BRAIN CONECTIONS

大脑连接

基本信息

  • 批准号:
    7627510
  • 负责人:
  • 金额:
    $ 1.08万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-04-01 至 2008-03-31
  • 项目状态:
    已结题

项目摘要

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. OBJECTIVES: The three specific aims of this study are 1) to determine the change in continuous measures of cognitive function over time among patients with a recent diagnosis of SLE; 2) to determine the predictive value of neuroimaging for decline in continuous measures of cognitive function in newly diagnosed SLE patients; 3) to determine the predictive value of serologic factors for decline in continuous measures of cognitive function in newly diagnosed SLE patients. METHODS: Thirty patients will undergo a baseline MRI with gadolinium and brain FDG PET, standard neuropsychological testing, disease activity will be assessed by the physician, and a blood sample will be taken. There will be quarterly visits for 3 1/2 to 4 years, depending on entry time. At each visit, the following will be repeated: disease activity measures, serum, plasma, and DNA storage, ANAM, depression inventory, fibromyalgia tender points, AIMS pain scale and ACR NPSLE case definitions. EXPECTED OUTCOME: We hope to find a moderate to severe decline in a clinically relevant number of newly diagnosed SLE patients using continuous measures of cognitive function independent of race, education, socioeconomic status and co-morbid conditions; imaging abnormalities will be more common in cognitively impaired subjects; and abnormalities observed in levels of Antiphospholipid antibodies, cytokines and soluble adhesion molecules will be associated with poorer cognitive function. CLINICAL RELEVANCE: Neuropsychiatric manifestations of Systemic Lupus Erythematosus (NPSLE) are both common and an important source of morbidity. Of the case definitions for NPSLE syndromes that have recently been developed, cognitive dysfunction appears to be the most prevalent. Little is know about the influence of co-morbidities or ethnicity/race on disease outcomes or the underlying pathogenesis of this important NPSLE syndrome. Perhaps most importantly, no rational therapeutic approach for the treatment of SLE-related cognitive dysfunction currently exists and is unlikely to be developed without a better understanding of neuropathological mechanisms. New brain imaging techniques using both structural and functional analyses have the potential to uncover mechanisms underlying NPSLE syndrome, particularly if specific syndromes are targeted.
这个子项目是许多研究子项目中利用 资源由NIH/NCRR资助的中心拨款提供。子项目和 调查员(PI)可能从NIH的另一个来源获得了主要资金, 并因此可以在其他清晰的条目中表示。列出的机构是 该中心不一定是调查人员的机构。 目的:本研究的三个具体目的是:1)确定新近诊断的SLE患者认知功能连续指标随时间的变化;2)确定神经影像对新诊断SLE患者认知功能连续指标下降的预测价值;3)确定血清学因素对新诊断SLE患者认知功能连续指标下降的预测价值。 方法:30例患者将接受Gd和脑FDG PET的基线MRI检查,进行标准的神经心理测试,由医生评估疾病的活动性,并采集血样。根据参赛时间的不同,将在三年半至四年内每季度访问一次。在每次就诊时,将重复以下内容:疾病活动性测量、血清、血浆和DNA存储、ANAM、抑郁症清单、纤维肌痛压痛点、AIMS疼痛评分和ACR NPSLE病例定义。 预期结果:我们希望使用与种族、教育、社会经济地位和合并症无关的认知功能连续测量方法,发现临床上相关的新诊断SLE患者数量出现中度至严重下降;成像异常将在认知受损的受试者中更为常见;在抗磷脂抗体、细胞因子和可溶性黏附分子水平观察到的异常将与较差的认知功能相关。 临床意义:系统性红斑狼疮(NPSLE)的神经精神症状很常见,也是发病率的重要来源。在最近开发的NPSLE综合征的病例定义中,认知功能障碍似乎是最普遍的。关于这一重要的NPSLE综合征的共病或种族/种族对疾病结局或潜在发病机制的影响,人们知之甚少。也许最重要的是,目前还没有合理的治疗方法来治疗SLE相关的认知功能障碍,如果不能更好地了解神经病理机制,也不太可能开发出这种方法。使用结构和功能分析的新的脑成像技术有可能揭示NPSLE综合征的潜在机制,特别是如果特定的综合征是有针对性的。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

ROBIN L BREY其他文献

ROBIN L BREY的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('ROBIN L BREY', 18)}}的其他基金

COGNITIVE FUNCTION IN SLE
SLE 的认知功能
  • 批准号:
    7718718
  • 财政年份:
    2008
  • 资助金额:
    $ 1.08万
  • 项目类别:
BRAIN CONECTIONS
大脑连接
  • 批准号:
    7718715
  • 财政年份:
    2008
  • 资助金额:
    $ 1.08万
  • 项目类别:
CLINICAL AND SEROLOGIC PREDICTORS OF NEUROPSYCHIATRIC SLE
神经精神系统性红斑狼疮的临床和血清学预测因素
  • 批准号:
    7718713
  • 财政年份:
    2008
  • 资助金额:
    $ 1.08万
  • 项目类别:
SALUD BONE MINERAL DENSITY SUB-STUDY
Salud 骨矿物质密度子研究
  • 批准号:
    7718714
  • 财政年份:
    2008
  • 资助金额:
    $ 1.08万
  • 项目类别:
ANTIPHOSPHOLIPID SYNDROME COLLABORATIVE REGISTRY
抗磷脂综合征合作登记
  • 批准号:
    7627508
  • 财政年份:
    2007
  • 资助金额:
    $ 1.08万
  • 项目类别:
COGNITIVE FUNCTION IN SLE
SLE 的认知功能
  • 批准号:
    7627514
  • 财政年份:
    2007
  • 资助金额:
    $ 1.08万
  • 项目类别:
CLINICAL AND SEROLOGIC PREDICTORS OF NEUROPSYCHIATRIC SLE
神经精神系统性红斑狼疮的临床和血清学预测因素
  • 批准号:
    7627507
  • 财政年份:
    2007
  • 资助金额:
    $ 1.08万
  • 项目类别:
SALUD BONE MINERAL DENSITY SUB-STUDY
Salud 骨矿物质密度子研究
  • 批准号:
    7627509
  • 财政年份:
    2007
  • 资助金额:
    $ 1.08万
  • 项目类别:
BRAIN CONECTIONS
大脑连接
  • 批准号:
    7378175
  • 财政年份:
    2006
  • 资助金额:
    $ 1.08万
  • 项目类别:
Cognitive Function in SLE (COGNITION)
SLE 的认知功能 (COGNITION)
  • 批准号:
    7222712
  • 财政年份:
    2006
  • 资助金额:
    $ 1.08万
  • 项目类别:

相似海外基金

Synergistic effects of antiphospholipid antibodies and oxidative stress that increase the risk of thrombosis in antiphospholipid syndrome
抗磷脂抗体和氧化应激的协同作用会增加抗磷脂综合征中血栓形成的风险
  • 批准号:
    18K16117
  • 财政年份:
    2018
  • 资助金额:
    $ 1.08万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
origin of antiphospholipid antibodies
抗磷脂抗体的起源
  • 批准号:
    390959600
  • 财政年份:
    2017
  • 资助金额:
    $ 1.08万
  • 项目类别:
    Research Grants
15th International Congress on Antiphospholipid Antibodies
第十五届国际抗磷脂抗体大会
  • 批准号:
    9193925
  • 财政年份:
    2016
  • 资助金额:
    $ 1.08万
  • 项目类别:
A comprehensive study of antiphospholipid antibodies in autoimmune diseases for which existing autoantibodies are unspecified
现有自身抗体未明确的自身免疫性疾病中抗磷脂抗体的综合研究
  • 批准号:
    16K10031
  • 财政年份:
    2016
  • 资助金额:
    $ 1.08万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Antiphospholipid antibodies and lupus: new molecular targets for treatment
抗磷脂抗体和狼疮:治疗的新分子靶点
  • 批准号:
    8035933
  • 财政年份:
    2010
  • 资助金额:
    $ 1.08万
  • 项目类别:
Antiphospholipid antibodies and lupus: new molecular targets for treatment
抗磷脂抗体和狼疮:治疗的新分子靶点
  • 批准号:
    8634020
  • 财政年份:
    2010
  • 资助金额:
    $ 1.08万
  • 项目类别:
Antiphospholipid antibodies and lupus: new molecular targets for treatment
抗磷脂抗体和狼疮:治疗的新分子靶点
  • 批准号:
    8231469
  • 财政年份:
    2010
  • 资助金额:
    $ 1.08万
  • 项目类别:
Antiphospholipid antibodies and lupus: new molecular targets for treatment
抗磷脂抗体和狼疮:治疗的新分子靶点
  • 批准号:
    8438259
  • 财政年份:
    2010
  • 资助金额:
    $ 1.08万
  • 项目类别:
Antiphospholipid antibodies and lupus: new molecular targets for treatment
抗磷脂抗体和狼疮:治疗的新分子靶点
  • 批准号:
    7889648
  • 财政年份:
    2010
  • 资助金额:
    $ 1.08万
  • 项目类别:
Proteomics to identify the targets of antiphospholipid antibodies in women with recurrent pregnancy loss
蛋白质组学确定反复流产女性抗磷脂抗体的靶标
  • 批准号:
    20791171
  • 财政年份:
    2008
  • 资助金额:
    $ 1.08万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了