Fusaro Maria, Aghi Andrea, Marino Carmela, Mallamaci Francesca, Plebani Mario, Zaninotto Martina, Grano Maria, Colucci Silvia, Gallieni Maurizio, Nickolas Thomas L, Giannini Sandro, Sella Stefania, Simioni Paolo, Bazzocchi Alberto, Guglielmi Giuseppe, Taddei Fulvia, Schileo Enrico, Versace Maria Carmela, Tripepi Giovanni
National Research Council (CNR), Institute of Clinical Physiology (IFC), 56124 Pisa, Italy.
Department of Medicine, University of Padova, 35128 Padova, Italy.
J Clin Med. 2024 Oct 2;13(19):5888. doi: 10.3390/jcm13195888.
Chronic kidney disease and mineral bone disorders (CKD-MBD) are frequently associated with an increased risk of both vascular calcifications (VCs) and bone fractures (BFs). The complex pathogenesis of VCs and BFs involves various factors such as calcium overload, phosphate imbalance, and secondary hyperparathyroidism. Key players, such as the vitamin K-dependent proteins (VKDPs) matrix Gla protein (MGP) and bone Gla protein (BGP), have pivotal roles both for VCs and BFs. The VIKI study highlighted that hemodialysis patients treated with calcimimetics had higher levels of total BGP and MGP compared to those untreated, suggesting a potential protective effect of these drugs on BFs and VCs beyond the beneficial effect of reducing PTH levels. ETERNITY-ITA is a multi-center, comparative effectiveness, observational, longitudinal study that will enroll 160 hemodialysis patients (80 patients treated with Etelcalcetide and 80 age- and sex-matched patients treated with calcitriol or vitamin D analogs). Nephrologists will tailor the target dose of Etelcalcetide on an individual level to achieve the KDIGO PTH target. In the Etelcalcetide-treated group, the addition of calcitriol will be allowed when required by clinical practice (for correction of hypocalcemia). This study will evaluate the real-world effect of Etelcalcetide on VKDP levels, such as BGP and MGP, at 3, 9, and 18 months from baseline. The resulting preservation of vascular and bone health will be assessed for the first time by examining aortic and iliac artery calcifications and vertebral fractures, respectively.
慢性肾脏病和矿物质骨病(CKD-MBD)常与血管钙化(VC)和骨折(BF)风险增加相关。VC和BF的复杂发病机制涉及多种因素,如钙超载、磷失衡和继发性甲状旁腺功能亢进。关键因子,如维生素K依赖蛋白(VKDPs)、基质Gla蛋白(MGP)和骨Gla蛋白(BGP),在VC和BF中均起关键作用。VIKI研究强调,与未接受治疗的血液透析患者相比,接受拟钙剂治疗的患者总BGP和MGP水平更高,这表明这些药物除了具有降低甲状旁腺激素水平的有益作用外,对BF和VC可能还有潜在的保护作用。ETERNITY-ITA是一项多中心、比较有效性、观察性纵向研究,将纳入160例血液透析患者(80例接受依特卡肽治疗,80例年龄和性别匹配的患者接受骨化三醇或维生素D类似物治疗)。肾病学家将根据个体情况调整依特卡肽的目标剂量,以实现KDIGO甲状旁腺激素目标。在依特卡肽治疗组中,根据临床实践需要(用于纠正低钙血症)可加用骨化三醇。本研究将评估依特卡肽在基线后3个月、9个月和18个月时对VKDP水平(如BGP和MGP)的实际影响。首次分别通过检查主动脉和髂动脉钙化以及椎体骨折来评估由此产生的血管和骨骼健康保护情况。