首页> 外文OA文献 >Potential Effects of Alendronate on Fibroblast Growth Factor 23 Levels and Effective Control of Hypercalciuria in an Adult with Jansen's Metaphyseal Chondrodysplasia
【2h】

Potential Effects of Alendronate on Fibroblast Growth Factor 23 Levels and Effective Control of Hypercalciuria in an Adult with Jansen's Metaphyseal Chondrodysplasia

机译:阿仑膦酸钠对成年Jansen干phy端软骨发育不良的成纤维细胞生长因子23水平和高钙尿症的有效控制的潜在作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Context: Jansen's metaphyseal chondrodysplasia (JMC) is a rare autosomal dominant disorder caused by activating mutations in the PTH 1 receptor (PTH1R; PTH/PTHrP receptor), leading to chronic hypercalcemia and hypercalciuria. Hypophosphatemia is also a hallmark of JMC, and recently, increased fibroblast growth factor 23 (FGF23) levels have been reported in this syndrome. Hypercalcemia has been associated with increased cardiovascular risk; however, cardiovascular disease has not been extensively investigated in JMC patients. Objective: The aim of the study was to describe the long-term follow-up of a JMC patient with regard to the management of hypercalciuria, the evaluation of FGF23 levels under bisphosphonate treatment, and the investigation of cardiovascular repercussion of chronic hypercalcemia. Results: The diagnosis of JCM was confirmed by molecular analysis (p.H223R mutation in PTH1R). The patient was followed from 5 to 27 yr of age. Asymptomatic nephrolithiasis was diagnosed at 18 yr of age, prompting pharmacological management of hypercalciuria. Treatment with alendronate reduced hypercalciuria; however, normocalciuria was only obtained with the association of thiazide diuretic. Serum FGF23 levels, measured under alendronate treatment, were repeatedly within the normal range. Subclinical cardiovascular disease was investigated when the patient was 26 yr old, after 19 yr of sustained mild hypercalcemia; carotid and vertebral artery ultrasonography was normal, as well as coronary computed tomography angiography (calcium score = 0). Conclusion: The long-term follow-up of our JMC patient has provided insight on therapeutic strategies to control hypercalciuria, on the potential effects of alendronate on FGF23 levels, and on the lack of detectable cardiovascular disease at young adulthood after prolonged exposure to hypercalcemia. (J Clin Endocrinol Metab 97: 1098-1103, 2012)
机译:背景:Jansen的干dy端软骨发育不良(JMC)是一种罕见的常染色体显性遗传疾病,由PTH 1受体(PTH1R; PTH / PTHrPP受体)的激活突变引起,导致慢性高钙血症和高钙尿症。低磷血症也是JMC的标志,最近,据报道该综合征的成纤维细胞生长因子23(FGF23)水平升高。高钙血症与心血管风险增加有关;然而,尚未在JMC患者中广泛研究心血管疾病。目的:该研究的目的是描述一名JMC患者在高钙尿症的治疗,双膦酸盐治疗下FGF23水平的评估以及对慢性高钙血症的心血管反应的调查方面的长期随访。结果:通过分子分析(PTH1R中的p.H223R突变)证实了JCM的诊断。随访了5至27岁的患者。在18岁时被诊断为无症状肾结石,这促使高钙尿症的药理学治疗。阿仑膦酸盐治疗可减少高钙尿症;然而,降钙尿症仅与噻嗪类利尿剂有关。在阿仑膦酸盐治疗下测得的血清FGF23水平反复在正常范围内。持续轻度高钙血症19年后,患者26岁时进行了亚临床心血管疾病调查;颈动脉和椎动脉超声检查正常,冠状动脉计算机断层造影血管造影正常(钙评分= 0)。结论:我们的JMC患者的长期随访为控制高钙尿症的治疗策略,阿仑膦酸盐对FGF23水平的潜在作用以及长期暴露于高钙血症后年轻成年期缺乏可检测到的心血管疾病提供了见识。 (J Clin Endocrinol Metab 97:1098-1103,2012)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号