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  • 1
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2020
    In:  Neurology Vol. 94, No. 15_supplement ( 2020-04-14)
    In: Neurology, Ovid Technologies (Wolters Kluwer Health), Vol. 94, No. 15_supplement ( 2020-04-14)
    Type of Medium: Online Resource
    ISSN: 0028-3878 , 1526-632X
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2020
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2010
    In:  Cognitive and Behavioral Neurology Vol. 23, No. 1 ( 2010-03), p. 1-7
    In: Cognitive and Behavioral Neurology, Ovid Technologies (Wolters Kluwer Health), Vol. 23, No. 1 ( 2010-03), p. 1-7
    Type of Medium: Online Resource
    ISSN: 1543-3633
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2010
    detail.hit.zdb_id: 2063084-0
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  • 3
    Online Resource
    Online Resource
    Informa UK Limited ; 2004
    In:  Neurocase Vol. 10, No. 1 ( 2004-02), p. 3-18
    In: Neurocase, Informa UK Limited, Vol. 10, No. 1 ( 2004-02), p. 3-18
    Type of Medium: Online Resource
    ISSN: 1355-4794 , 1465-3656
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2004
    detail.hit.zdb_id: 1497469-1
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  • 4
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Alzheimer's & Dementia Vol. 15, No. 7S_Part_19 ( 2019-07)
    In: Alzheimer's & Dementia, Wiley, Vol. 15, No. 7S_Part_19 ( 2019-07)
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2201940-6
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  • 5
    In: Alzheimer's & Dementia, Wiley, Vol. 16, No. S5 ( 2020-12)
    Abstract: Speech is a complex activity requiring proper function and connectivity of multiple brain networks and as such is sensitive to focal neurodegeneration. We have previously reported on acoustic markers of dysprosody in speech samples of speakers with frontotemporal dementia (FTD) phenotypes. In the current study we explore the longitudinal changes in acoustic‐prosodic markers in FTD. Method We analyzed 102 speech samples of picture descriptions from 46 participants with FTD (Table 1): 8 with non‐fluent/agrammatic primary progressive aphasia (naPPA), 14 with semantic variant PPA (svPPA), 10 with logopenic aphasia (lvPPA) and 14 with behavioral FTD (bvFTD). We automatically segmented the acoustic signal into segments of continuous speech or silence, measured their durations, and derived other measures. We used linear mixed effects (lme) models to test changes over time for each acoustic measure, controlling for sex, education, and random intercepts. We also examined any interaction between phenotypes and disease duration. Result bvFTD speakers increased their pause duration by 0.27 seconds per year and their pause rate by 3.9 pauses per minute (ppm) each year. Their speech segment duration shortened by 0.1 seconds per year (p=0.041), decreasing their total speech time by 6.6 seconds (p=0.003) per year. Thus, bvFTD patients reduced the proportion of speech in their samples by 5.16 percent per year (p=0.008). svPPA speakers increased their pause rate similarly, but in contrast, their pause duration decreased by 0.097 seconds per year and they increased their speech segment frequency by 8.32 per minute each year (p=0.054). naPPA and lvPPA speakers increased their pause rate over time and spent less total time (speech + pause) describing the picture (by 5.6 seconds per year; p=0.018). They did not differ from bvFTD and svPPA in these two acoustic measures. Conclusion In our study all FTD speakers became more dysfluent and produced shorter descriptions with time, however, only bvFTD speakers actually exhibited reduced speech production. In contrast, svPPA speech had more frequent pauses and speech segments over time, rendering it “fragmented” and inefficient. These findings support the role of automated acoustic analysis in characterizing speech longitudinally in neurodegeneration.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2201940-6
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  • 6
    In: Alzheimer's & Dementia, Wiley, Vol. 18, No. S5 ( 2022-12)
