Literature DB >> 30599136

Genetic screen in a large series of patients with primary progressive aphasia.

Eliana Marisa Ramos1, Deepika Reddy Dokuru1, Victoria Van Berlo1, Kevin Wojta1, Qing Wang1, Alden Y Huang2, Zachary A Miller3, Anna M Karydas3, Eileen H Bigio4, Emily Rogalski4, Sandra Weintraub4, Benjamin Rader4, Bruce L Miller3, Maria Luisa Gorno-Tempini3, Marek-Marsel Mesulam4, Giovanni Coppola5.   

Abstract

INTRODUCTION: Primary progressive aphasia (PPA) is a neurological syndrome, associated with both frontotemporal dementia and Alzheimer's disease, in which progressive language impairment emerges as the most salient clinical feature during the initial stages of disease.
METHODS: We screened the main genes associated with Alzheimer's disease and frontotemporal dementia for pathogenic and risk variants in a cohort of 403 PPA cases.
RESULTS: In this case series study, 14 (3.5%) cases carried (likely) pathogenic variants: four C9orf72 expansions, nine GRN, and one TARDBP mutation. Rare risk variants, TREM2 R47H and MAPT A152T, were associated with a three- to seven-fold increase in risk for PPA. DISCUSSION: Our results show that while pathogenic variants within the most common dementia genes were rarely associated with PPA, these were found almost exclusively in GRN and C9orf72, suggesting that PPA is more TDP43- than tau-related in our series. This is consistent with the finding that PPA frequency in dominantly inherited dementias is the highest in kindreds with GRN variants.
Copyright © 2019 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  C9orf72; GRN; Genetics; Primary progressive aphasia; TARDBP

Mesh:

Substances:

Year:  2019        PMID: 30599136      PMCID: PMC6480353          DOI: 10.1016/j.jalz.2018.10.009

Source DB:  PubMed          Journal:  Alzheimers Dement        ISSN: 1552-5260            Impact factor:   21.566


  62 in total

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2.  Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.

Authors:  Giovanni Coppola; Subashchandrabose Chinnathambi; Jason JiYong Lee; Beth A Dombroski; Matt C Baker; Alexandra I Soto-Ortolaza; Suzee E Lee; Eric Klein; Alden Y Huang; Renee Sears; Jessica R Lane; Anna M Karydas; Robert O Kenet; Jacek Biernat; Li-San Wang; Carl W Cotman; Charles S Decarli; Allan I Levey; John M Ringman; Mario F Mendez; Helena C Chui; Isabelle Le Ber; Alexis Brice; Michelle K Lupton; Elisavet Preza; Simon Lovestone; John Powell; Neill Graff-Radford; Ronald C Petersen; Bradley F Boeve; Carol F Lippa; Eileen H Bigio; Ian Mackenzie; Elizabeth Finger; Andrew Kertesz; Richard J Caselli; Marla Gearing; Jorge L Juncos; Bernardino Ghetti; Salvatore Spina; Yvette M Bordelon; Wallace W Tourtellotte; Matthew P Frosch; Jean Paul G Vonsattel; Chris Zarow; Thomas G Beach; Roger L Albin; Andrew P Lieberman; Virginia M Lee; John Q Trojanowski; Vivianna M Van Deerlin; Thomas D Bird; Douglas R Galasko; Eliezer Masliah; Charles L White; Juan C Troncoso; Didier Hannequin; Adam L Boxer; Michael D Geschwind; Satish Kumar; Eva-Maria Mandelkow; Zbigniew K Wszolek; Ryan J Uitti; Dennis W Dickson; Jonathan L Haines; Richard Mayeux; Margaret A Pericak-Vance; Lindsay A Farrer; Owen A Ross; Rosa Rademakers; Gerard D Schellenberg; Bruce L Miller; Eckhard Mandelkow; Daniel H Geschwind
Journal:  Hum Mol Genet       Date:  2012-05-03       Impact factor: 6.150

3.  Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

Authors:  M Baker; I Litvan; H Houlden; J Adamson; D Dickson; J Perez-Tur; J Hardy; T Lynch; E Bigio; M Hutton
Journal:  Hum Mol Genet       Date:  1999-04       Impact factor: 6.150

4.  Frontotemporal Dementia due to the Novel GRN Arg161GlyfsX36 Mutation.

Authors:  Stefano Gazzina; Silvana Archetti; Antonella Alberici; Elisa Bonomi; Maura Cosseddu; Diego Di Lorenzo; Alessandro Padovani; Barbara Borroni
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5.  From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

Authors:  Chiara Cerami; Alessandra Marcone; Daniela Galimberti; Chiara Villa; Elio Scarpini; Stefano F Cappa
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6.  Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

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Journal:  J Alzheimers Dis       Date:  2016-09-06       Impact factor: 4.472

7.  Asymmetry and heterogeneity of Alzheimer's and frontotemporal pathology in primary progressive aphasia.

Authors:  M-Marsel Mesulam; Sandra Weintraub; Emily J Rogalski; Christina Wieneke; Changiz Geula; Eileen H Bigio
Journal:  Brain       Date:  2014-02-25       Impact factor: 13.501

Review 8.  Progranulin mutations as risk factors for Alzheimer disease.

Authors:  David C Perry; Manja Lehmann; Jennifer S Yokoyama; Anna Karydas; Jason Jiyong Lee; Giovanni Coppola; Lea T Grinberg; Dan Geschwind; William W Seeley; Bruce L Miller; Howard Rosen; Gil Rabinovici
Journal:  JAMA Neurol       Date:  2013-06       Impact factor: 18.302

9.  Cognition and anatomy in three variants of primary progressive aphasia.

Authors:  Maria Luisa Gorno-Tempini; Nina F Dronkers; Katherine P Rankin; Jennifer M Ogar; La Phengrasamy; Howard J Rosen; Julene K Johnson; Michael W Weiner; Bruce L Miller
Journal:  Ann Neurol       Date:  2004-03       Impact factor: 10.422

10.  Characteristics of frontotemporal dementia patients with a Progranulin mutation.

Authors:  Edward D Huey; Jordan Grafman; Eric M Wassermann; Pietro Pietrini; Michael C Tierney; Bernardino Ghetti; Salvatore Spina; Matt Baker; Mike Hutton; Joshua W Elder; Stephen L Berger; Kyle A Heflin; John Hardy; Parastoo Momeni
Journal:  Ann Neurol       Date:  2006-09       Impact factor: 10.422

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2.  Neuropathological fingerprints of survival, atrophy and language in primary progressive aphasia.

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4.  Diagnostic Assessment in Primary Progressive Aphasia: An Illustrative Case Example.

Authors:  Eduardo Europa; Leonardo Iaccarino; David C Perry; Elizabeth Weis; Ariane E Welch; Gil D Rabinovici; Bruce L Miller; Maria Luisa Gorno-Tempini; Maya L Henry
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7.  Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations.

Authors:  Andrew E Arrant; Jonathan R Roth; Nicholas R Boyle; Shreya N Kashyap; Madelyn Q Hoffmann; Charles F Murchison; Eliana Marisa Ramos; Alissa L Nana; Salvatore Spina; Lea T Grinberg; Bruce L Miller; William W Seeley; Erik D Roberson
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9.  A novel temporal-predominant neuro-astroglial tauopathy associated with TMEM106B gene polymorphism in FTLD/ALS-TDP.

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10.  The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han Patients.

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  10 in total

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