An incidence cohort of 308 multiple sclerosis patients was followed up
repeatedly during at least 25 years of disease. In the patients with
acute onset, multivariate survival analyses were performed and predict
ive models created. The endpoints DSS 6 and start of progressive disea
se were used. A number of variables were tested. The most important of
these for prediction and therefore included in these models were: age
at onset, sex, degree of remission after relapse, mono- or polyregion
al symptoms, type of affected nerve fibres, number of affected neurolo
gical systems. The relapse rate did not correlate with prognosis. In t
he predictive models, coefficients and risk ratios are provided that c
an be used for calculating the risk of progression and DSS 6 or to pre
dict the median time for these endpoints in individual patients. It wa
s also found that the risk of progression is not constant, but has a m
aximum a certain time after disease onset. For a patient with early on
set, the risk is low in the beginning, but reaches a maximum level, wh
ich is several times higher, after about 15 years. The patient with a
late onset has a much higher risk of endpoint immediately after onset,
but reaches the maximum in a few years, and after that the risk decre
ases