potentially clinically relevant increases in serum calcium, offering an effective and well-tolerated treatment option for the management of SHPT in patients with ND-CKD.

Funder

Vifor Pharma

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference28 articles.

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2. FGF23 And the PTH response to paricalcitol in chronic kidney disease;D'Arrigo;Eur J Clin Invest,2020

3. Changes in fibroblast growth factor 23 during treatment of secondary hyperparathyroidism with alfacalcidol or paricalcitol;Hansen;Nephrol Dial Transplant,2012

4. Paricalcitol and endothelial function in chronic kidney disease trial;Zoccali;Hypertension,2014

5. Vitamin D therapy and cardiac structure and function in patients with chronic kidney disease: the PRIMO randomized controlled trial;Thadhani;JAMA,2012

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