Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina 60, 20132, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.
J Neurol. 2024 Jul;271(7):4203-4215. doi: 10.1007/s00415-024-12338-9. Epub 2024 Apr 10.
Semantic behavioral variant frontotemporal dementia (sbvFTD) is a neurodegenerative condition presenting with specific behavioral and semantic derangements and predominant atrophy of the right anterior temporal lobe (ATL). The objective was to evaluate clinical, neuropsychological, neuroimaging, and genetic features of an Italian sbvFTD cohort, defined according to recently proposed guidelines, compared to semantic variant primary progressive aphasia (svPPA) and behavioral variant FTD (bvFTD) patients.
Fifteen sbvFTD, sixty-three bvFTD, and twenty-five svPPA patients and forty controls were enrolled. Patients underwent clinical, cognitive evaluations, and brain MRI. Symptoms of bvFTD patients between onset and first visit were retrospectively recorded and classified as early and late. Grey matter atrophy was investigated using voxel-based morphometry.
sbvFTD experienced early criteria-specific symptoms: world, object and person-specific semantic loss (67%), complex compulsions and rigid thought (60%). Sequentially, more behavioral symptoms emerged (apathy/inertia, loss of empathy) along with non-criteria-specific symptoms (anxiety, suspiciousness). sbvFTD showed sparing of attentive/executive functions, especially compared to bvFTD and better language functions compared to svPPA. All sbvFTD patients failed at the famous face recognition test and more than 80% failed in understanding written metaphors and humor. At MRI, sbvFTD had predominant right ATL atrophy, almost specular to svPPA. Three sbvFTD patients presented pathogenic genetic variants.
We replicated the application of sbvFTD diagnostic guidelines in an independent Italian cohort, demonstrating that the presence of person-specific semantic knowledge loss and mental rigidity, along with preserved executive functions and a predominant right ATL atrophy with sparing of frontal lobes, should prompt a diagnosis of sbvFTD.
语义行为变异额颞叶痴呆(sbvFTD)是一种神经退行性疾病,表现为特定的行为和语义障碍,以及右前颞叶(ATL)的主要萎缩。目的是根据最近提出的指南,评估意大利 sbvFTD 队列的临床、神经心理学、神经影像学和遗传学特征,与语义变异原发性进行性失语症(svPPA)和行为变异额颞叶痴呆(bvFTD)患者进行比较。
纳入了 15 名 sbvFTD、63 名 bvFTD 和 25 名 svPPA 患者和 40 名对照者。患者接受了临床、认知评估和脑部 MRI。回顾性记录了 bvFTD 患者从发病到首次就诊的早期和晚期症状,并进行了分类。使用基于体素的形态计量学研究灰质萎缩。
sbvFTD 经历了早期的特定症状:世界、物体和人物特定的语义丧失(67%)、复杂的强迫和僵化思维(60%)。随后,出现了更多的行为症状(冷漠/惰性、同理心丧失)以及非特定症状(焦虑、多疑)。sbvFTD 保留了注意力/执行功能,尤其是与 bvFTD 相比,语言功能也更好。所有 sbvFTD 患者都未能通过著名的面孔识别测试,超过 80%的患者无法理解书面隐喻和幽默。在 MRI 上,sbvFTD 出现了右侧 ATL 明显的萎缩,几乎与 svPPA 相同。3 名 sbvFTD 患者携带致病性基因突变。
我们在一个独立的意大利队列中复制了 sbvFTD 诊断指南的应用,证明了特定的人物语义知识丧失和精神僵化,以及保留的执行功能和右 ATL 主要萎缩,而额叶不受影响,应提示 sbvFTD 的诊断。