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原发性进行性言语失用症的韵律和语音亚型

Prosodic and phonetic subtypes of primary progressive apraxia of speech.

作者信息

Utianski Rene L, Duffy Joseph R, Clark Heather M, Strand Edythe A, Botha Hugo, Schwarz Christopher G, Machulda Mary M, Senjem Matthew L, Spychalla Anthony J, Jack Clifford R, Petersen Ronald C, Lowe Val J, Whitwell Jennifer L, Josephs Keith A

机构信息

Department of Neurology, Division of Speech Pathology, Mayo Clinic, Rochester, MN, USA.

Department of Neurology, Division of Speech Pathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Brain Lang. 2018 Sep;184:54-65. doi: 10.1016/j.bandl.2018.06.004. Epub 2018 Jul 4.

Abstract

Primary progressive apraxia of speech (PPAOS) is a clinical syndrome in which apraxia of speech is the initial indication of neurodegenerative disease. Prior studies of PPAOS have identified hypometabolism, grey matter atrophy, and white matter tract degeneration in the frontal gyri, precentral cortex, and supplementary motor area (SMA). Recent clinical observations suggest two distinct subtypes of PPAOS may exist. Phonetic PPAOS is characterized predominantly by distorted sound substitutions. Prosodic PPAOS is characterized predominantly by slow, segmented speech. Demographic, clinical, and neuroimaging data (MRI, DTI, and FDG-PET) were analyzed to validate these subtypes and explore anatomic correlates. The Phonetic subtype demonstrated bilateral involvement of the SMA, precentral gyrus, and cerebellar crus. The Prosodic subtype demonstrated more focal involvement in the SMA and right superior cerebellar peduncle. The findings provide converging evidence that differences in the reliably determined predominant clinical characteristics of AOS are associated with distinct imaging patterns, independent of severity.

摘要

原发性进行性言语失用症(PPAOS)是一种临床综合征,其中言语失用症是神经退行性疾病的初始表现。先前对PPAOS的研究已经确定了额回、中央前回和辅助运动区(SMA)存在代谢减低、灰质萎缩和白质束变性。最近的临床观察表明,PPAOS可能存在两种不同的亚型。语音性PPAOS主要表现为声音替代失真。韵律性PPAOS主要表现为语速缓慢、言语不连贯。对人口统计学、临床和神经影像学数据(MRI、DTI和FDG-PET)进行分析,以验证这些亚型并探索其解剖学相关性。语音性亚型表现为SMA、中央前回和小脑脚双侧受累。韵律性亚型表现为SMA和右侧小脑上脚受累更为局限。这些发现提供了一致的证据,表明AOS可靠确定的主要临床特征的差异与不同的影像学模式相关,与严重程度无关。

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