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It has been recently reported that a large proportion of patients with familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are associated with a hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72. We have assessed 1757 Italian sporadic ALS cases, 133 from Sardinia, 101 from Sicily, and 1523 from mainland Italy. Sixty (3.7%) of 1624 mainland Italians and Sicilians and 9 (6.8%) of the 133 Sardinian sporadic ALS cases carried the pathogenic repeat expansion. None of the 619 regionally matched control samples (1238 chromosomes) carried the expansion. Twenty-five cases (36.2%) had behavioral FTD in addition to ALS. FTD or unspecified dementia was also detected in 19 pedigrees (27.5%) in first-degree relatives of ALS patients. Cases carrying the C9ORF72 hexanucleotide expansion survived 1 year less than cases who did not carry this mutation. In conclusion, we found that C9ORF72 hexanucleotide repeat expansions represents a sizeable proportion of apparent sporadic ALS in the Italian and Sardinian population, representing by far the most common mutation in Italy and the second most common in Sardinia.

Original publication

DOI

10.1016/j.neurobiolaging.2012.02.011

Type

Journal article

Journal

Neurobiol Aging

Publication Date

08/2012

Volume

33

Pages

1848.e15 - 1848.e20

Keywords

Amyotrophic Lateral Sclerosis, C9orf72 Protein, Female, Genetic Markers, Genetic Predisposition to Disease, Genetic Variation, Humans, Italy, Male, Middle Aged, Polymorphism, Single Nucleotide, Prevalence, Proteins, Repetitive Sequences, Nucleic Acid, Risk Factors