Literature DB >> 33004608

Neural correlates of naming errors across different neurodegenerative diseases: An FDG-PET study.

Eleonora Catricalà1, Cristina Polito1, Luca Presotto1, Valentina Esposito1, Arianna Sala1, Francesca Conca1, Celeste Gasparri1, Valentina Berti1, Massimo Filippi1, Alberto Pupi1, Sandro Sorbi1, Sandro Iannaccone1, Giuseppe Magnani1, Stefano F Cappa2, Daniela Perani1.   

Abstract

OBJECTIVE: To investigate the types of errors produced in a picture naming task by patients with neurodegenerative dementia due to different etiologies and their neural correlates.
METHODS: The same standardized picture naming test was administered to a consecutive sample of patients (n = 148) who had been studied with [18F] FDG-PET. The errors were analyzed in 3 categories (visual, semantic, and phonologic). The PET data were analyzed using an optimized single-subject procedure, and the statistical parametric mapping multiple regression design was used to explore the correlation between each type of error and brain hypometabolism in the whole group. Metabolic connectivity analyses were run at the group level on 7 left hemisphere cortical areas corresponding to an a priori defined naming network.
RESULTS: Semantic errors were predominant in most patients, independent of clinical diagnosis. In the whole group analysis, visual errors correlated with hypometabolism in the right inferior occipital lobe and in the left middle occipital lobe. Semantic errors correlated with hypometabolism in the left fusiform gyrus, the inferior and middle temporal gyri, and the temporal pole. Phonologic errors were associated with hypometabolism in the left superior and middle temporal gyri. Both positive (occipital-posterior fusiform) and negative (anterior fusiform gyrus and the superior anterior temporal lobe) connectivity changes were associated with semantic errors.
CONCLUSIONS: Naming errors reflect the dysfunction of separate stages of the naming process and are specific markers for different patterns of brain involvement. These correlations are not limited to primary progressive aphasia but extend to other neurodegenerative dementias.
© 2020 American Academy of Neurology.

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Year:  2020        PMID: 33004608     DOI: 10.1212/WNL.0000000000010967

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  5 in total

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2.  Auditory Verb Generation Performance Patterns Dissociate Variants of Primary Progressive Aphasia.

Authors:  Sladjana Lukic; Abigail E Licata; Elizabeth Weis; Rian Bogley; Buddhika Ratnasiri; Ariane E Welch; Leighton B N Hinkley; Z Miller; Adolfo M Garcia; John F Houde; Srikantan S Nagarajan; Maria Luisa Gorno-Tempini; Valentina Borghesani
Journal:  Front Psychol       Date:  2022-06-24

3.  Clinical, Imaging, and Pathologic Characteristics of Patients With Right vs Left Hemisphere-Predominant Logopenic Progressive Aphasia.

Authors:  Marina Buciuc; Joseph R Duffy; Mary M Machulda; Jonathan Graff-Radford; Nha Trang Thu Pham; Peter R Martin; Matthew L Senjem; Clifford R Jack; Nilüfer Ertekin-Taner; Dennis W Dickson; Val J Lowe; Jennifer L Whitwell; Keith Anthony Josephs
Journal:  Neurology       Date:  2021-06-04       Impact factor: 11.800

4.  Cortical hypometabolism reflects local atrophy and tau pathology in symptomatic Alzheimer's disease.

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5.  Cerebral perfusion mediated by thalamo-cortical functional connectivity in non-dominant thalamus affects naming ability in aphasia.

Authors:  Jie Zhang; Zhen Zhou; Lingling Li; Jing Ye; Desheng Shang; Shuchang Zhong; Bo Yao; Cong Xu; Yamei Yu; Fangping He; Xiangming Ye; Benyan Luo
Journal:  Hum Brain Mapp       Date:  2021-10-26       Impact factor: 5.038

  5 in total

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