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Published in: European Journal of Epidemiology 7/2018

01-07-2018 | META-ANALYSIS

Age-specific ALS incidence: a dose–response meta-analysis

Authors: Benoît Marin, Andrea Fontana, Simona Arcuti, Massimilano Copetti, Farid Boumédiene, Philippe Couratier, Ettore Beghi, Pierre Marie Preux, Giancarlo Logroscino

Published in: European Journal of Epidemiology | Issue 7/2018

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Abstract

To evaluate the association between worldwide ALS incidence rates and age, using a dose–response meta-analysis. We reviewed Medline and Embase up to July 2016 and included all population-based studies of newly-diagnosed cases, using multiple sources for case ascertainment. A dose–response meta-analysis was performed. A meta-regression investigated potential sources of heterogeneity. Of 3254 articles identified in the literature, we included 41 incidence studies covering 42 geographical areas. Overall, the fit between observed and predicted age-specific rates was very good. The expected variation of ALS incidence with age was characterized, in each study, by a progressive increase in the incidence from the 40s leading to a peak in the 60s or 70s, followed by a sharp decrease. Cochran’s Q test suggested a significant heterogeneity between studies. Overall, estimated patterns of ALS age-specific incidence (at which the peak was reached) were similar among subcontinents of Europe and North America: peak of ALS incidence ranged in these areas between 6.98 and 8.17/100,000 PYFU, which referred to age in the range 71.6–77.4 years. The relationship between age and ALS incidence appeared different for Eastern Asia which was characterized by a peak of ALS incidence at 2.20/100,000 PYFU around 75 years of age. This study confirms the consistency of the age-specific ALS incidence pattern within different subcontinents. Age-specific incidence appears lower in Eastern Asia as compared to Europe and North America.
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Literature
1.
go back to reference Beghi E, Logroscino G, Chio A, Hardiman O, Mitchell D, Swingler R, Traynor BJ. The epidemiology of ALS and the role of population-based registries. Biochem Biophys Acta. 2006;1762:1150–7.PubMed Beghi E, Logroscino G, Chio A, Hardiman O, Mitchell D, Swingler R, Traynor BJ. The epidemiology of ALS and the role of population-based registries. Biochem Biophys Acta. 2006;1762:1150–7.PubMed
2.
go back to reference Logroscino G, Tortelli R, Rizzo G, Marin B, Preux PM, Malaspina A. Amyotrophic lateral sclerosis: an aging-related disease. Curr Geriatr Rep. 2015;4:142–53.CrossRef Logroscino G, Tortelli R, Rizzo G, Marin B, Preux PM, Malaspina A. Amyotrophic lateral sclerosis: an aging-related disease. Curr Geriatr Rep. 2015;4:142–53.CrossRef
3.
go back to reference Logroscino G, Traynor BJ, Hardiman O, Chio A, Couratier P, Mitchell JD, Swingler RJ, Beghi E. Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues. J Neurol Neurosurg Psychiatry. 2008;79:6–11.CrossRefPubMed Logroscino G, Traynor BJ, Hardiman O, Chio A, Couratier P, Mitchell JD, Swingler RJ, Beghi E. Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues. J Neurol Neurosurg Psychiatry. 2008;79:6–11.CrossRefPubMed
4.
go back to reference Marin B, Boumediene F, Logroscino G, Couratier P, Babron MC, Leutenegger AL, Copetti M, Preux PM, Beghi E. Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis. Int J Epidemiol. 2017;46:57–74.PubMed Marin B, Boumediene F, Logroscino G, Couratier P, Babron MC, Leutenegger AL, Copetti M, Preux PM, Beghi E. Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis. Int J Epidemiol. 2017;46:57–74.PubMed
5.
go back to reference Marin B, Logroscino G, Boumediene F, Labrunie A, Couratier P, Babron MC, Leutenegger AL, Preux PM, Beghi E. Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin. Eur J Epidemiol. 2016;31:229–45.CrossRefPubMed Marin B, Logroscino G, Boumediene F, Labrunie A, Couratier P, Babron MC, Leutenegger AL, Preux PM, Beghi E. Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin. Eur J Epidemiol. 2016;31:229–45.CrossRefPubMed
6.
go back to reference Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, Moher D, Becker BJ, Sipe TA, Thacker SB. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis of Observational Studies in Epidemiology (MOOSE) Group. JAMA. 2000;283:2008–12.CrossRefPubMed Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, Moher D, Becker BJ, Sipe TA, Thacker SB. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis of Observational Studies in Epidemiology (MOOSE) Group. JAMA. 2000;283:2008–12.CrossRefPubMed
7.
