Literature DB >> 58973

Amyotrophic lateral sclerosis: a population study.

E Kahana, M Alter, S Feldman.   

Abstract

A country-wide study of the frequency of amyotrophic lateral sclerosis (ALS) was undertaken in Israel for the period 1960-1970. Israel was chosen for this study because of its excellent medical facilities and detailed demographic information. Moreover, the population includes representative groups from all parts of the world for comparison of frequency. A wide variety of motor system disease was screened in all hospitals, clinics, and chronic care facilities in the country, death certificates were reviewed and physicians with a neurological practice were contacted to derive a tentative list of cases. Only those who fit strict clinical diagnostic criteria or had autopsy confirmation were included in estimates of prevalence and incidence. On January 1, 1965, the mid-point of the study, 62 patients with ALS were living in Israel. The age-adjusted prevalence of ALS on that date was 3 per 100,000 population. The average annual age-adjusted incidence for the period 1960-1970 was 0.78 per 100000 population )0.86 in males, 0.46 in females; ratio 1.9:1). There was no appreciable change in trend of incidence over the study interval. Age-specific incidence rates were similar in native-born inhabitants of Israel, immigrants from Europe and immigrants from Afro-Asian countries. The range in age-adjusted incidence among subgroups of immigrants to Israel from various countries was 0.25 to 1.20 per 100000 population but small numbers precluded testing the statistical significance of these rather narrow differences. Mean age at onset was 55.4 years for males and 52.4 years for females. The mean age at death was 60.2 for males and 58.0 for females. The average annual mortality from ALS was 0.58 per 100000 population. There were no familial aggregates of ALS in Israel and autopsy data showed no neurofibrillary changes, granulovacuolar or inclusion bodies. There are only a few other population studies of ALS in different regions of the world. The average annual incidence in these other studies ranged from 0.4 to 1.4 per 100000 population. Thus, the incidence in Israel falls within this narrow range. The present study lends further support to the impression that ALS has a remarkably uniform geographic distribution with Guam and the Kii peninsula of Japan being the only known areas with significantly high rates. If an environmental factor contributes to the pathogenesis of ALS, the factor must also have a uniform geographic distribution.

Entities:  

Mesh:

Year:  1976        PMID: 58973     DOI: 10.1007/bf00314523

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  12 in total

1.  Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.

Authors:  L T KURLAND; D W MULDER
Journal:  Neurology       Date:  1955-03       Impact factor: 9.910

2.  Amyotrophic lateral sclerosis among Guamanians in California.

Authors:  J TORRES; L L IRIARTE; L T KURLAND
Journal:  Calif Med       Date:  1957-06

Review 3.  Epidemiology of motor-neuron diseases.

Authors:  A R Bobowick; J A Brody
Journal:  N Engl J Med       Date:  1973-05-17       Impact factor: 91.245

4.  Neurological disease in an English city.

Authors:  M Brewis; D C Poskanzer; C Rolland; H Miller
Journal:  Acta Neurol Scand       Date:  1966       Impact factor: 3.209

5.  Amyotrophic lateral sclerosis mortality among native-born and migrant residents of California and Washington.

Authors:  A H Edgar; J A Brody; R Detels
Journal:  Neurology       Date:  1973-01       Impact factor: 9.910

6.  Epidemiologic study of amyotrophic lateral sclerosis in Hawaii. Identification of high incidence among Filipino men.

Authors:  N Matsumoto; R M Worth; L T Kurland; H Okazaki
Journal:  Neurology       Date:  1972-09       Impact factor: 9.910

7.  Mexican "resistance" to amyotrophic lateral sclerosis.

Authors:  L Olivares; E S Estéban; M Alter
Journal:  Arch Neurol       Date:  1972-11

8.  The prevalence of some neurological diseases in Iceland.

Authors:  K R Gudmundsson
Journal:  Acta Neurol Scand       Date:  1968       Impact factor: 3.209

9.  Neurologic disease in the western Pacific islands, with a report on the focus of amyotrophic lateral sclerosis found in the Kii peninsula, Japan.

Authors:  Y Yase
Journal:  Am J Trop Med Hyg       Date:  1970-01       Impact factor: 2.345

10.  [Epidemiological analysis of amyotrophic lateral sclerosis in Poznan District in Western Poland].

Authors:  W Cendrowski; M Wender; M Owsianowski
Journal:  Acta Neurol Scand       Date:  1970       Impact factor: 3.209

View more
  5 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.  The epidemiology of motor neurone disease in two counties in the southwest of England.

Authors:  Ibrahim Imam; Susan Ball; Dave Wright; C Oliver Hanemann; John Zajicek
Journal:  J Neurol       Date:  2010-01-22       Impact factor: 4.849

3.  Amyotrophic lateral sclerosis. A study of its presentation and prognosis.

Authors:  S S Gubbay; E Kahana; N Zilber; G Cooper; S Pintov; Y Leibowitz
Journal:  J Neurol       Date:  1985       Impact factor: 4.849

4.  Evidence of underdiagnosis of myasthenia gravis in older people.

Authors:  A Vincent; L Clover; C Buckley; J Grimley Evans; P M Rothwell
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-08       Impact factor: 10.154

Review 5.  The epidemiology of primary degenerative dementia and related neurological disorders.

Authors:  B Cooper
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.