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dc.contributor.otherProducción Científica UCH 2023-
dc.contributor.otherUCH. Departamento de Medicina y Cirugía-
dc.creatorD'Marco Gascón, Luis Gerardo-
dc.creatorCheca Ros, Ana-
dc.creatorGamero, Dionilux-
dc.creatorSoto, Carlos-
dc.creatorSalazar, Juan-
dc.creatorNava, Manuel-
dc.creatorBermúdez, Valmore-
dc.creatorDapena, Fabiola-
dc.date.accessioned2024-09-13T16:22:01Z-
dc.date.available2024-09-13T16:22:01Z-
dc.date.issued2023-01-26-
dc.identifier.citationD'Marco, L., Checa-Ros, A., Gamero, D., Soto, C., Salazar, J., Nava, M., Bermúdez, V. & Dapena, F. (2023). Etelcalcetide and Paricalcitol in Chronic Kidney Disease: when the target is inflammation. Healthcare, vol. 11, i. 1, art. 72 (26 dec. 2022). DOI: https://doi.org/10.3390/healthcare11010072es_ES
dc.identifier.issn2227-9032 (Electrónico)-
dc.identifier.urihttp://hdl.handle.net/10637/16164-
dc.descriptionEste artículo pertenece al número especial "Exploring the Link between Cardiorenal and Metabolic Diseases".es_ES
dc.description.abstractIntroduction: Secondary hyperparathyroidism (SHP) is frequent in patients with chronic kidney disease (CKD), particularly in those in dialysis. To treat this complication, the current options available include phosphorus restriction, phosphate binders, the inhibition of parathyroid hormone (PTH) synthesis and secretion by the supplementation of vitamin D or VDR activators, or the use of calcimimetics. Beyond the control of PTH, the effects of the treatment of SHP on other biomarkers of risk may represent an additional benefit for this population. In this study, we explore the benefits of current SHP treatment options, mainly paricalcitol and/or etelcalcetide in the inflammatory state of hemodialysis (HD) patients. Results: the study finally included 142 maintenance HD patients (5 patients were excluded) followed for 6 months (dialysis vintage 26 ± 30 months, mean age 70 years old, 73% women, 81% Spanish white, 47% diabetic). In this case, 52 patients were on regular treatment with paricalcitol for SHP and 25 patients were eligible to initiate etelcalcetide. The baseline serum levels of Ca, P, PTH, Ferritin, albumin, C-reactive protein (CRP), and other variables were measured. We found serum PTH levels showed an improvement after the treatment with etelcalcetide again paricalcitol and no treatment (p < 0.04). Of note, serum levels of CRP were significantly lower in a small group of patients (n = 11) receiving paricalcitol + etelcalcetide compared to paricalcitol or etelcalcetide alone. The proportion of patients with CRP within target ranges (≤1.0 mg/dL) increased significantly after combined treatment (p < 0.001). Conclusions: etelcalcetide proved to safely reduce the PTH levels without significant adverse events and the possibility of a synergic anti-inflammatory effect with the simultaneous use of Paricalcitol in HD patients.es_ES
dc.language.isoenes_ES
dc.publisherMDPIes_ES
dc.relation.ispartofHealthcare, vol. 11, i. 1-
dc.rightshttp://creativecommons.org/licenses/by/4.0/deed.es-
dc.rightsOpen Access-
dc.subjectEnfermedades_ES
dc.subjectDiseaseses_ES
dc.subjectAparato urinarioes_ES
dc.subjectUrinary systemes_ES
dc.subjectParatiroideses_ES
dc.subjectParathyroides_ES
dc.subjectTratamiento médicoes_ES
dc.subjectMedical treatmentes_ES
dc.subjectEtelcalcetidees_ES
dc.subjectParicalcitoles_ES
dc.titleEtelcalcetide and Paricalcitol in Chronic Kidney Disease: when the target is inflammationes_ES
dc.typeArtículoes_ES
dc.identifier.doihttps://doi.org/10.3390/healthcare11010072-
dc.centroUniversidad Cardenal Herrera-CEU-
Aparece en las colecciones: Dpto. Medicina y Cirugía




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