Spatial clustering of amyotrophic lateral sclerosis in Sardinia, Italy: The contribution of age, sex, and genetic factors

Author:

Borghero Giuseppe1,Sechi Maria Margherita12,Vasta Rosario3,Pierri Vincenzo2,Pili Francesca1,Pateri Ida12,Pilotto Silvy12,Ercoli Tommaso2ORCID,Muroni Antonella1,Chiò Adriano3,Defazio Giovanni124

Affiliation:

1. Institute of Neurology, University Hospital of Cagliari Cagliari Italy

2. Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy

3. Amyotrophic Lateral Sclerosis Center University of Turin Turin Italy

4. Amyotrophic Lateral Sclerosis Center University of Cagliari Cagliari Italy

Abstract

AbstractIntroduction/AimsSeveral microgeographic clusters of higher/lower incidence of amyotrophic lateral sclerosis (ALS) have been identified worldwide. Differences in the distribution of local factors were proposed to explain the excess ALS risk, whereas the contribution of known genetic/epigenetic factors remains unclear. The aim is to identify restricted areas of higher risk in Sardinia and to assess whether age, sex, and the most common causative genetic mutations in Sardinia (C9orf72 and TARDBP mutations) contributed to the variation in the ALS risk.MethodsWe performed an ad hoc analysis of the 10‐y population‐based incident cohort of ALS cases from a recent study of a large Sardinian area. Cluster analysis was performed by age‐ and sex‐adjusted Kulldorff's spatial scan statistic.ResultsWe identified a statistically significant cluster of higher ALS incidence in a relatively large area including 34 municipalities and >100,000 individuals. The investigated genetic mutations were more frequent in the cluster area than outside. Regardless of the genetic mutations, the excess of ALS risk was significantly associated with either sex or with age ≥ 65 y. Finally, an additive interaction between older age and male sex contributed to the excess of ALS risk in the cluster area but not outside.DiscussionOur analysis demonstrated that known genetic factors, age, and sex may contribute to microgeographic variation in ALS incidence. The significant additive interaction between older age and male sex we found in the high‐incidence cluster could suggest the presence of a third factor connecting the analyzed risk factors.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

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