Changes in Bone Quality after Treatment with Etelcalcetide

Author:

Khairallah Pascale1,Cherasard Jenna2ORCID,Sung Joshua3,Agarwal Sanchita3ORCID,Aponte Maria Alejandra3ORCID,Bucovsky Mariana3,Fusaro Maria4,Silberzweig Jeffrey5ORCID,Frumkin Gail N.5,El Hachem Karim5ORCID,Schulman Linda5,McMahon Donald3,Allen Matthew R.6,Metzger Corinne E.6ORCID,Surowiec Rachel K.6ORCID,Wallace Joseph6ORCID,Nickolas Thomas L.3ORCID

Affiliation:

1. Baylor College of Medicine, Houston, Texas

2. City University of New York School of Medicine, New York, New York

3. Columbia University Irving Medical Center, New York, New York

4. CNR, University of Padua, Padua, Italy

5. Rogosin Institute, NewYork-Presbyterian Hospital, New York, New York

6. Indiana University School of Medicine, Indianapolis, Indiana

Abstract

Introduction Secondary hyperparathyroidism is associated with osteoporosis and fractures. Etelcalcetide is an intravenous calcimimetic for the control of hyperparathyroidism in patients on hemodialysis. Effects of etelcalcetide on the skeleton are unknown. Methods In a single-arm, open-label, 36-week prospective trial, we hypothesized that etelcalcetide improves bone quality and strength without damaging bone–tissue quality. Participants were 18 years or older, on hemodialysis ≥1 year, without calcimimetic exposure within 12 weeks of enrollment. We measured pretreatment and post-treatment areal bone mineral density by dual-energy X-ray absorptiometry, central skeleton trabecular microarchitecture by trabecular bone score, and peripheral skeleton volumetric bone density, geometry, microarchitecture, and estimated strength by high-resolution peripheral quantitative computed tomography. Bone–tissue quality was assessed using quadruple-label bone biopsy in a subset of patients. Paired t tests were used in our analysis. Results Twenty-two participants were enrolled; 13 completed follow-up (mean±SD age 51±14 years, 53% male, and 15% White). Five underwent bone biopsy (mean±SD age 52±16 years and 80% female). Over 36 weeks, parathyroid hormone levels declined 67%±9% (P < 0.001); areal bone mineral density at the spine, femoral neck, and total hip increased 3%±1%, 7%±2%, and 3%±1%, respectively (P < 0.05); spine trabecular bone score increased 10%±2% (P < 0.001); and radius stiffness and failure load trended to a 7%±4% (P = 0.05) and 6%±4% increase (P = 0.06), respectively. Bone biopsy demonstrated a decreased bone formation rate (mean difference −25±4 µm3/µm2 per year; P < 0.01). Conclusions Treatment with etelcalcetide for 36 weeks was associated with improvements in central skeleton areal bone mineral density and trabecular quality and lowered bone turnover without affecting bone material properties. Clinical Trial registry name and registration number: The Effect of Etelcalcetide on CKD-MBD (Parsabiv-MBD), NCT03960437

Funder

Amgen

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

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