Ohm Daniel T, Rhodes Emma, Bahena Alejandra, Capp Noah, Lowe MaKayla, Sabatini Philip, Trotman Winifred, Olm Christopher A, Phillips Jeffrey, Prabhakaran Karthik, Rascovsky Katya, Massimo Lauren, McMillan Corey, Gee James, Tisdall M Dylan, Yushkevich Paul A, Lee Edward B, Grossman Murray, Irwin David J
Penn Digital Neuropathology Laboratory, Department of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
Penn Frontotemporal Degeneration Center, Department of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
Front Neurol. 2023 Oct 11;14:1245886. doi: 10.3389/fneur.2023.1245886. eCollection 2023.
Frontotemporal dementia (FTD) is a spectrum of clinically and pathologically heterogenous neurodegenerative dementias. Clinical and anatomical variants of FTD have been described and associated with underlying frontotemporal lobar degeneration (FTLD) pathology, including tauopathies (FTLD-tau) or TDP-43 proteinopathies (FTLD-TDP). FTD patients with predominant degeneration of anterior temporal cortices often develop a language disorder of semantic knowledge loss and/or a social disorder often characterized by compulsive rituals and belief systems corresponding to predominant left or right hemisphere involvement, respectively. The neural substrates of these complex social disorders remain unclear. Here, we present a comparative imaging and postmortem study of two patients, one with FTLD-TDP (subtype C) and one with FTLD-tau (subtype Pick disease), who both developed new rigid belief systems. The FTLD-TDP patient developed a complex set of values centered on positivity and associated with specific physical and behavioral features of pigs, while the FTLD-tau patient developed compulsive, goal-directed behaviors related to general themes of positivity and spirituality. Neuroimaging showed left-predominant temporal atrophy in the FTLD-TDP patient and right-predominant frontotemporal atrophy in the FTLD-tau patient. Consistent with antemortem cortical atrophy, histopathologic examinations revealed severe loss of neurons and myelin predominantly in the anterior temporal lobes of both patients, but the FTLD-tau patient showed more bilateral, dorsolateral involvement featuring greater pathology and loss of projection neurons and deep white matter. These findings highlight that the regions within and connected to anterior temporal lobes may have differential vulnerability to distinct FTLD proteinopathies and serve important roles in human belief systems.
额颞叶痴呆(FTD)是一系列临床和病理表现均异质性的神经退行性痴呆。FTD的临床和解剖学变异已被描述,并与潜在的额颞叶变性(FTLD)病理相关,包括tau蛋白病(FTLD-tau)或TDP-43蛋白病(FTLD-TDP)。以颞叶前部皮质为主的FTD患者通常会出现语义知识丧失的语言障碍和/或社交障碍,这些社交障碍通常分别表现为强迫性仪式和信仰体系,分别对应于左半球或右半球的主要受累情况。这些复杂社交障碍的神经基础仍不清楚。在此,我们展示了对两名患者的比较影像学和尸检研究,一名患有FTLD-TDP(C亚型),另一名患有FTLD-tau(匹克病亚型),他们都发展出了新的僵化信仰体系。FTLD-TDP患者发展出了一套以积极向上为核心、与猪的特定身体和行为特征相关的复杂价值观,而FTLD-tau患者则发展出了与积极向上和灵性等一般主题相关的强迫性、目标导向行为。神经影像学显示,FTLD-TDP患者左侧颞叶萎缩为主,FTLD-tau患者右侧额颞叶萎缩为主。与生前皮质萎缩一致,组织病理学检查显示,两名患者主要是颞叶前部神经元和髓鞘严重缺失,但FTLD-tau患者表现出更双侧、背外侧受累,病理改变更严重,投射神经元和深部白质损失更多。这些发现突出表明,颞叶前部内部及与之相连的区域可能对不同的FTLD蛋白病具有不同的易损性,并在人类信仰体系中发挥重要作用。