Literature DB >> 22819134

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.

Livia Bernardi1, Francesca Frangipane1, Nicoletta Smirne1, Rosanna Colao1, Gianfranco Puccio1, Sabrina Am Curcio1, Maria Mirabelli1, Raffaele Maletta1, Maria Anfossi1, Maura Gallo1, Silvana Geracitano1, Maria Elena Conidi1, Raffale Di Lorenzo1, Alessandra Clodomiro1, Chiara Cupidi1, Sandra Marzano2, Francesco Comito2, Vincenzo Valenti2, Maria Angela Zirilli2, Mahdi Ghani3, Zhengrui Xi3, Christine Sato3, Danielle Moreno3, Annelisa Borelli4, Rosa Anna Leone4, Peter St George-Hyslop3,5,6, Ekaterina Rogaeva3,5, Amalia C Bruni1.   

Abstract

The objectives of this study were to estimate frontotemporal dementia (FTD) prevalence, identify FTD-related mutations, and correlate FTD phenotype with mutations in a southern Italian population. The study population consisted of subjects ≥ 50 years of age residing in the Community of Biv. on January 1, 2004, and a door-to-door 2-phase design was used. Genetic and biochemical analyses were done on samples collected from 32 patients. Prevalence rates were 0.6 for Alzheimer's disease, 0.4 for vascular dementia (VD), 3.5 for FTD, 0.2 for Parkinson dementia, and 1.2 for unspecified dementia. Three GRN (1 known and 2 novel) mutations with reduced plasma protein levels were found associated to 3 distinct phenotypes (behavioral, affective, and delirious type). We report an unusually high FTD prevalence in the investigated population, but a low prevalence of Alzheimer's disease. We confirm the heterogeneity of FTD phenotype associated with different GRN mutations.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22819134      PMCID: PMC5019339          DOI: 10.1016/j.neurobiolaging.2012.06.017

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  29 in total

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Authors:  Manabu Ikeda; Tomohisa Ishikawa; Hirotaka Tanabe
Journal:  Dement Geriatr Cogn Disord       Date:  2004       Impact factor: 2.959

2.  Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.

Authors:  Mariely DeJesus-Hernandez; Ian R Mackenzie; Bradley F Boeve; Adam L Boxer; Matt Baker; Nicola J Rutherford; Alexandra M Nicholson; NiCole A Finch; Heather Flynn; Jennifer Adamson; Naomi Kouri; Aleksandra Wojtas; Pheth Sengdy; Ging-Yuek R Hsiung; Anna Karydas; William W Seeley; Keith A Josephs; Giovanni Coppola; Daniel H Geschwind; Zbigniew K Wszolek; Howard Feldman; David S Knopman; Ronald C Petersen; Bruce L Miller; Dennis W Dickson; Kevin B Boylan; Neill R Graff-Radford; Rosa Rademakers
Journal:  Neuron       Date:  2011-09-21       Impact factor: 17.173

3.  Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern Italy.

Authors:  Giovanni Cizza; Livia Bernardi; Nicoletta Smirne; Raffaele Maletta; Carmine Tomaino; Angela Costanzo; Maura Gallo; John G Lewis; Silvana Geracitano; Maria Beatrice Grasso; Giuseppe Potenza; Cosimo Monteleone; Giacomino Brancati; Jui T Ho; David J Torpy; Amalia C Bruni
Journal:  J Clin Endocrinol Metab       Date:  2011-07-27       Impact factor: 5.958

4.  Progranulin null mutations in both sporadic and familial frontotemporal dementia.

Authors:  Isabelle Le Ber; Julie van der Zee; Didier Hannequin; Ilse Gijselinck; Dominique Campion; Michèle Puel; Annie Laquerrière; Tim De Pooter; Agnès Camuzat; Marleen Van den Broeck; Bruno Dubois; François Sellal; Lucette Lacomblez; Martine Vercelletto; Catherine Thomas-Antérion; Bernard-François Michel; Véronique Golfier; Mira Didic; François Salachas; Charles Duyckaerts; Marc Cruts; Patrice Verpillat; Christine Van Broeckhoven; Alexis Brice
Journal:  Hum Mutat       Date:  2007-09       Impact factor: 4.878

5.  Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.

