An event-based model for disease progression and its application in familial Alzheimer's disease and Huntington's disease

被引:172
作者
Fonteijn, Hubert M. [1 ,2 ,3 ]
Modat, Marc [2 ,4 ]
Clarkson, Matthew J. [2 ,4 ,5 ]
Barnes, Josephine [5 ]
Lehmann, Manja [5 ]
Hobbs, Nicola Z. [6 ]
Scahill, Rachael I. [6 ]
Tabrizi, Sarah J. [6 ,7 ]
Ourselin, Sebastien [2 ,4 ,5 ]
Fox, Nick C. [5 ,7 ]
Alexander, Daniel C. [2 ,3 ]
机构
[1] Max Planck Inst Psycholinguist, NL-6500 HB Nijmegen, Netherlands
[2] UCL, Ctr Med Image Comp, London WC1E 6BT, England
[3] UCL, Dept Comp Sci, London WC1E 6BT, England
[4] UCL, Dept Med Phys & Bioengn, London WC1E 6BT, England
[5] UCL, UCL Inst Neurol, Dementia Res Ctr, London WC1N 3AR, England
[6] UCL, UCL Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
[7] Natl Hosp Neurol & Neurosurg, Dept Clin Neurol, London WC1N 3BG, England
基金
英国工程与自然科学研究理事会;
关键词
Disease progression; MRI; Alzheimer's disease; Huntington's disease; COGNITIVE IMPAIRMENT; ENTORHINAL CORTEX; CEREBRAL-CORTEX; ATROPHY; HIPPOCAMPUS; DIAGNOSIS; MILD;
D O I
10.1016/j.neuroimage.2012.01.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Understanding the progression of neurological diseases is vital for accurate and early diagnosis and treatment planning. We introduce a new characterization of disease progression, which describes the disease as a series of events, each comprising a significant change in patient state. We provide novel algorithms to learn the event ordering from heterogeneous measurements over a whole patient cohort and demonstrate using combined imaging and clinical data from familial Alzheimer's and Huntington's disease cohorts. Results provide new detail in the progression pattern of these diseases, while confirming known features, and give unique insight into the variability of progression over the cohort. The key advantage of the new model and algorithms over previous progression models is that they do not require a priori division of the patients into clinical stages. The model and its formulation extend naturally to a wide range of other diseases and developmental processes and accommodate cross-sectional and longitudinal input data. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1880 / 1889
页数:10
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