Sex Differences in trauma-related psychopathology: a critical review of neuroimaging literature (2014–2017)
Open accessAbstract
Purpose of review Sex differences in the epidemiology and clinical presentation of trauma-related psychopathology have long been documented. Multiple underlying mechanisms have been examined, both psychosocial and biological. Among the most promising biological mechanisms are neural substrates of trauma-related psychopathology that have been uncovered in recent years.Recent findings Neuroimaging studies of sex-related heterogeneity published over the past 3 years (2014-2017) demonstrate an interaction between sex and type, timing, and load of trauma exposure. These studies suggest that, for males, early trauma exposure may involve a loss of gray matter in the limbic system, including the prefrontal cortex (PFC), amygdala, and hippocampus, and an over-activity and increased connectivity of salience hubs, and particularly dorsal anterior cingulate cortex (dACC). For females, however, early trauma exposure may involve overactive and possibly an enlarged amygdala, as well as decreased connectivity of salience hubs such as the dACC. Underlying mechanisms may include interaction with several endocrine systems and result in differential neural response to naturally occurring and added endocrine ligands, as well as sex-specific genetic and epigenetic risk and resilience factors. This complex interaction between multiple biological systems may be associated with sex-specific behavioral patterns, in turn associated with trauma-related psychopathology. While substantial number of published studies present preliminary evidence for neural mechanisms of sex-specific posttraumatic responses, there is a paucity of research directly designed to examine sex as a biological factor in trauma-related psychopathology. Specific foci for future studies aiming to bridge current gaps in the literature are discussed.
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
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?
Males lose more grey matter after stress in limbic system structures (prefrontal cortex, amygdala and hippocampus).
“In addition, males lose more grey matter after stress in limbic system structures (prefrontal cortex, amygdala and the hippocampus (275).”
From Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma (2019) · cites this paper as [275]
The Discussion says early trauma exposure in males may involve gray-matter loss in the PFC, amygdala, and hippocampus. The claim drops both the early-trauma condition and the uncertainty, presenting the loss as a general effect of stress. The Structural MRI section also says sex-specific structural patterns have not been found following traumatic stress in adulthood. Page numbers were not supplied. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Diagnostic and Statistical Manual of Mental Disorders, 5th Edition
(2013) · American Psychiatric Association Publishing eBooks · doi:10.1176/appi.books.9780890425596.893619 · Cited by 4,390 · see citing works
Emotional processing in anterior cingulate and medial prefrontal cortex
Etkin, A., Egner, T., & Kalisch, R. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.11.004 · Cited by 3,059 · cited 1× · see citing works
“The PFC is involved in executive functions [27] and includes sub-regions such as the orbitofrontal (OFC; implicated in emotional processing [28]) and anterior cingulate (ACC; associated with monitoring [29]) cortices.”
BackgroundTolin, D. F., & Foa, E. B. (2006) · Psychological Bulletin · doi:10.1037/0033-2909.132.6.959 · Cited by 2,197 · see citing works
Benjet, C., Bromet, E., Karam, E. G., Kessler, R. C., McLaughlin, K. A., Ruscio, A. M., Shahly, V., Stein, D. J., Petukhova, M., Hill, E., et al. (2016) · Psychological Medicine · doi:10.1017/s0033291715001981 · Cited by 1,458 · see citing works
Neurobiological Basis of Failure to Recall Extinction Memory in Posttraumatic Stress Disorder
Milad, M. R., Pitman, R. K., Ellis, C. B., Gold, A. L., Shin, L. M., Lasko, N. B., Zeidan, M. A., Handwerger, K., Orr, S. P., & Rauch, S. L. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.06.026 · Cited by 1,339 · see citing works
Amygdala–frontal connectivity during emotion regulation
Banks, S. J., Eddy, K. T., Angstadt, M., Nathan, P. J., & Phan, K. L. (2007) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsm029 · Cited by 1,187 · cited 1× · see citing works
“Most commonly, these regions have included the amygdala, limbic and salience hub linked to emotional processing and response [24, 25], hippocampus, associated with learning and memory [26], insula, a major salience hub implicated in self-referential processing [20], and prefrontal cortex (PFC).”
BackgroundDepression, Stress, and Anhedonia: Toward a Synthesis and Integrated Model
Pizzagalli, D. A. (2014) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050212-185606 · Cited by 1,155 · cited 2× · see citing works
“DA is involved in the experience of pleasure and has been implicated in multiple trauma-related pathologies such as depression [31] and substance use [32].”
BackgroundPubertal hormones organize the adolescent brain and behavior
Sisk, C. L., & Zehr, J. L. (2005) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2005.10.003 · Cited by 1,082 · see citing works
Gender differences in posttraumatic stress disorder.
Olff, M., Langeland, W., Draijer, N., & Gersons, B. P. R. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.2.183 · Cited by 1,058 · cited 1× · see citing works
“Empirical examination of the mechanisms underlying this disproportion has included type and load of the traumatic exposure, cognitive factors, coping strategies, and biological factors related to sex [12 – 15].”
