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This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The purpose of this novel study is to elucidate the relationship between abnormalities in prefrontal structure and impairments in executive functioning by conducting a study of schizophrenia patients compared to controls using multi-modal magnetic resonance imaging (MRI) techniques. Background: Genes associated with vulnerability to schizophrenia may affect neurodevelopment and result in abnormalities in prefrontal structure and function. The prefrontal cortex occupies approximately one quarter of the human cortex and is part of the brain that is most unique to humans. It is the one of the last parts of the brain to mature, but is typically also the first part of the brain to suffer with age. The prefrontal cortex regulates executive processes such as attention, planning, judgment, impulse control, self-monitoring, and problem solving. Studies have demonstrated reduced prefrontal gray matter in schizophrenia patients and their healthy relatives compared to controls suggesting a genetic component (Cannon et al., 1998). In addition, problems in executive functioning are a fairly robust correlate of the schizophrenia diathesis (Snitz et al., 2006) and reduced prefrontal brain activity is also a reliable correlate of schizophrenia (Snitz et al., 2005). To date, most studies have analyzed structural and functional data in isolation. The purpose of this study is to examine the relationship between abnormalities in prefrontal cortical structure and BOLD response in schizophrenia patients, first-degree biological relatives of schizophrenia patients, and control subjects. We hypothesize that schizophrenia patients with prefrontal abnormalities in either structure or hemodynamic responses will have a similar regional abnormality in the complementary domain. Similar regional associations between structure and BOLD response will be observed in first-degree biological relatives of schizophrenia patients suggesting the abnormalities are related to the diathesis for schizophrenia. Covariation of structure and hemodynamic response will be less robust in control subjects.
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Neural Disconnection and Errant Visual Perception in Psychotic Psychopathology
  • 批准号:
    10372412
  • 项目类别:
  • 资助金额:
    $38.96万
  • 财政年份:
    2021
  • 负责人:
    Scott R Sponheim
  • 依托单位:
Translational Neurophysiology Core
  • 批准号:
    10597080
  • 项目类别:
  • 资助金额:
    $55.86万
  • 财政年份:
    2020
  • 负责人:
    Scott R Sponheim
  • 依托单位:
Deviant Synchronization of Neural Functions in Schizophrenia
  • 批准号:
    10426230
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2019
  • 负责人:
    Scott R Sponheim
  • 依托单位:
Deviant Synchronization of Neural Functions in Schizophrenia
  • 批准号:
    9850860
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2019
  • 负责人:
    Scott R Sponheim
  • 依托单位:
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: