Imaging Biomarkers of Social Cognition and Pharmacologic Target Engagement in ASD

自闭症谱系障碍 (ASD) 中社会认知和药理学目标参与的成像生物标志物

• 批准号: 9453091
• 负责人: David M. Cochran
• 金额: $ 18.88万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-09-15 至 2021-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9453091
• 关键词: Adolescent; Adult; Affect; Age; Aminobutyric Acids; Anterior; Anticonvulsants; Area; Award; Behavior; Biochemical; Biological Markers; Biometry; Brain; Brain imaging; Caring; Child; Clinical; Clinical Research; Clinical Trials; Cognitive deficits; Complex; Data; Data Analyses; Data Set; Development; Disease; Dose; Economics; Emotional; Employment Opportunities; Epilepsy; Female; Foundations; Functional disorder; Funding; Future; Gender; Glutamates; Glutamine; Goals; Imaging Techniques; Imaging technology; Impairment; Individual; Intervention; Investigation; Knowledge; Lead; Life; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Measurement; Measures; Medical; Mental disorders; Mentored Patient-Oriented Research Career Development Award; Mentors; Mentorship; Methodology; Methods; Molecular Target; Monitor; National Institute of Mental Health; Neurobiology; Neurodevelopmental Disorder; Neurotransmitters; Occipital lobe; Outcome; Pathway interactions; Pattern; Pharmaceutical Preparations; Pharmacology; Physicians; Prevalence; Productivity; Protons; Public Health; Quality of life; Research; Research Methodology; Research Personnel; Role; Scientist; Social Functioning; Social Interaction; Speed; Stimulus; Techniques; Technology; Time; Training; Translations; Work; autism spectrum disorder; career; cingulate cortex; experience; gabapentin; gamma-Aminobutyric Acid; imaging biomarker; imaging modality; improved; interest; life time cost; male; mouse model; neural correlate; neuroimaging; neurotransmission; new therapeutic target; novel; novel therapeutic intervention; predicting response; predictive of treatment response; response; social; social cognition; social communication; symposium; targeted agent; treatment response

Project Summary/Abstract This Mentored Patient-Oriented Research Career Development Award will develop the candidate into an independent physician-scientist with expertise in neuroimaging investigations of biomarkers of social cognition that may predict treatment response and facilitate identification of novel therapeutic targets and approaches for individuals with autism spectrum disorders (ASD). ASD is a neurodevelopmental disorder that is increasing in prevalence, and is characterized by deficits in social communication and interaction across multiple contexts, and restricted, repetitive patterns of behavior, interests, or activities. The majority of individuals with ASD have poor outcomes in the area of social functioning; however, there are no medical treatments available that target the core social communication deficits. The goal of the proposed research is to understand the neurobiological role of an imbalance in excitatory (glutamate) and inhibitory (gamma-aminobutyric acid, GABA) neurotransmission in the social cognition deficits in ASD, and to develop proton magnetic resonance spectroscopy as a measurement of target engagement to measure the ability of a medication, gabapentin, to increase cortical GABA levels. Spectrally-edited proton magnetic resonance spectroscopy (1H-MRS) provides an ideal method for measuring cortical GABA levels. All proposed studies will be in 70 adolescents (male and female) with ASD (age 13 to 17 years). Specific Aim 1: To measure correlations of 1H-MRS GABA levels in the anterior cingulate cortex (ACC) and occipital cortex (OC) with clinical measures of social cognition at baseline. Specific Aim 2: To measure the effect of an initial one time dose of gabapentin on 1H-MRS GABA levels in the ACC and OC. The application also outlines a detailed training plan involving didactic coursework, seminars, scientific conferences, and mentored experiences to provide the candidate with training in: (1) advanced neuroimaging techniques to study the neural correlates of social cognition in ASD; (2) clinical trials research methodology with a goal of integrating neuroimaging wraparound studies into the methods; and (3) advanced biostatistics and data analysis of complex neuroimaging datasets and clinical trials data. This NIMH K23 is the bridge (i.e. pathway for training and mentorship) for this early stage investigator to develop into an independently-funded researcher with the expertise to conduct neuroimaging studies of social cognition in ASD and contribute to the development and understanding of novel therapeutic approaches in these disorders.

项目总结/文摘