Literature DB >> 886364

Changing mortality patterns of motor neuron disease in Japan.

K Kondo, T Tsubaki.   

Abstract

The age-adjusted female death rate from motor neuron disease in Japan was noted to rise after 1952 and to fall rapidly since about 1960. A similar trend was also noticed in the males. Further study will show whether this was a part of a cyclical change or whether the mortality of the disease has entered a period of prolonged decline in that country. Death rates for neurological diseases in various countries were reported previously for 1953-58. Updating this study for 1966-71, a rising trend of deaths from motor neuron disease was identified in European countries, but the rate has been stationary in the United States. The rapidly changing patterns of the mortality seemed incompatible with a purely genetic causation of the disease. This indicates the need for extensive epidemiological studies to identify the extrinsic factors which induced such a trend, and were thus possibly the cause of the disease. In view of the results of the re-evaluation of the diagnosis in death certificates, mortality figures of motor neuron disease in females appeared reasonably reliable for an epidemiological study.

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Year:  1977        PMID: 886364     DOI: 10.1016/0022-510x(77)90023-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  8 in total

1.  Adult onset motor neuron disease: worldwide mortality, incidence and distribution since 1950.

Authors:  A M Chancellor; C P Warlow
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-12       Impact factor: 10.154

2.  Changing mortality for motor neuron disease in France (1968-2007): an age-period-cohort analysis.

Authors:  Paul H Gordon; Fanny Artaud; Albertine Aouba; Françoise Laurent; Vincent Meininger; Alexis Elbaz
Journal:  Eur J Epidemiol       Date:  2011-06-15       Impact factor: 8.082

3.  Validating population-based registers for ALS: how accurate is death certification?

Authors:  Loraine Yeo; Catherine Lynch; Orla Hardiman
Journal:  J Neurol       Date:  2010-02-12       Impact factor: 4.849

4.  Utility of Scottish morbidity and mortality data for epidemiological studies of motor neuron disease.

Authors:  A M Chancellor; R J Swingler; H Fraser; J A Clarke; C P Warlow
Journal:  J Epidemiol Community Health       Date:  1993-04       Impact factor: 3.710

5.  Motor neurone disease in the Lothian Region of Scotland 1961-81.

Authors:  S M Holloway; J D Mitchell
Journal:  J Epidemiol Community Health       Date:  1986-12       Impact factor: 3.710

6.  Accuracy of death certificate diagnosis of amyotrophic lateral sclerosis.

Authors:  A Chiò; C Magnani; E Oddenino; G Tolardo; D Schiffer
Journal:  J Epidemiol Community Health       Date:  1992-10       Impact factor: 3.710

7.  Familial amyotrophic lateral sclerosis: features of multisystem degeneration.

Authors:  J Tanaka; H Nakamura; Y Tabuchi; K Takahashi
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

8.  Analysis of incidence of motor neuron disease in England 1998-2019: use of three linked datasets.

Authors:  Judith M Burchardt; Xue W Mei; Tom Ranger; Christopher J McDermott; Aleksandar Radunovic; Carol Coupland; Julia Hippisley-Cox
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2022-02-01       Impact factor: 3.528

  8 in total

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