BackgroundChildhood abuse and lifetime psychopathology in a community sample
MacMillan, H. L., Fleming, J. E., Streiner, D. L., Lin, E., Boyle, M. H., Jamieson, E., Duku, E. K., Walsh, C. A., Wong, M. Y.-Y., & Beardslee, W. R. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.11.1878 · Cited by 1,035 · see citing works
The effects of sex and hormonal status on the physiological response to acute psychosocial stress
Kajantie, E., & Phillips, D. I. W. (2006) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2005.07.002 · Cited by 1,035 · see citing works
depue, R. A., & morrone-strupinsky, J. V. (2005) · Behavioral and Brain Sciences · doi:10.1017/s0140525x05000063 · Cited by 958 · see citing works
The Epidemiology of Trauma, PTSD, and Other Posttrauma Disorders
Breslau, N. (2009) · Trauma, Violence, & Abuse · doi:10.1177/1524838009334448 · Cited by 810 · see citing works
Post-traumatic stress disorder is associated with PACAP and the PAC1 receptor
Ressler, K. J., Mercer, K. B., Bradley, B., Jovanovic, T., Mahan, A., Kerley, K., Norrholm, S. D., Kilaru, V., Smith, A. K., Myers, A. J., et al. (2011) · Nature · doi:10.1038/nature09856 · Cited by 800 · see citing works
Post-traumatic stress disorder: the neurobiological impact of psychological trauma
Sherin, J. E., & Nemeroff, C. B. (2011) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2011.13.2/jsherin · Cited by 750 · see citing works
Traumatic stress: effects on the brain
Bremner, J. D. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/jbremner · Cited by 738 · see citing works
Individual Differences in Reward Drive Predict Neural Responses to Images of Food
Beaver, J. D., Lawrence, A. D., van Ditzhuijzen, J., Davis, M. H., Woods, A., & Calder, A. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0350-06.2006 · Cited by 594 · see citing works
Sex differences in brain activation to emotional stimuli: A meta-analysis of neuroimaging studies
Stevens, J. S., & Hamann, S. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.011 · Cited by 588 · see citing works
The influence of puberty on subcortical brain development
Goddings, A., Mills, K. L., CLASEN, L. S., Giedd, J. N., Viner, R., & Blakemore, S. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.073 · Cited by 556 · see citing works
Johnson, H., & Thompson, A. (2008) · Clinical Psychology Review · doi:10.1016/j.cpr.2007.01.017 · Cited by 530 · see citing works
Presence and acquired origin of reduced recall for fear extinction in PTSD: Results of a twin study
Milad, M. R., Orr, S. P., Lasko, N. B., Chang, Y., Rauch, S. L., & Pitman, R. K. (2008) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2008.01.017 · Cited by 512 · see citing works
de Kloet, C. S., Vermetten, E., Geuze, E., Kavelaars, A., Heijnen, C. J., & Westenberg, H. G. M. (2006) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2005.08.002 · Cited by 503 · see citing works
Generalized Anxiety Disorder Is Associated With Overgeneralization of Classically Conditioned Fear
Lissek, S. M., Kaczkurkin, A. N., Rabin, S. J., Geraci, M. F., Pine, D. S., & Grillon, C. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.07.025 · Cited by 462 · see citing works
Woon, F. L., Sood, S., & Hedges, D. W. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.06.016 · Cited by 410 · see citing works
O'Doherty, D. C. M., Chitty, K. M., Saddiqui, S., Bennett, M. R., & Lagopoulos, J. (2015) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2015.01.002 · Cited by 375 · see citing works
Hypothalamic Oxytocin Mediates Social Buffering of the Stress Response
Smith, A. S., & Wang, Z. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.09.017 · Cited by 359 · see citing works
Ansell, E. B., Rando, K., Tuit, K., Guarnaccia, J., & Sinha, R. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.022 · Cited by 354 · see citing works
Childhood Trauma Exposure Disrupts the Automatic Regulation of Emotional Processing
Marusak, H. A., Martin, K. R., Etkin, A., & Thomason, M. E. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.311 · Cited by 343 · see citing works
Perroud, N., Rutembesa, E., Paoloni-Giacobino, A., Mutabaruka, J., Mutesa, L., Stenz, L., Malafosse, A., & Karege, F. (2014) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2013.866693 · Cited by 336 · see citing works
Pruessner, J. C., Dedovic, K., Pruessner, M., Lord, C., Buss, C., Collins, L., Dagher, A., & Lupien, S. J. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.02.016 · Cited by 333 · see citing works
Sex Differences in Anxiety Disorders: Interactions between Fear, Stress, and Gonadal Hormones
Maeng, L. Y., & Milad, M. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.04.002 · Cited by 323 · see citing works
Amygdala Volume Changes in Posttraumatic Stress Disorder in a Large Case-Controlled Veterans Group
Morey, R. A., Gold, A. L., LaBar, K. S., Beall, S. K., Brown, V. M., Haswell, C. C., Nasser, J. D., Wagner, H. R., McCarthy, G., & Mid-Atlantic MIRECC Workgroup, F. T. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.50 · Cited by 289 · see citing works
Potenza, M. N., Hong, K., Lacadie, C., Fulbright, R. K., Tuit, K. L., & Sinha, R. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11020289 · Cited by 288 · see citing works
Estrogen Levels Are Associated with Extinction Deficits in Women with Posttraumatic Stress Disorder
Glover, E. M., Jovanović, T., Mercer, K. B., Kerley, K. A., Bradley, B., Ressler, K. J., & Norrholm, S. D. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.02.031 · Cited by 259 · see citing works
The impact of developmental timing for stress and recovery
Gee, D. G., & Casey, B. J. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2015.02.001 · Cited by 245 · cited 1× · see citing works
“Studies examining the neural mechanisms of development and maintenance of trauma-related psychopathology have focused mainly on circuits implicated in fear processing [17 – 19], emotional regulation [20, 21], and stress response [22, 23], including cortical, limbic, and salience regions.”
