TY - JOUR
T1 - Neurobiological Divergence of the Positive and Negative Schizophrenia Subtypes Identified on a New Factor Structure of Psychopathology Using Non-negative Factorization
T2 - An International Machine Learning Study
AU - Pharmacotherapy Monitoring and Outcome Survey (PHAMOUS) Investigators
AU - Chen, Ji
AU - Patil, Kaustubh R.
AU - Weis, Susanne
AU - Sim, Kang
AU - Nickl-Jockschat, Thomas
AU - Zhou, Juan
AU - Aleman, André
AU - Sommer, Iris E.
AU - Liemburg, Edith J.
AU - Hoffstaedter, Felix
AU - Habel, Ute
AU - Derntl, Birgit
AU - Liu, Xiaojin
AU - Fischer, Jona M.
AU - Kogler, Lydia
AU - Regenbogen, Christina
AU - Diwadkar, Vaibhav A.
AU - Stanley, Jeffrey A.
AU - Riedl, Valentin
AU - Jardri, Renaud
AU - Gruber, Oliver
AU - Sotiras, Aristeidis
AU - Davatzikos, Christos
AU - Eickhoff, Simon B.
AU - Bartels-Velthuis, Agna A.
AU - Bruggeman, Richard
AU - Castelein, Stynke
AU - Jörg, Frederike
AU - Pijnenborg, Gerdina H.M.
AU - Knegtering, Henderikus
AU - Visser, Ellen
N1 - Funding Information:
This study was supported by the Deutsche Forschungsgemeinschaft (Grant No. EI 816/4-1 [to SBE]), the National Institute of Mental Health (Grant No. R01-MH074457 [to SBE]), the Helmholtz Portfolio Theme “Supercomputing and Modeling for the Human Brain,” and the European Union’s Horizon 2020 Research and Innovation Programme (Grant Nos. 720270 [HBP SGA1] [to SBE] and 785907 [HBP SGA2] [to SBE]). JC received a Ph.D. fellowship from the Chinese Scholarship Council (Grant No. CSC201609350006 ). VAD acknowledges support from the National Institutes of Mental Health (Grant No. 1R01 MH111177 ), and the Cohen Neuroscience Endowment.
Funding Information:
This study was supported by the Deutsche Forschungsgemeinschaft (Grant No. EI 816/4-1 [to SBE]), the National Institute of Mental Health (Grant No. R01-MH074457 [to SBE]), the Helmholtz Portfolio Theme “Supercomputing and Modeling for the Human Brain,” and the European Union's Horizon 2020 Research and Innovation Programme (Grant Nos. 720270 [HBP SGA1] [to SBE] and 785907 [HBP SGA2] [to SBE]). JC received a Ph.D. fellowship from the Chinese Scholarship Council (Grant No. CSC201609350006). VAD acknowledges support from the National Institutes of Mental Health (Grant No. 1R01 MH111177), and the Cohen Neuroscience Endowment. We acknowledge Asadur Chowdury (Brain Imaging Research Division, Wayne State University School of Medicine, Detroit, Michigan), who contributed to the early arrangement and communication of the Wayne State dataset. Acknowledgments also go to Laura Waite (Institute of Neuroscience and Medicine, Brain and Behaviour [INM-7], Research Center Jülich, Jülich, Germany) for proofreading. A Dimensions and Clustering Tool for assessing schizophrenia Symptomatology (DCTS) is available at http://webtools.inm7.de/sczDCTS/. The authors report no biomedical financial interests or potential conflicts of interest.
Publisher Copyright:
© 2019 Society of Biological Psychiatry
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Background: Disentangling psychopathological heterogeneity in schizophrenia is challenging, and previous results remain inconclusive. We employed advanced machine learning to identify a stable and generalizable factorization of the Positive and Negative Syndrome Scale and used it to identify psychopathological subtypes as well as their neurobiological differentiations. Methods: Positive and Negative Syndrome Scale data from the Pharmacotherapy Monitoring and Outcome Survey cohort (1545 patients; 586 followed up after 1.35 ± 0.70 years) were used for learning the factor structure by an orthonormal projective non-negative factorization. An international sample, pooled from 9 medical centers across Europe, the United States, and Asia (490 patients), was used for validation. Patients were clustered into psychopathological subtypes based on the identified factor structure, and the neurobiological divergence between the subtypes was assessed by classification analysis on functional magnetic resonance imaging connectivity patterns. Results: A 4-factor structure representing negative, positive, affective, and cognitive symptoms was identified as the most stable and generalizable representation of psychopathology. It showed higher internal consistency than the original Positive and Negative Syndrome Scale subscales and previously proposed factor models. Based on this representation, the positive–negative dichotomy was confirmed as the (only) robust psychopathological subtypes, and these subtypes were longitudinally stable in about 80% of the repeatedly assessed patients. Finally, the individual subtype could be predicted with good accuracy from functional connectivity profiles of the ventromedial frontal cortex, temporoparietal junction, and precuneus. Conclusions: Machine learning applied to multisite data with cross-validation yielded a factorization generalizable across populations and medical systems. Together with subtyping and the demonstrated ability to predict subtype membership from neuroimaging data, this work further disentangles the heterogeneity in schizophrenia.
AB - Background: Disentangling psychopathological heterogeneity in schizophrenia is challenging, and previous results remain inconclusive. We employed advanced machine learning to identify a stable and generalizable factorization of the Positive and Negative Syndrome Scale and used it to identify psychopathological subtypes as well as their neurobiological differentiations. Methods: Positive and Negative Syndrome Scale data from the Pharmacotherapy Monitoring and Outcome Survey cohort (1545 patients; 586 followed up after 1.35 ± 0.70 years) were used for learning the factor structure by an orthonormal projective non-negative factorization. An international sample, pooled from 9 medical centers across Europe, the United States, and Asia (490 patients), was used for validation. Patients were clustered into psychopathological subtypes based on the identified factor structure, and the neurobiological divergence between the subtypes was assessed by classification analysis on functional magnetic resonance imaging connectivity patterns. Results: A 4-factor structure representing negative, positive, affective, and cognitive symptoms was identified as the most stable and generalizable representation of psychopathology. It showed higher internal consistency than the original Positive and Negative Syndrome Scale subscales and previously proposed factor models. Based on this representation, the positive–negative dichotomy was confirmed as the (only) robust psychopathological subtypes, and these subtypes were longitudinally stable in about 80% of the repeatedly assessed patients. Finally, the individual subtype could be predicted with good accuracy from functional connectivity profiles of the ventromedial frontal cortex, temporoparietal junction, and precuneus. Conclusions: Machine learning applied to multisite data with cross-validation yielded a factorization generalizable across populations and medical systems. Together with subtyping and the demonstrated ability to predict subtype membership from neuroimaging data, this work further disentangles the heterogeneity in schizophrenia.
KW - Brain imaging
KW - Machine learning
KW - Multivariate classification
KW - Non-negative factorization
KW - Schizophrenia
KW - Subtyping
UR - http://www.scopus.com/inward/record.url?scp=85075452072&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2019.08.031
DO - 10.1016/j.biopsych.2019.08.031
M3 - Article
C2 - 31748126
AN - SCOPUS:85075452072
SN - 0006-3223
VL - 87
SP - 282
EP - 293
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 3
ER -