Renal Osteodystrophy: A Fresh Approach

肾性骨营养不良：一种新方法

• 批准号: 9096749
• 负责人: Hartmut H Malluche
• 金额: $ 64.17万
• 依托单位: UNIVERSITY OF KENTUCKY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-03-01 至 2020-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9096749
• 关键词: Address; Affect; Age; Alendronate; Alkaline Phosphatase; Aorta; Biochemical; Blood; Blood Tests; Bone Density; Bone Diseases; Bone Pain; Bone Resorption; Categories; Chronic; Chronic Kidney Failure; Clinical; Control Groups; Coronary; Data; Dialysis procedure; Disease; End stage renal failure; Endocrine System Diseases; Enrollment; Event; FDA approved; Forteo; Fracture; Funding; Gender; General Population; Goals; Health; Heart Arrest; Heart Valves; Hip Fractures; Histologic; Individual; Kidney Diseases; Link; Malignant Neoplasms; Measures; Metabolic Diseases; Minerals; Mission; Monitor; Morbidity - disease rate; Myocardial Infarction; N-terminal; Operative Surgical Procedures; Osteogenesis; Osteoporosis; PTH gene; Pathway interactions; Patients; Physicians; Postmenopausal Osteoporosis; Procollagen; Quality of life; Race; Randomized; Randomized Controlled Trials; Renal Osteodystrophy; Renal function; Research; Risk; Safety; Science; Serum; Severities; Staging; Stroke; Telephone; Testing; Therapeutic; Time; Treatment Cost; Treatment Protocols; United States; United States National Institutes of Health; Vascular calcification; Visit; X-Ray Computed Tomography; arm; base; bone; bone loss; bone mass; bone turnover; calcification; cardiovascular risk factor; cinacalcet; clinical practice; coronary artery calcification; cost; detector; fibroblast growth factor 23; high risk; improved; individualized medicine; mortality; novel; response; socioeconomics; tartrate-resistant acid phosphatase; treatment group

 DESCRIPTION (provided by applicant): Renal osteodystrophy (ROD) represents the bone histologic abnormalities resulting from loss of renal function. It starts early during the loss of kidney function and is seen in virtually all chronic end stage kidney disease patients on dialysis (CKD-5D). A major component of ROD is bone loss leading to CKD-associated osteoporosis. Debilitating hip fractures occur in patients with CKD at a rate 4.4 times higher than in the general population, with associated high costs, morbidity and an annual mortality of 64%. CKD osteoporosis is distinctly different from post-menopausal osteoporosis. Presently, no uniformly accepted CKD osteoporosis treatment protocol exists because of challenges related to racially specific bone turnover states. Therefore, most physicians are reluctant to treat this disorder despite the profound impact on health and quality of life, and its association with vascular calcifications. These vascular calcifications confer an increased risk for cardiovascular events which are the major cause of the over 20% annual mortality rate in CKD-5D patients. The goal of the proposed controlled randomized study is to test the concept that CKD osteoporosis can be successfully treated when treatment is individualized by patients' turnover status. The study will demonstrate that reversal of bone loss can be achieved by increasing bone formation in low turnover patients, and by reducing bone resorption in normal or high turnover patients. A second aim of this study is to provide new information whether these treatments will also retard progression of vascular calcifications. Blood tests measuring FGF23, indicators of Wnt pathway activity, bone resorption and formation will be followed to understand potential mechanisms and to evaluate their usefulness for prediction of changes in bone mass and vascular calcifications. CKD-5D patients with established osteoporosis will be enrolled into one of two treatment arms based on bone turnover status. Each arm will be adaptively randomized by race, age and gender into treatment or control groups. In the low turnover arm, teriparatide combined with cinacalcet will be given, and in the normal or high turnover arm, alendronate will be administered. Bone mineral density will be measured at baseline and after one year of treatment by quantitative computed tomography. Calcifications of the coronaries, aorta and heart valves will also be measured at the same times by multi-detector computed tomography. If this proof-of-concept study is successful, it will offer a heretofore unavailable treatment for osteoporosis i CKD-5D patients thus changing the prevailing clinical practice paradigm. This will provide immediate benefit to CKD patients by reducing fracture risk, bone pain, and cardiovascular risk, while greatly improving their quality of life. These improvements will also convey major socioeconomic benefits by decreasing the high associated treatment costs. The proposed study is highly relevant to the NIDDK's mission of disseminating science-based information to improve the health and quality of life for patients with endocrine, metabolic and kidney diseases.

 描述(申请人提供)：肾性骨营养不良(Rod)代表肾功能丧失引起的骨组织学异常。它开始于肾功能丧失的早期，几乎见于所有慢性终末期肾病患者的透析(CKD-5D)。Rod的一个主要成分是骨丢失，导致CKD相关的骨质疏松。衰弱的髋部骨折在慢性肾脏病患者中的发生率是普通人群的4.4倍，相关的高成本、发病率和年死亡率为%。CKD骨质疏松症与绝经后骨质疏松症有明显不同。目前，还没有统一接受的CKD骨质疏松症治疗方案，因为存在与种族特定的骨转换状态相关的挑战。因此，大多数医生不愿治疗这种疾病，尽管它对健康和生活质量产生了深远的影响，并与血管钙化有关。这些血管钙化增加了心血管事件的风险，心血管事件是CKD-5D患者年死亡率超过20%的主要原因。这项拟议的对照随机研究的目的是测试这样一个概念，即当治疗根据患者的周转状况进行个体化治疗时，CKD骨质疏松症可以成功地治疗。这项研究将证明，通过增加低周转率患者的骨形成，以及通过减少正常或高周转率患者的骨吸收，可以逆转骨丢失。这项研究的第二个目的是提供新的信息，看看这些治疗是否也会延缓血管钙化的进展。随后将进行血液测试，测量FGF23、Wnt途径活性、骨吸收和形成的指标，以了解潜在的机制，并评估它们对预测骨量和血管钙化变化的有效性。确诊为骨质疏松症的CKD-5D患者将根据骨转换状况被纳入两个治疗分支之一。每组受试者将根据种族、年龄和性别自适应地随机分为治疗组或对照组。低周转组给予特派拉替联用桂皮钙片，正常周转组或高周转组给予阿仑磷酸钠。骨密度将在基线和治疗一年后通过定量计算机断层扫描进行测量。冠状动脉、主动脉和心脏瓣膜的钙化也将通过多探测器计算机断层扫描同时测量。如果这项概念验证研究成功，它将为骨质疏松症I CKD-5D患者提供一种迄今为止不可用的治疗方法，从而改变流行的临床实践范式。这将通过降低骨折风险、骨痛和心血管风险为CKD患者带来直接好处，同时极大地提高他们的生活质量。这些改进还将通过降低相关的高额治疗成本来传递重大的社会经济效益。这项拟议的研究与NIDDK的使命高度相关，即传播基于科学的信息，以改善内分泌、代谢和肾脏疾病患者的健康和生活质量。