The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.
Parsing Heterogeneity in the Brain Connectivity of Depressed and Healthy Adults During Positive Mood
Open accessAbstract
Background There is well-known heterogeneity in affective mechanisms in depression that may extend to positive affect. We used data-driven parsing of neural connectivity to reveal subgroups present across depressed and healthy individuals during positive processing, informing targets for mechanistic intervention.Methods Ninety-two individuals (68 depressed patients, 24 never-depressed control subjects) completed a sustained positive mood induction during functional magnetic resonance imaging. Directed functional connectivity paths within a depression-relevant network were characterized using Group Iterative Multiple Model Estimation (GIMME), a method shown to accurately recover the direction and presence of connectivity paths in individual participants. During model selection, individuals were clustered using community detection on neural connectivity estimates. Subgroups were externally tested across multiple levels of analysis.Results Two connectivity-based subgroups emerged: subgroup A, characterized by weaker connectivity overall, and subgroup B, exhibiting hyperconnectivity (relative to subgroup A), particularly among ventral affective regions. Subgroup predicted diagnostic status (subgroup B contained 81% of patients; 50% of control subjects; χ 2 = 8.6, p = .003) and default mode network connectivity during a separate resting-state task. Among patients, subgroup B members had higher self-reported symptoms, lower sustained positive mood during the induction, and higher negative bias on a reaction-time task. Symptom-based depression subgroups did not predict these external variables.Conclusions Neural connectivity-based categorization travels with diagnostic category and is clinically predictive, but not clinically deterministic. Both patients and control subjects showed heterogeneous, and overlapping, profiles. The larger and more severely affected patient subgroup was characterized by ventrally driven hyperconnectivity during positive processing. Data-driven parsing suggests heterogeneous substrates of depression and possible resilience in control subjects in spite of biological overlap.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Equally noteworthy, however, is the marked heterogeneity of depressed patients, which is evident at the neural network 143,144 , cognitive 145 , information processing 145,146 , and clinical 147 levels, and may help to explain the fact that no known intervention strategy is effective for all depressed patients.”
From Neuroplasticity in cognitive and psychological mechanisms of depression: an integrative model (2020) · cites this paper as [144]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Karalunas, S. L., Fair, D., Musser, E. D., Aykes, K., Iyer, S. P., & Nigg, J. T. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.763 · Cited by 340
RetractedDiagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,845
(1975) · Medical Entomology and Zoology · Cited by 7,245
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
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
Gottesman, I. I., & Gould, T. D. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.4.636 · Cited by 5,615
Cognitive Therapy and the Emotional Disorders
Jaffe, B. (1977) · Psychosomatics · doi:10.1016/s0033-3182(77)71107-7 · Cited by 4,730
Functional connectome fingerprinting: Identifying individuals using patterns of brain connectivity
Finn, E. S., Shen, X., Scheinost, D., Rosenberg, M. D., Huang, J., Chun, M. M., Papademetris, X., & Constable, R. T. (2015) · Nature Neuroscience · doi:10.1038/nn.4135 · Cited by 2,747
Functional and effective connectivity in neuroimaging: a synthesis
Friston, K. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020107 · Cited by 2,452
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320
Kaiser, R. H., Andrews-Hanna, J. R., Wager, T. D., & Pizzagalli, D. A. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0071 · Cited by 2,281
Drevets, W. C., Price, J. L., & Furey, M. L. (2008) · Brain Structure and Function · doi:10.1007/s00429-008-0189-x · Cited by 2,241
Greicius, M. D., Flores, B. H., Menon, V., Glover, G. H., Solvason, H. B., Kenna, H., Reiss, A. L., & Schatzberg, A. F. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.09.020 · Cited by 2,214
Organization, development and function of complex brain networks
SPORNS, O., CHIALVO, D., KAISER, M., & HILGETAG, C. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.07.008 · Cited by 2,055
Network modelling methods for FMRI
Smith, S. M., Miller, K. L., Salimi-Khorshidi, G., Webster, M., Beckmann, C. F., Nichols, T. E., Ramsey, J. D., & Woolrich, M. W. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.063 · Cited by 1,878
Computing Communities in Large Networks Using Random Walks
Pons, P., & Matthieu Latapy, B. (2006) · Journal of Graph Algorithms and Applications · doi:10.7155/jgaa.00124 · Cited by 1,600
Sheline, Y. I., Price, J. L., Yan, Z., & Mintun, M. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000446107 · Cited by 1,196
Creative Cognition and Brain Network Dynamics
Beaty, R. E., Benedek, M., Silvia, P. J., & Schacter, D. L. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.004 · Cited by 1,105
The new person-specific paradigm in psychology
Molenaar, P. C. M., & Campbell, C. G. (2009) · Current Directions in Psychological Science · doi:10.1111/j.1467-8721.2009.01619.x · Cited by 1,088
Fried, E. I., & Nesse, R. M. (2015) · Journal of Affective Disorders · doi:10.1016/j.jad.2014.10.010 · Cited by 1,043
Depressive rumination, the default-mode network, and the dark matter of clinical neuroscience
Hamilton, J. P., Farmer, M., Fogelman, P., & Gotlib, I. H. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.02.020 · Cited by 952
A meta-analysis of emotional reactivity in major depressive disorder
Bylsma, L. M., Morris, B. H., & Rottenberg, J. (2008) · Clinical Psychology Review · doi:10.1016/j.cpr.2007.10.001 · Cited by 933
Siegle, G. J., Steinhauer, S. R., Thase, M. E., Stenger, V. A., & Carter, C. S. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01314-8 · Cited by 859
Self-citationSiegle, G. J., Thompson, W., Carter, C. S., Steinhauer, S. R., & Thase, M. E. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.05.048 · Cited by 857
Self-citationIdentification 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
Zhu, X., Wang, X., Xiao, J., Liao, J., Zhong, M., Wang, W., & Yao, S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.10.035 · Cited by 638
Emotional information processing in mood disorders: a review of behavioral and neuroimaging findings
Leppänen, J. M. (2006) · Current Opinion in Psychiatry · doi:10.1097/01.yco.0000191500.46411.00 · Cited by 632
Attentional bias in generalized anxiety disorder versus depressive disorder.
