Amyotrophic Lateral Sclerosis · 2012 · 46 citations · 11 references
MedicineNeurologyClinical EpidemiologyDisease SurveillanceEpidemiologyAmyotrophic Lateral SclerosisAnalytic EpidemiologyCase DefinitionDisease IncidenceMotor Neuron DiseasesAnnual IncidenceDisease Incidence RateIncidence RateIncidence Rate EstimationIncidence Rate RatioNeurodegenerative Disease EpidemiologyNeurological Disease Cases
Our objective was to investigate incidence of amyotrophic lateral sclerosis (ALS) in Sicily, southern Italy, by means of a population based study. We included people with ALS resident in five Sicilian provinces, whose onset occurred in the two-year period 2005-2006 (population at 31 December 2006: 3,481,096 inhabitants). A multisource case-finding procedure was adopted and patients were classified as affected by ALS according to revised El Escorial criteria. During the two-year surveillance period, 97 patients meeting eligibility criteria included 57 males (58.8%) and 40 females (41.2%). Crude annual incidence rate was 1.4/100,000 person years (95% CI 1.33-1.47). The incidence rate was higher in males (1.71/100,000; CI 1.61-1.81) than in females (1.11/100,000; CI 1.01-1.21). Standardized incidence rate for the total population in the 45-74-years-old age group was 3.22 (CI 3.11-3.33). Prevalence rate was 6.0/100,000 (CI 5.97-6.03), higher in males (7.1/100,000; CI 7.02-7.18) than females (4.9/100,000; CI 4.86-4.94). In conclusion, ALS rates observed in the present study are higher in males than females, with a peak of incidence at 70 years of age in both genders. These findings are consistent with those of other population based European studies.
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Incidence of amyotrophic lateral sclerosis in Europe
Giancarlo Logroscino, Bryan Traynor, Orla Hardiman et al. · Journal of Neurology Neurosurgery & Psychiatry · 2009 · 751 citations