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DESCRIPTION (provided by applicant): Vitamin K has an emerging role in bone health. However, little is known about the vitamin K metabolism, particularly in regards to aging, and maintenance of bone mass. Such limited understanding about vitamin K metabolism currently impedes the ability to establish dietary recommendations for vitamin K, and interpret the results from recent clinical trials on vitamin K supplementation and bone health currently being conducted in primarily women of a narrow age group. The proposed study will be the first to assess the role of dietary and non-dietary factors that influence the response to measures of vitamin K status and bone turnover to vitamin K depletion and repletion in younger and older men and women. This study will also compare the absorption efficiency of vitamin K, relative to current vitamin K status. Men and women [21 younger (21-40y) and 21 older (60-80y)] will participate in a 65-d metabolic study, with a 5-d run-in period, followed by a 30 d dietary vitamin K restriction period (10 mu/ g/d), and ending with a 30 d dietary vitamin K supplementation period (500 mu g/d). Serial measurements of markers of vitamin K status (plasma phylloquinone, urinary Gla, serum %ucOC and plasma PIVKA-II) and bone turnover (serum osteocalcin and NTx) will provide information on their response to dietary manipulation of vitamin K for both age groups under identical controlled dietary conditions. A stable isotope tracer (deuterium-labeled vitamin K in collards) will be used to compare the absorption of vitamin K during a vitamin K-deplete state (21 d of dietary vitamin K depletion) to that of a vitamin K-replete state (21 d of dietary vitamin K repletion). Because vitamin K is transported in triglyceride-rich lipoproteins, which may vary among individuals due to differences in adiposity, measurement of body composition by DXA and plasma lipids (total and individual lipoproteins) will provide insight into the role of lipids in absorption and transport of vitamin K. The findings of the proposed study are critical for the interpretation of the epidemiologic and clinical data used to determine optimal intakes at which vitamin K may have a protective role in bone health.
期刊论文(6)
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DOI: 10.1002/jbmr.289
发表时间: 2011-05
期刊: JOURNAL OF BONE AND MINERAL RESEARCH
影响因子: 6.2
作者: [Zwart, Sara R., Booth, Sarah L., Peterson, James W., Wang, Zuwei, Smith, Scott M.]
通讯作者: Smith, Scott M.
Age group and sex do not influence responses of vitamin K biomarkers to changes in dietary vitamin K.
年龄组和性别不会影响维生素 K 生物标志物对膳食维生素 K 变化的反应。
DOI: 10.3945/jn.111.154807
发表时间: 2012
期刊: The Journal of nutrition
影响因子: --
作者: [Truong,JenniferT, Fu,Xueyan, Saltzman,Edward, AlRajabi,Ala, Dallal,GerardE, Gundberg,CarenM, Booth,SarahL]
通讯作者: Booth,SarahL
α-Tocopherol disappearance rates from plasma depend on lipid concentrations: studies using deuterium-labeled collard greens in younger and older adults.
血浆中α-生育酚的消失率取决于脂质浓度:在年轻人和老年人中使用氘标记的羽衣甘蓝进行的研究。
DOI: 10.3945/ajcn.114.100966
发表时间: 2015
期刊: The American journal of clinical nutrition
影响因子: --
作者: [Traber,MaretG, Leonard,ScottW, Bobe,Gerd, Fu,Xueyan, Saltzman,Edward, Grusak,MichaelA, Booth,SarahL]
通讯作者: Booth,SarahL
Effects of Vitamin K on Lower-extremity Function in Adults with Osteoarthritis: a Randomized Controlled Pilot Trial
  • 批准号:
    10708005
  • 项目类别:
  • 资助金额:
    $27.14万
  • 财政年份:
    2022
  • 负责人:
    SARAH Louise BOOTH
  • 依托单位:
Effects of Vitamin K on Lower-extremity Function in Adults with Osteoarthritis: a Randomized Controlled Pilot Trial
  • 批准号:
    10516989
  • 项目类别:
  • 资助金额:
    $28.36万
  • 财政年份:
    2022
  • 负责人:
    SARAH Louise BOOTH
  • 依托单位:
Significance of UBIAD1 in Regulation of HMG CoA Reductase Degradation, Mevalonate Metabolism, and Menaquinone-4 Synthesis
  • 批准号:
    10474511
  • 项目类别:
  • 资助金额:
    $47.53万
  • 财政年份:
    2021
  • 负责人:
    SARAH Louise BOOTH
  • 依托单位:
Significance of UBIAD1 in Regulation of HMG CoA Reductase Degradation, Mevalonate Metabolism, and Menaquinone-4 Synthesis
  • 批准号:
    10626858
  • 项目类别:
  • 资助金额:
    $47.29万
  • 财政年份:
    2021
  • 负责人:
    SARAH Louise BOOTH
  • 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: