Genetic and Neurobiologic Risk Factors for Bipolar Disorder Development

双相情感障碍发展的遗传和神经生物学危险因素

• 批准号: 7201893
• 负责人: KIKI D CHANG
• 金额: $ 58.78万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-02-08 至 2012-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7201893
• 关键词: Adolescence; Adolescent; Adult; Affect; Affective; Age; Alcohol or Other Drugs use; Alleles; Amygdaloid structure; Anxiety Disorders; Attention deficit hyperactivity disorder; Behavior; Behavioral; Biological; Biological Markers; Bipolar Disorder; Blood; Brain; Candidate Disease Gene; Characteristics; Child; Child Support; Childhood; Chronic; Code; Collaborations; Comorbidity; Control Groups; Cross-Sectional Studies; Data; Development; Disease; Disruptive Behavior Disorder; Early identification; Environment; Environmental Risk Factor; Etiology; Evaluation; Event; Factor Va; Family; Family Study; Family history of; First Degree Relative; Foundations; Functional Magnetic Resonance Imaging; Functional disorder; Future; Genes; Genetic; Genetic Polymorphism; Genetic Predisposition to Disease; Genetic Variation; Genotype; Growth Factor; Growth Factor Gene; Health Care Costs; Heritability; Hippocampus (Brain); Human; Hyperactive behavior; Individual; Inherited; Intervention; Interview; Laboratories; Lead; Life; Life Stress; Link; Longitudinal Studies; Major Depressive Disorder; Manic; Mental Depression; Mood Disorders; Moods; Morbidity - disease rate; Neurobiology; Neurotransmitter Receptor; Normal Range; Numbers; Other Finding; Outcome; Parents; Pathogenesis; Patients; Personal Satisfaction; Pharmaceutical Preparations; Population; Population Study; Positioning Attribute; Prevention; Principal Investigator; Psychiatry; Psychosocial Factor; Questionnaires; Range; Rate; Recurrence; Relative (related person); Reporting; Research; Research Personnel; Resources; Retrospective Studies; Risk; Risk Factors; Risk Marker; Sampling; Scanning; Severities; Severity of illness; Siblings; Stress; Structure; Substance abuse problem; Suicide; Suicide attempt; Symptoms; Testing; Twin Multiple Birth; United States National Institutes of Health; Work; accomplished suicide; base; brain-derived growth factor; cohort; design; early onset; endophenotype; executive function; experience; follow-up; genetic analysis; gray matter; mortality; neural circuit; neuroimaging; prevent; proband; programs; psychosocial; receptor density; repository; response; serotonin transporter; size; stressor; suicidal risk; tool; trait

DESCRIPTION (provided by applicant): Bipolar disorder (BD) commonly begins during childhood or adolescence, and those with early onset typically have greater severity of illness and suicidality. Early identification of this disorder is paramount for implementing psychosocial and pharmacologic interventions that might prevent the full disorder. Due to the nonspecificity of early symptoms of BD, such as hyperactivity or depression, biologic markers that signify highest-risk for BD would aid in early identification as well as contribute to the understanding of BD pathogenesis. Children with BD have abnormalities in amygdalar volume and prefrontal-limbic circuits, but it is unclear if these abnormalities are present before the development of BD. Furthermore, polymorphisms of the serotonin transporter (5-HTT) and brain-derived neurotrophic growth factor (BDNF) genes may adversely affect these circuits and be risk factors for BD. In order to study the trait-status of these neurobiological abnormalities and their relationship to genetic polymorphisms, it is necessary to study a high-risk group of children before the development of BD, such as children of parents with BD ("bipolar offspring"). We propose to study 100 offspring from families having one or more parents with BD, comprised of 50 sibling pairs discordant for putative prodromal BD ("Prodromal Siblings"), and 30 singleton healthy controls. Prodromal Siblings will be children with depression and/or ADHD + moderate mood symptoms. All subjects will be carefully assessed by semi-structured interviews, clinician rated scales, and questionnaires relevant to family function and life stressors. Blood will be obtained from parents and siblings for genotyping polymorphism status of the 5-HTT and BNDF genes. Subjects will be scanned on a high-field (3T) magnet, obtaining amygdalar morphometric and functional MRI data in response to two separate affective probes designed to elicit activation of prefrontal-amygdalar circuits. Finally, subjects will be reassessed by interview 3 years after initial evaluation to assess for development of BD. By studying genetic and brain characteristics of high-risk discordant siblings before the development of full BD, we will be able to determine non-environmental risk factors for BD that are not caused by later events, such as substance abuse or recurrent mood episodes. We will also be able to determine possible gene-effects on brain structure and function in this cohort and create a repository for genetic and neuroimaging data that can be used for future longitudinal studies.

描述（由申请人提供）：双相情感障碍（BD）通常始于儿童或青少年时期，早期发作的患者通常具有更严重的疾病和自杀倾向。这种疾病的早期识别是至关重要的实施心理和药物干预，可能会防止全面的障碍。由于BD早期症状的非特异性，如多动症或抑郁症，表明BD最高风险的生物标志物将有助于早期识别以及有助于理解BD发病机制。患有BD的儿童在杏仁核体积和前额叶边缘回路方面存在异常，但尚不清楚这些异常是否在BD发展之前存在。此外，5-羟色胺转运体（5-HTT）和脑源性神经营养生长因子（BDNF）基因的多态性可能会对这些回路产生不利影响，并成为BD的危险因素。为了研究这些神经生物学异常的特征状态及其与遗传多态性的关系，有必要研究BD发生前的高危儿童群体，例如BD父母的子女（“双相后代”）。我们建议研究100个后代的家庭有一个或多个父母与BD，包括50个兄弟姐妹对不一致的推定前驱BD（“前驱Sixomal”），和30个单例健康对照。前驱症状发作将是患有抑郁症和/或ADHD +中度情绪症状的儿童。所有受试者将通过半结构化访谈、临床医生评定量表和与家庭功能和生活压力相关的问卷进行仔细评估。将从父母和兄弟姐妹处采集血液，用于5-HTT和BNDF基因的基因分型多态性状态。受试者将在高场（3 T）磁体上进行扫描，获得杏仁核形态测量和功能MRI数据，以响应两个单独的情感探针，旨在引起前额叶-杏仁核回路的激活。最后，将在初始评价后3年通过访谈对受试者进行重新评估，以评估BD的发展。通过在完全BD发生之前研究高风险不一致兄弟姐妹的遗传和大脑特征，我们将能够确定BD的非环境风险因素，这些因素不是由后来的事件（例如药物滥用或复发性情绪发作）引起的。我们还将能够确定该队列中基因对大脑结构和功能的可能影响，并创建一个遗传和神经成像数据库，可用于未来的纵向研究。