Advertisement
Research Article| Volume 298, ISSUE 1-2, P78-84, November 15, 2010

Download started.

Ok

Temporal trends and geographic clusters of mortality from amyotrophic lateral sclerosis in Japan, 1995–2004

Published:September 01, 2010DOI:https://doi.org/10.1016/j.jns.2010.08.004

      Abstract

      The present study examined temporal trends and geographic clustering of amyotrophic lateral sclerosis (ALS) mortality in Japan, during 1995–2004, using vital statistics based on death certificates. ALS was usually diagnosed by neurologists according to clinical guidelines that complied with the El Escorial Criteria. The underlying cause of death for ALS was coded as G12.2A. Regression analysis was used to examine temporal trends. Spatial scan statistic was used to detect any area of elevated risk as a cluster. A total of 12,173 (6864 male and 5309 female) ALS deaths were reported. Annual crude mortality rate per 100,000 population was 1.07 (1.26 for males and 0.89 for females) in 2004. Although the overall temporal trend was stable, the trend increased in the 70+years age group (p for trend, <0.001 in males and <0.05 in females), while it declined in the under 70 years age group (p for trend, <0.01 for both sexes). Male preponderance and M/F ratio remained nearly constant over time. Three clusters were detected: two (p<0.005 in males and p<0.05 in females) in northeast and one (p<0.05 in males) in west-central Japan. Further research is needed to clarify contributing factors for the observed trends and clusters in ALS mortality.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Journal of the Neurological Sciences
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Rowland L.P.
        • Shneider N.A.
        Amyotrophic lateral sclerosis.
        N Engl J Med. 2001; 344: 1688-1700
        • Armon C.
        An evidence-based medicine approach to the evaluation of the role of exogenous risk factors in sporadic amyotrophic lateral sclerosis.
        Neuroepidemiology. 2003; 22: 217-228
        • Beghi E.
        • Logroscino G.
        • Chiò A.
        • Hardiman O.
        • Mitchell D.
        • Swingler R.
        • et al.
        • EURALS Consortium
        The epidemiology of ALS and the role of population-based registries.
        Biochim Biophys Acta. 2006; 1762: 1150-1157
        • McGuire V.
        • Nelson L.M.
        Epidemiology of ALS.
        in: Mitsumoto H. Przedbroski S. Gordon P. Amyotrophic lateral sclerosis. Taylor & Francis, New York2006: 17-41
        • Noonan C.W.
        • White M.C.
        • Thurman D.
        • Wong L.Y.
        Temporal and geographic variation in United States motor neuron disease mortality, 1969–1998.
        Neurology. 2005; 64: 1215-1221
        • Chancellor A.M.
        • Warlow C.P.
        Adult onset motor neuron disease: worldwide mortality, incidence and distribution since 1950.
        J Neurol Neurosurg Psychiatry. 1992; 55: 1106-1115
        • Román G.C.
        Neuroepidemiology of amyotrophic lateral sclerosis: clues to aetiology and pathogenesis.
        J Neurol Neurosurg Psychiatry. 1996; 61: 131-137
        • Seljeseth Y.M.
        • Vollset S.E.
        • Tysnes O.B.
        Increasing mortality from amyotrophic lateral sclerosis in Norway?.
        Neurology. 2000; 55: 1262-1266
        • Worms P.M.
        The epidemiology of motor neuron diseases: a review of recent studies.
        J Neurol Sci. 2001; 191: 3-9
        • Day T.G.
        • Scott M.
        • Perring R.
        • Doyle P.
        Motor neuron disease mortality in Great Britain continues to rise: examination of mortality rates 1975–2004.
        Amyotroph Lateral Scler. 2007; 8: 337-342
        • Kondo K.
        • Tsubaki T.
        Changing mortality patterns of motor neuron disease in Japan.
        J Neurol Sci. 1977; 32: 411-424
        • Neilson S.
        • Robinson I.
        • Kondo K.
        A new analysis of mortality from motor neurone disease in Japan, 1950–1990: rise and fall in the postwar years.
        J Neurol Sci. 1993; 117: 46-53
        • Okamoto K.
        • Kobashi G.
        • Washio M.
        • Sasaki S.
        • Yokoyama T.
        • Miyake Y.
        • et al.
        Descriptive epidemiology of amyotrophic lateral sclerosis in Japan, 1995–2001.
        J Epidemiol. 2005; 15: 20-23
        • Kusui K.
        Epidemiological study on amyotrophic lateral sclerosis (ALS) and other neighboring motor neuron diseases in Kii Peninsula.
        Psychiatr Neurol Jpn. 1962; 64 (in Japanese): 85-99
        • Wiederholt W.C.
        Neuroepidemiologic research initiatives on Guam: past and present.
        Neuroepidemiology. 1999; 18: 279-291
        • Kuzuhara S.
        • Kokubo Y.
        Atypical parkinsonism of Japan: amyotrophic lateral sclerosis–parkinsonism-dementia complex of the Kii peninsula of Japan (Muro disease): an update.
        Mov Disord. 2005; 20: S108-S113
        • Yoshida S.
        • Uebayashi Y.
        • Kihira T.
        • Kohmoto J.
        • Wakayama I.
        • Taguchi S.
        • et al.
        Epidemiology of motor neuron disease in the Kii Peninsula of Japan, 1989–1993: active or disappearing focus?.
        J Neurol Sci. 1998; 155: 146-155
        • Brooks B.R.
        El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial “Clinical limits of amyotrophic lateral sclerosis” workshop contributors.
        J Neurol Sci. 1994; 124: 96-107
        • Research Committee on Neurodegenerative Diseases of Intractable Diseases
        • the Ministry of Health
        • Labour and Welfare, Japan
        Amyotrophic lateral sclerosis.
        in: Disease Prevention Study Group Guidelines of diagnoses and treatments for intractable diseases. 3rd ed. Tokyo Roppo Publishing, Tokyo2005: 80-89 (in Japanese)
        • Kim H.J.
        • Fay M.P.
        • Feuer E.J.
        • Midthune D.N.
        Permutation tests for joinpoint regression with applications to cancer rates.
        Stat Med. 2000; 19: 335-351
      1. National Cancer Institute, U. S. National Institutes of Health. Statistical Research and Applications: Joinpoint Regression Program Version 3.4.2. Available from: http://srab.cancer.gov/joinpoint/.

