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1.
Neurology ; 72(19): 1640-5, 2009 May 12.
Article in English | MEDLINE | ID: mdl-19433736

ABSTRACT

OBJECTIVE: To describe ALS mortality rates in the well-characterized ethnically mixed Cuban population over a 6-year period. BACKGROUND: There have been few population-based epidemiologic studies of ALS in non-Europeans. Preliminary data from the United States suggest a lower frequency of ALS in Hispanic and African groups compared with those of European descent. The Cuban population of 11 million comprises three main ancestral groups classified by skin color as white (65%), mixed (24%), and (black 10%). Medical care is of a high standard and is free. Cuba is ideally placed to establish the frequency of ALS in an admixed population of diverse ethnic origin. METHODS: Multiple-cause mortality files from the Central Statistics office in Cuba for the years 2001 through to 2006 were searched for codes corresponding to ALS. Age-adjusted mortality rates were calculated by sex, race/ethnicity, age, and geographic region at time of death. RESULTS: Four hundred thirty-two patients with a diagnosis of ALS were identified. The mean age at death was 63.7 years. There was a slight male predominance (1.1:1). The adjusted death rate from ALS for the total population older than 15 years was 0.83 per 100,000. The adjusted mortality rate per 100,000 was considerably lower in the mixed population (0.55; confidence interval [CI] 0.4-0.72) than in whites (0.93; CI 0.83-1.03) and blacks (0.87; CI 0.62-1.17). There was no correlation between the number of neurologists in each region and the mortality rate from ALS (r = 0.268, p = 0.335). CONCLUSIONS: The overall mortality rate from ALS in Cuba is similar to that described in Hispanic populations in the United States and is lower than in Northern European populations. Mortality from ALS is lowest in a population of mixed ancestry. Ancestral origin is likely to play a role in ALS susceptibility.


Subject(s)
Amyotrophic Lateral Sclerosis/ethnology , Amyotrophic Lateral Sclerosis/genetics , Amyotrophic Lateral Sclerosis/mortality , Genetic Predisposition to Disease/genetics , Racial Groups/genetics , Age of Onset , Cohort Studies , Confidence Intervals , Cuba/epidemiology , Cuba/ethnology , Female , Hispanic or Latino/ethnology , Hispanic or Latino/genetics , Hispanic or Latino/statistics & numerical data , Humans , Incidence , Male , Middle Aged , Mortality/ethnology , Racial Groups/statistics & numerical data , Registries , White People/ethnology , White People/genetics , White People/statistics & numerical data
2.
Neurology ; 65(4): 636-8, 2005 Aug 23.
Article in English | MEDLINE | ID: mdl-16116135

ABSTRACT

The authors reviewed all cases of type I spinal muscular atrophy (SMA) in Cuba over a 6-year period. The incidence of SMA type I was 3.53 per 100,000 livebirths. When the population was classified according to self-reported ethnicity, the incidence was eight per 100,000 for whites; 0.89 per 100,000 for blacks, and 0.96 per 100,000 for those of mixed ethnicity. Type 1 SMA may occur less frequently in individuals of African ancestry.


Subject(s)
Genetic Predisposition to Disease/genetics , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Spinal Muscular Atrophies of Childhood/epidemiology , Black People/genetics , Chromosomes, Human, Pair 5/genetics , Cohort Studies , Cuba/epidemiology , Cyclic AMP Response Element-Binding Protein/genetics , DNA Mutational Analysis , Exons/genetics , Female , Genetic Testing , Genetic Variation/genetics , Heterozygote , Humans , Incidence , Infant , Infant, Newborn , Male , Mutation/genetics , Nerve Tissue Proteins/genetics , Prevalence , RNA-Binding Proteins/genetics , SMN Complex Proteins , Sex Distribution , Spinal Muscular Atrophies of Childhood/ethnology , Spinal Muscular Atrophies of Childhood/genetics , White People/genetics
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