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@ARTICLE{Rubbert:862440,
author = {Rubbert, Christian and Mathys, Christian and Jockwitz,
Christiane and Hartmann, Christian J and Eickhoff, Simon and
Hoffstaedter, Felix and Caspers, Svenja and Eickhoff,
Claudia and Sigl, Benjamin and Teichert, Nikolas A and
Südmeyer, Martin and Turowski, Bernd and Schnitzler, Alfons
and Caspers, Julian},
title = {{M}achine-learning identifies parkinson's disease patients
based on resting-state between-network functional
connectivity},
journal = {The British journal of radiology},
volume = {92},
number = {1101},
issn = {1748-880X},
address = {London},
publisher = {Inst.},
reportid = {FZJ-2019-02752},
pages = {20180886},
year = {2019},
note = {Data were provided in part by the Human Connectome Project,
WU-Minn Consortium(Principal Investigators: David Van Essen
and Kamil Ugurbil; 1U54MH091657) funded by the16 NIH
Institutes and Centers that support the NIH Blueprint for
Neuroscience Research; andby the McDonnell Center for
Systems Neuroscience at Washington University.},
abstract = {OBJECTIVES:Evaluation of a data-driven, model-based
classification approach to discriminate idiopathic
Parkinson's disease (PD) patients from healthy controls (HC)
based on between-network connectivity in whole-brain
resting-state functional MRI (rs-fMRI).METHODS:Whole-brain
rs-fMRI (EPI/TR = 2.2 s/TE = 30 ms/flip angle =
90°/resolution = 3.1 × 3.1 × 3.1 mm/acquisition
time≈11 min) was assessed in 42 PD patients (medical
OFF) and 47 HC matched for age and gender. Between-network
connectivity based on full and L2-regularized partial
correlation measures were computed for each subject based on
canonical functional network architectures of two cohorts at
different levels of granularity (Human Connectome Project:
15/25/50/100/200 networks; 1000BRAINS: 15/25/50/70
networks). A Boosted Logistic Regression model was trained
on the correlation matrices using a nested cross-validation
(CV) with 10 outer and 10 inner folds for an unbiased
performance estimate, treating the canonical functional
network architecture and the type of correlation as
hyperparameters. The number of boosting iterations was fixed
at 100. The model with the highest mean accuracy over the
inner folds was trained using an non-nested 10- fold
20-repeats CV over the whole dataset to determine feature
importance.RESULTS:Over the outer folds the mean accuracy
was found to be 76.2 $\%$ (median $77.8\%,$ SD 18.2, IQR
69.4 - 87.1 $\%).$ Mean sensitivity was 81 $\%$ (median
$80\%,$ SD 21.1, IQR 75 - 100 $\%)$ and mean specificity was
72.7 $\%$ (median $75\%,$ SD 20.4, IQR 66.7 - 80 $\%).$ The
1000BRAINS 50-network-parcellation, using full correlations,
performed best over the inner folds. The top features
predominantly included sensorimotor as well as sensory
networks.CONCLUSIONS:A rs-fMRI whole-brain-connectivity,
data-driven, model-based approach to discriminate PD
patients from healthy controls shows a very good accuracy
and a high sensitivity. Given the high sensitivity of the
approach, it may be of use in a screening setting.ADVANCES
IN KNOWLEDGE:Resting-state functional MRI could prove to be
a valuable, non-invasive neuroimaging biomarker for
neurodegenerative diseases. The current model-based,
data-driven approach on whole-brain between-network
connectivity to discriminate Parkinson's disease patients
from healthy controls shows promising results with a very
good accuracy and a very high sensitivity.},
cin = {INM-7 / INM-1},
ddc = {610},
cid = {I:(DE-Juel1)INM-7-20090406 / I:(DE-Juel1)INM-1-20090406},
pnm = {571 - Connectivity and Activity (POF3-571)},
pid = {G:(DE-HGF)POF3-571},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30994036},
UT = {WOS:000482099400005},
doi = {10.1259/bjr.20180886},
url = {https://juser.fz-juelich.de/record/862440},
}