Bone Turnover and Fracture Risk in Men
Bone Turnover and Fracture Risk in Men
批准号:
7101551
负责人:
Douglas C Bauer
金额:
$27.34万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-04-20 至 2009-01-31
关键词:
anthropometrybiomarkerbone densitybone fractureclinical researchcollagendisease /disorder proneness /riskhealth behaviorhuman datahuman old age (65+)human tissuelongitudinal human studymaleosteoporosispathologic bone resorptionpathologic processpatient oriented researchphoton absorptiometrysex hormones
中文摘要
描述(由申请人提供):尽管人们对男性骨质疏松症的兴趣越来越大,但关于男性骨折的发病机制和危险因素的数据很少,也没有有效的诊断策略。为了解决这些问题,正在进行的男性骨质疏松症研究(mro)已经成功地从6个美国临床中心招募了6000多名65岁以上的男性。核磁共振成像收集了大量人体测量和健康习惯的基线测量数据,以及轴向密度测量和侧位腰骶脊柱x线片。臀部和脊柱的基线QCT,以及性激素的亚组测量。自基线随访以来,随访对象的新骨折发生情况,截至2005年2月,有46例髋部骨折和256例非脊柱骨折被报告并集中裁决。研究参与者将在平均随访4.5年之后,于2005年1月返回临床中心进行脊柱x光检查和密度测量。在这项mri辅助研究中,我们计划使用基线存档的血清和尿液标本,并采用有效的巢式病例队列研究设计,对骨转换与椎体、髋关节和任何非脊柱骨折之间的关系进行前瞻性分析。我们的抽样方案将利用mro中许多现有的测量方法,包括DXA、QCT和性激素水平。此外,我们将分析一种新的无创骨胶原质量生化指标,1型胶原异构化与椎体、髋关节和任何非脊柱骨折之间的关系。对老年妇女的前瞻性研究表明,骨转换和拼贴异构化与骨折风险独立相关,但这种关系尚未在男性中研究。最后,我们计划研究骨转换和骨质流失,并确定哪些人体测量、历史和健康习惯因素与骨转换相关。这些分析将解决关于男性脊柱和非脊柱骨折发病机制的关键问题,并将确定骨转换测量在这一人群中的临床应用。
英文摘要
DESCRIPTION (provided by applicant): Despite growing interest about osteoporosis in men, there is little data regarding the pathogenesis and risk factors for fracture in men, or effective diagnostic strategies in this population. To address these issues, the ongoing Osteoporosis in Men Study (MrOS) has successfully recruited over 6000 men over age 65 from 6 US clinical centers. MrOS collected extensive baseline measurements of anthropometric and health habits, as well as axial densitometry and lateral lumbosacral spine radiographs. Baseline QCT of the hip and spine, and sex hormones have been measured in subsets. Since the baseline visit, subjects have been followed for the occurrence of new fractures, and as of February 2005, 46 hip fractures and a total of 256 non-spine fractures have been reported and centrally adjudicated. Study participants will return to the clinical centers for repeat spine x-rays and densitometry beginning January, 2005, after a mean follow-up of 4.5 years. In this MrOS ancillary study, we plan to use archived serum and urine specimens from baseline and propose a prospective analysis of the relationship between bone turnover and incident vertebral, hip and any non-spine fracture using an efficient nested case-cohort study design. Our sampling scheme will take advantage of the many existing measurements in MrOS, including DXA, QCT and sex hormone levels. In addition, we will analyze the relationship between a new non-invasive biochemical index of bone collagen quality, type 1 collagen isomerization, and incident vertebral, hip and any non-spine fracture. Propective studies among older women suggest that both bone turnover and collage isomerization are independently associated with fracture risk, but such relationships have not been studied in men. Lastly, we plan to study bone turnover and bone loss, and determine which anthropometric, historical and health habit factors are associated with bone turnover. These analyses will address critical questions about the pathogenesis of spine and non-spine fracture in men, and will determine the clinical utility of bone turnover measurements in this population.
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