MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
批准号:
2825574
负责人:
Laura Kristin NEWBY
金额:
$12.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-04-01 至 2004-03-31
关键词:
blood coagulation cardiovascular disorder prevention clinical research clinical trials combination chemotherapy coronary disorder estrogens female hormone therapy human subject human therapy evaluation information systems meta analysis postmenopause progesterone progestins smoking vascular endothelium women's health
中文摘要
非对立雌激素联合雌孕激素治疗卵巢癌的临床研究
冠心病事件的一级预防和二级预防
更年期女性在美国越来越受欢迎。对此的支持
实践在很大程度上是基于减少的流行病学关联
在人群中死亡和非致命性心肌梗死的风险
服用雌激素的女性中,大多数以前没有冠状动脉疾病
原因多种多样。雌激素中添加孕激素的作用
都没有得到很好的研究。因为潜在的公共卫生影响来自
激素替代疗法对绝经后妇女的治疗作用
预防冠状动脉疾病事件是巨大的,它是
当务之急是建立知识基金,支持和帮助
临床试验数据的解释,以帮助建立小组
或者应该向哪些群体推荐治疗以及应该在什么时候
已启动。为实现这些目标,我们建议:
1.使用血管反应性的无创性测量,以量化
补肾活血方对血管内皮功能的影响
绝经后合并黄体酮和黄体酮的妇女的孕酮和雌激素治疗
没有冠状动脉疾病。
2.研究绝经后妇女不同组合的治疗效果
激素治疗对凝血系统的影响。
3.利用积累的临床试验数据库进行临床研究
影响激素替代疗法疗效的因素
用于绝经后冠心病的二级预防
女人。
拟议工作将提供对该机制的进一步了解
雌激素对内皮功能的作用(这被认为是
雌激素有益作用的主要机制)和
雌激素替代疗法中添加孕激素的效果。
英文摘要
The use of unopposed estrogen of combined estrogen/progestin therapy for
primary and secondary prevention of coronary disease events in post-
menopausal women is gaining favor in the United States. Support for this
practice is based largely on epidemiological association of a reduction
in the risk of death and non-fatal myocardial infarction in populations
of women mostly without prior coronary artery disease who took estrogen
for a variety of reasons. The effects of adding a progestin to estrogen
are less well studied. Because the potential public health impact from
treatment of post-menopausal women with hormone replacement therapy for
prevention of coronary artery disease events is enormous, it is
imperative to establish a fund of knowledge that supports and aids in
the interpretation of clinical trials data to help establish the group
or groups for whom treatment should be recommended and when it should be
initiated. To accomplish these goals we propose:
1. Using non-invasive measurement of vascular reactivity, to quantify
the effect on vascular endothelial function of the addition of
progesterone to estrogen therapy in post-menopausal women with and
without coronary artery disease.
2. To study the effect of various combinations of post-menopausal
hormone therapy on the coagulation system.
3. To use accumulated clinical trials databases to study clinical
factors that may influence the efficacy of hormone replacement therapy
for secondary prevention of coronary artery disease in post-menopausal
women.
The propose work will provide additional understanding of the mechanism
of estrogen action on endothelial function (which is postulated to be
the major mechanism of the beneficial effects of estrogen) and the
effects of adding progestins to estrogen replacement regimens.
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会议论文
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批准号:10021553
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资助金额:$146.05万
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财政年份:2019
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批准号:10259720
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资助金额:$86.62万
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PREVENTABLE Biorepository and Laboratory
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财政年份:2016
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负责人:Laura Kristin NEWBY
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ACT-NOW Data Sustainability - ECHO Administrative Supplement
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批准号:10628516
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资助金额:$9.99万
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财政年份:2016
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依托单位:
ECHO Administrative Supplement - Neonatal Opioid Trials
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资助金额:$199.97万
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财政年份:2016
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依托单位:
ECHO Coordinating Center
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批准号:10261552
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项目类别:
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资助金额:$1750.29万
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财政年份:2016
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依托单位:
ECHO Steering Committee Support and Communications Component
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资助金额:$382.96万
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ECHO Steering Committee Support and Communications Component
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批准号:10015361
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资助金额:$328.42万
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财政年份:2016
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依托单位:
ECHO Administrative Supplement - Neonatal Opioid Trials
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批准号:10459783
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资助金额:$150.0万
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财政年份:2016
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依托单位:
MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
-
批准号:6388523
-
项目类别:
-
资助金额:$12.78万
-
财政年份:1999
-
负责人:Laura Kristin NEWBY
-
依托单位:
MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
-
批准号:6638089
-
项目类别:
-
资助金额:$12.97万
-
财政年份:1999
-
负责人:Laura Kristin NEWBY
-
依托单位:
MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
-
批准号:6182895
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项目类别:
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资助金额:$10.95万
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财政年份:1999
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负责人:Laura Kristin NEWBY
-
依托单位:
MECHANISMS OF HORMONE THERAPY IN POSTMENOPAUSAL WOMEN
-
批准号:6536548
-
项目类别:
-
资助金额:$12.87万
-
财政年份:1999
-
负责人:Laura Kristin NEWBY
-
依托单位: