TY - JOUR
T1 - Generalizability of the disease state index prediction model for identifying patients progressin from mild cognitive impariment to Alzheimer's disease
AU - Hall, Anette
AU - Muñoz-Ruiz, Miguel
AU - Mattila, Jussi
AU - Koikkalainen, Juha
AU - Tsolaki, Magda
AU - Mecocci, Patrizia
AU - Kloszewska, Iwona
AU - Vellas, Bruno
AU - Lovestone, Simon
AU - Visser, Pieter Jelle
AU - Lötjönen, Jyrki
AU - Soininen, Hilkka
PY - 2015
Y1 - 2015
N2 - Background: The Disease State Index (DSI) prediction
model measures the similarity of patient data to
diagnosed stable and progressive mild cognitive
impairment (MCI) cases to identify patients who are
progressing to Alzheimer's disease. Objectives: We
evaluated how well the DSI generalizes across four
different cohorts: DESCRIPA, ADNI, AddNeuroMed, and the
Kuopio MCI study. Methods: The accuracy of the DSI in
predicting progression was examined for each cohort
separately using 10 * 10-fold cross-validation and for
inter-cohort validation using each cohort as a test set
for the model built from the other independent cohorts
using bootstrapping with 10 repetitions. Altogether 875
subjects were included in the analysis. The analyzed data
included a comprehensive set of age and gender corrected
magnetic resonance imaging (MRI) features from
hippocampal volumetry, multi-template tensor-based
morphometry, and voxel-based morphometry as well as
Mini-Mental State Examination (MMSE), APOE genotype, and
additional cohort specific data from neuropsychological
tests and cerebrospinal fluid measurements (CSF).
Results: The DSI model was used to classify the patients
into stable and progressive MCI cases. AddNeuroMed had
the highest classification results of the cohorts, while
ADNI and Kuopio MCI exhibited the lowest values. The MRI
features alone achieved a good classification performance
for all cohorts. For ADNI and DESCRIPA, adding MMSE, APOE
genotype, CSF, and neuropsychological data improved the
results. Conclusions: The results reveal that the
prediction performance of the combined cohort is close to
the average of the individual cohorts. It is feasible to
use different cohorts as training sets for the DSI, if
they are sufficiently similar.
AB - Background: The Disease State Index (DSI) prediction
model measures the similarity of patient data to
diagnosed stable and progressive mild cognitive
impairment (MCI) cases to identify patients who are
progressing to Alzheimer's disease. Objectives: We
evaluated how well the DSI generalizes across four
different cohorts: DESCRIPA, ADNI, AddNeuroMed, and the
Kuopio MCI study. Methods: The accuracy of the DSI in
predicting progression was examined for each cohort
separately using 10 * 10-fold cross-validation and for
inter-cohort validation using each cohort as a test set
for the model built from the other independent cohorts
using bootstrapping with 10 repetitions. Altogether 875
subjects were included in the analysis. The analyzed data
included a comprehensive set of age and gender corrected
magnetic resonance imaging (MRI) features from
hippocampal volumetry, multi-template tensor-based
morphometry, and voxel-based morphometry as well as
Mini-Mental State Examination (MMSE), APOE genotype, and
additional cohort specific data from neuropsychological
tests and cerebrospinal fluid measurements (CSF).
Results: The DSI model was used to classify the patients
into stable and progressive MCI cases. AddNeuroMed had
the highest classification results of the cohorts, while
ADNI and Kuopio MCI exhibited the lowest values. The MRI
features alone achieved a good classification performance
for all cohorts. For ADNI and DESCRIPA, adding MMSE, APOE
genotype, CSF, and neuropsychological data improved the
results. Conclusions: The results reveal that the
prediction performance of the combined cohort is close to
the average of the individual cohorts. It is feasible to
use different cohorts as training sets for the DSI, if
they are sufficiently similar.
KW - Alzheimer's disease
KW - computer-assisted diagnosis
KW - dementia
KW - magnetic resonance imaging (MRI)
KW - mild cognitive impairment
U2 - 10.3233/JAD-140942
DO - 10.3233/JAD-140942
M3 - Article
SN - 1387-2877
VL - 44
SP - 79
EP - 92
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 1
ER -