Changes in Bone Quality after Treatment with Etelcalcetide

dc.contributor.authorKhairallah, Pascale
dc.contributor.authorCherasard, Jenna
dc.contributor.authorSung, Joshua
dc.contributor.authorAgarwal, Sanchita
dc.contributor.authorAponte, Maria Alejandra
dc.contributor.authorBucovsky, Mariana
dc.contributor.authorFusaro, Maria
dc.contributor.authorSilberzweig, Jeffrey
dc.contributor.authorFrumkin, Gail N.
dc.contributor.authorEl Hachem, Karim
dc.contributor.authorSchulman, Linda
dc.contributor.authorMcMahon, Donald
dc.contributor.authorAllen, Matthew R.
dc.contributor.authorMetzger, Corinne E.
dc.contributor.authorSurowiec, Rachel K.
dc.contributor.authorWallace, Joseph
dc.contributor.authorNickolas, Thomas L.
dc.contributor.departmentAnatomy, Cell Biology and Physiology, School of Medicine
dc.date.accessioned2024-12-12T11:23:55Z
dc.date.available2024-12-12T11:23:55Z
dc.date.issued2023
dc.description.abstractIntroduction: 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.
dc.eprint.versionFinal published version
dc.identifier.citationKhairallah P, Cherasard J, Sung J, et al. Changes in Bone Quality after Treatment with Etelcalcetide. Clin J Am Soc Nephrol. 2023;18(11):1456-1465. doi:10.2215/CJN.0000000000000254
dc.identifier.urihttps://hdl.handle.net/1805/44965
dc.language.isoen_US
dc.publisherWolters Kluwer
dc.relation.isversionof10.2215/CJN.0000000000000254
dc.relation.journalClinical Journal of the American Society of Nephrology
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectPhoton absorptiometry
dc.subjectBone density
dc.subjectPeptides
dc.titleChanges in Bone Quality after Treatment with Etelcalcetide
dc.typeArticle
ul.alternative.fulltexthttps://pmc.ncbi.nlm.nih.gov/articles/PMC10637456/
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