Geographic distribution of amyotrophic lateral sclerosis through motor neuron disease mortality data

Amyotrophic lateral sclerosis (ALS) is a rare and devastating neurological disorder of the adult age with a prognosis of about 2–3 years from the onset of the disease. No clear cause has been identified but it seems to be a multifactorial disease with genetic and environmental components involved. I...

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Veröffentlicht in:European journal of epidemiology 2007-11, Vol.22 (11), p.781-790
Hauptverfasser: Uccelli, Raffaella, Binazzi, Alessandra, Altavista, Pierluigi, Belli, Stefano, Comba, Pietro, Mastrantonio, Marina, Vanacore, Nicola
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container_end_page 790
container_issue 11
container_start_page 781
container_title European journal of epidemiology
container_volume 22
creator Uccelli, Raffaella
Binazzi, Alessandra
Altavista, Pierluigi
Belli, Stefano
Comba, Pietro
Mastrantonio, Marina
Vanacore, Nicola
description Amyotrophic lateral sclerosis (ALS) is a rare and devastating neurological disorder of the adult age with a prognosis of about 2–3 years from the onset of the disease. No clear cause has been identified but it seems to be a multifactorial disease with genetic and environmental components involved. Increments of mortality rates were observed since 1980 both in Italy and in many other countries. The objective of the present study is to describe the distribution of ALS mortality in Italy in the period 1980–2001 detecting single municipalities or clusters with high mortality levels for motor neuron disease (MND). ALS represents the main part (85%) of the MND group which is globally identified by the IX ICD (International Classification of Diseases and Causes of Death) 335.2 code. Death numbers and standardized mortality ratios (SMR) for MND were calculated for all Italian municipalities through the ENEA mortality database system (data source: National Institute of Statistics—ISTAT), using national mortality rates as reference. Subsequently, in order to detect municipal clusters, spatial analysis was performed. Out of the 8,099 Italian municipalities, 132 where characterized by SMR values higher than expected. Moreover 16 clusters with significant high relative risk values (RR) were identified, 12 out of them including only a single municipality. Only 22 of the municipalities with high SMR were included in the clusters. In conclusion, the two different epidemiological methodologies demonstrated to be widely complementary in detecting the geographical distribution of the disease in terms of risk for populations. A first selection of the priority areas where analytical studies should be carried on, in order to identify risk factors associated to ALS, is tentatively suggested.
doi_str_mv 10.1007/s10654-007-9173-7
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A first selection of the priority areas where analytical studies should be carried on, in order to identify risk factors associated to ALS, is tentatively suggested.</description><subject>Aged</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - mortality</subject><subject>Biological and medical sciences</subject><subject>Cluster Analysis</subject><subject>Death certificates</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. 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No clear cause has been identified but it seems to be a multifactorial disease with genetic and environmental components involved. Increments of mortality rates were observed since 1980 both in Italy and in many other countries. The objective of the present study is to describe the distribution of ALS mortality in Italy in the period 1980–2001 detecting single municipalities or clusters with high mortality levels for motor neuron disease (MND). ALS represents the main part (85%) of the MND group which is globally identified by the IX ICD (International Classification of Diseases and Causes of Death) 335.2 code. Death numbers and standardized mortality ratios (SMR) for MND were calculated for all Italian municipalities through the ENEA mortality database system (data source: National Institute of Statistics—ISTAT), using national mortality rates as reference. Subsequently, in order to detect municipal clusters, spatial analysis was performed. 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subjects Aged
Amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis - mortality
Biological and medical sciences
Cluster Analysis
Death certificates
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Disease risk
Epidemiology
Female
General aspects
Geographic regions
Geographical distribution
Geography
Humans
Italy - epidemiology
Male
Medical genetics
Medical sciences
Miscellaneous
Mortality
Motor neuron disease
Nervous system diseases
Neurological disorders
Neurology
NEURO–EPIDEMIOLOGY
Public health. Hygiene
Public health. Hygiene-occupational medicine
Risk factors
Spatial analysis
Statistical analysis
title Geographic distribution of amyotrophic lateral sclerosis through motor neuron disease mortality data
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