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RGS4 Polymorphisms and Neurobiology of Schizophrenia

RGS4 Polymorphisms and Neurobiology of Schizophrenia
RGS4 多态性与精神分裂症的神经生物学
批准号:
7643982
负责人:
Konasale M Prasad
金额:
$17.56万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-08-05 至 2011-07-31

项目摘要

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This Research Career Development plan proposes a program of training and research designed to clarify the in vivo biological impact of variations in the gene encoding regulator of G-protein signaling subtype 4 (RGS4) polymorphisms in schizophrenia patients, individuals at risk for schizophrenia and matched healthy subjects. Demonstrating an association between genetic variations and intermediate phenotypes provides an important additional support for genetic association. RGS4 underexpression in the dorsolateral prefrontal cortex (DLPFC) of schizophrenia patients is reported. Subsequently, an association of RGS4 gene with schizophrenia has been reported in 7 independently ascertained populations in USA, Europe, india and Brazil. Our preliminary studies showed smaller DLPFC in schizophrenia patients homozygous for allele T of SNP4 and allele A of SNP18 but not in healthy subjects suggesting an interaction with other illness related variables. According to the neurodevelopmental hypothesis of schizophrenia pathogenic process starts prior to the emergence of clinical symptoms. Therefore, studying cerebral changes in persons at genetically high risk for developing schizophrenia who have not yet manifested the illness could minimize the confounds due to the illness. Smaller DLPFC was also observed in schizophrenia subjects homozygous for Val allele of the COMT gene that has also been associated with schizophrenia. The proposed study plans to utilize structural MRI and phosphorus magnetic resonance spectroscopy to characterize the differences in morphometry and membrane chemical (phosphomonoesters and phosphodiesters) concentrations associated with RGS4 variations in these study groups. We will explore the associations of these imaging measures with COMT polymorphisms. Characterizing intermediate phenotypes using "cross-longitudinal" design helps in delineating longitudinal trajectory of cerebral correlates of genetic polymorphisms, designing novel medications and early detection.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
Neuroscience in psychiatry training: how much do residents need to know?
精神病学培训中的神经科学:住院医师需要了解多少?
DOI: 10.1176/ajp.2006.163.5.919
发表时间: 2006
期刊: The American journal of psychiatry
影响因子: --
作者: [Roffman,JoshuaL, Simon,AsherB, Prasad,KonasaleM, Truman,ChristineJ, Morrison,Jason, Ernst,CarrieL]
通讯作者: Ernst,CarrieL
DOI: 10.1007/s11920-004-0080-2
发表时间: 2004-08-01
期刊: Current psychiatry reports
影响因子: 6.7
作者: [Diwadkar, Vaibhav A, Prasad, Konasale M, Keshavan, Matcheri S]
通讯作者: Keshavan, Matcheri S
DOI: 10.1016/j.neuroimage.2012.08.030
发表时间: 2012-11-15
期刊: NEUROIMAGE
影响因子: 5.7
作者: [Stolz, Erin, Pancholi, Krishna M., Goradia, Dhruman D., Paul, Sarah, Keshavan, Matcheri S., Nimgaonkar, Vishwajit L., Prasad, Konasale M.]
通讯作者: Prasad, Konasale M.
DOI: 10.1016/j.schres.2014.09.045
发表时间: 2015-01
期刊: SCHIZOPHRENIA RESEARCH
影响因子: 4.5
作者: [Prasad, Konasale M., Upton, Catherine H., Schirda, Claudiu S., Nimgaonkar, Vishwajit L., Keshavan, Matcheri S.]
通讯作者: Keshavan, Matcheri S.
8
    Neural Circuitry Resilience in Psychotic Disorders: A Multimodal Ultra-High Field Neuroimaging Study
    • 批准号:
      10467980
    • 项目类别:
    • 资助金额:
      $0.0万
    • 财政年份:
      2021
    • 负责人:
      Konasale M Prasad
    • 依托单位:
    Neural Circuitry Resilience in Psychotic Disorders: A Multimodal Ultra-High Field Neuroimaging Study
    • 批准号:
      10013729
    • 项目类别:
    • 资助金额:
      $0.0万
    • 财政年份:
      2021
    • 负责人:
      Konasale M Prasad
    • 依托单位:
    Synaptic Pruning and Complement Gene in Schizophrenia: Imaging & Cellular Studies
    Synaptic Pruning and Complement Gene in Schizophrenia: Imaging & Cellular Studies
    海外基金