go back to reference Fiest KM, Pringsheim T, Patten SB, Svenson LW, Jette N. The role of systematic reviews and meta-analyses of incidence and prevalence studies in neuroepidemiology. Neuroepidemiology. 2014;42:16–24.CrossRefPubMed Fiest KM, Pringsheim T, Patten SB, Svenson LW, Jette N. The role of systematic reviews and meta-analyses of incidence and prevalence studies in neuroepidemiology. Neuroepidemiology. 2014;42:16–24.CrossRefPubMed
8.
go back to reference Mitsumoto H, Chad AD, Pioro EP. Amyotrophic lateral sclerosis. Philadelphia: FA Davis; 1998. Mitsumoto H, Chad AD, Pioro EP. Amyotrophic lateral sclerosis. Philadelphia: FA Davis; 1998.
11.
go back to reference Plato CC, Garruto RM, Galasko D, Craig UK, Plato M, Gamst A, Torres JM, Wiederholt W. Amyotrophic lateral sclerosis and parkinsonism-dementia complex of Guam: changing incidence rates during the past 60 years. Am J Epidemiol. 2003;157:149–57.CrossRefPubMed Plato CC, Garruto RM, Galasko D, Craig UK, Plato M, Gamst A, Torres JM, Wiederholt W. Amyotrophic lateral sclerosis and parkinsonism-dementia complex of Guam: changing incidence rates during the past 60 years. Am J Epidemiol. 2003;157:149–57.CrossRefPubMed
12.
go back to reference Murphy M, Quinn S, Young J, Parkin P, Taylor B. Increasing incidence of ALS in Canterbury, New Zealand: a 22-year study. Neurology. 2008;71:1889–95.CrossRefPubMed Murphy M, Quinn S, Young J, Parkin P, Taylor B. Increasing incidence of ALS in Canterbury, New Zealand: a 22-year study. Neurology. 2008;71:1889–95.CrossRefPubMed
13.
go back to reference Gunnarsson LG, Lindberg G, Soderfelt B, Axelson O. The mortality of motor neuron disease in Sweden. Arch Neurol. 1990;47:42–6.CrossRefPubMed Gunnarsson LG, Lindberg G, Soderfelt B, Axelson O. The mortality of motor neuron disease in Sweden. Arch Neurol. 1990;47:42–6.CrossRefPubMed
14.
go back to reference Murros K, Fogelholm R. Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study. Acta Neurol Scand. 1983;67:41–7.CrossRefPubMed Murros K, Fogelholm R. Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study. Acta Neurol Scand. 1983;67:41–7.CrossRefPubMed
15.
go back to reference Hudson AJ, Davenport A, Hader WJ. The incidence of amyotrophic lateral sclerosis in southwestern Ontario, Canada. Neurology. 1986;36:1524–8.CrossRefPubMed Hudson AJ, Davenport A, Hader WJ. The incidence of amyotrophic lateral sclerosis in southwestern Ontario, Canada. Neurology. 1986;36:1524–8.CrossRefPubMed
16.
go back to reference Bettini M, Gargiulo-Monachelli GM, Rodriguez G, Rey RC, Peralta LM, Sica RE. Epidemiology of amyotrophic lateral sclerosis patients in a centre in Buenos Aires. Arq Neuropsiquiatr. 2011;69:867–70.CrossRefPubMed Bettini M, Gargiulo-Monachelli GM, Rodriguez G, Rey RC, Peralta LM, Sica RE. Epidemiology of amyotrophic lateral sclerosis patients in a centre in Buenos Aires. Arq Neuropsiquiatr. 2011;69:867–70.CrossRefPubMed
17.
go back to reference Bonaparte JP, Grant IA, Benstead TJ, Murray TJ, Smith M. ALS incidence in Nova Scotia over a 20-year-period: a prospective study. Can J Neurol Sci. 2007;34:69–73.CrossRefPubMed Bonaparte JP, Grant IA, Benstead TJ, Murray TJ, Smith M. ALS incidence in Nova Scotia over a 20-year-period: a prospective study. Can J Neurol Sci. 2007;34:69–73.CrossRefPubMed
20.
go back to reference Il’yasova D, Hertz-Picciotto I, Peters U, Berlin JA, Poole C. Choice of exposure scores for categorical regression in meta-analysis: a case study of a common problem. Cancer Causes Control. 2005;16:383–8.CrossRefPubMed Il’yasova D, Hertz-Picciotto I, Peters U, Berlin JA, Poole C. Choice of exposure scores for categorical regression in meta-analysis: a case study of a common problem. Cancer Causes Control. 2005;16:383–8.CrossRefPubMed
21.
