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

被引:26
作者
Doi, Yuriko [1 ]
Yokoyama, Testuji [2 ]
Tango, Toshiro [3 ]
Takahashi, Kunihiko [3 ]
Fujimoto, Kenichi [4 ]
Nakano, Imaharu [4 ]
机构
[1] Natl Inst Publ Hlth, Dept Educ & Training Technol, Wako, Saitama 3510197, Japan
[2] Natl Inst Publ Hlth, Dept Human Resources Dev, Wako, Saitama 3510197, Japan
[3] Natl Inst Publ Hlth, Dept Technol Assessment & Biostat, Wako, Saitama 3510197, Japan
[4] Jichi Med Univ, Sch Med, Dept Med, Div Neurol, Shimotsuke, Tochigi, Japan
关键词
Amyotrophic lateral sclerosis; ALS; Motor neuron disease; Mortality; Trends; Cluster analysis; Epidemiology; Japan; MOTOR-NEURON DISEASE; DESCRIPTIVE EPIDEMIOLOGY; KII PENINSULA; COMPLEX; RATES; RISE; ALS;
D O I
10.1016/j.jns.2010.08.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
相关论文
共 38 条
  • [1] [Anonymous], 2013, Statistical methods in spatial epidemiology
  • [2] [Anonymous], 2010, OECD HLTH DAT 2010
  • [3] An evidence-based medicine approach to the evaluation of the role of exogenous risk factors in sporadic amyotrophic lateral sclerosis
    Armon, C
    [J]. NEUROEPIDEMIOLOGY, 2003, 22 (04) : 217 - 228
  • [4] Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis
    Atsuta, Naoki
    Watanabe, Hirohisa
    Ito, Mizuki
    Tanaka, Fumiaki
    Tamakoshi, Akiko
    Nakano, Imaharu
    Aoki, Masashi
    Tsuji, Shoji
    Yuasa, Tatsuhiko
    Takano, Hirold
    Hayashi, Hideaki
    Kuzuhara, Shigeld
    Sobue, Gen
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 276 (1-2) : 163 - 169
  • [5] The epidemiology of ALS and the role of population-based registries
    Beghi, Ettore
    Logroscino, Giancarlo
    Chio, Adriano
    Hardiman, Orla
    Mitchell, Douglas
    Swingler, Robert
    Traynor, Bryan J.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2006, 1762 (11-12): : 1150 - 1157
  • [6] Discontinuation of mechanical ventilation in patients with amyotrophic lateral sclerosis
    Borasio, GD
    Voltz, R
    [J]. JOURNAL OF NEUROLOGY, 1998, 245 (11) : 717 - 722
  • [8] ADULT ONSET MOTOR-NEURON DISEASE - WORLDWIDE MORTALITY, INCIDENCE AND DISTRIBUTION SINCE 1950
    CHANCELLOR, AM
    WARLOW, CP
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (12) : 1106 - 1115
  • [9] Epidemiology of ALS in Italy A 10-year prospective population-based study
    Chio, A.
    Mora, G.
    Calvo, A.
    Mazzini, L.
    Bottacchi, E.
    Mutani, R.
    [J]. NEUROLOGY, 2009, 72 (08) : 725 - 731
  • [10] Motor neuron disease mortality in Great Britain continues to rise: Examination of mortality rates 1975-2004
    Day, Thomas G.
    Scott, Martin
    Perring, Roslyn
    Doyle, Pat
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2007, 8 (06): : 337 - 342