Authors:  A C Bruni; L Bernardi; R Colao; E Rubino; N Smirne; F Frangipane; B Terni; S A M Curcio; M Mirabelli; A Clodomiro; R Di Lorenzo; R Maletta; M Anfossi; M Gallo; S Geracitano; C Tomaino; M G Muraca; A Leotta; S G Lio; L Pinessi; I Rainero; S Sorbi; L Nee; G Milan; S Pappatà; A Postiglione; N Abbamondi; G Forloni; P St George Hyslop; E Rogaeva; O Bugiani; G Giaccone; J F Foncin; M G Spillantini; G Puccio
Journal:  Neurology       Date:  2010-02-17       Impact factor: 9.910

6.  Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.

Authors:  Chiara Fenoglio; Daniela Galimberti; Francesca Cortini; John S K Kauwe; Carlos Cruchaga; Eliana Venturelli; Chiara Villa; Maria Serpente; Diego Scalabrini; Kevin Mayo; Laura M Piccio; Francesca Clerici; Diego Albani; Claudio Mariani; Gianluigi Forloni; Nereo Bresolin; Alison M Goate; Elio Scarpini
Journal:  J Alzheimers Dis       Date:  2009       Impact factor: 4.472

7.  Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

Authors:  Julie van der Zee; Isabelle Le Ber; Sebastian Maurer-Stroh; Sebastiaan Engelborghs; Ilse Gijselinck; Agnès Camuzat; Nathalie Brouwers; Rik Vandenberghe; Kristel Sleegers; Didier Hannequin; Bart Dermaut; Joost Schymkowitz; Dominique Campion; Patrick Santens; Jean-Jacques Martin; Lucette Lacomblez; Tim De Pooter; Karin Peeters; Maria Mattheijssens; Martine Vercelletto; Marleen Van den Broeck; Marc Cruts; Peter P De Deyn; Frederic Rousseau; Alexis Brice; Christine Van Broeckhoven
Journal:  Hum Mutat       Date:  2007-04       Impact factor: 4.878

8.  Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.

Authors:  Jennifer Gass; Ashley Cannon; Ian R Mackenzie; Bradley Boeve; Matt Baker; Jennifer Adamson; Richard Crook; Stacey Melquist; Karen Kuntz; Ron Petersen; Keith Josephs; Stuart M Pickering-Brown; Neill Graff-Radford; Ryan Uitti; Dennis Dickson; Zbigniew Wszolek; John Gonzalez; Thomas G Beach; Eileen Bigio; Nancy Johnson; Sandra Weintraub; Marsel Mesulam; Charles L White; Bryan Woodruff; Richard Caselli; Ging-Yuek Hsiung; Howard Feldman; Dave Knopman; Mike Hutton; Rosa Rademakers
Journal:  Hum Mol Genet       Date:  2006-09-01       Impact factor: 6.150

9.  Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics.

Authors:  Mahdi Ghani; Dalila Pinto; Joseph H Lee; Yakov Grinberg; Christine Sato; Danielle Moreno; Stephen W Scherer; Richard Mayeux; Peter St George-Hyslop; Ekaterina Rogaeva
Journal:  G3 (Bethesda)       Date:  2012-01-01       Impact factor: 3.154

10.  A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Authors:  Jonathan Beck; Jonathan D Rohrer; Tracy Campbell; Adrian Isaacs; Karen E Morrison; Emily F Goodall; Elizabeth K Warrington; John Stevens; Tamas Revesz; Janice Holton; Safa Al-Sarraj; Andrew King; Rachael Scahill; Jason D Warren; Nick C Fox; Martin N Rossor; John Collinge; Simon Mead
Journal:  Brain       Date:  2008-01-29       Impact factor: 13.501

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  17 in total

Review 1.  The behavioral variant of frontotemporal dementia: linking neuropathology to social cognition.

Authors:  Chiara Cerami; Stefano F Cappa
Journal:  Neurol Sci       Date:  2013-02-03       Impact factor: 3.307

Review 2.  The epidemiology of frontotemporal dementia.

