Changes in Bone Quality after Treatment with Etelcalcetide

医学 骨矿物 股骨颈 泌尿科 骨质疏松症 甲状旁腺功能亢进 骨密度 骨重建 骨小梁评分 定量计算机断层扫描 前瞻性队列研究 继发性甲状旁腺功能亢进 活检 甲状旁腺激素 外科 内科学
作者
Pascale Khairallah,Jenna Cherasard,Joshua C. Sung,Sanchita Agarwal,Maria Alejandra Aponte,Mariana Bucovsky,Maria Fusaro,Jeffrey Silberzweig,Gail N. Frumkin,Karim El Hachem,Linda Schulman,Donald J. McMahon,Matthew R. Allen,Corinne E. Metzger,Rachel K. Surowiec,Joseph M. Wallace,Thomas L. Nickolas
出处
期刊:Clinical Journal of The American Society of Nephrology [Lippincott Williams & Wilkins]
卷期号:18 (11): 1456-1465 被引量:24
标识
DOI:10.2215/cjn.0000000000000254
摘要

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 µ m 3 / µ m 2 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
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