Olfactory Function in Schizophrenia: A Lifespan Analysis
Olfactory Function in Schizophrenia: A Lifespan Analysis
批准号:
8059714
负责人:
PAUL J MOBERG
金额:
$47.24万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-12-07 至 2013-02-28
关键词:
Acoustic RhinometryAdolescentAdultAffectAnteriorBehavioralBiologicalBrainBrain regionCerebrumComplexDevelopmentDevelopmental ProcessDiseaseDoseDysmorphologyFaceFamily memberFirst Degree RelativeFunctional disorderHereditary DiseaseImageImpairmentLifeLongevityMagnetic Resonance ImagingMapsMeasurementMeasuresMediatingMethodsModelingMorphogenesisMorphologyNasal cavityNerve DegenerationNeurobiologyNoseOlfactory CortexOlfactory EpitheliumOlfactory tractOralOral cavityPalatePatientsPerformancePeripheralPharmaceutical PreparationsPhotographyProcessPsychophysicsPsychophysiologyPsychotic DisordersRelative (related person)ResolutionRiskSamplingSchizophreniaSmell PerceptionStructureSymptomsSystemTemporal LobeThree-dimensional analysisWorkbasebehavior testcraniofacialcraniumdigital imagingendophenotypefetalfollow-upfunctional disabilityhealthy volunteerhigh riskinsightintimate behaviorneurodevelopmentneurogenesisneuron developmentnovelolfactory bulbprobandsynaptogenesis
中文摘要
描述(由申请人提供):精神分裂症目前被认为是一种复杂的遗传疾病,可能在生命的早期就改变了神经元的发育,对决定易感性很重要。神经发生和神经发育发生在成人嗅觉上皮中,嗅觉系统的探针可能为这种疾病中神经发育改变的神经生物学基础提供见解。事实上,对精神分裂症患者的研究已经证明嗅觉系统存在严重的行为、结构和功能障碍。我们和其他人的研究表明,大脑嗅觉区域受到神经退行性和遗传介导的神经发育过程的影响。这个项目代表了从生命周期的角度来检查这些化学感觉障碍的基础的唯一系统的努力。迄今为止,我们的努力已经确定:1)精神分裂症患者一生中普遍存在稳定的嗅觉缺陷;2)未见明显用药效果;3)患者一级亲属存在类似的心理生理、结构和功能缺陷;4)鼻、腭体积等面部基础结构异常。在胎儿早期,大脑形态发生与颅面形态发生在胚胎学上密切相关。因此,颅面和大脑畸形的定量分析以及嗅觉系统的详细心理物理评估可能提供有关精神分裂症发育起源的重要信息。在这个应用中,我们建议从早期神经发育的角度对嗅觉系统的结构和功能异常进行深入评估。我们将研究40名精神分裂症患者、40名健康的一级家庭成员、40名不相关的健康对照者和40名出现精神病早期症状的高危受试者。新的方法将被用于检查神经发育对患者化学感觉功能障碍的贡献,包括鼻/腭体积,结构MRI和面部形态学的定量检查。这些损伤的预测效用将通过检查精神病发展风险增加的受试者来探讨。我们的工作模型是,嗅觉障碍反映了神经发生和突触形成的发育障碍过程,这些措施可能代表了精神分裂症潜在的胚胎发育异常的特定标记。精神分裂症目前被认为是一种复杂的遗传疾病,具有大脑结构和功能的早期发育异常,是决定疾病易感性的重要因素。这项研究将检查精神分裂症患者嗅觉能力的变化,同时对鼻腔和口腔进行详细测量,并绘制面部和大脑结构和地形图。我们认为,在患者中发现的强烈嗅觉损伤反映了早期发育过程的紊乱,对这些功能和结构的分析可能为精神分裂症的发育起源提供重要信息。
英文摘要
DESCRIPTION (provided by applicant): Schizophrenia is currently thought to be a complex genetic disorder, with altered neuronal development, perhaps very early in life, important in determining vulnerability. Neurogenesis and neurodevelopment occur in the adult olfactory epithelium, and probes of the olfactory system may provide insights into the neuro-biological basis of altered neurodevelopment in this disorder. Indeed, studies of patients with schizophrenia have demonstrated robust behavioral, structural, and functional impairments of the olfactory system. Our work, along with others', has indicated that olfactory brain regions are affected by both neurodegenerative and genetically-mediated neurodevelopmental processes. This project represents the only systematic effort to examine the underpinnings of these chemosensory impairments from a life-span perspective. To date, our efforts have established that: 1)pervasive and stable olfactory deficits exist across the lifespan in schizophrenia; 2)no significant medication effects are seen; 3)similar psychophysical, structural, and functional deficits exist in first-degree relatives of patients; and 4)underlying facial structures such as nasal and palate volumes are abnormal. Over early fetal life, cerebral morphogenesis proceeds in embryological intimacy with craniofacial morphogenesis. As such, quantitative analysis of craniofacial and cerebral dysmorphology along with a detailed psychophysical assessment of the olfactory system may provide important information concerning the developmental origins of schizophrenia. In this application, we propose an in-depth assessment of the structural and functional abnormalities of the olfactory system from an early neurodevelopmental perspective. We will study 40 schizophrenia patients, 40 otherwise healthy first-degree family members, 40 unrelated healthy controls, and 40 high-risk subjects who present with early symptoms of psychosis. New methods will be utilized to examine the neurodevelopmental contributions to chemosensory dysfunction in patients including nasal/palate volume, structural MRI, and quantitative examination of facial morphology. Predictive utility of these impairments will be probed by examining subjects at increased risk for the development of psychosis. Our working model is that olfactory impairment reflects developmentally disturbed processes of neurogenesis and synapse formation and that these measures may represent specific markers of embryological dysmorphogenesis underlying schizophrenia. Schizophrenia is currently thought to be a complex genetic disorder, with early developmental abnormalities in brain structure and function, being important in determining vulnerability to illness. This study will examine changes in smell abilities in schizophrenia along with detailed measurements of the nasal and oral cavities and mapping of facial and brain structure and topography. We believe that robust olfactory impairment seen in patients reflects a disturbance of an early developmental process and that the analysis of these functions and structures may provide important information concerning the developmental origins of schizophrenia.
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