Authors:  Chiadi U Onyike; Janine Diehl-Schmid
Journal:  Int Rev Psychiatry       Date:  2013-04

3.  GRN and MAPT Mutations in 2 Frontotemporal Dementia Research Centers in Brazil.

Authors:  Leonel T Takada; Valeria S Bahia; Henrique C Guimarães; Thais V M M Costa; Thiago C Vale; Roberta D Rodriguez; Fabio H G Porto; João C B Machado; Rogério G Beato; Karolina G Cesar; Jerusa Smid; Camila F Nascimento; Lea T Grinberg; Sonia M D Brucki; Jessica R Maximino; Sarah T Camargos; Gerson Chadi; Paulo Caramelli; Ricardo Nitrini
Journal:  Alzheimer Dis Assoc Disord       Date:  2016 Oct-Dec       Impact factor: 2.703

Review 4.  Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis.

Authors:  Ashley F Curtis; Mario Masellis; Ging-Yuek Robin Hsiung; Rahim Moineddin; Kathy Zhang; Bonnie Au; Geneva Millett; Ian Mackenzie; Ekaterina Rogaeva; Mary C Tierney
Journal:  Neurology       Date:  2017-09-15       Impact factor: 9.910

Review 5.  Cognitive Profile of C9orf72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Authors:  Anjali N Patel; Jacinda B Sampson
Journal:  Curr Neurol Neurosci Rep       Date:  2015-09       Impact factor: 5.081

6.  Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.

Authors:  Celeste M Karch; Lubov Ezerskiy; Veronica Redaelli; Anna Rita Giovagnoli; Pietro Tiraboschi; Giuseppe Pelliccioni; Paolo Pelliccioni; Dimos Kapetis; Ilaria D'Amato; Elena Piccoli; Maria Giulia Ferretti; Fabrizio Tagliavini; Giacomina Rossi
Journal:  Neurobiol Aging       Date:  2015-11-02       Impact factor: 4.673

7.  Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

Authors:  Raffaele Ferrari; Mario Grassi; Francesca Graziano; Fernando Palluzzi; Silvana Archetti; Elisa Bonomi; Amalia C Bruni; Raffaele G Maletta; Livia Bernardi; Chiara Cupidi; Rosanna Colao; Innocenzo Rainero; Elisa Rubino; Lorenzo Pinessi; Daniela Galimberti; Elio Scarpini; Maria Serpente; Benedetta Nacmias; Irene Piaceri; Silvia Bagnoli; Giacomina Rossi; Giorgio Giaccone; Fabrizio Tagliavini; Luisa Benussi; Giuliano Binetti; Roberta Ghidoni; Andrew Singleton; John Hardy; Parastoo Momeni; Alessandro Padovani; Barbara Borroni
Journal:  J Alzheimers Dis       Date:  2017       Impact factor: 4.472

8.  Comparative study of subcortical atrophy in patients with frontotemporal dementia and dementia with extrapyramidal signs.

Authors:  Leonardo Caixeta; Renata Teles Vieira; Flávia Paes; Mauro Giovanni Carta; Antonio Egidio Nardi; Oscar Arias-Carrión; Nuno B F Rocha; Henning Budde; Sergio Machado
Journal:  Clin Pract Epidemiol Ment Health       Date:  2015-03-31

9.  Hippocampal neurobiology and function in an aged mouse model of TDP-43 proteinopathy in an APP/PSEN1 background.

Authors:  Sanaz Arezoumandan; Xuezhu Cai; Praveen Kalkarni; Stephani A Davis; Katherine Wilson; Craig F Ferris; Nigel J Cairns; Michael A Gitcho
Journal:  Neurosci Lett       Date:  2021-06-09       Impact factor: 3.197

10.  Somatic comorbidities and Alzheimer's disease treatment.

Authors:  Alessandra Clodomiro; Pietro Gareri; Gianfranco Puccio; Francesca Frangipane; Roberto Lacava; Alberto Castagna; Valeria Graziella Laura Manfredi; Rosanna Colao; Amalia Cecilia Bruni
Journal:  Neurol Sci       Date:  2013-02-01       Impact factor: 3.307

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