Jenkins Peter O, Mehta Mitul A, Sharp David J
1 The Division of Brain Sciences, The Department of Medicine, Imperial College London, UK.
2 Department of Neuroimaging, Institute of Psychiatry, Psychology & Neuroscience, King's College London, UK.
Brain. 2016 Sep;139(Pt 9):2345-71. doi: 10.1093/brain/aww128. Epub 2016 Jun 2.
Cognitive problems are one of the main causes of ongoing disability after traumatic brain injury. The heterogeneity of the injuries sustained and the variability of the resulting cognitive deficits makes treating these problems difficult. Identifying the underlying pathology allows a targeted treatment approach aimed at cognitive enhancement. For example, damage to neuromodulatory neurotransmitter systems is common after traumatic brain injury and is an important cause of cognitive impairment. Here, we discuss the evidence implicating disruption of the catecholamines (dopamine and noradrenaline) and review the efficacy of catecholaminergic drugs in treating post-traumatic brain injury cognitive impairments. The response to these therapies is often variable, a likely consequence of the heterogeneous patterns of injury as well as a non-linear relationship between catecholamine levels and cognitive functions. This individual variability means that measuring the structure and function of a person's catecholaminergic systems is likely to allow more refined therapy. Advanced structural and molecular imaging techniques offer the potential to identify disruption to the catecholaminergic systems and to provide a direct measure of catecholamine levels. In addition, measures of structural and functional connectivity can be used to identify common patterns of injury and to measure the functioning of brain 'networks' that are important for normal cognitive functioning. As the catecholamine systems modulate these cognitive networks, these measures could potentially be used to stratify treatment selection and monitor response to treatment in a more sophisticated manner.
认知问题是创伤性脑损伤后持续性残疾的主要原因之一。所受损伤的异质性以及由此产生的认知缺陷的变异性使得治疗这些问题变得困难。确定潜在的病理状况有助于采取针对性的治疗方法以促进认知功能。例如,神经调节性神经递质系统受损在创伤性脑损伤后很常见,并且是认知障碍的重要原因。在此,我们讨论涉及儿茶酚胺(多巴胺和去甲肾上腺素)紊乱的证据,并综述儿茶酚胺能药物治疗创伤性脑损伤后认知障碍的疗效。对这些疗法的反应通常存在差异,这可能是损伤模式异质性以及儿茶酚胺水平与认知功能之间非线性关系的结果。这种个体差异意味着测量一个人的儿茶酚胺能系统的结构和功能可能会带来更精确的治疗。先进的结构和分子成像技术有可能识别儿茶酚胺能系统的破坏,并直接测量儿茶酚胺水平。此外,结构和功能连接性测量可用于识别常见的损伤模式,并测量对正常认知功能很重要的脑“网络”的功能。由于儿茶酚胺系统调节这些认知网络,这些测量有可能用于更精细地分层治疗选择并监测治疗反应。