Neural Mechanisms of Chemotherapy-Induced Cognitive Dis
Neural Mechanisms of Chemotherapy-Induced Cognitive Dis
批准号:
7106608
负责人:
ANDREW J SAYKIN
金额:
$41.28万
依托单位:
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:
2003-08-01 至 2007-05-31
关键词:
adult human (21+)apolipoprotein Ebioimaging /biomedical imagingbrain imaging /visualization /scanningbreast neoplasmsclinical researchcognition disordersfunctional magnetic resonance imaginggenetic susceptibilityhuman genetic material taghuman subjectmemoryneoplasm /cancer chemotherapyneuropsychological testspatient oriented researchpolymerase chain reactionquestionnaires
中文摘要
描述(由申请方提供):全身性癌症化疗与认知和记忆缺陷相关,可能是长期的(Ahles,Saykin et al,2002)。有很少的前瞻性研究的认知变化和潜在的病理生理机制还没有得到系统的检查。脑成像可以帮助确定这些机制,但目前还没有前瞻性的、对照良好的研究。我们将通过采用磁共振成像(MRI)和分析技术的集成来确定与化疗相关的脑结构和功能的特定变化,从而解决这一知识差距。影像学研究将建立在我们团队在NCI赞助的化疗认知研究(CA 87845)的经验基础上。我们的具体目标是:(i)确定接受化疗的患者脑结构和组织组成的短期和长期变化的频率、数量和特征,(ii)使用功能磁共振成像检测和表征记忆处理期间脑激活的变化,以评估任务相关回路,以及(iii)。系统地检查关键治疗、疾病和个体差异因素(例如,化疗方案、遗传风险、年龄、教育、基线功能)作为认知缺陷和恢复的预测因子,以促进未来的模型构建。参与者将包括接受化疗(n=50)或仅接受局部治疗(n=50)的乳腺癌患者和30名健康对照。将在化疗前和化疗后1个月和12个月(或同等时间间隔)获得测量结果。综合MRI检查将检测和测量:局灶性炎症/脱髓鞘(FLAIR)和分布的灰质和白色物质变化(基于体素的形态测定法)、记忆关键结构的完整性(海马3D体积和形状分析)和白色物质完整性和连接性(扩散张量成像,DTI)以及工作和情景记忆处理期间的大脑激活模式(功能性MRI,fMRI)。预期结果:该研究将确定哪些成像测量对化疗最敏感、信息量最大和特异性最强。认知变化机制的识别和新措施的引入将有助于推动神经系统副作用评估和风险/获益分析的进展,并将为神经保护剂、神经药理学治疗和康复方法的设计和评价提供基础。
英文摘要
DESCRIPTION (provided by applicant): Systemic cancer chemotherapy has been associated with cognitive and memory deficits that may be long-lasting (Ahles, Saykin et al, 2002). There are very few prospective studies of cognitive changes and the underlying pathophysiological mechanisms have not been systematically examined. Brain imaging could help to identify these mechanisms, yet there are no prospective, well-controlled studies. We will address this knowledge gap by employing an ensemble of magnetic resonance imaging (MRI) and analysis techniques to identify specific changes in brain structure and function associated with chemotherapy. The imaging study will build on our team's experience with NCI-sponsored cognitive studies of chemotherapy (CA87845). Our specific aims are to: (i) Determine the frequency, quantity and characteristics of short and long term changes in brain structure and tissue composition in patients undergoing chemotherapy, (ii) Detect and characterize alterations in brain activation during memory processing using fMRI to assess task-relevant circuits and (iii). Systematically examine key treatment, disease and individual difference factors (e.g., chemotherapy regimen, genetic risk, age, education, baseline functioning) as predictors of cognitive deficits and recovery, to facilitate future model building. Participants will include breast cancer patients undergoing chemotherapy (n=50) or local therapy only (n=50), and 30 healthy controls. Measures will be obtained before and 1 and 12 months after chemotherapy (or equivalent intervals). An integrated MRI exam will detect and measure: focal inflammation/demyelination (FLAIR) and distributed gray and white matter changes (voxel-based morphometry), the integrity of memory critical structures (hippocampal 3D volume and shape analysis) and white matter integrity and connectivity (diffusion tensor imaging, DTI), and brain activation patterns during working and episodic memory processing (functional MRI, fMRI). Expected outcomes: The study will determine which imaging measures are most sensitive, informative and specific to chemotherapy. Identification of the mechanisms of cognitive changes and introduction of new measures will help to drive advances in assessment of neurological side effects and risk/benefit analyses, and it will provide a foundation for design and evaluation of neuroprotective agents, neuropharmacologic treatment and rehabilitative approaches.
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