Mogg, K., & Bradley, B. P. (2005) · Cognitive Therapy and Research · doi:10.1007/s10608-005-1646-y · Cited by 565
Johansen-Berg, H., Gutman, D. A., Behrens, T. E. J., Matthews, P. M., Rushworth, M. F. S., Katz, E., Lozano, A. M., & Mayberg, H. S. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm167 · Cited by 561
Negative thinking in depression: cause, effect, or reciprocal relationship?
Teasdale, J. D. (1983) · Advances in Behaviour Research and Therapy · doi:10.1016/0146-6402(83)90013-9 · Cited by 541
Gates, K. M., & Molenaar, P. C. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.026 · Cited by 478
Self-citationDiscrete Neural Signatures of Basic Emotions
Saarimäki, H., Gotsopoulos, A., Jääskeläinen, I. P., Lampinen, J., Vuilleumier, P. O., Hari, R., Sams, M. E., & Nummenmaa, L. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv086 · Cited by 451
Heller, A. S., Johnstone, T., Shackman, A. J., Light, S. N., Peterson, M. J., Kolden, G. G., Kalin, N. H., & Davidson, R. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910651106 · Cited by 444
Toward an information-processing analysis of depression
Ingram, R. E. (1984) · Cognitive Therapy and Research · doi:10.1007/bf01173284 · Cited by 417
Research review: altered reward function in adolescent depression: what, when and how?
Forbes, E. E., & Dahl, R. E. (2012) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2011.02477.x · Cited by 350
Mental illness, suicide and creativity: 40-Year prospective total population study
Kyaga, S., Landén, M., Boman, M., Hultman, C. M., Långström, N., & Lichtenstein, P. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2012.09.010 · Cited by 303
Neural Responses to Happy Facial Expressions in Major Depression Following Antidepressant Treatment
Fu, C. H. Y., Williams, S. C. R., Brammer, M. J., Suckling, J., Kim, J., Cleare, A. J., Walsh, N. D., Mitterschiffthaler, M. T., Andrew, C. M., Pich, E. M., et al. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.4.599 · Cited by 288
Discovering imaging endophenotypes for major depression
Hasler, G., & Northoff, G. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.23 · Cited by 274
Kim, J., Zhu, W., Chang, L., Bentler, P. M., & Ernst, T. (2007) · Human Brain Mapping · doi:10.1002/hbm.20259 · Cited by 236
Psychopathology and pathophysiology of the self in depression-Neuropsychiatric hypothesis
Northoff, G. (2007) · Journal of Affective Disorders · doi:10.1016/j.jad.2007.02.012 · Cited by 209
Toward Clinically Useful Neuroimaging in Depression Treatment
Siegle, G. J., Thompson, W. K., Collier, A. B., Berman, S., Feldmiller, J., Thase, M. E., & Friedman, E. S. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.65 · Cited by 206
Self-citationA resilience framework for promoting stable remission from depression
Waugh, C. E., & Koster, E. H. W. (2015) · Clinical Psychology Review · doi:10.1016/j.cpr.2014.05.004 · Cited by 202
Computing communities in large networks using random walks (long version)Preprint
Pons, P., & Matthieu Latapy, B. (2005) · arXiv (Cornell University) · doi:10.48550/arxiv.physics/0512106 · Cited by 178
Miller, M. B., Horn, J. D. V., Wolford, G., Handy, T. C., Valsangkar-Smyth, M., Inati, S., Grafton, S. T., & Gazzaniga, M. S. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902760807203 · Cited by 158
Childhood Antecedents and Risk for Adult Mental Disorders
Pine, D. S., & Fox, N. A. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015038 · Cited by 149
Architectural Representation of Valence in the Limbic System
Namburi, P., Al‐Hasani, R., Calhoon, G. G., Bruchas, M. R., & Tye, K. M. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.358 · Cited by 148
Unsupervised Classification During Time-Series Model Building
Gates, K. M., Lane, S., Varangis, E. M. L., Giovanello, K. S., & Guiskewicz, K. (2016) · Multivariate Behavioral Research · doi:10.1080/00273171.2016.1256187 · Cited by 145
Self-citationAlcaro, A., Panksepp, J., Witczak, J., Hayes, D. J., & Northoff, G. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.11.023 · Cited by 144
Bayesian networks for fMRI: A primer
Mumford, J. A., & Ramsey, J. D. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.10.020 · Cited by 132
