SCHIZOTYPAL DISORDER: BIOL BASIS USING NEUROPSYCHOLOGICAL & MRI METHODS
SCHIZOTYPAL DISORDER: BIOL BASIS USING NEUROPSYCHOLOGICAL & MRI METHODS
批准号:
6123559
负责人:
Robert W McCarley
金额:
$1.96万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-09-30 至 1999-07-31
中文摘要
分裂型人格障碍(SPD)是一种内在的兴趣,
人格障碍 理论上和实验上也是
作为精神分裂症谱的可能组成部分,
疾病:最近的遗传流行病学研究提供了强有力的
SPD和精神分裂症(SZ)之间存在联系的证据,从而
强调SPD研究策略的实用性,
检查SZ频谱异常而不使其复杂化,以及
SZ中经常存在混杂变量,如慢性疾病,
长期用药和长期住院治疗。 SPD受试者因此
我们相信,这可能会提供一个更不混淆和更清晰的观点,
至少一些“原发性”频谱异常和/或
比SZ受试者更脆弱。 因此,本申请
建议扩展我们的多学科研究计划,
SZ对SPD研究的生物学基础。 我们认为这种专注
关于SPD的研究是特别及时的,因为SPD的许多生物
相关因素仍未得到研究。 我们开发了临床,
神经心理学的 事件相关电位(ERP)和磁
共振成像(NM)方法,与我们的
我们认为,概念和理论方法已被证明是
在SZ研究方面非常有成果。 我们认为,这种方法将SPD
证明同样富有成效,因为我们自己和其他人的数据强烈
这表明,至少有一些功能,临床和大脑
SZ的异常也可能存在于该谱系障碍中。
我们新的初步和多学科SPD数据提供了我们
相信是惊人的和令人兴奋的证据一致,
深圳出现异常,我们认为这可能是
主要分布在颞叶和前额叶 皮质和
他们的联合系统。 SPD受试者表现出:1)相对特异性
语言学习的缺陷(主要是语义聚类)
加州语言学习测试(CVLT)和威斯康星州的趋势
卡片分类任务(WCST)异常; 2)P300事件相关
潜在的整体振幅降低和左<右颞
区域电压不对称(P300测量处理异常
刺激);和3)NM证据左侧体积减少
海马体/杏仁核前部和邻近的
颞角 本申请旨在确认并延长
这些发现是在一项对25名男性和25名女性右撇子进行的为期5年的研究中得出的
患有DSM-III-R SPD诊断的个体和50名年龄、性别和父母
所有SES匹配的正常对照。 这种应用的可行性
雄心勃勃的技术和理论目标,我们相信,
凭借我们在深圳的丰富经验,
research.
英文摘要
Schizotypal personality disorder (SPD) is of intrinsic interest as
a personality disorder. It is also theoretically and experimentally
important as a likely component of the schizophrenia spectrum
disorders: recent genetic-epidemiologic studies have provided strong
evidence of a link between SPD and schizophrenia (SZ), thereby
emphasizing the utility of the strategy of studying SPD in order to
examine the SZ spectrum abnormalities without the complicating, and
often confounding variables present in SZ, such as chronic illness,
chronic medication, and chronic hospitalization. SPD subjects thus
may, we believe, provide a more non-confounded and clearer view of at
least some of the "primary" spectrum abnormalities and/or markers of
vulnerability than SZ subjects. Accordingly, this application
proposes to extend our multidisciplinary research program for probing
the biological bases of SZ to the study of SPD. We think this focus
on SPD is particularly timely because many of SPD's biologic
correlates remain unexamined. We have developed clinical,
neuropsychological. event-related potential (ERP) and magnetic
resonance imaging (NM) methodologies which, together with our
conceptual and theoretical approach, have, we believe, proven to be
very fruitful in SZ studies. We believe this approach to SPD will
prove equally fruitful, since our own and others' data strongly
suggest that at least some of the functional, clinical and brain
abnormalities of SZ may also be present in this spectrum disorder.
