Motor neuron disease in the province of Turin, Italy, 1966-1980. Survival analysis in an unselected population

J Neurol Sci. Nov-Dec 1984;66(2-3):165-73. doi: 10.1016/0022-510x(84)90004-2.

Abstract

We performed a population based survival analysis of all incident cases (220) of motor neuron disease (MND) in the province of Turin, Italy, during the period 1966-1980. 175 cases were diagnosed as amyotrophic lateral sclerosis (ALS), 43 as progressive muscular atrophy (PMA) and 2 as progressive bulbar palsy (PBP). The life-tables of MND, adjusted as to the "expected" mortality, showed a survival rate of 27.8% and 22.0% at 5 and 10 years, respectively. The course of PMA and ALS cases was different, with a 5-year survival rate of 66.8% and 17.7%, respectively. Nevertheless both life-tables showed a similar pattern with a rapidly fatal outcome in the first 3 years after diagnosis and a slower death rate in the following years. In each curve, the slopes suggested the presence of 2 subgroups with different prognosis. It is to be stressed that a percentage of PMA patients (25.7%) showed a rapidly fatal outcome and that a subgroup of ALS patients (26.6%) showed a relatively benign course. This might suggest a different individual susceptibility to the disease.

MeSH terms

  • Adult
  • Aged
  • Amyotrophic Lateral Sclerosis / mortality
  • Bulbar Palsy, Progressive / mortality
  • Female
  • Follow-Up Studies
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Motor Neurons*
  • Muscular Atrophy / mortality
  • Neuromuscular Diseases / mortality*