go back to reference Berlin JA, Longnecker MP, Greenland S. Meta-analysis of epidemiologic dose-response data. Epidemiology. 1993;4:218–28.CrossRefPubMed Berlin JA, Longnecker MP, Greenland S. Meta-analysis of epidemiologic dose-response data. Epidemiology. 1993;4:218–28.CrossRefPubMed
22.
go back to reference Greenland S. Quantitative methods in the review of epidemiologic literature. Epidemiol Rev. 1987;9:1–30.CrossRefPubMed Greenland S. Quantitative methods in the review of epidemiologic literature. Epidemiol Rev. 1987;9:1–30.CrossRefPubMed
23.
go back to reference Heinzl H, Mittlböck M. Pseudo R-squared measures for Poisson regression models with over- or underdispersion. Comput Stat Data Anal. 2003;44:253–71.CrossRef Heinzl H, Mittlböck M. Pseudo R-squared measures for Poisson regression models with over- or underdispersion. Comput Stat Data Anal. 2003;44:253–71.CrossRef
24.
go back to reference Fontana A, Spadaro S, Copetti M, Spoto B, Salvemini L, Pizzini P, Frittitta L, Mallamaci F, Pellegrini F, Trischitta V, et al. Association between resistin levels and all-cause and cardiovascular mortality: a new study and a systematic review and meta-analysis. PLoS ONE. 2015;10:e0120419.CrossRefPubMedPubMedCentral Fontana A, Spadaro S, Copetti M, Spoto B, Salvemini L, Pizzini P, Frittitta L, Mallamaci F, Pellegrini F, Trischitta V, et al. Association between resistin levels and all-cause and cardiovascular mortality: a new study and a systematic review and meta-analysis. PLoS ONE. 2015;10:e0120419.CrossRefPubMedPubMedCentral
25.
go back to reference van Houwelingen HC, Arends LR, Stijnen T. Advanced methods in meta-analysis: multivariate approach and meta-regression. Stat Med. 2002;21:589–624.CrossRefPubMed van Houwelingen HC, Arends LR, Stijnen T. Advanced methods in meta-analysis: multivariate approach and meta-regression. Stat Med. 2002;21:589–624.CrossRefPubMed
27.
go back to reference Borenstein M, Hedges L, Higgins J, Rothstein H. Introduction to meta-analysis. Chichester: Wiley; 2009.CrossRef Borenstein M, Hedges L, Higgins J, Rothstein H. Introduction to meta-analysis. Chichester: Wiley; 2009.CrossRef
28.
go back to reference Uenal H, Rosenbohm A, Kufeldt J, Weydt P, Goder K, Ludolph A, Rothenbacher D, Nagel G, A.L.S.r.S. Group. Incidence and geographical variation of amyotrophic lateral sclerosis (ALS) in Southern Germany–completeness of the ALS registry Swabia. PLoS ONE. 2014;9:e93932.CrossRefPubMedPubMedCentral Uenal H, Rosenbohm A, Kufeldt J, Weydt P, Goder K, Ludolph A, Rothenbacher D, Nagel G, A.L.S.r.S. Group. Incidence and geographical variation of amyotrophic lateral sclerosis (ALS) in Southern Germany–completeness of the ALS registry Swabia. PLoS ONE. 2014;9:e93932.CrossRefPubMedPubMedCentral
29.
go back to reference Logroscino G, Traynor BJ, Hardiman O, Chio A, Mitchell D, Swingler RJ, Millul A, Benn E, Beghi E. Incidence of amyotrophic lateral sclerosis in Europe. J Neurol Neurosurg Psychiatry. 2010;81:385–90.CrossRefPubMed Logroscino G, Traynor BJ, Hardiman O, Chio A, Mitchell D, Swingler RJ, Millul A, Benn E, Beghi E. Incidence of amyotrophic lateral sclerosis in Europe. J Neurol Neurosurg Psychiatry. 2010;81:385–90.CrossRefPubMed
30.
go back to reference Matsumoto N, Worth RM, Kurland LT, Okazaki H. Epidemiologic study of amyotrophic lateral sclerosis in Hawaii. Identification of high incidence among Filipino men. Neurology. 1972;22:934–40.CrossRefPubMed Matsumoto N, Worth RM, Kurland LT, Okazaki H. Epidemiologic study of amyotrophic lateral sclerosis in Hawaii. Identification of high incidence among Filipino men. Neurology. 1972;22:934–40.CrossRefPubMed
31.