Our new preliminary and multidisciplinary SPD data provide what we
believe is striking and exciting evidence for congruence with the
abnormalities present in SZ, and which we think are likely to be
primarily referable to temporal lobe, to prefrontal. cortex and to
their joint systems. SPD subjects show: 1) a relatively specific
deficit in verbal learning (primarily semantic clustering) on the
California Verbal Learning Test (CVLT) and a trend toward Wisconsin
Card Sorting Task (WCST) abnormalities; 2) P300 event-related
potential overall amplitude reduction and a left < right temporal
region voltage asymmetry (the P300 measures processing of unusual
stimuli); and 3) NM evidence for left-lateralized reduction in volume
of the anterior hippocampus/amygdala and enlargement of adjacent
temporal horn. This application proposes to confirm and to extend
these findings in a 5-year study of 25 male and 25 female right-handed
individuals with DSM-III-R SPD diagnoses and 50 age-, sex-, and parent
al SES-matched normal controls. The feasibility of this application's
ambitious technical and theoretical goals, is, we believe, validated
by our extensive experience with the methodology and approach in SZ
research.
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会议论文
Basal Forebrain Cellular Mechanisms of Cortical Activation
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批准号:8242210
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项目类别:
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资助金额:$0.0万
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财政年份:2011
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负责人:Robert W McCarley
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依托单位:
Basal Forebrain Cellular Mechanisms of Cortical Activation
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批准号:8413399
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项目类别:
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资助金额:$0.0万
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财政年份:2011
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负责人:Robert W McCarley
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依托单位:
Basal Forebrain Cellular Mechanisms of Cortical Activation
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批准号:8598052
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项目类别:
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资助金额:$0.0万
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财政年份:2011
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负责人:Robert W McCarley
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依托单位:
PROJECT 3: ELECTROPHYSIOLOGICAL & GRAY MATTER MARKERS & PREDICTORS OF PROGRESSION
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批准号:8136028
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项目类别:
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资助金额:$12.53万
-
财政年份:2010
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负责人:Robert W McCarley
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依托单位:
CORE 1: OPERATIONS AND CLINICAL ASSESSMENT
-
批准号:8136030
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项目类别:
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资助金额:$24.09万
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财政年份:2010
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负责人:Robert W McCarley
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依托单位:
Project 3 HMS - VA sub
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批准号:9304306
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项目类别:
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资助金额:$31.21万
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财政年份:2010
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负责人:Robert W McCarley
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依托单位:
Project 3 HMS - VA sub
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批准号:8794523
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项目类别:
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资助金额:$33.06万
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财政年份:2010
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负责人:Robert W McCarley
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依托单位:
MRI Anatomy of Schizophrenia
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批准号:8586849
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项目类别:
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资助金额:$0.0万
-
财政年份:2009
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负责人:Robert W McCarley
-
依托单位:
MRI Anatomy of Schizophrenia
-
批准号:7906935
-
项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Robert W McCarley
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依托单位:
Vulnerability to Progression Schizophrenia
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批准号:7929313
-
项目类别:
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资助金额:$30.5万
-
财政年份:2009
-
负责人:Robert W McCarley
-
依托单位:
MRI Anatomy of Schizophrenia
-
批准号:8195955
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2009
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负责人:Robert W McCarley
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依托单位:
Neurophysiological Studies of Schizophrenia
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批准号:7809830
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项目类别:
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资助金额:$42.0万
-
财政年份:2009
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负责人:Robert W McCarley
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依托单位:
MRI Anatomy of Schizophrenia
-
批准号:7792783
-
项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Robert W McCarley
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依托单位:
MRI Anatomy of Schizophrenia
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批准号:8390426
-
项目类别:
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资助金额:$0.0万
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财政年份:2009
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负责人:Robert W McCarley
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依托单位:
CLINICAL STATUS AND BRAIN FUNCTIONING IN ADOLESCENTS AND ADULTS
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批准号:7718948
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项目类别:
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资助金额:$0.09万
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财政年份:2008
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负责人:Robert W McCarley
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依托单位:
Vulnerability to Progression Schizophrenia
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批准号:7920849
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项目类别:
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资助金额:$191.29万
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财政年份:2007
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负责人:Robert W McCarley
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依托单位:
Vulnerability to Progression Schizophrenia
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批准号:8136034
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项目类别:
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资助金额:$183.86万
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财政年份:2007
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负责人:Robert W McCarley
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依托单位:
Vulnerability to Progression Schizophrenia
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批准号:7498415
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项目类别:
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资助金额:$194.2万
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财政年份:2007
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负责人:Robert W McCarley
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依托单位:
CORE 1: OPERATIONS AND CLINICAL ASSESSMENT
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批准号:7279685
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项目类别:
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资助金额:$10.79万
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财政年份:2007
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负责人:Robert W McCarley
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依托单位:
Vulnerability to Progression Schizophrenia
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批准号:7684159
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项目类别:
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资助金额:$194.2万
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财政年份:2007
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负责人:Robert W McCarley
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依托单位:
海外基金