Searching for Endophenotypes of Bipolar Disorder

寻找双相情感障碍的内表型

基本信息

批准号：
8670769
负责人：
JAIR C SOARES
金额：
$ 57.68万
依托单位：
UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-09-12 至 2017-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8670769
关键词：
Address Affective Amygdaloid structure Anisotropy Anterior Atrophic Behavioral Bipolar Disorder Brain Brain Pathology Brain imaging Brain region Case-Control Studies Controlled Study Data Diffusion Magnetic Resonance Imaging Dizygotic Twins Emotional Enrollment Epidemiologic Studies Etiology Female Functional disorder Gender Genes Genetic Genetic Predisposition to Disease Health Heritability Hippocampus (Brain)Impairment Lateral Magnetic Resonance Imaging Major Mental Illness Measures Medial Memory Moods N-acetylaspartate Neurocognitive Pathology Patients Performance Population Prefrontal Cortex Risk Role Scanning Siblings Spectrum Analysis Symptoms Temporal Lobe cognitive neuroscience density design endophenotype executive function gray matter indexing male neurocognitive test neuroimaging proband public health relevance tool white matter

项目摘要

DESCRIPTION (provided by applicant): The causes of bipolar disorder (BD) are unknown, but neuroimaging studies have identified abnormalities in fronto-limbic brain (FLB) regions, which parallel findings of neurocognitive impairment. There is growing evidence to support abnormalities in sub- regions of the prefrontal cortex (PFC) and medial temporal lobe. In particular, the most consistent findings implicate the dorsolateral PFC, anterior cingulate, amygdala and hippocampus. These brain regions are interlinked and abnormalities could result in emotional instability, behavioral activation and other symptoms seen in BD patients. The primary aim of our study is to determine the extent to which FLB pathology in BD is attributable to genetic effects. The relationship between FLB abnormalities and BD will be addressed in a control study of same-gender sibling pairs discordant for BD type I. We will enroll 60 male and female sibling pairs discordant for BD and 60 matched controls, in a 3 group design (BD probands, unaffected siblings and healthy controls). Each subject will undergo brain magnetic resonance imaging (MRI), spectroscopy (MRS), diffusion tensor imaging (DTI) scans and neurocognitive testing. We will examine the relationship between BD and FLB abnormalities, neurocognitive function and genetic vulnerability. We will use state-of-the art tools from brain imaging and cognitive neuroscience to study the contribution of familial factors in determining FLB impairment in sibling pairs discordant for BD. The study will further elucidate the pathophysiology of BD and the role of genetic factors in the genesis of such abnormalities. If our hypotheses are confirmed, this will indicate that FLB abnormalities in BD are heritable and could be viable endophenotypes in the search for the specific genes involved. PUBLIC HEALTH RELEVANCE: Bipolar disorder is a very prevalent psychiatric illness and a major health problem worldwide. This study will examine the role of heritability on key brain abnormalities involved in causation of bipolar disorder (BD). If our hypotheses are confirmed, this will indicate that abnormalities in fronto-limbic brain regions in patients with BD are heritable and could be utilized as "endophenotypes" to guide future research on the specific genes involved.

描述（由申请人提供）：双相情感障碍（BD）的原因是未知的，但是神经影像学研究已经确定了额 - 膜脑（FLB）区域的异常，这与神经认知障碍的发现相似。越来越多的证据支持前额叶皮层（PFC）和内侧颞叶的子区域异常。特别是，最一致的发现暗示了背外侧PFC，前扣带回，杏仁核和海马。这些大脑区域是相互联系的，异常可能导致情绪不稳定，行为激活和BD患者的其他症状。我们研究的主要目的是确定BD中FLB病理的程度归因于遗传效应。 FLB异常与BD之间的关系将在BD类型I的同性同学对的控制研究中得到解决。我们将在BD的60个男性和女性兄弟姐妹对中，在BD和60个匹配的对照组中，在3组设计中（BD探测器，未受影响的兄弟姐妹和健康的对照组）。每个受试者将接受大脑磁共振成像（MRI），光谱法（MRS），扩散张量成像（DTI）扫描和神经认知测试。我们将研究BD和FLB异常，神经认知功能和遗传脆弱性之间的关系。我们将使用从脑成像和认知神经科学中的最先进的工具来研究家族因素在确定BD兄弟姐妹对中的FLB损害方面的贡献。该研究将进一步阐明BD的病理生理学以及遗传因素在此类异常起源中的作用。如果我们的假设得到证实，这将表明BD中的FLB异常是可遗传的，并且在寻找所涉及的特定基因时可能是可行的内型型。公共卫生相关性：双相情感障碍是一种非常普遍的精神病和全球重大健康问题。这项研究将研究遗传力对躁郁症因果关系（BD）涉及的关键大脑异常的作用。如果我们的假设得到证实，这将表明BD患者额膜脑区域的异常是遗传的，并且可以用作“内型型”来指导对所涉及的特定基因的未来研究。