go back to reference Forbes RB, Colville S, Parratt J, Swingler RJ. The incidence of motor nueron disease in Scotland. J Neurol. 2007;254:866–9.CrossRefPubMed Forbes RB, Colville S, Parratt J, Swingler RJ. The incidence of motor nueron disease in Scotland. J Neurol. 2007;254:866–9.CrossRefPubMed
32.
go back to reference Gross-Paju K, Oopik M, Luus SM, Kalbe I, Puksa L, Lepik T, Kaasik AE. Motor neurone disease in South Estonia. Diagnosis and incidence rate. Acta Neurol Scand. 1998;98:22–8.CrossRefPubMed Gross-Paju K, Oopik M, Luus SM, Kalbe I, Puksa L, Lepik T, Kaasik AE. Motor neurone disease in South Estonia. Diagnosis and incidence rate. Acta Neurol Scand. 1998;98:22–8.CrossRefPubMed
33.
go back to reference O’Toole O, Traynor BJ, Brennan P, Sheehan C, Frost E, Corr B, Hardiman O. Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004. J Neurol Neurosurg Psychiatry. 2008;79:30–2.CrossRefPubMed O’Toole O, Traynor BJ, Brennan P, Sheehan C, Frost E, Corr B, Hardiman O. Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004. J Neurol Neurosurg Psychiatry. 2008;79:30–2.CrossRefPubMed
34.
go back to reference Marin B, Hamidou B, Couratier P, Nicol M, Delzor A, Raymondeau M, Druet-Cabanac M, Lautrette G, Boumediene F, Preux PM, et al. Population-based epidemiology of amyotrophic lateral sclerosis (ALS) in an ageing Europe—the French register of ALS in Limousin (FRALim register). Eur J Neurol. 2014;21:1292–300.CrossRefPubMed Marin B, Hamidou B, Couratier P, Nicol M, Delzor A, Raymondeau M, Druet-Cabanac M, Lautrette G, Boumediene F, Preux PM, et al. Population-based epidemiology of amyotrophic lateral sclerosis (ALS) in an ageing Europe—the French register of ALS in Limousin (FRALim register). Eur J Neurol. 2014;21:1292–300.CrossRefPubMed
35.
go back to reference Mandrioli J, Biguzzi S, Guidi C, Venturini E, Sette E, Terlizzi E, Ravasio A, Casmiro M, Salvi F, Liguori R, et al. Epidemiology of amyotrophic lateral sclerosis in Emilia Romagna Region (Italy): a population based study. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:262–8.CrossRefPubMed Mandrioli J, Biguzzi S, Guidi C, Venturini E, Sette E, Terlizzi E, Ravasio A, Casmiro M, Salvi F, Liguori R, et al. Epidemiology of amyotrophic lateral sclerosis in Emilia Romagna Region (Italy): a population based study. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:262–8.CrossRefPubMed
36.
go back to reference Bandettini di Poggio M, Sormani MP, Truffelli R, Mandich P, Origone P, Verdiani S, Mantero V, Scialo C, Schenone A, Mancardi GL, et al. Clinical epidemiology of ALS in Liguria, Italy. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:52–7.CrossRefPubMed Bandettini di Poggio M, Sormani MP, Truffelli R, Mandich P, Origone P, Verdiani S, Mantero V, Scialo C, Schenone A, Mancardi GL, et al. Clinical epidemiology of ALS in Liguria, Italy. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:52–7.CrossRefPubMed
37.
go back to reference Logroscino G, Beghi E, Zoccolella S, Palagano R, Fraddosio A, Simone IL, Lamberti P, Lepore V, Serlenga L. Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study. J Neurol Neurosurg Psychiatry. 2005;76:1094–8.CrossRefPubMedPubMedCentral Logroscino G, Beghi E, Zoccolella S, Palagano R, Fraddosio A, Simone IL, Lamberti P, Lepore V, Serlenga L. Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study. J Neurol Neurosurg Psychiatry. 2005;76:1094–8.CrossRefPubMedPubMedCentral
38.
go back to reference Pugliatti M, Parish LD, Cossu P, Leoni S, Ticca A, Saddi MV, Ortu E, Traccis S, Borghero G, Puddu R, et al. Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995–2009. J Neurol. 2013;260:572–9.CrossRefPubMed Pugliatti M, Parish LD, Cossu P, Leoni S, Ticca A, Saddi MV, Ortu E, Traccis S, Borghero G, Puddu R, et al. Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995–2009. J Neurol. 2013;260:572–9.CrossRefPubMed
39.