    Abstract: Mild cognitive impairment (MCI) and mild Alzheimer’s disease (mAD) are characterized by decline in memory and other cognitive domains, including language. Previous studies have shown that MCI and mAD patients produce impaired speech. In this study, we investigated longitudinal changes in lexical and acoustic speech features from natural speech of MCI and mAD patients using highly reliable automated methods. Method We analyzed 116 digitized 1‐minute picture descriptions produced by 24 MCI (65.8±9.2y, 9 females, mean mini‐mental state exam (MMSE) score at the first recording (T1)=25.4±1.1) and 19 mAD patients (66.9±8.8y, 5 females, mean MMSE at T1=21.9±1.1). The groups did not differ in demographic characteristics, disease duration, and mean inter‐sample interval. Using automated pipelines, we tagged the part‐of‐speech categories of all words, rated words for word frequency, familiarity, concreteness, and semantic ambiguity, and counted partial words and total number of words. Speech samples were segmented into speech and silent pause segments to calculate mean speech segment duration, pause rate, percent of speech out of total time, and articulation rate. Linear mixed‐effects models examined changes over time for each measure, controlling for disease duration at T1. The difference between the first and the last recordings (mean=24±10.9 months) in each measure was related to changes in MMSE, covarying for disease duration at T1. Result Patients’ adjectives (beta=‐0.04, p =0.006) and determiners (beta=‐0.06, p =0.01) decreased over time, whereas pronouns increased (beta=0.06, p =0.014). Patients produced more frequent (beta=0.004, p =0.043) and more familiar (beta=0.001, p =0.046) words over time. Patients articulated more slowly (beta=‐0.02, p =0.001) and produced more partial words (beta=0.04, p =0.004) and fewer total words (beta=‐0.9, p =0.018) over time. Patients produced shorter speech segments (beta=0.008, p =0.021), paused more frequently (beta=0.32, p =0.001), and produced less speech (beta=‐0.35, p 〈 0.001) over time. All measures showed no group interaction. Patients whose MMSE scores decreased spoke more slowly (beta=2.25, p =0.04) and produced higher‐frequency words (beta=‐6.4, p =0.043) and more partial words (beta=‐0.72, p =0.028) compared with patients whose MMSE scores did not change. Conclusion MCI and mAD patients’ language changed over time, and this was significantly related to patients’ cognitive decline. These findings support the use of automated speech analyses in studying longitudinal changes in neurodegeneration.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2201940-6
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  • 7
    In: Neurology, Ovid Technologies (Wolters Kluwer Health), Vol. 88, No. 24 ( 2017-06-13), p. 2276-2284
    Abstract: To determine whether logopenic features of phonologic loop dysfunction reflect Alzheimer disease (AD) neuropathology in primary progressive aphasia (PPA). Methods: We performed a retrospective case-control study of 34 patients with PPA with available autopsy tissue. We compared baseline and longitudinal clinical features in patients with primary AD neuropathology to those with primary non-AD pathologies. We analyzed regional neuroanatomic disease burden in pathology-defined groups using postmortem neuropathologic data. Results: A total of 19/34 patients had primary AD pathology and 15/34 had non-AD pathology (13 frontotemporal lobar degeneration, 2 Lewy body disease). A total of 16/19 (84%) patients with AD had a logopenic spectrum phenotype; 5 met published criteria for the logopenic variant (lvPPA), 8 had additional grammatical or semantic deficits (lvPPA+), and 3 had relatively preserved sentence repetition (lvPPA−). Sentence repetition was impaired in 68% of patients with PPA with AD pathology; forward digit span (DF) was impaired in 90%, substantially higher than in non-AD PPA (33%, p 〈 0.01). Lexical retrieval difficulty was common in all patients with PPA and did not discriminate between groups. Compared to non-AD, PPA with AD pathology had elevated microscopic neurodegenerative pathology in the superior/midtemporal gyrus, angular gyrus, and midfrontal cortex ( p 〈 0.01). Low DF scores correlated with high microscopic pathologic burden in superior/midtemporal and angular gyri ( p ≤ 0.03). Conclusions: Phonologic loop dysfunction is a central feature of AD-associated PPA and specifically correlates with temporoparietal neurodegeneration. Quantitative measures of phonologic loop function, combined with modified clinical lvPPA criteria, may help discriminate AD-associated PPA.
