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      Environmental and Occupational Risk Factors of Amyotrophic Lateral Sclerosis: A Population-Based Case-Control Study

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          Abstract

          Objectives: Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease with still unknown etiology. We aimed at investigating the association between environmental and occupational factors with ALS risk. Methods: We performed a population-based case-control study in four Italian provinces (Catania, Modena, Novara, and Reggio Emilia) by administration of tailored questionnaires to ALS cases ( n = 95) and randomly selected population referents ( n = 135). We estimated ALS risk by calculating the odds ratio (OR) with its 95% confidence interval (CI) using an unconditional logistic regression model. Results: We found a positive association with disease risk for history of occupation in the agricultural sector (OR = 2.09, 95% CI 0.79–7.54), especially for longer than 10 years (OR = 2.72, 95% 1.02–7.20). Overall occupational exposure to solvents also suggested a positive association, especially for thinners (OR = 2.27, 95% CI 1.14–4.54) and paint removers (OR = 2.01, 95% CI 0.90–4.48). Both occupational and environmental exposure to electromagnetic fields show a slightly increased risk with OR = 1.69 (95% CI 0.70–4.09) and 2.41 (95% CI 1.13–5.12), respectively. Occupational but not environmental exposure to pesticides (OR = 1.22, 95% CI 0.63–2.37), particularly fungicides, and exposure to metals (OR = 4.20, 95% CI 1.88–9.38), particularly lead, mercury, and selenium, showed an imprecise but positive association. Finally, there was an indication of increased risk for living in proximity to water bodies. Conclusions: Despite the caution that needs to be used due to some study limitations, such as the low number of exposed subjects and the possibility of recall bias, these results suggest the potential role of some environmental and occupational factors in ALS etiology.

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          Most cited references72

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          Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature

          Background: Amyotrophic lateral sclerosis (ALS) is relatively rare, yet the economic and social burden is substantial. Having accurate incidence and prevalence estimates would facilitate efficient allocation of healthcare resources. Objective: To provide a comprehensive and critical review of the epidemiological literature on ALS. Methods: MEDLINE and EMBASE (1995-2011) databases of population-based studies on ALS incidence and prevalence reporting quantitative data were analyzed. Data extracted included study location and time, design and data sources, case ascertainment methods and incidence and/or prevalence rates. Medians and interquartile ranges (IQRs) were calculated, and ALS case estimates were derived using 2010 population estimates. Results: In all, 37 articles met the inclusion criteria. In Europe, the median incidence rate (/100,000 population) was 2.08 (IQR 1.47-2.43), corresponding to an estimated 15,355 (10,852-17,938) cases. Median prevalence (/100,000 population) was 5.40 (IQR 4.06-7.89), or 39,863 (29,971-58,244) prevalent cases. Conclusions: Disparity in rates among ALS incidence and prevalence studies may be due to differences in study design or true variations in population demographics such as age and geography, including environmental factors and genetic predisposition. Additional large-scale studies that use standardized case ascertainment methods are needed to more accurately assess the true global burden of ALS.
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            ALS: A bucket of genes, environment, metabolism and unknown ingredients.

            The scientific scenario of amyotrophic lateral sclerosis (ALS) has dramatically changed since TDP-43 aggregates were discovered in 2006 as the main component of the neuronal inclusions seen in the disease, and more recently, when the implication of C9ORF72 expansion in familial and sporadic cases of ALS and frontotemporal dementia was confirmed. These discoveries have enlarged an extense list of genes implicated in different cellular processes such as RNA processing or autophagia among others and have broaden the putative molecular targets of the disease. Some of ALS-related genes such as TARDBP or SOD1 among others have important roles in the regulation of glucose and fatty acids metabolism, so that an impairment of fatty acids (FA) consumption and ketogenic deficits during exercise in ALS patients would connect the physiopathology with some of the more intriguing epidemiological traits of the disease. The current understanding of ALS as part of a continuum with other neurodegenerative diseases and a crossroads between genetic, neurometabolic and environmental factors represent a fascinating model of interaction that could be translated to other neurodegenerative diseases. In this review we summarize the most relevant data obtained in the ten last years and the key lines for future research in ALS.
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              Environmental Selenium and Human Health: an Update

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                Author and article information

                Journal
                Int J Environ Res Public Health
                Int J Environ Res Public Health
                ijerph
                International Journal of Environmental Research and Public Health
                MDPI
                1661-7827
                1660-4601
                22 April 2020
                April 2020
                : 17
                : 8
                : 2882
                Affiliations
                [1 ]CREAGEN-Environmental, Genetic and Nutritional Epidemiology Research Center, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, 41125 Modena, Italy; carlotta.malagoli@ 123456unimore.it (C.M.); federica.violi@ 123456unimore.it (F.V.); l.iacuzio@ 123456ausl.mo.it (L.I.); elisa.arcolin@ 123456gmail.com (E.A.); marco.vinceti@ 123456unimore.it (M.V.)
                [2 ]Department of Biomedical, Surgical and Dental Sciences, University of Milan, 20122 Milan, Italy; marina.tesauro@ 123456unimi.it (M.T.); michela.consonni@ 123456unimi.it (M.C.)
                [3 ]Department of Medical, Surgical Sciences and Advanced Technologies “G. F. Ingrassia”, Catania University, 95123 Catania, Italy; mfiore@ 123456unict.it (M.F.); olivericonti@ 123456unict.it (G.O.C.); antonio.cristaldi81@ 123456gmail.com (A.C.); pietro.zuccarello@ 123456unict.it (P.Z.); patti@ 123456unict.it (F.P.); marfer@ 123456unict.it (M.F.)
                [4 ]Azienda USL-IRCCS di Reggio Emilia, 42122 Reggio Emilia, Italy
                [5 ]Department of Public Health, Local Health Unit, 41121 Modena, Italy
                [6 ]Neurology Unit, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, 41125 Modena, Italy; elibettizucchi@ 123456gmail.com
                [7 ]ALS Centre Department of Neurology, ‘Maggiore della Carità’ University Hospital, 28100 Novara, Italy; letizia.mazzini@ 123456uniupo.it (L.M.); ileanagagliardi91@ 123456gmail.com (I.G.)
                [8 ]Neurological Rehabilitation Division, Policlinico San Marco di Zingonia, 24046 Zingonia (BG), Italy; fabrizio.pisano@ 123456grupposandonato.it
                [9 ]Neurology Unit, Department of Neuroscience, S. Agostino Estense Hospital, Azienda Ospedaliero Universitaria di Modena, 41126 Modena, Italy; mandrioli.jessica@ 123456aou.mo.it
                [10 ]Department of Epidemiology, Boston University School of Public Health, Boston, MA 02118, USA
                Author notes
                Author information
                https://orcid.org/0000-0003-2100-0344
                https://orcid.org/0000-0001-5542-5119
                https://orcid.org/0000-0002-5078-0135
                https://orcid.org/0000-0003-1857-8612
                https://orcid.org/0000-0002-6923-0846
                https://orcid.org/0000-0002-9244-9782
                https://orcid.org/0000-0001-7596-2464
                https://orcid.org/0000-0002-0551-2473
                Article
                ijerph-17-02882
                10.3390/ijerph17082882
                7216189
                32331298
                d8c1c6ed-2323-46f8-b6ea-c1c7288f6cf1
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 March 2020
                : 20 April 2020
                Categories
                Article

                Public health
                amyotrophic lateral sclerosis,occupational factors,environmental factors,case-control study

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