go back to reference Ragonese P, Cellura E, Aridon P, D’Amelio M, Spataro R, Taiello AC, Maimone D, La Bella V, Savettieri G. Incidence of amyotrophic lateral sclerosis in Sicily: a population based study. Amyotroph Lateral Scler. 2012;13:284–7.CrossRefPubMed Ragonese P, Cellura E, Aridon P, D’Amelio M, Spataro R, Taiello AC, Maimone D, La Bella V, Savettieri G. Incidence of amyotrophic lateral sclerosis in Sicily: a population based study. Amyotroph Lateral Scler. 2012;13:284–7.CrossRefPubMed
40.
go back to reference McGuire V, Longstreth WT Jr, Koepsell TD, van Belle G. Incidence of amyotrophic lateral sclerosis in three counties in western Washington state. Neurology. 1996;47:571–3.CrossRefPubMed McGuire V, Longstreth WT Jr, Koepsell TD, van Belle G. Incidence of amyotrophic lateral sclerosis in three counties in western Washington state. Neurology. 1996;47:571–3.CrossRefPubMed
41.
go back to reference Radhakrishnan K, Ashok PP, Sridharan R, Mousa ME. Descriptive epidemiology of motor neuron disease in Benghazi, Libya. Neuroepidemiology. 1986;5:47–54.CrossRefPubMed Radhakrishnan K, Ashok PP, Sridharan R, Mousa ME. Descriptive epidemiology of motor neuron disease in Benghazi, Libya. Neuroepidemiology. 1986;5:47–54.CrossRefPubMed
42.
go back to reference Fong GC, Cheng TS, Lam K, Cheng WK, Mok KY, Cheung CM, Chim CS, Mak W, Chan KH, Tsang KL, et al. An epidemiological study of motor neuron disease in Hong Kong. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005;6:164–8.CrossRefPubMed Fong GC, Cheng TS, Lam K, Cheng WK, Mok KY, Cheung CM, Chim CS, Mak W, Chan KH, Tsang KL, et al. An epidemiological study of motor neuron disease in Hong Kong. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005;6:164–8.CrossRefPubMed
43.
go back to reference Sajjadi M, Etemadifar M, Nemati A, Ghazavi H, Basiri K, Khoundabi B, Mousavi SA, Kabiri P, Maghzi AH. Epidemiology of amyotrophic lateral sclerosis in Isfahan, Iran. Eur J Neurol. 2010;17:984–9.CrossRefPubMed Sajjadi M, Etemadifar M, Nemati A, Ghazavi H, Basiri K, Khoundabi B, Mousavi SA, Kabiri P, Maghzi AH. Epidemiology of amyotrophic lateral sclerosis in Isfahan, Iran. Eur J Neurol. 2010;17:984–9.CrossRefPubMed
44.
go back to reference Imam I, Ball S, Wright D, Hanemann CO, Zajicek J. The epidemiology of motor neurone disease in two counties in the southwest of England. J Neurol. 2010;257:977–81.CrossRefPubMed Imam I, Ball S, Wright D, Hanemann CO, Zajicek J. The epidemiology of motor neurone disease in two counties in the southwest of England. J Neurol. 2010;257:977–81.CrossRefPubMed
45.
go back to reference Chio A, Mora G, Calvo A, Mazzini L, Bottacchi E, Mutani R. Epidemiology of ALS in Italy: a 10-year prospective population-based study. Neurology. 2009;72:725–31.CrossRefPubMed Chio A, Mora G, Calvo A, Mazzini L, Bottacchi E, Mutani R. Epidemiology of ALS in Italy: a 10-year prospective population-based study. Neurology. 2009;72:725–31.CrossRefPubMed
46.
go back to reference Drigo D, Verriello L, Clagnan E, Eleopra R, Pizzolato G, Bratina A, D’Amico D, Sartori A, Mase G, Simonetto M, et al. The incidence of amyotrophic lateral sclerosis in Friuli Venezia Giulia, Italy, from 2002 to 2009: a retrospective population-based study. Neuroepidemiology. 2013;41:54–61.CrossRefPubMed Drigo D, Verriello L, Clagnan E, Eleopra R, Pizzolato G, Bratina A, D’Amico D, Sartori A, Mase G, Simonetto M, et al. The incidence of amyotrophic lateral sclerosis in Friuli Venezia Giulia, Italy, from 2002 to 2009: a retrospective population-based study. Neuroepidemiology. 2013;41:54–61.CrossRefPubMed
47.
