{"title":"La inhibición del RANKL en el tratamiento de la osteoporosis: denosumab","authors":"Luis Pérez Edo","doi":"10.1016/j.semreu.2010.11.003","DOIUrl":null,"url":null,"abstract":"<div><p>Denosumab is a human monoclonal antibody IgG2 against RANKL that prevents the coupling of the RANKL with its receptor RANK on osteoclast and osteoclast precursors, which is essential for the formation, activity and survival of osteoclasts, disabling the bone resorption. The action of the Denosumab on bone remodeling is rapid, sustained and reversible. The recommended dose is of 60<!--> <!-->mg for subcutaneous route every 6 months. The reduction of the relative risk of new vertebral fractures is of 68% (2.3% vs 7.2%, p<!--> <!--><<!--> <!-->0.0001), 20% (6.5% vs 8.0%) in non vertebral fractures and 40% (0.7% vs 1.2%) in the case of the of hip. At 36 months the lumbar bone mineral density increased 9.2% and 6.2% in the total hip, in comparison with the placebo. It is a safe drug with a low incident of cutaneous effects. The frequency and route of administration can be useful to improve the compliance of the osteoporosis treatment.</p></div>","PeriodicalId":101152,"journal":{"name":"Seminarios de la Fundación Espa?ola de Reumatología","volume":"12 1","pages":"Pages 27-30"},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.semreu.2010.11.003","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminarios de la Fundación Espa?ola de Reumatología","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S157735661100011X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Denosumab is a human monoclonal antibody IgG2 against RANKL that prevents the coupling of the RANKL with its receptor RANK on osteoclast and osteoclast precursors, which is essential for the formation, activity and survival of osteoclasts, disabling the bone resorption. The action of the Denosumab on bone remodeling is rapid, sustained and reversible. The recommended dose is of 60 mg for subcutaneous route every 6 months. The reduction of the relative risk of new vertebral fractures is of 68% (2.3% vs 7.2%, p < 0.0001), 20% (6.5% vs 8.0%) in non vertebral fractures and 40% (0.7% vs 1.2%) in the case of the of hip. At 36 months the lumbar bone mineral density increased 9.2% and 6.2% in the total hip, in comparison with the placebo. It is a safe drug with a low incident of cutaneous effects. The frequency and route of administration can be useful to improve the compliance of the osteoporosis treatment.
Denosumab是一种针对RANKL的人单克隆抗体IgG2,可阻止RANKL与其受体RANK在破骨细胞和破骨细胞前体上的偶联,这对于破骨细胞的形成、活性和存活至关重要,从而使骨吸收丧失。Denosumab对骨重塑的作用是快速、持续和可逆的。推荐剂量为每6个月皮下注射60毫克。新椎体骨折的相对风险降低68% (2.3% vs 7.2%, p <0.0001),非椎体骨折为20% (6.5% vs 8.0%),髋部骨折为40% (0.7% vs 1.2%)。在36个月时,与安慰剂组相比,腰椎骨矿物质密度增加了9.2%,全髋增加了6.2%。它是一种安全的药物,皮肤效应发生率低。给药的频率和途径有助于提高骨质疏松症治疗的依从性。