Extended unified SEM approach for modeling event-related fMRI data
Gates, K. M., Molenaar, P. C. M., Hillary, F. G., & Slobounov, S. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.051 · Cited by 125
Self-citationA Comparison of Community Detection Algorithms on Artificial Networks
Orman, G. K., & Labatut, V. (2009) · Lecture notes in computer science · doi:10.1007/978-3-642-04747-3_20 · Cited by 109
Gates, K. M., Molenaar, P. C. M., Iyer, S. P., Nigg, J. T., & Fair, D. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091322 · Cited by 107
Self-citationCorticostriatal pathways contribute to the natural time course of positive mood
Admon, R., & Pizzagalli, D. A. (2015) · Nature Communications · doi:10.1038/ncomms10065 · Cited by 57
Brain Network Informed Subject Community Detection In Early-Onset Schizophrenia
Yang, Z., Xu, Y., Xu, T., Hoy, C. W., Handwerker, D. A., Chen, G., Northoff, G., Zuo, X., & Bandettini, P. (2014) · Scientific Reports · doi:10.1038/srep05549 · Cited by 56
Social anhedonia and medial prefrontal response to mutual liking in late adolescents
Healey, K. L., Morgan, J., Musselman, S. C., Olino, T. M., & Forbes, E. E. (2014) · Brain and Cognition · doi:10.1016/j.bandc.2013.12.004 · Cited by 53
Horner, M. S., Siegle, G. J., Schwartz, R. M., Price, R. B., Haggerty, A. E., Collier, A. B., & Friedman, E. S. (2014) · Depression and Anxiety · doi:10.1002/da.22244 · Cited by 46
Self-citationMorgan, J. K., Shaw, D. S., Olino, T. M., Musselman, S. C., Kurapati, N. T., & Forbes, E. E. (2015) · Journal of Clinical Child & Adolescent Psychology · doi:10.1080/15374416.2015.1030753 · Cited by 36
Flagged first, then by citations
Cited by
Sorted by citations
Building better biomarkers: brain models in translational neuroimaging
Woo, C.-W., Chang, L. J., Lindquist, M. A., & Wager, T. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4478 · Cited by 1,056
Neuroplasticity in cognitive and psychological mechanisms of depression: an integrative model
Price, R. B., & Duman, R. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0615-x · Cited by 739
Self-citationPersonalized Models of Psychopathology
Wright, A. G. C., & Woods, W. C. (2020) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-102419-125032 · Cited by 308
Dissecting diagnostic heterogeneity in depression by integrating neuroimaging and genetics
Buch, A. M., & Liston, C. M. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00789-3 · Cited by 289
Zhang, Y., Wu, W., Toll, R. T., Naparstek, S., Maron-Katz, A., Watts, M., Gordon, J., Jeong, J., Astolfi, L., Shpigel, E., et al. (2020) · Nature Biomedical Engineering · doi:10.1038/s41551-020-00614-8 · Cited by 241
Metadata
- Authors
- Price, R. B., Lane, S., Gates, K., Kraynak, T. E., Horner, M. S., Thase, M. E., & Siegle, G. J.
- Affiliations
- University of Pittsburgh (US)
- University of North Carolina at Chapel Hill (US)
- Philadelphia VA Medical Center (US)
- Corresponding author
- Price, Rebecca B.
- ORCID
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2017-02
- Volume
- 81
- Issue
- 4
- Pages
- 347-357
- ISSN
- 0006-3223 (ISSN-L)
- PMC
- PMC5215983
- OpenAlex
- W2463383187
- Cited by
- 106
- References
- 56
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 7 · 2023: 15 · 2022: 9 · 2021: 18 · 2020: 17 · 2019: 9 · 2018: 10 · 2017: 8
- FWCI
- 6.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (T32HL007560)
- National Institute of Mental Health (R01MH069618, K02MH082998, R01MH058397, K23MH100259, R01MH074807, R01MH058356)
- National Institute of Biomedical Imaging and Bioengineering (R21EB015573)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Mental Health Research Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- depression, positive mood, neuronal heterogeneity, directed functional connectivity, GIMME, community detection, default mode network, mood induction, negative bias, resilience
- MeSH terms
- Adult, Affect, Brain, Brain Mapping, Depressive Disorder, Major, Major Depressive Disorder, Female, Humans, Magnetic Resonance Imaging, Male, Neural Pathways, Psychiatric Status Rating Scales, Resilience, Psychological
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review