go back to reference Wolf J, Wohrle JC, Palm F, Nix WA, Maschke M, Safer A, Becher H, Grau AJ. Incidence of amyotrophic lateral sclerosis in Rhineland-Palatinate, Germany. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:269–74.CrossRefPubMed Wolf J, Wohrle JC, Palm F, Nix WA, Maschke M, Safer A, Becher H, Grau AJ. Incidence of amyotrophic lateral sclerosis in Rhineland-Palatinate, Germany. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:269–74.CrossRefPubMed
48.
go back to reference Beghi E, Millul A, Micheli A, Vitelli E, Logroscino G. Incidence of ALS in Lombardy, Italy. Neurology. 2007;68:141–5.CrossRefPubMed Beghi E, Millul A, Micheli A, Vitelli E, Logroscino G. Incidence of ALS in Lombardy, Italy. Neurology. 2007;68:141–5.CrossRefPubMed
49.
go back to reference Freer C, Hylton T, Jordan HM, Kaye WE, Singh S, Huang Y. Results of Florida’s Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011. BMJ Open. 2015;5:e007359.CrossRefPubMedPubMedCentral Freer C, Hylton T, Jordan HM, Kaye WE, Singh S, Huang Y. Results of Florida’s Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011. BMJ Open. 2015;5:e007359.CrossRefPubMedPubMedCentral
50.
go back to reference Jordan H, Fagliano J, Rechtman L, Lefkowitz D, Kaye W. Population-based surveillance of amyotrophic lateral sclerosis in New Jersey, 2009–2011. Neuroepidemiology. 2014;43:49–56.CrossRefPubMedPubMedCentral Jordan H, Fagliano J, Rechtman L, Lefkowitz D, Kaye W. Population-based surveillance of amyotrophic lateral sclerosis in New Jersey, 2009–2011. Neuroepidemiology. 2014;43:49–56.CrossRefPubMedPubMedCentral
51.
52.
go back to reference Valle J, Roberts E, Paulukonis S, Collins N, English P, Kaye W. Epidemiology and surveillance of amyotrophic lateral sclerosis in two large metropolitan areas in California. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16:209–15.CrossRefPubMedPubMedCentral Valle J, Roberts E, Paulukonis S, Collins N, English P, Kaye W. Epidemiology and surveillance of amyotrophic lateral sclerosis in two large metropolitan areas in California. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16:209–15.CrossRefPubMedPubMedCentral
53.
go back to reference Lannuzel A, Mecharles S, Tressieres B, Demoly A, Alhendi R, Hedreville-Tablon MA, Alecu C. Clinical varieties and epidemiological aspects of amyotrophic lateral sclerosis in the Caribbean island of Guadeloupe: a new focus of ALS associated with Parkinsonism. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16:216–23.CrossRefPubMed Lannuzel A, Mecharles S, Tressieres B, Demoly A, Alhendi R, Hedreville-Tablon MA, Alecu C. Clinical varieties and epidemiological aspects of amyotrophic lateral sclerosis in the Caribbean island of Guadeloupe: a new focus of ALS associated with Parkinsonism. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16:216–23.CrossRefPubMed
54.
go back to reference Pradas J, Puig T, Rojas-Garcia R, Viguera ML, Gich I, Logroscino G, Group A-C. Amyotrophic lateral sclerosis in Catalonia: a population based study. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:278–83.CrossRefPubMed Pradas J, Puig T, Rojas-Garcia R, Viguera ML, Gich I, Logroscino G, Group A-C. Amyotrophic lateral sclerosis in Catalonia: a population based study. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:278–83.CrossRefPubMed
55.
go back to reference Huisman MH, de Jong SW, van Doormaal PT, Weinreich SS, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH. Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology. J Neurol Neurosurg Psychiatry. 2011;82:1165–70.CrossRefPubMed Huisman MH, de Jong SW, van Doormaal PT, Weinreich SS, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH. Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology. J Neurol Neurosurg Psychiatry. 2011;82:1165–70.CrossRefPubMed
56.
go back to reference Joensen P. Incidence of amyotrophic lateral sclerosis in the Faroe Islands. Acta Neurol Scand. 2012;126:62–6.CrossRefPubMed Joensen P. Incidence of amyotrophic lateral sclerosis in the Faroe Islands. Acta Neurol Scand. 2012;126:62–6.CrossRefPubMed
57.
go back to reference Murros K, Fogelholm R. Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study. Acta Neurol Scand. 1983;67:41–7.CrossRefPubMed Murros K, Fogelholm R. Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study. Acta Neurol Scand. 1983;67:41–7.CrossRefPubMed
58.
