Data on amyotrophic lateral sclerosis (Lou Gehrig's disease) from Section 17.2. There are 1822 observations on individuals with ALS. The goal is to predict the rate of progression dFRS of a functional rating score, using 369 predictors based on measurements (and derivatives of these) obtained from patient visits.
Format
A data frame with 1822 rows and 371 variables. The key variables are
testset (logical indicator for training/test split) and dFRS
(response: rate of progression of the ALS functional rating score). The 369
predictor variables include:
Demographics:
Age,Sex.Male,Sex.Female, and race indicators (Race...Caucasian,Race...Asian, etc.)Family history of neurological diseases in relatives (e.g.,
Father,Mother,Brother,Sister)Neurological disease indicators (e.g.,
Neurological.Disease.ALS,Neurological.Disease.PARKINSON.S.DISEASE)Site of onset (
Site.of.Onset.Onset..Bulbar,Site.of.Onset.Onset..Limb)Symptoms (
Symptom.Atrophy,Symptom.Cramps,Symptom.Fasciculations,Symptom.Speech, etc.)Study arm indicators (
Study.Arm.ACTIVE,Study.Arm.PLACEBO)Clinical measurements with summary statistics (first, last, min, max, mean, sd, slope): ALSFRS scores, blood pressure, forced/slow vital capacity (
fvc.liters,svc.liters), respiratory rate, weight, heightALSFRS subscale items:
climbing.stairs,cutting,dressing,handwriting,salivation,speech,swallowing,turning,walking