    Type of Medium: Online Resource
    ISSN: 0028-3878 , 1526-632X
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2017
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  • 8
    Online Resource
    Online Resource
    American Speech Language Hearing Association ; 2018
    In:  Journal of Speech, Language, and Hearing Research Vol. 61, No. 7 ( 2018-07-13), p. 1691-1699
    In: Journal of Speech, Language, and Hearing Research, American Speech Language Hearing Association, Vol. 61, No. 7 ( 2018-07-13), p. 1691-1699
    Abstract: Early cognitive symptoms such as word-finding difficulty (WFD) in daily conversation are common in Parkinson's disease (PD), but studies have been limited by a lack of feasible, quantitative measures. Linguistic analysis, focused on pauses in speech, may yield markers of impairment of cognition and communication in PD. The objective of this study was to evaluate the relationship of linguistic markers in semistructured speech to WFD symptoms and cognitive function in PD. Method Speech recordings of description of the Cookie Theft picture in 53 patients with PD without dementia and 23 elderly controls were analyzed with Praat software. Montreal Cognitive Assessment (MoCA; Nasreddine et al., 2005), category naming fluency, and confrontation naming tests were administered. Questionnaires rating WFD symptoms and cognitive instrumental activities of daily living were completed. We determined the relationships between (a) pause length and location, (b) MoCA score, and (c) WFD symptoms, using Pearson's correlations and multivariate regression models. Results Compared with controls, patients with PD had more pauses within utterances as well as fewer words per minute and a lower percentage of well-formed sentences. Pauses within utterances differed significantly between PD–mild cognitive impairment and normal cognition ( p 〈 .001). Words per minute and percentage of well-formed sentences were predictive of MoCA in multivariate regression models. Pauses before verbs were associated with patient-reported severity of WFD symptoms ( p = .006). Conclusions Linguistic markers including pauses within utterances distinguish patients with PD with mild cognitive symptoms from elderly controls. These markers are associated with global cognitive function before the onset of dementia. Pauses before verbs and grammatical markers may index early cognitive symptoms such as WFD that may interfere with functional communication. Supplemental Material https://doi.org/10.23641/asha.6615401
    Type of Medium: Online Resource
    ISSN: 1092-4388 , 1558-9102
    Language: English
    Publisher: American Speech Language Hearing Association
    Publication Date: 2018
    detail.hit.zdb_id: 2070420-3
    SSG: 5,2
    SSG: 7,11
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  • 9
    In: Journal of Alzheimer's Disease Reports, IOS Press, Vol. 7, No. 1 ( 2023-06-08), p. 589-604
    Abstract: Background: Apraxia of speech (AOS) is a core feature of nonfluent/agrammatic primary progressive aphasia (naPPA), but its precise characteristics and the prevalence of AOS features in spontaneous speech are debated. Objective: To assess the frequency of features of AOS in the spontaneous, connected speech of individuals with naPPA and to evaluate whether these features are associated with an underlying motor disorder such as corticobasal syndrome or progressive supranuclear palsy. Methods: We examined features of AOS in 30 patients with naPPA using a picture description task. We compared these patients to 22 individuals with behavioral variant frontotemporal dementia and 30 healthy controls. Each speech sample was evaluated perceptually for lengthened speech segments and quantitatively for speech sound distortions, pauses between and within words, and articulatory groping. We compared subgroups of naPPA with and without at least two features of AOS to assess the possible contribution of a motor impairment to speech production deficits. Results: naPPA patients produced both speech sound distortions and other speech sound errors. Speech segmentation was found in 27/30 (90%) of individuals. Distortions were identified in 8/30 (27%) of individuals, and other speech sound errors occurred in 18/30 (60%) of individuals. Frequent articulatory groping was observed in 6/30 (20%) of individuals. Lengthened segments were observed rarely. There were no differences in the frequencies of AOS features among naPPA subgroups as a function of extrapyramidal disease. Conclusion: Features of AOS occur with varying frequency in the spontaneous speech of individuals with naPPA, independently of an underlying motor disorder.
    Type of Medium: Online Resource
    ISSN: 2542-4823
    Language: Unknown
    Publisher: IOS Press
    Publication Date: 2023
    detail.hit.zdb_id: 2955863-3
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  • 10
    In: Brain and Language, Elsevier BV, Vol. 120, No. 3 ( 2012-03), p. 290-302
    Type of Medium: Online Resource
    ISSN: 0093-934X
    RVK:
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2012
    detail.hit.zdb_id: 1462477-1
    SSG: 5,2
    SSG: 7,11
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