go back to reference Højer-Pedersen E, Christensen PB, Jensen NB. Incidence and prevalence of motor neuron disease in two Danish counties. Neuroepidemiology. 1989;8:151–9.CrossRefPubMed Højer-Pedersen E, Christensen PB, Jensen NB. Incidence and prevalence of motor neuron disease in two Danish counties. Neuroepidemiology. 1989;8:151–9.CrossRefPubMed
59.
go back to reference Annegers JF, Appel S, Lee JRJ, Perkins P. Incidence and prevalence of amyotrophic lateral sclerosis in Harris County, Texas, 1985–1988. Arch Neurol. 1991;48:589–93.CrossRefPubMed Annegers JF, Appel S, Lee JRJ, Perkins P. Incidence and prevalence of amyotrophic lateral sclerosis in Harris County, Texas, 1985–1988. Arch Neurol. 1991;48:589–93.CrossRefPubMed
60.
go back to reference Forsgren L, Almay BGL, Holmgren G, Wall S. Epidemiology of motor neuron disease in northern Sweden. Acta Neurol Scand. 1983;68:20–9.CrossRefPubMed Forsgren L, Almay BGL, Holmgren G, Wall S. Epidemiology of motor neuron disease in northern Sweden. Acta Neurol Scand. 1983;68:20–9.CrossRefPubMed
61.
go back to reference Lai CH, Tseng HF. Epidemiology and medical expenses of motor neuron diseases in Taiwan. Neuroepidemiology. 2008;31:159–66.CrossRefPubMed Lai CH, Tseng HF. Epidemiology and medical expenses of motor neuron diseases in Taiwan. Neuroepidemiology. 2008;31:159–66.CrossRefPubMed
62.
go back to reference Okumura H. Epidemiological and clinical patterns of western pacific amyotrophic lateral sclerosis (ALS) in Guam and sporadic ALS in Rochester, Minnesota, U.S.A. and Hokkaido, Japan: a comparative study. Hokkaido Igaku Zasshi. 2003;78:187–95.PubMed Okumura H. Epidemiological and clinical patterns of western pacific amyotrophic lateral sclerosis (ALS) in Guam and sporadic ALS in Rochester, Minnesota, U.S.A. and Hokkaido, Japan: a comparative study. Hokkaido Igaku Zasshi. 2003;78:187–95.PubMed
63.
go back to reference Vazquez MC, Ketzoian C, Legnani C, Rega I, Sanchez N, Perna A, Penela M, Aguirrezabal X, Druet-Cabanac M, Medici M. Incidence and prevalence of amyotrophic lateral sclerosis in Uruguay: a population-based study. Neuroepidemiology. 2008;30:105–11.CrossRefPubMed Vazquez MC, Ketzoian C, Legnani C, Rega I, Sanchez N, Perna A, Penela M, Aguirrezabal X, Druet-Cabanac M, Medici M. Incidence and prevalence of amyotrophic lateral sclerosis in Uruguay: a population-based study. Neuroepidemiology. 2008;30:105–11.CrossRefPubMed
64.
go back to reference Sorenson EJ, Stalker AP, Kurland LT, Windebank AJ. Amyotrophic lateral sclerosis in Olmsted County, Minnesota, 1925 to 1998. Neurology. 2002;59:280–2.CrossRefPubMed Sorenson EJ, Stalker AP, Kurland LT, Windebank AJ. Amyotrophic lateral sclerosis in Olmsted County, Minnesota, 1925 to 1998. Neurology. 2002;59:280–2.CrossRefPubMed
65.
go back to reference Abhinav K, Stanton B, Johnston C, Hardstaff J, Orrell RW, Howard R, Clarke J, Sakel M, Ampong MA, Shaw CE, et al. Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry). Neuroepidemiology. 2007;29:44–8.CrossRefPubMed Abhinav K, Stanton B, Johnston C, Hardstaff J, Orrell RW, Howard R, Clarke J, Sakel M, Ampong MA, Shaw CE, et al. Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry). Neuroepidemiology. 2007;29:44–8.CrossRefPubMed
66.
go back to reference Scialo C, Novi G, Bandettini di Poggio M, Canosa A, Sormani MP, Mandich P, Origone P, Truffelli R, Mancardi GL, Caponnetto C. Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: an update of LIGALS register. Amyotroph Lateral Scler Frontotemporal Degener 2016;17:535–542.CrossRefPubMed Scialo C, Novi G, Bandettini di Poggio M, Canosa A, Sormani MP, Mandich P, Origone P, Truffelli R, Mancardi GL, Caponnetto C. Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: an update of LIGALS register. Amyotroph Lateral Scler Frontotemporal Degener 2016;17:535–542.CrossRefPubMed
67.
