TOURETTE'S SYNDROME & RELATED DISORDERS: STUDY OF HIGH DENSITY FAMILIES
TOURETTE'S SYNDROME & RELATED DISORDERS: STUDY OF HIGH DENSITY FAMILIES
批准号:
6301836
负责人:
DAVID L PAULS
金额:
$20.59万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-03-05 至 2001-02-28
关键词:
Tourette's syndrome adolescence (12-20) adult human (21+) behavioral /social science research tag child psychology clinical research cognition disease /disorder onset family genetics gene environment interaction gene expression genetic susceptibility human subject interview linkage mapping longitudinal human study mental disorder diagnosis middle childhood (6-11) obsessive compulsive disorder pathologic process perinatal phenotype preschool child (1-5) psychometrics
中文摘要
该项目的长期目标是获得更好的
了解遗传和环境因素在其中的作用
发展性神经精神障碍的研究
抽动秽语综合征(TS)。来的研究
在过去的十年里,我们在认识上取得了一些显著的进展,
TS和相关条件:1)有一个更大范围的表型
包括慢性抽动和强迫症在内的TS表达); 2)TS和相关
疾病比以前想象的要普遍得多; 3)
该综合征似乎是作为常染色体显性性状传播的。
此外,TS和相关疾病的患病率及其
对那些受折磨的人的衰弱影响使这些条件成为主要的
公共卫生问题。了解TS的遗传学和相关的
行为将直接受益于患者关注
在他们的家庭中复发;最终,澄清遗传学
这些情况可以阐明其发病机理。我们工作的结果
提示:1)TS在家庭内传播的模式
符合常染色体显性遗传; 2)有一个
TS与强迫症的病因关系; 3)家庭环境是
与其他相关行为的表达相关联;以及4)
具体的环境因素可能与
病在本项目中,我们的目标是具体研究以下方面的作用:
基因和环境在TS的表达和相关行为中的作用。
我们计划对未受影响的幼儿进行一项前瞻性研究,
确定家庭进行连锁研究,招募约60名
在这些高风险地区,
密度家族这些数据将使我们有可能描述更多
完全理解TS和其他性状之间的关系。
这项研究还将有助于确定重要的“非遗传”因素,
TS和相关疾病的发作和可变表达。因此,在本发明中,
这项前瞻性研究样本的数据将有助于确定具体的
与变量表达相关的遗传和环境因素
的TS。此外,这些家庭中的所有成年人和青少年将被
重新评价以更新诊断信息并收集持续的
表型数据的测量,将被纳入随后的
数据分析旨在更好地描述遗传表型,
这些家庭。三种类型的信息将从所有
家庭成员:1)通过直接结构化收集的诊断数据
评估; 2)神经心理学数据,侧重于以下领域
注意力、抑制力和强迫性; 3)家庭的测量
环境和家庭功能。这些新数据将被纳入
表型分析旨在更好地了解遗传TS
表型以及连锁分析,旨在检查假说,
一个假设的基因或该表型的基因与
已知的多态标记。
英文摘要
The long term objective of this project is to obtain a better
understanding of the role of genetic and environmental factors in
developmental neuropsychiatric disorders through the study of the
specific disorder, Gilles de la Tourette's syndrome (TS). Research over
the last decade has led to several notable advances in our understanding
of TS and related conditions: 1) there is a greater range of phenotypic
expression for TS including chronic tics and OCD); 2) TS and related
disorders are much more common than had previously been thought; and 3)
the syndrome appears to be transmitted as an autosomal dominant trait.
Furthermore,the prevalence of TS and associated illnesses and their
debilitating effects on those afflicted makes these conditions a major
public health problem. Understanding the genetics of TS and associated
behaviors will be of direct benefit to patients concerned about
recurrence in their families; ultimately, clarifying the genetics of
these conditions may elucidate their pathogenesis. Findings from our work
suggest: 1) that TS is transmitted within families in a pattern
consistent with autosomal dominant inheritance; 2) that there is an
etiologic relationship between TS and OCD; 3) that family environment is
associated with the expression of other associated behaviors; and 4) that
specific environmental factors may be related to the severity of the
illness. In this Project, we aim to examine specifically the role of
genes and environment in the expression of TS and associated behaviors.
We plan to conduct a prospective study of young unaffected children in
families ascertained for linkage studies, enrolling approximately 60
additional children at risk to TS and associated conditions in these high
density families. These data will make it possible to characterize more
completely the nature of the relationship between TS and other traits.
This study will also help to identify "non-genetic" factors important for
the onset and variable expressions of TS and related disorders. Thus,
data from this prospective study sample will help identify specific
genetic and environmental factors associated with the variable expression
of TS. In addition, all adults and adolescents in these families will be
re-evaluated to update diagnostic information and to collect continuous
measures of phenotypic data that will be incorporated into subsequent
data analyses designed to delineate better the inherited phenotype in
these families. Three types of information will be obtained from all
family members: 1) diagnostic data collected via direct structured
assessments; 2) neuropsychological data focusing on the domains of
attention, inhibition, and compulsivity; and 3) measures of home
environment and family functioning. These new data will be incorporated
into phenotypic analyses designed to understand better the inherited TS
phenotype as well as linkage analyses designed to examine hypotheses of
genetic linkage of a hypothetical gene or genes for this phenotype to
known polymorphic makers.
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会议论文
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资助金额:$0.0万
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资助金额:$11.91万
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批准号:7877706
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资助金额:$0.0万
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项目类别:
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资助金额:$4.93万
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OC Foundation Genetics Collaborative Conference
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批准号:6887981
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项目类别:
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资助金额:$11.53万
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OC Foundation Genetics Collaborative Conference
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批准号:6950704
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资助金额:$11.77万
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财政年份:2004
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依托单位:
OC Foundation Genetics Collaborative Conference
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批准号:7455778
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项目类别:
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资助金额:$11.8万
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财政年份:2004
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负责人:DAVID L PAULS
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依托单位:
TOURETTE'S SYNDROME & RELATED DISORDERS: STUDY OF HIGH DENSITY FAMILIES
-
批准号:6579412
-
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资助金额:$20.59万
-
财政年份:2002
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负责人:DAVID L PAULS
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依托单位:
FAMILY GENETICS OF AUTISM AND ASPERGER DISORDER
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资助金额:$17.24万
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财政年份:2001
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资助金额:$18.66万
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财政年份:2000
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负责人:DAVID L PAULS
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依托单位:
A GENETIC LINKAGE STUDY OF GTS
-
批准号:6529548
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