Amyotrophic lateral sclerosis (ALS) is a disorder marked by loss of motoneu
rons. We hypothesized that subjects with ALS would have an altered gait rhy
thm, with an increase in both the magnitude of the stride-to-stride fluctua
tions and perturbations in the fluctuation dynamics. To test for this locom
otor instability, we quantitatively compared the gait rhythm of subjects wi
th ALS with that of normal controls and with that of subjects with Parkinso
n's disease (PD) and Huntington's disease (HD), pathologies of the basal ga
nglia. Subjects walked for 5 min at, their usual pace wearing an ankle-worn
recorder that enabled determination of the duration of each stride and of
stride-to-stride fluctuations. We found that the gait of patients with ALS
is less steady and more temporally disorganized compared with that of healt
hy controls. In addition, advanced ALS, HD, and PD were associated with cer
tain common, as well as apparently distinct, features of altered stride dyn
amics. Thus stride-to-stride control of gait rhythm is apparently compromis
ed with ALS. Moreover, a matrix of markers based on gait dynamics may be us
eful in characterizing certain pathologies of motor control and, possibly,
in quantitatively monitoring disease progression and evaluating therapeutic
interventions.