RISKS AND BENEFITS OF MODERATE ALCOHOL
RISKS AND BENEFITS OF MODERATE ALCOHOL
批准号:
2769195
负责人:
Carol A. Shively
金额:
$25.49万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-09-30 至 2001-08-31
关键词:
Macaca fascicularis aggression alcoholic beverage consumption atherosclerosis atherosclerotic plaque biological models bone density bone metabolism breast neoplasms cancer risk cardiovascular pharmacology dietary lipid disease /disorder proneness /risk estradiol female hormone regulation /control mechanism immunocytochemistry lipid metabolism longitudinal animal study nutrition related tag osteoporosis ovariectomy postmortem preneoplastic state psychological stressor skeletal pharmacology
中文摘要
申请者摘要:虽然过量饮酒的有害影响
饮酒是公认的,适度饮酒的影响
都没有被很好地理解。目前,人们认为中度酒精
消费可降低患冠心病的风险,增加骨骼
密度,具有抗焦虑作用,并促进社会互动。因此,在那里
目前看来,适度饮酒有一些好处。更多
令人担忧的是,适度饮酒可能会增加
乳腺癌的风险,它还可能导致过量饮酒
消费。因此,适度可能存在风险/利益权衡。
饮酒。我们建议评估中度酒精的影响
卵巢切除患者的冠心病、骨质疏松症和乳腺癌风险
雌性食蟹猴(猕猴)是一种有用的动物模型
这些端点中的每一个。这种动物模型将允许随机分配
中度酒精或安慰剂治疗组,从而避免了问题
自我选择的人群和自我报告的固有饮酒量
在人类研究中。拟议中的实验还提供了对
酒精剂量、饮食和其他已知影响疾病终点的变量。
在拟议的实验中,酒精作用的假想机制将
在疾病发展的早期和中期阶段应予以解决
使用人类受试者是不可能的。因此,这种动物的使用
模型消除了等待相对罕见的临床事件发生的需要
以获得可靠的疾病风险衡量标准。我们的长期目标是
通过以下方式确定适度饮酒的相对风险/好处
同时评估冠心病、骨质疏松症和乳腺癌的风险。
英文摘要
APPLICANT'S ABSTRACT: While the deleterious effects of excessive alcohol
consumption are well recognized, the effects of moderate alcohol consumption
are not well understood. Currently, it is thought that moderate alcohol
consumption reduces the risk of coronary heart disease (CHD), increases bone
density, is anxiolytic, and promotes social interaction. Thus, there
currently appears to be some benefit to moderate alcohol consumption. More
worrisome is the possibility that moderate alcohol consumption may increase
breast cancer risk, and that it may also lead to excessive alcohol
consumption. Hence, there may be a risk/benefit trade-off to moderate
alcohol consumption. We propose to assess the effects of moderate alcohol
consumption on CHD, osteoporosis, and breast cancer risk in ovariectomized
female cynomolgus monkeys (Macaca fascicularis), a useful animal model for
each of these endpoints. This animal model will allow randomized assignment
to moderate alcohol or placebo treatment groups, thus avoiding the problems
of self-selected populations and self-reported alcohol consumption inherent
in human studies. The proposed experiment also offers complete control over
alcohol dose, diet, and other variables known to affect disease endpoints.
In the proposed experiment, hypothesized mechanisms of alcohol action will
be addressed during the early and middle stages of disease development which
is not possible using human subjects. Consequently, the use of this animal
model obviates the need to wait for relatively rare clinical events to occur
in order to obtain reliable measures of disease risk. Our long-term goal is
to determine the relative risks/benefits of moderate alcohol consumption by
simultaneous assessment of CHD, osteoporosis, and breast cancer risk.
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