Network anatomy in logopenic variant of primary progressive aphasia

Author:

Mandelli Maria Luisa1ORCID,Lorca‐Puls Diego L.12,Lukic Sladjana13,Montembeault Maxime14,Gajardo‐Vidal Andrea15,Licata Abigail1,Scheffler Aaron6,Battistella Giovanni17,Grasso Stephanie M.8,Bogley Rian1,Ratnasiri Buddhika M.1,La Joie Renaud1,Mundada Nidhi S.1,Europa Eduardo9,Rabinovici Gil1,Miller Bruce L.1,De Leon Jessica1,Henry Maya L.8,Miller Zachary1,Gorno‐Tempini Maria Luisa1

Affiliation:

1. Memory and Aging Center, Department of Neurology University of California San Francisco California USA

2. Sección de Neurología, Departamento de Especialidades, Facultad de Medicina Universidad de Concepción Concepción Chile

3. Department of Communication Sciences and Disorders Adelphi University Garden City New York USA

4. Department of Psychiatry Douglas Mental Health University Institute, McGill University Montréal Canada

5. Faculty of Health Sciences Universidad del Desarrollo Concepción Chile

6. Department of Epidemiology and Biostatistics University of California San Francisco California USA

7. Department of Otolaryngology Head and Neck Surgery, Massachusetts Eye and Ear and Harvard Medical School Boston Massachusetts USA

8. Department of Speech, Language, and Hearing Sciences University of Texas Austin Texas USA

9. Department of Communicative Disorders and Sciences San Jose State University San Jose California USA

Abstract

AbstractThe logopenic variant of primary progressive aphasia (lvPPA) is a neurodegenerative syndrome characterized linguistically by gradual loss of repetition and naming skills resulting from left posterior temporal and inferior parietal atrophy. Here, we sought to identify which specific cortical loci are initially targeted by the disease (epicenters) and investigate whether atrophy spreads through predetermined networks. First, we used cross‐sectional structural MRI data from individuals with lvPPA to define putative disease epicenters using a surface‐based approach paired with an anatomically fine‐grained parcellation of the cortical surface (i.e., HCP‐MMP1.0 atlas). Second, we combined cross‐sectional functional MRI data from healthy controls and longitudinal structural MRI data from individuals with lvPPA to derive the epicenter‐seeded resting‐state networks most relevant to lvPPA symptomatology and ascertain whether functional connectivity in these networks predicts longitudinal atrophy spread in lvPPA. Our results show that two partially distinct brain networks anchored to the left anterior angular and posterior superior temporal gyri epicenters were preferentially associated with sentence repetition and naming skills in lvPPA. Critically, the strength of connectivity within these two networks in the neurologically‐intact brain significantly predicted longitudinal atrophy progression in lvPPA. Taken together, our findings indicate that atrophy progression in lvPPA, starting from inferior parietal and temporoparietal junction regions, predominantly follows at least two partially nonoverlapping pathways, which may influence the heterogeneity in clinical presentation and prognosis.

Funder

Foundation for the National Institutes of Health

Larry L. Hillblom Foundation

John Douglas French Alzheimer's Foundation

Agencia Nacional de Investigación y Desarrollo

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

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