SLEEP & MENTAL FUNCTION IN THE AGED--ANABOLIC INFLUENCE
睡觉
基本信息
- 批准号:2054751
- 负责人:
- 金额:$ 15.11万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1994
- 资助国家:美国
- 起止时间:1994-09-30 至 1997-08-31
- 项目状态:已结题
- 来源:
- 关键词:attention body composition brain electrical activity clinical chemistry cognition cortisol electrical impedance electroencephalography high performance liquid chromatography hormone regulation /control mechanism human old age (65+) human subject insulinlike growth factor memory neurobiology neuropsychological tests radioimmunoassay sex hormones sleep somatotropin thyroid hormones wakefulness
项目摘要
Older adults complain of memory loss, sleep disorders, frailty, and loss
of lean body mass; age-related decreases in cognitive ability, sleep
quantity and quality, lean body mass (LBM), and anabolic hormones such
as growth hormone (GH) are well-documented. Preliminary evidence from
our database suggests that these changes may be interrelated. We
observed that anabolic status (as indexed by plasma insulin-like growth
factor, or IGF), correlates significantly and positively with better
sleep quality (increased slow wave sleep, decreased wakefulness, and
decreased fragmentation of sleep) and with cognition, particularly memory
and attention in healthy seniors. These preliminary results lead us to
hypothesize that measures of peripheral anabolic status (e.g., sex
hormones, LBM, and particularly GH and IGF) may index central nervous
system (CNS) status in older adults. While GH and IGF are well-known to
index somatic status, their relationship to CNS function has been largely
ignored. There are no such studies in the elderly, who are more likely
to suffer from impaired sleep and cognition and have lower GH and IGF
levels than the young. The proposed study will expand our existing data
base to clarify the relationships among anabolic hormone status, sleep
quality and cognitive function in subsets of controls drawn from our
already-existing samples of healthy older control adults (n=280).
Our hypotheses will be tested in approximately 140 control subjects. To
evaluate anabolic status, blood will be sampled via slow withdrawal pump
across 24-hours. Pooled plasma will be assayed for integrated 24-hour
levels of GH, IGF, cortisol, free testosterone (in men), and thyroid
hormones (T3,T4). Binding proteins for GH and testosterone will also be
measured. Twenty-four hour urinary estrone and estradiol will be
measured in women. Lean body mass will be determined via bio-impedance.
Sleep variables will include stages of sleep and wakefulness, sleep
fragmentation (stage changes) and consolidated (sleep period time), as
well as total EEG delta activity (computer derived). Relationships
between anabolic status and sleep will be identified using multiple
regression techniques. Cognitive tests will include Rivermead Behavioral
Memory, Dementia Rating Scale, a paired associates learning task, a
working memory task (Verbal Sets), a selective attention task (Brief Test
of Attention), and a verbal fluency test. Relationships between anabolic
status and cognition will also be identified using multiple regression
techniques. These studies will identify levels of anabolic hormones that
are associated with high sleep quality and good cognitive function in
senior adults. They will also foster the design of appropriate GH and
IGF intervention studies targeted at improving cognition/sleep in
seniors. Our larger long-term objective is to elucidate the role of GH
and IGF and related hormones in the neurobiology of aging.
老年人抱怨记忆力减退、睡眠障碍、虚弱和丧失
瘦体重;与年龄相关的认知能力下降,睡眠
数量和质量,瘦体重(LBM)和合成代谢激素,
生长激素(GH)是有据可查的。 初步证据来自
我们的数据库显示,这些变化可能是相互关联的。 我们
观察到合成代谢状态(如血浆胰岛素样生长指数
因子,或IGF),与更好的
睡眠质量(增加慢波睡眠,减少觉醒,
睡眠碎片减少)和认知,特别是记忆
注意力集中在健康的老年人身上。 这些初步结果使我们
假设外周合成代谢状态的测量(例如,性
激素,LBM,特别是GH和IGF)可能指示中枢神经系统
老年人的中枢神经系统(CNS)状态。 虽然GH和IGF是众所周知的,
指标躯体状态,它们与CNS功能的关系在很大程度上
忽视 在老年人中没有这样的研究,
睡眠和认知能力受损,GH和IGF水平较低
水平比年轻人。 这项研究将扩大我们现有的数据。
基础,以澄清合成代谢激素状态,睡眠
质量和认知功能的控制子集从我们的
现有的健康老年对照成人样本(n=280)。
我们的假设将在大约140名对照受试者中进行测试。 到
评估合成代谢状态,将通过缓慢抽取泵采集血液样本
在24小时内。 将分析合并血浆的24小时积分
GH、IGF、皮质醇、游离睾酮(男性)和甲状腺激素水平
激素(T3、T4)。 生长激素和睾酮的结合蛋白也将被
测定了 24小时尿雌酮和雌二醇
以女性为衡量标准。 将通过生物阻抗测定瘦体重。
睡眠变量将包括睡眠和清醒的阶段,睡眠
分段(阶段变化)和巩固(睡眠期时间),如
以及总EEG δ活动(计算机导出)。 关系
之间的合成代谢状态和睡眠将确定使用多个
回归技术 认知测试将包括Rivermead行为测试
记忆,痴呆评定量表,配对联想学习任务,
工作记忆任务(Verbal Sets),选择性注意任务(Brief Test
注意力)和语言流畅性测试。 合成代谢之间的关系
还将使用多元回归确定状态和认知
技术. 这些研究将确定合成代谢激素的水平,
与高睡眠质量和良好的认知功能有关,
老年人。 他们还将促进适当的生长激素的设计,
针对改善认知/睡眠的IGF干预研究
前辈 我们更大的长期目标是阐明生长激素的作用,
IGF和相关激素在衰老的神经生物学中的作用。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Patricia N Prinz其他文献
Patricia N Prinz的其他文献
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{{ truncateString('Patricia N Prinz', 18)}}的其他基金
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMER'S DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
2244348 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
SLEEP AND EEG DISCRIMINATION OF DEMENTIA FROM DEPRESSION
睡眠和脑电图区分痴呆和抑郁
- 批准号:
3375435 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
SLEEP AND EEG DISCRIMINATION OF DEMENTIA FROM DEPRESSION
睡眠和脑电图区分痴呆和抑郁
- 批准号:
3375434 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMERS DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
3486483 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMERS DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
3486480 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMERS DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
3486478 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMERS DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
3486481 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
BIOMARKERS FOR EARLY EXPRESSION OF ALZHEIMER'S DISEASE
阿尔茨海默病早期表达的生物标志物
- 批准号:
2392870 - 财政年份:1979
- 资助金额:
$ 15.11万 - 项目类别:
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