TY - JOUR
T1 - Probabilistic disease progression modeling to characterize diagnostic uncertainty
T2 - Application to staging and prediction in Alzheimer's disease
AU - for the Alzheimer's Disease Neuroimaging Initiative
AU - Lorenzi, Marco
AU - Filippone, Maurizio
AU - Frisoni, Giovanni B.
AU - Alexander, Daniel C.
AU - Ourselin, Sebastien
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2019/4/15
Y1 - 2019/4/15
N2 - Disease progression modeling (DPM) of Alzheimer's disease (AD) aims at revealing long term pathological trajectories from short term clinical data. Along with the ability of providing a data-driven description of the natural evolution of the pathology, DPM has the potential of representing a valuable clinical instrument for automatic diagnosis, by explicitly describing the biomarker transition from normal to pathological stages along the disease time axis. In this work we reformulated DPM within a probabilistic setting to quantify the diagnostic uncertainty of individual disease severity in an hypothetical clinical scenario, with respect to missing measurements, biomarkers, and follow-up information. We show that the staging provided by the model on 582 amyloid positive testing individuals has high face validity with respect to the clinical diagnosis. Using follow-up measurements largely reduces the prediction uncertainties, while the transition from normal to pathological stages is mostly associated with the increase of brain hypo-metabolism, temporal atrophy, and worsening of clinical scores. The proposed formulation of DPM provides a statistical reference for the accurate probabilistic assessment of the pathological stage of de-novo individuals, and represents a valuable instrument for quantifying the variability and the diagnostic value of biomarkers across disease stages.
AB - Disease progression modeling (DPM) of Alzheimer's disease (AD) aims at revealing long term pathological trajectories from short term clinical data. Along with the ability of providing a data-driven description of the natural evolution of the pathology, DPM has the potential of representing a valuable clinical instrument for automatic diagnosis, by explicitly describing the biomarker transition from normal to pathological stages along the disease time axis. In this work we reformulated DPM within a probabilistic setting to quantify the diagnostic uncertainty of individual disease severity in an hypothetical clinical scenario, with respect to missing measurements, biomarkers, and follow-up information. We show that the staging provided by the model on 582 amyloid positive testing individuals has high face validity with respect to the clinical diagnosis. Using follow-up measurements largely reduces the prediction uncertainties, while the transition from normal to pathological stages is mostly associated with the increase of brain hypo-metabolism, temporal atrophy, and worsening of clinical scores. The proposed formulation of DPM provides a statistical reference for the accurate probabilistic assessment of the pathological stage of de-novo individuals, and represents a valuable instrument for quantifying the variability and the diagnostic value of biomarkers across disease stages.
KW - Alzheimer's disease
KW - Clinical trials
KW - Diagnosis
KW - Disease progression modeling
KW - Gaussian process
UR - http://www.scopus.com/inward/record.url?scp=85034615495&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2017.08.059
DO - 10.1016/j.neuroimage.2017.08.059
M3 - Review article
C2 - 29079521
AN - SCOPUS:85034615495
SN - 1053-8119
VL - 190
SP - 56
EP - 68
JO - NeuroImage
JF - NeuroImage
ER -