The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Classification of schizophrenia and bipolar patients using static and dynamic resting-state fMRI brain connectivity
Open accessAbstract
Recently, functional network connectivity (FNC, defined as the temporal correlation among spatially distant brain networks) has been used to examine the functional organization of brain networks in various psychiatric illnesses. Dynamic FNC is a recent extension of the conventional FNC analysis that takes into account FNC changes over short periods of time. While such dynamic FNC measures may be more informative about various aspects of connectivity, there has been no detailed head-to-head comparison of the ability of static and dynamic FNC to perform classification in complex mental illnesses. This paper proposes a framework for automatic classification of schizophrenia, bipolar and healthy subjects based on their static and dynamic FNC features. Also, we compare cross-validated classification performance between static and dynamic FNC. Results show that the dynamic FNC significantly outperforms the static FNC in terms of predictive accuracy, indicating that features from dynamic FNC have distinct advantages over static FNC for classification purposes. Moreover, combining static and dynamic FNC features does not significantly improve the classification performance over the dynamic FNC features alone, suggesting that static FNC does not add any significant information when combined with dynamic FNC for classification purposes. A three-way classification methodology based on static and dynamic FNC features discriminates individual subjects into appropriate diagnostic groups with high accuracy. Our proposed classification framework is potentially applicable to additional mental disorders.
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Citations
Cites
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Consistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326
A method for making group inferences from functional MRI data using independent component analysis
Calhoun, V. D., Adali, T., Pearlson, G. D., & Pekar, J. J. (2001) · Human Brain Mapping · doi:10.1002/hbm.1048 · Cited by 2,994
Self-citationTracking whole-brain connectivity dynamics in the resting state
Allen, E. A., Damaraju, E., Plis, S. M., Erhardt, E. B., Eichele, T., & Calhoun, V. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs352 · Cited by 2,992
Self-citationResting-state functional connectivity in neuropsychiatric disorders
Greicius, M. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e328306f2c5 · Cited by 1,180
Identification of Distinct Psychosis Biotypes Using Brain-Based Biomarkers
Clementz, B. A., Sweeney, J. A., Hamm, J. P., Ivleva, E. I., Ethridge, L. E., Pearlson, G. D., Keshavan, M. S., & Tamminga, C. A. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.14091200 · Cited by 768
Self-citationBeyond Phrenology: What Can Neuroimaging Tell Us About Distributed Circuitry?
Friston, K. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142846 · Cited by 465
Imaging human connectomes at the macroscale
Craddock, R. C., Jbabdi, S., Yan, C.-G., Vogelstein, J. T., Castellanos, F. X., Di Martino, A., Kelly, C., Heberlein, K., Colcombe, S., & Milham, M. P. (2013) · Nature Methods · doi:10.1038/nmeth.2482 · Cited by 419
An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia
Altshuler, L. L., Bartzokis, G., Grieder, T., Curran, J., Jimenez, T., Leight, K., Wilkins, J., Gerner, R., & Mintz, J. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00836-2 · Cited by 369
Functional connectivity in the developing brain: a longitudinal study from 4 to 9months of age
Damaraju, E., Caprihan, A., Lowe, J. R., Allen, E. A., Calhoun, V. D., & Phillips, J. P. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.038 · Cited by 103 · cited 3×
“We expected some connectivity measures to be better captured in a static model and others in a dynamic model (Damaraju et al., 2014).”
BackgroundSelf-citationSpoletini, I., Cherubini, A., Di Paola, M., Banfi, G., Rüsch, N., Martinotti, G., Bria, P., Rubino, I. A., Siracusano, A., Caltagirone, C., et al. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2008.11.011 · Cited by 62
Cited by
Questions and controversies in the study of time-varying functional connectivity in resting fMRI
Lurie, D. J., Kessler, D., Bassett, D. S., Betzel, R. F., Breakspear, M., Kheilholz, S., Kucyi, A., Liégeois, R., Lindquist, M. A., McIntosh, A. R., et al. (2020) · Network Neuroscience · doi:10.1162/netn_a_00116 · Cited by 648
Self-citationLi, J., Duan, X., Cui, Q., Chen, H., & Liao, W. (2019) · Psychological Medicine · doi:10.1017/s0033291718001502 · Cited by 208
Data-Driven Subgroups in Depression Derived from Directed Functional Connectivity Paths at Rest
Price, R. B., Gates, K., Kraynak, T. E., Thase, M. E., & Siegle, G. J. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.97 · Cited by 98
Li, Y., Zhu, Y., Nguchu, B. A., Wang, Y., Wang, H., Qiu, B., & Wang, X. (2020) · Autism Research · doi:10.1002/aur.2212 · Cited by 95
The Necessity of Leave One Subject Out (LOSO) Cross Validation for EEG Disease Diagnosis
Kunjan, S., Grummett, T. S., Pope, K. J., Powers, D. M. W., Fitzgibbon, S. P., Bastiampillai, T., Battersby, M., & Lewis, T. W. (2021) · Lecture Notes in Computer Science · doi:10.1007/978-3-030-86993-9_50 · Cited by 80
Metadata
- Authors
- Rashid, B., Arbabshirani, M. R., Damaraju, E., Cetin, M. S., Miller, R., Pearlson, G. D., & Calhoun, V. D.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2016-07
- Volume
- 134
- Pages
- 645-657
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2336687820
- Cited by
- 334
- References
- 13
- FWCI
- 21.35
- Type
- journal article
- Language
- en
- Open access
- green
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