Journal of the Neurological Sciences
Volume 298, Issue 1 , Pages 78-84, 15 November 2010

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

  • Yuriko Doi

      Affiliations

    • Department of Education and Training Technology, National Institute of Public Health, 2-3-6 Minami, Wako, Saitama 351-0197, Japan
    • Corresponding Author InformationCorresponding author. Tel.: +81 48 458 6111x6148; fax: +81 48 469 0213.
  • ,
  • Testuji Yokoyama

      Affiliations

    • Department of Human Resources Development, National Institute of Public Health, Saitama, Japan
  • ,
  • Toshiro Tango

      Affiliations

    • Department of Technology Assessment and Biostatistics, National Institute of Public Health, Saitama, Japan
  • ,
  • Kunihiko Takahashi

      Affiliations

    • Department of Technology Assessment and Biostatistics, National Institute of Public Health, Saitama, Japan
  • ,
  • Kenichi Fujimoto

      Affiliations

    • Division of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan
  • ,
  • Imaharu Nakano

      Affiliations

    • Division of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan

Received 29 March 2010; received in revised form 5 August 2010; accepted 5 August 2010. published online 01 September 2010.

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 70years 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: Amyotrophic lateral sclerosis, ALS, Motor neuron disease, Mortality, Trends, Cluster analysis, Epidemiology, Japan

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PII: S0022-510X(10)00353-9

doi:10.1016/j.jns.2010.08.004

Journal of the Neurological Sciences
Volume 298, Issue 1 , Pages 78-84, 15 November 2010