TY - JOUR
T1 - Prevalence of Huntington's disease in Southern Sardinia, Italy
AU - Muroni, Antonella
AU - Murru, Maria Rita
AU - Sechi, Margherita
AU - Ercoli, Tommaso
AU - Marrosu, Francesco
AU - Bentivoglio, Anna Rita
AU - Petracca, Martina
AU - Maria Scaglione, Cesa Lorella
AU - Soliveri, Paola
AU - Cocco, Eleonora
AU - Pedron, Monica
AU - Murgia, Moreno
AU - Deriu, Marcello
AU - Cuccu, Stefania
AU - Ulgheri, Lucia
AU - Zuccato, Chiara
AU - Defazio, Giovanni
PY - 2020
Y1 - 2020
N2 - Background: The frequency of Huntington's disease (HD) may vary considerably, with higher estimates in non Asian populations. In Italy, two recent studies performed in Ferrara county and Molise provided different prevalence estimates, varying from 4.2 × 105 to 10.8 × 105. Here we present a study performed in the Southern part of Sardinia, a large Italian mediterranean island that is considered a genetic isolate. Methods: The study area included the two neighbouring counties of South Sardinia and Cagliari with 353,830 and 431,955 inhabitants respectively on December 31st, 2017 (prevalence date). Case-patients were ascertained through multiple sources in Sardinia and Italy. Results: We identified 54 individuals with HD, of whom 47 were alive on prevalence date. The resulting prevalence rate was 5.98 × 105 in the overall study area, however with marked variations between South Sardinia and Cagliari (9.6 × 105 vs. 3.0 × 105, p = 0.02). In the two study areas, we found similar CAG repeat length in normal alleles (17.5 ± 2.1 vs. 17.7 ± 2.2, p = 0.5). Conclusions: The overall prevalence of HD in Sardinia is close to the correspondent estimates in Europeans. Our findings also highlighted the possibility of local microgeographic variations in the epidemiology of HD.
AB - Background: The frequency of Huntington's disease (HD) may vary considerably, with higher estimates in non Asian populations. In Italy, two recent studies performed in Ferrara county and Molise provided different prevalence estimates, varying from 4.2 × 105 to 10.8 × 105. Here we present a study performed in the Southern part of Sardinia, a large Italian mediterranean island that is considered a genetic isolate. Methods: The study area included the two neighbouring counties of South Sardinia and Cagliari with 353,830 and 431,955 inhabitants respectively on December 31st, 2017 (prevalence date). Case-patients were ascertained through multiple sources in Sardinia and Italy. Results: We identified 54 individuals with HD, of whom 47 were alive on prevalence date. The resulting prevalence rate was 5.98 × 105 in the overall study area, however with marked variations between South Sardinia and Cagliari (9.6 × 105 vs. 3.0 × 105, p = 0.02). In the two study areas, we found similar CAG repeat length in normal alleles (17.5 ± 2.1 vs. 17.7 ± 2.2, p = 0.5). Conclusions: The overall prevalence of HD in Sardinia is close to the correspondent estimates in Europeans. Our findings also highlighted the possibility of local microgeographic variations in the epidemiology of HD.
KW - Huntington's disease
KW - Prevalence
KW - Huntington's disease
KW - Prevalence
UR - http://hdl.handle.net/10807/182880
U2 - 10.1016/j.parkreldis.2020.09.011
DO - 10.1016/j.parkreldis.2020.09.011
M3 - Article
SN - 1353-8020
VL - 80
SP - 54
EP - 57
JO - PARKINSONISM & RELATED DISORDERS
JF - PARKINSONISM & RELATED DISORDERS
ER -