        • Lawson A.B.
        Statistical methods in spatial epidemiology.
        2nd ed. John Wiley & Sons, West Sussex2006
        • Tango T.
        • Takahashi K.
        A flexibly shaped spatial scan statistic for detecting clusters.
        Int J Health Geogr. 2005; 4 (Available from: http://www.ij-healthgeographics.com/content/4/1/11): 11
        • Doi Y.
        • Yokoyama T.
        • Sakai M.
        • Nakamura Y.
        • Tango T.
        • Takahashi K.
        Spatial clusters of Creutzfeldt–Jakob disease mortality in Japan between 1995 and 2004.
        Neuroepidemiology. 2008; 30: 222-228
        • Tango T.
        Statistical methods for disease clustering.
        in: Gail M. Krickeberg Samet J.M. Tsiatis A. Wong W. Springer, New York2010
      2. Department of Technology Assessment and Biostatistics, National Institute of Public Health, Japan. The Flexible Scan Statistics Version 3.0.5. Available from: http://www.niph.go.jp/soshiki/gijutsu/download/flexscan/index.html.

        • Chiò A.
        • Mora G.
        • Calvo A.
        • Mazzini L.
        • Bottacchi E.
        PARALS. Epidemiology of ALS in Italy: a 10-year prospective population-based study.
        Neurology. 2009; 72: 725-731
        • Atsuta N.
        • Watanabe H.
        • Ito M.
        • Tanaka F.
        • Tamakoshi A.
        • Nakano I.
        • et al.
        • Research Committee on the Neurodegenerative Diseases of Japan
        Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis.
        J Neurol Sci. 2009; 276: 163-169
        • Smyth A.
        • Riedl M.
        • Kimura R.
        • Olick R.
        • Siegler M.
        End of life decisions in amyotrophic lateral sclerosis: a cross-cultural perspective.
        J Neurol Sci. 1997; 152: S93-S96
        • Hayashi H.
        Ventilatory support: Japanese experience.
        J Neurol Sci. 1997; 152: S97-S100
        • Borasio G.D.
        • Gelinas D.F.
        • Yanagisawa N.
        Mechanical ventilation in amyotrophic lateral sclerosis: a cross-cultural perspective.
        J Neurol. 1998; 245: S7-S12
        • Sorenson E.J.
        • Stalker A.P.
        • Kurland L.T.
        • Windebank A.J.
        Amyotrophic lateral sclerosis in Olmsted County, Minnesota, 1925 to 1998.
        Neurology. 2002; 59: 280-282
        • Forbes R.B.
        • Colville S.
        • Cran G.W.
        • Scottish Motor Neurone Disease Register
        Unexpected decline in survival from amyotrophic lateral sclerosis/motor neuron disease.
        J Neurol Neurosurg Psychiatry. 2004; 75: 1753-1755
        • Logroscino G.
        • Traynor B.J.
        • Hardiman O.
        • Chio' A.
        • Couratier P.
        • Mitchell J.D.
        • et al.
        • EURALS
        Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues.
        J Neurol Neurosurg Psychiatry. 2008; 79: 6-11
        • OECD
        OECD Health Data 2010.
        June 2010 (Available from: http://www.oecd.org/document/16/0,3343,en_2649_34631_2085200_1_1_1_37407,00.html.)
        • Kihira T.
        • Yoshida S.
        • Hironishi M.
        • Miwa H.
        • Okamato K.
        • Kondo T.
        Changes in the incidence of amyotrophic lateral sclerosis in Wakayama, Japan.
        Amyotroph Lateral Scler Other Mot Neuron Disord. 2005; 6: 155-163
        • Statistics and Information Department
        • the Ministry of Health
        • Labour and Welfare, Japan
        Survey of physicians, dentists and pharmacists.
        2004 (Available from: http://www.mhlw.go.jp/toukei/saikin/hw/ishi/04/index.html. (in Japanese))
        • Simpson C.L.
        • Al-Chalabi A.
        Amyotrophic lateral sclerosis as a complex genetic disease.
        Biochim Biophys Acta. 2006; 1762: 973-985