Introduction: The analytical epidemiological information on amyotrophic lateral sclerosis (ALS) is extensive and is based on case-control studies, selective patient series and few cohort studies that analyze the risk factors for the disease.
Review: The studies found in the literature on analytical epidemiology have been reviewed in an attempt to analyze the methodology, compare their results and comment on the possible biases and confounding factors such as the different roles of the risk factors.
Conclusion: In spite of the extensive information available, the analytical epidemiology of ALS has still not clarified the etiological factors of the disease. This may be due to the influence of the genetic factors, but also to the variability of the methodological designs. However, the analytical factor that has the greatest consistency is that of exhibition to heavy metals. Greater physical activity or increased frequency in special situations such as is the cases from the first Gulf War could be suggested as a more than casual precipitating factor.
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Trials
January 2025
Department of Physiotherapy, Melbourne School of Health Science, University of Melbourne, Melbourne, Australia.
Background: Non-invasive ventilation (NIV) uses positive pressure to assist people with respiratory muscle weakness or severe respiratory compromise to breathe. Most people use this treatment during sleep when breathing is most susceptible to instability. The benefits of using NIV in motor neurone disease (MND) are well-established.
View Article and Find Full Text PDFSci Rep
December 2024
Neurogenetics Department, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Amyotrophic lateral sclerosis (ALS) is a devastating, uniformly lethal degenerative disease of motor neurons, presenting with relentlessly progressive muscle atrophy and weakness. More than fifty genes carrying causative or disease-modifying variants have been identified since the 1990s, when the first ALS-associated variant in the gene SOD1 was discovered. The most commonly mutated ALS genes in the European populations include the C9orf72, SOD1, TARDBP and FUS.
View Article and Find Full Text PDFAmyotroph Lateral Scler Frontotemporal Degener
December 2024
Rare Diseases Information System, Planning and Health Financing Department, Regional Health Council, Murcia, Spain.
Objective: To describe the epidemiology, characteristics, and factors associated with the evolution and survival in patients with amyotrophic lateral sclerosis (ALS) in a region of southeastern Spain.
Methods: An observational study was carried out in people with a diagnosis of ALS in the period 2008-2021 who were registered in the Information System of Rare Diseases of the Region of Murcia (SIER). We calculated crude and standardized incidence rate (SIR) using European Standard Population of 2013 and point prevalence.
Int J Mol Sci
November 2024
Department of Pathomorphology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 3 Maja St. 13, 41-800 Zabrze, Poland.
J Neurol
December 2024
Department of Neurology, Aarhus University Hospital, Aarhus, Denmark.
Background And Aim: Recent studies have suggested that the incidence rate (IR) and the rate of death (MR) of amyotrophic lateral sclerosis (ALS) are increasing. Still, it remains unclear whether this is due to improved case ascertainment or represents a true increase. We examined the development in the incidence and mortality of ALS in Denmark for 42 years.
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