Mutational Landscape of Alzheimer’s Disease and Frontotemporal Dementia: Regional Variances in Northern, Central, and Southern Italy

Author:

Saraceno Claudia1ORCID,Pagano Lorenzo1ORCID,Laganà Valentina2ORCID,Geviti Andrea3ORCID,Bagnoli Silvia4,Ingannato Assunta4ORCID,Mazzeo Salvatore56,Longobardi Antonio1ORCID,Fostinelli Silvia7ORCID,Bellini Sonia1ORCID,Montesanto Alberto8ORCID,Binetti Giuliano7,Maletta Raffaele2,Nacmias Benedetta49ORCID,Ghidoni Roberta1ORCID

Affiliation:

1. Molecular Markers Laboratory, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, 25125 Brescia, Italy

2. Department of Primary Care, Regional Neurogenetic Centre (CRN), ASP Catanzaro, 88046 Lamezia Terme, Italy

3. Service of Statistics, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, 25125 Brescia, Italy

4. Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, 50139 Florence, Italy

5. Vita-Salute San Raffaele University, 20132 Milan, Italy

6. IRCCS Policlinico San Donato, 20097 San Donato Milanese, Italy

7. MAC-Memory Clinic and Molecular Markers, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, 25125 Brescia, Italy

8. Department of Biology, Ecology and Earth Sciences, University of Calabria, 87036 Rende, Italy

9. IRCCS Fondazione Don Carlo Gnocchi, 50143 Florence, Italy

Abstract

Alzheimer’s Disease (AD) and Frontotemporal Dementia (FTD) are the two major neurodegenerative diseases with distinct clinical and neuropathological profiles. The aim of this report is to conduct a population-based investigation in well-characterized APP, PSEN1, PSEN2, MAPT, GRN, and C9orf72 mutation carriers/pedigrees from the north, the center, and the south of Italy. We retrospectively analyzed the data of 467 Italian individuals. We identified 21 different GRN mutations, 20 PSEN1, 11 MAPT, 9 PSEN2, and 4 APP. Moreover, we observed geographical variability in mutation frequencies by looking at each cohort of participants, and we observed a significant difference in age at onset among the genetic groups. Our study provides evidence that age at onset is influenced by the genetic group. Further work in identifying both genetic and environmental factors that modify the phenotypes in all groups is needed. Our study reveals Italian regional differences among the most relevant AD/FTD causative genes and emphasizes how the collaborative studies in rare diseases can provide new insights to expand knowledge on genetic/epigenetic modulators of age at onset.

Funder

European Union—Next Generation EU—NRRP M6C2—Investment 2.1 Enhancement and strengthening of biomedical research in the NHS

Publisher

MDPI AG

Reference72 articles.

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