Faculty of Psychology, eCampus University, Novedrate, Italy.
Clinical Psychology Service, Saint George Foundation, Cavallermaggiore, Italy.
Br J Clin Psychol. 2022 Jun;61(2):214-241. doi: 10.1111/bjc.12337. Epub 2021 Oct 14.
Huntington's disease (HD) is a dramatic neurodegenerative disorder encompassing severe motor symptoms coupled to significant cognitive and social cognition deficits. However, it is not clear whether and how patients' neuropsychological profile changes between the prodromal and the manifest stages of the condition. The aim of the present in-depth review is to consider cognitive and social cognition impairment in HD patients by differentiating deficits arising before diagnosis from those evident from the manifest phase onwards.
Electronic databases were searched between January 1 , 2010 and December 31 , 2020 by using multiple combinations of keywords related to the investigation of neuropsychological profile in HD for preliminary search, and by defining strict selection criteria for studies to be included.
Forty-two studies were included. Evidence suggests that the neuropsychological profile in HD reflects a complex pathological spectrum of deficits. It includes impairment in the realms of executive functions, memory, attention, information processing, and social cognition. Interestingly, patients' profiles differ significantly between the manifest and the prodromal stages of their condition, not only in quantitative terms but also from a qualitative point of view.
Researchers and clinicians should thus include in clinical routine timely and specific neuropsychological assessments in order to monitor patients' cognitive status as time goes by, with the ultimate goal to implement effective clinical management strategies.
The neuropsychological profile in HD encompasses a complex pathological spectrum of deficits. Patients' profiles differ significantly between the manifest and the prodromal stages of their condition. Clinicians should include in everyday practice a timely and specific neuropsychological assessment. Detecting patients' cognitive status during the early stages of the condition already can contribute significantly to implement effective clinical management strategies.
亨廷顿病(HD)是一种严重的神经退行性疾病,包括严重的运动症状以及显著的认知和社会认知缺陷。然而,目前尚不清楚患者的神经心理学特征在疾病的前驱期和显性期之间是否以及如何发生变化。本深入综述的目的是通过区分诊断前和显性期出现的缺陷,来考虑 HD 患者的认知和社会认知障碍。
通过使用与 HD 神经心理学特征研究相关的多个关键词组合进行初步搜索,并定义严格的纳入研究选择标准,在 2010 年 1 月 1 日至 2020 年 12 月 31 日期间检索电子数据库。
共纳入 42 项研究。有证据表明,HD 的神经心理学特征反映了一系列复杂的病理性缺陷。它包括执行功能、记忆、注意力、信息处理和社会认知领域的损伤。有趣的是,患者的特征在疾病的显性和前驱阶段之间存在显著差异,不仅在数量上,而且在质量上也存在显著差异。
因此,研究人员和临床医生应该在临床常规中纳入及时和特定的神经心理学评估,以便随着时间的推移监测患者的认知状态,最终目的是实施有效的临床管理策略。
HD 的神经心理学特征包括一系列复杂的病理性缺陷。患者的特征在疾病的显性和前驱阶段之间存在显著差异。临床医生应在日常实践中纳入及时和特定的神经心理学评估。在疾病的早期阶段检测到患者的认知状态可以显著有助于实施有效的临床管理策略。