go back to reference Lee JR, Annegers JF, Appel SH. Prognosis of amyotrophic lateral sclerosis and the effect of referral selection. J Neurol Sci. 1995;132:207–15.CrossRefPubMed Lee JR, Annegers JF, Appel SH. Prognosis of amyotrophic lateral sclerosis and the effect of referral selection. J Neurol Sci. 1995;132:207–15.CrossRefPubMed
68.
go back to reference Sorenson EJ, Mandrekar J, Crum B, Stevens JC. Effect of referral bias on assessing survival in ALS. Neurology. 2007;68:600–2.CrossRefPubMed Sorenson EJ, Mandrekar J, Crum B, Stevens JC. Effect of referral bias on assessing survival in ALS. Neurology. 2007;68:600–2.CrossRefPubMed
69.
go back to reference Logroscino G, Beghi E, Hardiman O, Chio A, Mitchell JD, Swingler RJ, Traynor B. Effect of referral bias on assessing survival in ALS. Neurology. 2007;69:939 (author reply 939–940).CrossRefPubMed Logroscino G, Beghi E, Hardiman O, Chio A, Mitchell JD, Swingler RJ, Traynor B. Effect of referral bias on assessing survival in ALS. Neurology. 2007;69:939 (author reply 939–940).CrossRefPubMed
70.
go back to reference Marin B, Hamidou B, Couratier P, Nicol M, Delzor A, Raymondeau M, Druet-Cabanac M, Lautrette G, Boumediene F, Preux PM, et al. Population-based epidemiology of amyotrophic lateral sclerosis (ALS) in an ageing Europe—the French register of ALS in Limousin (FRALim register). Eur J Neurol. 2014;21:1292–300.CrossRefPubMed Marin B, Hamidou B, Couratier P, Nicol M, Delzor A, Raymondeau M, Druet-Cabanac M, Lautrette G, Boumediene F, Preux PM, et al. Population-based epidemiology of amyotrophic lateral sclerosis (ALS) in an ageing Europe—the French register of ALS in Limousin (FRALim register). Eur J Neurol. 2014;21:1292–300.CrossRefPubMed
71.
go back to reference Forbes RB, Colville S, Swingler RJ. The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over. Age Ageing. 2004;33:131–4.CrossRefPubMed Forbes RB, Colville S, Swingler RJ. The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over. Age Ageing. 2004;33:131–4.CrossRefPubMed
72.
go back to reference Forbes RB, Colville S, Swingler RJ, A.L.S.M.N.D.R. Scottish. The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over. Age Ageing. 2004;33:131–4.CrossRefPubMed Forbes RB, Colville S, Swingler RJ, A.L.S.M.N.D.R. Scottish. The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over. Age Ageing. 2004;33:131–4.CrossRefPubMed
73.
go back to reference Dandaba M, Couratier P, Labrunie A, Nicol M, Hamidou B, Raymondeau M, Logroscino G, Preux PM, Marin B, Consortium F. Characteristics and prognosis of oldest old subjects with amyotrophic lateral sclerosis. Neuroepidemiology. 2017;49:64–73.CrossRefPubMed Dandaba M, Couratier P, Labrunie A, Nicol M, Hamidou B, Raymondeau M, Logroscino G, Preux PM, Marin B, Consortium F. Characteristics and prognosis of oldest old subjects with amyotrophic lateral sclerosis. Neuroepidemiology. 2017;49:64–73.CrossRefPubMed
74.
go back to reference Cronin S, Hardiman O, Traynor BJ. Ethnic variation in the incidence of ALS: a systematic review. Neurology. 2007;68:1002–7.CrossRefPubMed Cronin S, Hardiman O, Traynor BJ. Ethnic variation in the incidence of ALS: a systematic review. Neurology. 2007;68:1002–7.CrossRefPubMed
Metadata
Title
Age-specific ALS incidence: a dose–response meta-analysis
Authors
Benoît Marin
Andrea Fontana
Simona Arcuti
Massimilano Copetti
Farid Boumédiene
Philippe Couratier
Ettore Beghi
Pierre Marie Preux
Giancarlo Logroscino
Publication date
01-07-2018
Publisher
Springer Netherlands
Published in
European Journal of Epidemiology / Issue 7/2018
Print ISSN: 0393-2990
Electronic ISSN: 1573-7284
DOI
https://doi.org/10.1007/s10654-018-0392-x

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