TY - JOUR
T1 - White matter diffusion estimates in obsessive-compulsive disorder across 1653 individuals
T2 - machine learning findings from the ENIGMA OCD Working Group
AU - ENIGMA OCD Working Group
AU - Kim, Bo Gyeom
AU - Kim, Gakyung
AU - Abe, Yoshinari
AU - Alonso, Pino
AU - Ameis, Stephanie
AU - Anticevic, Alan
AU - Arnold, Paul D.
AU - Balachander, Srinivas
AU - Banaj, Nerisa
AU - Bargalló, Nuria
AU - Batistuzzo, Marcelo C.
AU - Benedetti, Francesco
AU - Bertolín, Sara
AU - Beucke, Jan Carl
AU - Bollettini, Irene
AU - Brem, Silvia
AU - Brennan, Brian P.
AU - Buitelaar, Jan K.
AU - Calvo, Rosa
AU - Castelo-Branco, Miguel
AU - Cheng, Yuqi
AU - Chhatkuli, Ritu Bhusal
AU - Ciullo, Valentina
AU - Coelho, Ana
AU - Couto, Beatriz
AU - Dallaspezia, Sara
AU - Ely, Benjamin A.
AU - Ferreira, Sónia
AU - Fontaine, Martine
AU - Fouche, Jean Paul
AU - Grazioplene, Rachael
AU - Gruner, Patricia
AU - Hagen, Kristen
AU - Hansen, Bjarne
AU - Hanna, Gregory L.
AU - Hirano, Yoshiyuki
AU - Höxter, Marcelo Q.
AU - Hough, Morgan
AU - Hu, Hao
AU - Huyser, Chaim
AU - Ikuta, Toshikazu
AU - Jahanshad, Neda
AU - James, Anthony
AU - Jaspers-Fayer, Fern
AU - Kasprzak, Selina
AU - Kathmann, Norbert
AU - Kaufmann, Christian
AU - Kim, Minah
AU - Koch, Kathrin
AU - Matsumoto, Koji
N1 - Publisher Copyright:
© The Author(s) 2024. corrected publication 2024.
PY - 2024/4
Y1 - 2024/4
N2 - White matter pathways, typically studied with diffusion tensor imaging (DTI), have been implicated in the neurobiology of obsessive-compulsive disorder (OCD). However, due to limited sample sizes and the predominance of single-site studies, the generalizability of OCD classification based on diffusion white matter estimates remains unclear. Here, we tested classification accuracy using the largest OCD DTI dataset to date, involving 1336 adult participants (690 OCD patients and 646 healthy controls) and 317 pediatric participants (175 OCD patients and 142 healthy controls) from 18 international sites within the ENIGMA OCD Working Group. We used an automatic machine learning pipeline (with feature engineering and selection, and model optimization) and examined the cross-site generalizability of the OCD classification models using leave-one-site-out cross-validation. Our models showed low-to-moderate accuracy in classifying (1) “OCD vs. healthy controls” (Adults, receiver operator characteristic-area under the curve = 57.19 ± 3.47 in the replication set; Children, 59.8 ± 7.39), (2) “unmedicated OCD vs. healthy controls” (Adults, 62.67 ± 3.84; Children, 48.51 ± 10.14), and (3) “medicated OCD vs. unmedicated OCD” (Adults, 76.72 ± 3.97; Children, 72.45 ± 8.87). There was significant site variability in model performance (cross-validated ROC AUC ranges 51.6–79.1 in adults; 35.9–63.2 in children). Machine learning interpretation showed that diffusivity measures of the corpus callosum, internal capsule, and posterior thalamic radiation contributed to the classification of OCD from HC. The classification performance appeared greater than the model trained on grey matter morphometry in the prior ENIGMA OCD study (our study includes subsamples from the morphometry study). Taken together, this study points to the meaningful multivariate patterns of white matter features relevant to the neurobiology of OCD, but with low-to-moderate classification accuracy. The OCD classification performance may be constrained by site variability and medication effects on the white matter integrity, indicating room for improvement for future research.
AB - White matter pathways, typically studied with diffusion tensor imaging (DTI), have been implicated in the neurobiology of obsessive-compulsive disorder (OCD). However, due to limited sample sizes and the predominance of single-site studies, the generalizability of OCD classification based on diffusion white matter estimates remains unclear. Here, we tested classification accuracy using the largest OCD DTI dataset to date, involving 1336 adult participants (690 OCD patients and 646 healthy controls) and 317 pediatric participants (175 OCD patients and 142 healthy controls) from 18 international sites within the ENIGMA OCD Working Group. We used an automatic machine learning pipeline (with feature engineering and selection, and model optimization) and examined the cross-site generalizability of the OCD classification models using leave-one-site-out cross-validation. Our models showed low-to-moderate accuracy in classifying (1) “OCD vs. healthy controls” (Adults, receiver operator characteristic-area under the curve = 57.19 ± 3.47 in the replication set; Children, 59.8 ± 7.39), (2) “unmedicated OCD vs. healthy controls” (Adults, 62.67 ± 3.84; Children, 48.51 ± 10.14), and (3) “medicated OCD vs. unmedicated OCD” (Adults, 76.72 ± 3.97; Children, 72.45 ± 8.87). There was significant site variability in model performance (cross-validated ROC AUC ranges 51.6–79.1 in adults; 35.9–63.2 in children). Machine learning interpretation showed that diffusivity measures of the corpus callosum, internal capsule, and posterior thalamic radiation contributed to the classification of OCD from HC. The classification performance appeared greater than the model trained on grey matter morphometry in the prior ENIGMA OCD study (our study includes subsamples from the morphometry study). Taken together, this study points to the meaningful multivariate patterns of white matter features relevant to the neurobiology of OCD, but with low-to-moderate classification accuracy. The OCD classification performance may be constrained by site variability and medication effects on the white matter integrity, indicating room for improvement for future research.
UR - http://www.scopus.com/inward/record.url?scp=85195457720&partnerID=8YFLogxK
U2 - 10.1038/s41380-023-02392-6
DO - 10.1038/s41380-023-02392-6
M3 - Article
C2 - 38326559
AN - SCOPUS:85195457720
SN - 1359-4184
VL - 29
SP - 1063
EP - 1074
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 4
ER -