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DESCRIPTION (provided by applicant): Symptomatic knee osteoarthritis has an incidence of 240/100,000 person years and is one of the most frequent causes of dependency in lower limb tasks, especially in the elderly. It causes 68 million work loss days per year and more than 5% of the annual retirement rate. Osteoarthritis is the most frequent reason for joint replacement at a cost to the community of billions of dollars per year. No effective medical remedies for osteoarthritis currently exist. However, the pharmaceutical industry is attempting to develop drugs that retard progression of OA. If efficacious, these proprietary medications will be expensive to employ in a population in which OA is endemic. Ironically, there is evidence that vitamin D supplementation, a simple non-proprietary intervention, may have efficacy in slowing progression of OA. Even if only modestly effective, it could have considerable impact in terms of reducing the societal burden of OA. Therefore, in the interests of public health, the efficacy of vitamin D supplementation as a disease-modifying treatment for OA needs to be tested in a rigorous clinical trial. Disease-modification trials for knee OA have been difficult due to limitations of the radiographic technique. However, MRI has emerged as a valid, precise and reproducible tool for obtaining volumetric measures of cartilage and joint structures. Our goal is to enroll 140 individuals with symptomatic knee OA into a 2-year randomized placebo controlled clinical trial of vitamin D, 14,000 ID / week. Outcomes will include the WOMAC questionnaire (primary clinical), cartilage volume loss (primary pathological), physical function tests, SF-36 and whole organ knee MRI OA severity scores. Bone density, calcium homeostasis and knee alignment will be tested as intermediary variables. We will test effectiveness of vitamin D using cross-sectional time series regression models with first-order autoregressive disturbance adjusting for informative dropouts.
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Constitutional and metabolic factors associated with the development of Hand OA
  • 批准号:
    8886165
  • 项目类别:
  • 资助金额:
    $77.04万
  • 财政年份:
    2015
  • 负责人:
    Timothy E McAlindon
  • 依托单位:
Constitutional and metabolic factors associated with the development of Hand OA
  • 批准号:
    9043813
  • 项目类别:
  • 资助金额:
    $70.37万
  • 财政年份:
    2015
  • 负责人:
    Timothy E McAlindon
  • 依托单位:
Constitutional and metabolic factors associated with the development of Hand OA
  • 批准号:
    9245652
  • 项目类别:
  • 资助金额:
    $71.51万
  • 财政年份:
    2015
  • 负责人:
    Timothy E McAlindon
  • 依托单位:
Periarticular Bone Density as a Biomarker for Early Knee OA
  • 批准号:
    8715314
  • 项目类别:
  • 资助金额:
    $46.13万
  • 财政年份:
    2012
  • 负责人:
    Timothy E McAlindon
  • 依托单位:
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: