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New Clinical Approaches to Creutzfeldt-Jakob Disease

New Clinical Approaches to Creutzfeldt-Jakob Disease
治疗克雅氏病的新临床方法
批准号:
7276628
负责人:
MICHAEL D GESCHWIND
金额:
$12.18万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-15 至 2008-08-31

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DESCRIPTION (provided by applicant): Creutzfeldt-Jakob disease (CJD)is a rapidly progressive, universally fatal, and transmissible neurodegenerative disease that imposes a terrible burden on patients and their families. The recent discovery that quinacrine may be a potential therapy for CJD could have enormous implications for patients. Unfortunately, patients are usually diagnosed in advanced stages of the disease - a time when available treatments may be ineffective. This delayed diagnosis is in part because current clinical criteria for sporadic CJD (sCJD) are based on a constellation of symptoms that often occur only late in a patient's course. Recently, neuroimaging has shown potential to improve the diagnosis of sCJD. Additionally, an elevated level of the protein 14-3-3 in the cerebrospinal fluid (CSF) has been touted as a sensitive and specific biomarker for sCJD and has recently been added to the diagnostic criteria for sCJD. Yet, no systematic study has been undertaken to identify the sensitivity and specificity of these two types of biomarkers in pathologically proven sCJD versus non-prion rapidly progressive dementias. The research goals of this proposal focus on identifying better ways for early diagnosis of CJD through a systematic analysis of clinical and imaging findings. The specific aims of this research will be as follows: 1 . To determine the sensitivity and specificity of diffusion-weighted imaging (DWI) sequence abnormalities in sporadic CJD, and 2. To determine the sensitivity and specificity of the CSF 14-3-3 protein as a marker for sporadic CJD. This research should provide new information on the early features of sCJD and thus facilitate diagnosis. In addition, this proposal will combine didactic teaching, mentoring, and clinical research experience to build upon Dr. Geschwind's training in behavioral neurology and neuroscience, thereby helping him to design and implement future clinical treatment studies for human prion disease and other dementias.
期刊论文(18)
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科研奖励(0)
会议论文
DOI: 10.1212/con.0000000000000251
发表时间: 2015-12
期刊: Continuum (Minneapolis, Minn.)
影响因子: --
作者: [Geschwind MD]
通讯作者: Geschwind MD
DOI: 10.1111/j.1528-1167.2009.02287.x
发表时间: 2010-03
期刊: Epilepsia
影响因子: 5.6
作者: [Barajas RF, Collins DE, Cha S, Geschwind MD]
通讯作者: Geschwind MD
DOI: 10.1097/nen.0b013e3181ffc39c
发表时间: 2010-12
期刊: Journal of neuropathology and experimental neurology
影响因子: 3.2
作者: [Tartaglia MC, Thai JN, See T, Kuo A, Harbaugh R, Raudabaugh B, Cali I, Sattavat M, Sanchez H, DeArmond SJ, Geschwind MD]
通讯作者: Geschwind MD
DOI: 10.1016/b978-0-444-63945-5.00020-9
发表时间: 2018-01-01
期刊: Handbook of clinical neurology
影响因子: --
作者: [Geschwind, Michael D, Murray, Katy]
通讯作者: Murray, Katy
12
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    Tracking longitudinal change in presymptomatic genetic prion disease (TLC-Pre-gPrD)
    Tracking longitudinal change in presymptomatic genetic prion disease (TLC-Pre-gPrD)
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