Strong Michael J, Abrahams Sharon, Goldstein Laura H, Woolley Susan, Mclaughlin Paula, Snowden Julie, Mioshi Eneida, Roberts-South Angie, Benatar Michael, HortobáGyi Tibor, Rosenfeld Jeffrey, Silani Vincenzo, Ince Paul G, Turner Martin R
a Department of Clinical Neurological Sciences, Schulich School of Medicine & Dentistry , London , Ontario , Canada.
b Department of Psychology, School of Philosophy, Psychology & Language Sciences , Euan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh , Edinburgh , UK.
Amyotroph Lateral Scler Frontotemporal Degener. 2017 May;18(3-4):153-174. doi: 10.1080/21678421.2016.1267768. Epub 2017 Jan 5.
This article presents the revised consensus criteria for the diagnosis of frontotemporal dysfunction in amyotrophic lateral sclerosis (ALS) based on an international research workshop on frontotemporal dementia (FTD) and ALS held in London, Canada in June 2015. Since the publication of the Strong criteria, there have been considerable advances in the understanding of the neuropsychological profile of patients with ALS. Not only is the breadth and depth of neuropsychological findings broader than previously recognised - - including deficits in social cognition and language - but mixed deficits may also occur. Evidence now shows that the neuropsychological deficits in ALS are extremely heterogeneous, affecting over 50% of persons with ALS. When present, these deficits significantly and adversely impact patient survival. It is the recognition of this clinical heterogeneity in association with neuroimaging, genetic and neuropathological advances that has led to the current re-conceptualisation that neuropsychological deficits in ALS fall along a spectrum. These revised consensus criteria expand upon those of 2009 and embrace the concept of the frontotemporal spectrum disorder of ALS (ALS-FTSD).
本文介绍了基于2015年6月在加拿大伦敦举行的额颞叶痴呆(FTD)和肌萎缩侧索硬化症(ALS)国际研究研讨会修订的ALS额颞叶功能障碍诊断共识标准。自斯特朗标准发布以来,在对ALS患者神经心理学特征的理解方面取得了相当大的进展。不仅神经心理学发现的广度和深度比以前认识的更广泛——包括社会认知和语言缺陷——而且可能会出现混合缺陷。现在有证据表明,ALS中的神经心理学缺陷极其异质,影响超过50%的ALS患者。当这些缺陷出现时,会对患者生存产生重大且不利的影响。正是认识到这种临床异质性与神经影像学、遗传学和神经病理学进展相结合,才导致了目前对ALS神经心理学缺陷呈谱系分布的重新概念化。这些修订后的共识标准在2009年标准的基础上进行了扩展,并纳入了ALS额颞叶谱系障碍(ALS-FTSD)的概念。