Mechanisms of chemotherapy-induced cognitive disorders: neuropsychological, pathophysiological, and neuroimaging perspectives.

Seminars in clinical neuropsychiatry Pub Date : 2003-10-01
Andrew J Saykin, Tim A Ahles, Brenna C McDonald
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Abstract

Recent studies have indicated the frequent occurrence of neuropsychologic deficits and cognitive complaints after systemic cancer chemotherapy. Most early reports were retrospective, but prospective longitudinal studies are underway. Although the available evidence suggests a fairly diffuse pattern of changes, memory and executive functions could be preferentially affected. Preliminary data also suggest that some individuals might be more vulnerable than others, leading to investigation of genetic and other risk factors. The greatest gap in our knowledge regarding chemotherapy-related cognitive changes is a lack of understanding of the mechanism or mechanisms that account for the observed changes. Several pathophysiological candidates include direct neurotoxic effects leading to atrophy of cerebral gray matter (GM) and/or demyelination of white matter (WM) fibers, secondary immunologic responses causing inflammatory reactions, and microvascular injury. Altered neurotransmitter levels and metabolites could constitute an additional mechanism related to neurotoxic effects. Advanced brain imaging techniques can directly or indirectly assess many of these mechanisms, but to date there has been very limited application of these tools. Morphometric magnetic resonance imaging (MRI), functional MRI (fMRI), diffusion tensor imaging (DTI), and MR spectroscopy (MRS) are noninvasive techniques that could yield important complementary data regarding the nature of neural changes after chemotherapy. Electrophysiological studies and targeted molecular imaging with positron emission tomography (PET) could also provide unique information. We review the minimal imaging data available at present and also note studies of other brain disorders or treatment effects that might serve as a model for imaging chemotherapy-induced changes. Large-scale prospective studies are needed to help isolate the pathophysiological mechanisms underlying the cognitive deficits associated with chemotherapy.

化疗引起的认知障碍的机制:神经心理学、病理生理学和神经影像学的观点。
最近的研究表明,系统性癌症化疗后经常出现神经心理缺陷和认知主诉。大多数早期的报告是回顾性的,但前瞻性的纵向研究正在进行中。尽管现有的证据表明,变化的模式相当分散,但记忆和执行功能可能优先受到影响。初步数据还表明,有些人可能比其他人更容易受到感染,因此需要对遗传和其他风险因素进行调查。关于化疗相关的认知变化,我们的知识中最大的空白是缺乏对观察到的变化的机制或机制的理解。几种病理生理学候选包括直接神经毒性作用导致脑灰质(GM)萎缩和/或白质(WM)纤维脱髓鞘,继发性免疫反应引起炎症反应和微血管损伤。改变的神经递质水平和代谢物可能构成与神经毒性作用相关的额外机制。先进的脑成像技术可以直接或间接地评估许多这些机制,但迄今为止,这些工具的应用非常有限。形态磁共振成像(MRI)、功能磁共振成像(fMRI)、弥散张量成像(DTI)和磁共振波谱(MRS)是无创技术,可以获得关于化疗后神经变化性质的重要补充数据。电生理研究和正电子发射断层扫描(PET)靶向分子成像也可以提供独特的信息。我们回顾了目前可用的最小成像数据,并注意到其他脑部疾病或治疗效果的研究,这些研究可能作为化疗引起的变化的成像模型。需要大规模的前瞻性研究来帮助分离与化疗相关的认知缺陷的病理生理机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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