Disrupted functional connectivity in primary progressive apraxia of speech

Autor: Nirubol Tosakulwong, Edythe A. Strand, David T.W. Jones, Mary M. Machulda, Hugo Botha, Heather M. Clark, Keith A. Josephs, Clifford R. Jack, David S. Knopman, Ronald C. Petersen, Jennifer L. Whitwell, Rene L. Utianski, Joseph R. Duffy
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Male
Audiology
Apraxia
MMSE
Mini-Mental State Examination

Intrinsic connectivity networks
lcsh:RC346-429
Functional connectivity
0302 clinical medicine
Degenerative disease
Gyrus
AES
Articulatory Error Score

Motor speech disorders
TOJ
Temporal-Occipital Junction

TT
Token Test

Language
Aged
80 and over

medicine.diagnostic_test
Supplementary motor area
05 social sciences
ICN
Intrinsic Connectivity Network

WAB
Western Aphasia Battery

Brain
Regular Article
NPI-S
Neuropsychiatric Inventory – Severity

SMA
Supplementary Motor Area

PFC
Prefrontal Cortex

Middle Aged
Magnetic Resonance Imaging
AOS
Apraxia Of Speech

UPDRS
Unified Parkinson Disease Rating Scale

medicine.anatomical_structure
Neurology
BNT
Boston Naming Test

lcsh:R858-859.7
Female
Psychology
medicine.medical_specialty
Apraxias
Cognitive Neuroscience
FBI
Frontal Behavioral Inventory

PCC
Posterior Cingulate Cortex

lcsh:Computer applications to medicine. Medical informatics
050105 experimental psychology
03 medical and health sciences
AQ
Aphasia Quotient

ASRS
Apraxia of Speech Severity Rating Scale

Apraxia of speech
medicine
Humans
0501 psychology and cognitive sciences
Radiology
Nuclear Medicine and imaging

lcsh:Neurology. Diseases of the nervous system
Aged
Working memory
medicine.disease
FAB
Frontal Assessment Battery

PPA
Primary Progressive Aphasia

NVOA
Nonverbal Oral Apraxia

Posterior cingulate
agPPA
Agrammatic/Nonfluent PPA

Neurology (clinical)
Nerve Net
Functional magnetic resonance imaging
030217 neurology & neurosurgery
Zdroj: NeuroImage: Clinical, Vol 18, Iss, Pp 617-629 (2018)
NeuroImage : Clinical
ISSN: 2213-1582
Popis: Apraxia of speech is a motor speech disorder thought to result from impaired planning or programming of articulatory movements. It can be the initial or only manifestation of a degenerative disease, termed primary progressive apraxia of speech (PPAOS). The aim of this study was to use task-free functional magnetic resonance imaging (fMRI) to assess large-scale brain network pathophysiology in PPAOS. Twenty-two PPAOS participants were identified from a prospective cohort of degenerative speech and language disorders patients. All participants had a comprehensive, standardized evaluation including an evaluation by a speech-language pathologist, examination by a behavioral neurologist and a multimodal imaging protocol which included a task-free fMRI sequence. PPAOS participants were age and sex matched to amyloid-negative, cognitively normal participants with a 1:2 ratio. We chose a set of hypothesis driven, predefined intrinsic connectivity networks (ICNs) from a large, out of sample independent component analysis and then used them to initialize a spatiotemporal dual regression to estimate participant level connectivity within these ICNs. Specifically, we evaluated connectivity within the speech and language, face and hand sensorimotor, left working memory, salience, superior parietal, supramarginal, insular and deep gray ICNs in a multivariate manner. The spatial maps for each ICN were then compared between PPAOS and control participants. We used clinical measures of apraxia of speech severity to assess for clinical-connectivity correlations for regions found to differ between PPAOS and control participants. Compared to controls, PPAOS participants had reduced connectivity of the right supplementary motor area and left posterior temporal gyrus to the rest of the speech and language ICN. The connectivity of the right supplementary motor area correlated negatively with an articulatory error score. PPAOS participants also had reduced connectivity of the left supplementary motor area to the face sensorimotor ICN, between the left lateral prefrontal cortex and the salience ICN and between the left temporal-occipital junction and the left working memory ICN. The latter connectivity correlated with the apraxia of speech severity rating scale, although the finding did not survive correction for multiple comparisons. Increased connectivity was noted in PPAOS participants between the dorsal posterior cingulate and the left working memory ICN. Our results support the importance of the supplementary motor area in the pathophysiology of PPAOS, which appears to be disconnected from speech and language regions. Supplementary motor area connectivity may serve as a biomarker of degenerative apraxia of speech severity.
Highlights • This is the first study of the network level connectivity changes underlying PPAOS. • We found changes in speech and language, face, working memory and salience networks. • Right SMA connectivity to speech and language areas correlated with AOS severity.
Databáze: OpenAIRE