International Cohort Collection for Bipolar Disorder
International Cohort Collection for Bipolar Disorder
批准号:
7911781
负责人:
PAMELA SKLAR
金额:
$210.13万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-30 至 2013-05-31
关键词:
AddressAffectiveAgeAlgorithmsArchitectureArtsAutoimmune DiseasesBiologyBipolar DisorderBlood specimenBostonCaliforniaCardiovascular DiseasesCatalogingCatalogsCollectionComorbidityComplexCopy Number PolymorphismDNADataData SetDetectionDevelopmentDiabetes MellitusDiagnosisDiagnosticDiseaseDissectionEuropeEuropeanEvaluationFundingGenderGenesGeneticGenetic DeterminismGenetic Predisposition to DiseaseGenomicsGenotypeHealth systemHealthcare SystemsHuman GeneticsIndividualInstitutesInternationalInterviewInvestmentsLos AngelesMalignant NeoplasmsMedicalMedical RecordsMental disordersMethodsModelingNatural Language ProcessingNon-Insulin-Dependent Diabetes MellitusPatientsPhenotypePopulationPopulation GeneticsPredispositionPsychotic DisordersResearchResearch PersonnelResourcesRestRiskRisk FactorsSamplingSchizophreniaScienceScreening procedureSiteSpecificityStatistical MethodsSusceptibility GeneSwedenTechnologyTimeUniversitiesValidationVariantcase controlcohortcostdesigndisability burdenearly onset disordereconomic costgenetic analysisgenetic resourcegenetic variantgenome wide association studygenotyping technologyinstrumentnovelphenomicspublic health prioritiesresponsesample collectionsuccesstreatment as usualvalidation studies
中文摘要
描述(由申请人提供):双相情感障碍(BPD)是一个主要的公共卫生优先事项,负责残疾,个人痛苦和经济成本的巨大负担。遗传易感性是BPD最强的已知危险因素,特异性易感基因的鉴定将对促进我们对BPD生物学的理解和揭示新的治疗靶点产生巨大影响。迄今为止,BPD遗传研究的有限成功是由于其复杂的遗传结构,可能包括许多影响不大的基因座。群体遗传学和基因分型技术的进步最近使像BPD这样的复杂疾病的遗传解剖成为一个可行的项目。全基因组关联研究(GWAS)已经确定了一系列其他常见医学疾病的易感性变异。然而,很明显,要取得这样的成功,BPD需要比目前可用的样本大得多的样本。本申请是国际研究者联盟对RFA-MH-08-130:“双相情感障碍和精神分裂症的基因组分析:美国和地球仪的大型队列研究”的回应。“拟议的双相情感障碍国际队列收集(ICCBD)将通过建立一个独特的大样本收集和来自BPD个体的数据来解决对大规模DNA和数据资源的需求。本申请的具体目的是:1)确定并收集大量BPD病例(N = 9000)和未受影响的对照组(N = 9000)在两个美国研究中心的5年内(波士顿和洛杉矶)使用新的高通量表型分型方法;和2)构建用于遗传研究的协调数据源,其将来自美国病例对照样品的表型数据与平行的,从英国和瑞典获得的单独资助的欧洲病例对照样本(10,000例病例和10,000例对照)。这些资源的单独资助的基因分型和遗传分析将充分表征完整样本中的常见多态性和拷贝数变异,以检测新的风险变异,并尝试复制最引人注目的先前发现。这一资源,通过现有的样本增强,将为发现BPD的遗传决定因素提供前所未有的平台。双相情感障碍(BPD)是一个主要的公共卫生优先事项,负责残疾,个人痛苦和经济成本的巨大负担。遗传易感性是BPD最强的已知危险因素,特异性易感基因的鉴定将对促进我们对BPD生物学的理解和揭示新的治疗靶点产生巨大影响。迄今为止,BPD遗传研究的有限成功是由于其复杂的遗传结构,可能包括许多影响不大的基因座。拟议的双相情感障碍国际队列收集(ICCBD)将通过建立一个独特的大样本收集和来自BPD个体的数据来解决对大规模DNA和数据资源的需求。
英文摘要
DESCRIPTION (provided by applicant): Bipolar disorder (BPD) is a major public health priority, responsible for a vast burden of disability, personal suffering, and economic cost. Genetic susceptibility is the strongest known risk factor for BPD, and the identification of specific susceptibility genes would have enormous implications for advancing our understanding of the biology of BPD and revealing novel targets for treatment. The limited success to date of genetic studies of BPD has been due to its complex genetic architecture that likely includes many contributing loci of modest effect. Advances in population genetics and genotyping technologies have recently made the genetic dissection of complex disorders like BPD a feasible project. Genomewide association studies (GWAS) have already identified susceptibility variants underlying a range of other common medical disorders. However, it has become clear that much larger samples than are currently available will be needed to achieve such successes for BPD. This application is a response by an international consortium of investigators to RFA-MH-08-130: "Genomic Parsing of Bipolar Disorder and Schizophrenia: Studies of Large Cohorts in the U.S. and Across the Globe." The proposed International Cohort Collection for Bipolar Disorder (ICCBD) will address the need for large-scale DNA and data resources by establishing a uniquely large collection of samples and data from individuals with BPD. The specific aims of this application are 1) to ascertain and collect a large cohort of BPD cases (N = 9000) and unaffected controls (N = 9000) over five years at two U.S. sites (Boston and Los Angeles) using novel high-throughput phenotyping methods; and 2) to construct a harmonized data resource for genetic studies combining phenotypic data from the U.S. case-control sample with a parallel, separately funded European case-control sample (10,000 cases and 10,000 controls) obtained from the UK and Sweden. Separately funded genotyping and genetic analyses of these resources will fully characterize common polymorphisms and copy number variants in the full sample to detect novel risk variants and attempt replication of the most compelling prior findings. This resource, augmented by existing samples, will provide an unprecedented platform for the discovery of the genetic determinants of BPD. Bipolar disorder (BPD) is a major public health priority, responsible for a vast burden of disability, personal suffering, and economic cost. Genetic susceptibility is the strongest known risk factor for BPD, and the identification of specific susceptibility genes would have enormous implications for advancing our understanding of the biology of BPD and revealing novel targets for treatment. The limited success to date of genetic studies of BPD has been due to its complex genetic architecture that likely includes many contributing loci of modest effect. The proposed International Cohort Collection for Bipolar Disorder (ICCBD) will address the need for large-scale DNA and data resources by establishing a uniquely large collection of samples and data from individuals with BPD.
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会议论文
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海外基金