Relaction ship btween occlusion function and bone mineral density of the mancibular condyle

下颌骨髁咬合功能与骨密度的关系

基本信息

  • 批准号:
    08835015
  • 负责人:
  • 金额:
    $ 1.34万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1996
  • 资助国家:
    日本
  • 起止时间:
    1996 至 1997
  • 项目状态:
    已结题

项目摘要

We conducted volunteer studies to assess age-related changes of the mandibular condyle bone mineral density (BMD) and its correlation to the spinal BMD.Quantitative computed tomography was performed on the condyles and spines (L1-3) of 210 healthy volunteers (114 men and 96 women ; aged 5 to 85 years). A separate study was performed on 73 young student subjects (39 men and 34 women, aged 23 to 25 years). The mandibular condyle BMDshowed age-related changes similar to those of the spinal BMD.However, when expressed by T-score, the age-related decrement rates of the mandibular condyle BMD in men and women were lesser in extent compared with those of the spine BMD.Correlations in BMD between the mandibular condyle and spine were high in women (r = 0.78, p<0.0001), but moderate in men (r= 0.58, p< 0.0001). Gender-related difference was more dramatic when assessed in the young student group ; the mandibular condyle and spinal BMDs were highly correlated in women (r=0.82, p<0.0001), but no correlation was found in men (r=0.22). Taken together, these results showed that the mandibular condyle BMD decreased with age in a similar fashion to the lumbar spine BMD,suggesting the same regulatory mechanisms as in the spinal BMD.However, aside from the lumbar spine BMD, additonal undefined factor (s) may be involved in maintaining the mandibular BMD.
为探讨下颌骨髁突骨密度(BMD)的增龄性变化及其与脊柱BMD的相关性,我们对210名健康志愿者(男性114名,女性96名;年龄5 ~ 85岁)的髁突和脊柱(L1-3)进行了定量计算机断层扫描。对73名年轻学生(39名男性和34名女性,年龄在23至25岁之间)进行了一项单独的研究。下颌骨髁状突BMD与脊柱BMD的增龄性变化相似,但以T值表示时,男性和女性下颌骨髁状突BMD的增龄性下降幅度均小于脊柱BMD,女性下颌骨髁状突BMD与脊柱BMD的相关性较高(r = 0.78,p<0.0001),但男性中度(r= 0.58,p< 0.0001)。在青年学生组中,性别相关性差异更为显著;女性下颌骨髁突和脊柱BMD高度相关(r=0.82,p<0.0001),但在男性中未发现相关性(r=0.22)。这些结果表明,下颌骨髁突骨密度随年龄增长而降低的规律与腰椎骨密度的变化规律相似,提示下颌骨密度的变化与腰椎骨密度的变化规律相同,但除腰椎骨密度外,下颌骨密度的维持可能还受到其他因素的影响。

项目成果

期刊论文数量(0)
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专利数量(0)
Nakamura T., et al: "Mandibular condyle BMD measurement by quantitative CT:A genderrelated difference in correlation to the spinal BMD" Bone. 30. 441-445 (1997)
Nakamura T. 等人:“通过定量 CT 测量下颌骨髁 BMD:与脊柱 BMD 相关的性别差异” Bone。
  • DOI:
  • 发表时间:
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    0
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  • 通讯作者:
Nakamura T.et al.: "Mandibular condyle BMD measurement by quantitative CT : A gender-related difference in correlation to the spinal BMD" Bone. 30. 441-445 (1997)
Nakamura T.et al.:“通过定量 CT 测量下颌骨髁 BMD:与脊柱 BMD 相关的性别差异”
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Nakamura T.,et at: "Mandibular condyle BMD measurement by quantitative CT:A gender-related difference in correlation to the spinal BMD" Bone. 30. 441-445 (1997)
Nakamura T. 等人:“通过定量 CT 测量下颌骨髁 BMD:与脊柱 BMD 相关的性别差异” 骨。
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HOTOKEZAKA Yuka其他文献

HOTOKEZAKA Yuka的其他文献

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{{ truncateString('HOTOKEZAKA Yuka', 18)}}的其他基金

the function of cPLA2 in progress and metastasis of tumor
cPLA2在肿瘤进展和转移中的作用
  • 批准号:
    16K11511
  • 财政年份:
    2016
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
dual-function stress response protein
双功能应激反应蛋白
  • 批准号:
    25462921
  • 财政年份:
    2013
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
ER stress pathway in apoptosis of DNA damage
DNA损伤细胞凋亡中的ER应激途径
  • 批准号:
    22592088
  • 财政年份:
    2010
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Identification of a noble ER stress pathway in hypoxia
缺氧中一条高贵的内质网应激途径的鉴定
  • 批准号:
    19592173
  • 财政年份:
    2007
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
A novel apoptotic pathway dependent on ribosome
依赖核糖体的新型凋亡途径
  • 批准号:
    17591967
  • 财政年份:
    2005
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Role of novel protein (p28^<nrp>) induced by ionizing radiation
电离辐射诱导的新型蛋白质 (p28^<nrp>) 的作用
  • 批准号:
    15591999
  • 财政年份:
    2003
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

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