Molecular Studies of Cognition in Chronic Alcoholism

慢性酒精中毒认知的分子研究

基本信息

项目摘要

DESCRIPTION (provided by applicant): Chronic alcoholism is generally regarded as a diverse and heterogeneous disorder that can be dichotomized into cognitively intact and cognitively impaired subgroups. The existence of neuropsychological deficits in chronic alcoholism subjects documented through the use of objective tests has been known since at least the 1960's. The rationale for the present study is to investigate possible molecular underpinnings for the cognitive impairment observed in some chronic alcoholism subjects using 31P magnetic resonance spectroscopic imaging (31P MRSI) and short echo time (TE) 'H MRSI and to correlate regional molecular findings with neuropsychological test scores and voxel molecular levels with voxel tissue composition. We propose to study by in vivo 31P MRSI and short TE 'H MRS molecular alterations in brain membrane phospholipid and high-energy phosphate metabolism, synaptic/transport vesicles and phosphorylated proteins as well as molecular alterations in metabolites with N-acetyl moieties, glutamate-glutamine, and gangliosides (by measuring 'H macromolecule resonances) in a chronic alcoholism cohort (N=80; 40 cognitively unimpaired, 40 cognitively impaired) compared to a normal control group of individuals (N=40) matched for all relevant demographic variables. Cognitive status will be determined on the basis of neuropsychological testing utilizing an Average Impairment Rating, a global index of cognitive function, as the criterion measure. Neuropsychological tests are used to assess abstract reasoning and problem solving, memory, attention, language, spatial abilities, sensory/perceptual, and motor function. The Addiction Severity Index will be used to assess the history and severity of the addiction and to match the two alcoholism cohorts. Given the increased morbidity associated with cognitive impairment in chronic alcoholism subjects, further insights into the molecular basis for the cognitive changes could lead the way to future therapeutic and preventative measures.
描述(由申请人提供):慢性酒精中毒通常被认为是一种多样性和异质性疾病,可分为认知完整和认知受损亚组。至少从20世纪60年代起,人们就知道慢性酒精中毒受试者存在神经心理学缺陷,这是通过客观测试记录下来的。本研究的基本原理是调查可能的分子基础的认知功能障碍中观察到的一些慢性酒精中毒受试者使用31 P磁共振波谱成像(31 P MRSI)和短回波时间(TE)的H MRSI和相关的区域分子结果与神经心理学测试分数和体素分子水平与体素组织成分。我们建议通过在体31 P MRSI和短TE 'H MRS研究脑膜磷脂和高能磷酸盐代谢、突触/转运囊泡和磷酸化蛋白的分子改变,以及N-乙酰基部分、谷氨酸-谷氨酰胺和神经节苷脂代谢产物的分子改变(通过测量'H大分子共振)在慢性酒精中毒队列(N=80; 40名认知未受损,40名认知受损)与所有相关人口统计学变量匹配的个体的正常对照组(N=40)相比。将根据神经心理学测试确定认知状态,使用平均损伤评级(认知功能的全球指数)作为标准测量。神经心理学测试用于评估抽象推理和解决问题、记忆、注意力、语言、空间能力、感觉/知觉和运动功能。成瘾严重程度指数将用于评估成瘾的历史和严重程度,并匹配两个酗酒队列。鉴于慢性酒精中毒受试者中与认知障碍相关的发病率增加,进一步了解认知变化的分子基础可能会为未来的治疗和预防措施开辟道路。

项目成果

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JAY W PETTEGREW其他文献

JAY W PETTEGREW的其他文献

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{{ truncateString('JAY W PETTEGREW', 18)}}的其他基金

PCr-based fMRSI Biomarker for Schizophrenia
基于 PCR 的 fMRSI 精神分裂症生物标志物
  • 批准号:
    8112970
  • 财政年份:
    2011
  • 资助金额:
    $ 5.9万
  • 项目类别:
PCr-based fMRSI Biomarker for Schizophrenia
基于 PCR 的 fMRSI 精神分裂症生物标志物
  • 批准号:
    8307297
  • 财政年份:
    2011
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Studies of Cognition in Chronic Alcoholism
慢性酒精中毒认知的分子研究
  • 批准号:
    7257881
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Studies of Cognition in Chronic Alcoholism
慢性酒精中毒认知的分子研究
  • 批准号:
    7470126
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Studies of Cognition in Chronic Alcoholism
慢性酒精中毒认知的分子研究
  • 批准号:
    6973392
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Studies of Cognition in Chronic Alcoholism
慢性酒精中毒认知的分子研究
  • 批准号:
    7127645
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
HUMAN 31P-1H MRSI AND MRI BRAIN STUDIES OF NICOTINE
人类 31P-1H MRSI 和 MRI 脑部尼古丁研究
  • 批准号:
    7201195
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Studies of Cognition in Chronic Alcoholism
慢性酒精中毒认知的分子研究
  • 批准号:
    7661708
  • 财政年份:
    2005
  • 资助金额:
    $ 5.9万
  • 项目类别:
Human 31P-1H MRSI and MRI Brain Studies of Nicotine
尼古丁的人类 31P-1H MRSI 和 MRI 脑研究
  • 批准号:
    6974795
  • 财政年份:
    2004
  • 资助金额:
    $ 5.9万
  • 项目类别:
Molecular Neurodevelopment: An In Vivo 31P-1H MRSI Study
分子神经发育:体内 31P-1H MRSI 研究
  • 批准号:
    6819710
  • 财政年份:
    2002
  • 资助金额:
    $ 5.9万
  • 项目类别:

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