BackgroundWells, T. S., LeardMann, C. A., Fortuna, S. O., Smith, B., Smith, T. C., Ryan, M. A. K., Boyko, E. J., Blazer, D. G., & for the Millennium Cohort Study Team (2009) · American Journal of Public Health · doi:10.2105/ajph.2008.155432 · Cited by 240 · see citing works
Trajectory of post-traumatic stress following traumatic injury: 6-year follow-up
Bryant, R. A., Nickerson, A., Creamer, M. C., O'Donnell, M. L., Forbes, D., Galatzer‐Levy, I. R., McFARLANE, A. C., & Silove, D. M. (2015) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.114.145516 · Cited by 232 · see citing works
Personality disorder in DSM-5: an oral history
Zachar, P., Krueger, R. F., & Kendler, K. S. (2016) · Psychological Medicine · doi:10.1017/s0033291715001543 · Cited by 206 · see citing works
Stress-induced cognitive dysfunction: hormone-neurotransmitter interactions in the prefrontal cortex
Shansky, R. M., & Lipps, J. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00123 · Cited by 205 · cited 1× · see citing works
“These sex differences appear not only to involve HPA response but also interaction with hypothalamic-pituitary-gonadal (HPG) axis activations, whereas estrogen, a gonadal steroid hormone, appears to modulate effects of both GC [104] and PAC1 [105].”
BackgroundCarrion, V. G., & Wong, S. S. (2012) · Journal of Adolescent Health · doi:10.1016/j.jadohealth.2012.04.010 · Cited by 205 · see citing works
Chronic stress and sex differences on the recall of fear conditioning and extinction
Baran, S. E., Armstrong, C. E., Niren, D. C., Hanna, J. J., & Conrad, C. D. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.11.005 · Cited by 200 · see citing works
Sex‐specific mechanisms for responding to stress
Bangasser, D. A., & Wicks, B. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23812 · Cited by 198 · see citing works
Neria, Y., Avi Besser, A., Kiper, D., & Westphal, M. (2010) · Journal of Traumatic Stress · doi:10.1002/jts.20522 · Cited by 185 · see citing works
Self-citationDifferential associations between childhood trauma subtypes and adolescent HPA-axis functioning
Kuhlman, K. R., Geiss, E. G., Vargas, I., & Lopez-Duran, N. L. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.01.020 · Cited by 178 · see citing works
Sex differences in PTSD resilience and susceptibility: Challenges for animal models of fear learning
Shansky, R. M. (2014) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.09.005 · Cited by 173 · see citing works
Van Dam, N. T., Rando, K., Potenza, M. N., Tuit, K., & Sinha, R. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.680 · Cited by 172 · see citing works
Vukojevic, V., Kolassa, I.-T., Fastenrath, M., Gschwind, L., Spalek, K., Milnik, A., Heck, A., Vogler, C., Wilker, S., Demougin, P., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1526-14.2014 · Cited by 168 · see citing works
Carrion, V. G., Weems, C. F., Watson, C., Eliez, S., Menon, V., & Reiss, A. L. (2009) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2008.07.008 · Cited by 165 · see citing works
Stress-induced sex differences: Adaptations mediated by the glucocorticoid receptor
Bourke, C. H., Harrell, C. S., & Neigh, G. N. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.02.024 · Cited by 158 · see citing works
Estrogen modulation of oxytocin and its relation to behavior.
McCarthy, M. M. (1995) · PubMed · Cited by 157 · see citing works
Shalev, A. Y., Videlock, E. J., Peleg, T., Segman, R. H., Pitman, R. K., & Yehuda, R. (2007) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145707008127 · Cited by 157 · see citing works
The effect of gonadal hormones and gender on anxiety and emotional learning
Toufexis, D. J., Myers, K. M., & Davis, M. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.06.020 · Cited by 144 · see citing works
Comprehensive Guide to Post-Traumatic Stress Disorder
(2014) · Springer eBooks · doi:10.1007/978-3-319-08613-2 · Cited by 136 · see citing works
Sex differences in stress effects on emotional learning
Merz, C. J., & Wolf, O. T. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23811 · Cited by 122 · see citing works
Au, T. M., Dickstein, B. D., Comer, J. S., Salters‐Pedneault, K., & Litz, B. T. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.01.026 · Cited by 121 · see citing works
Helpman, L., Marin, M.-F., Papini, S., Zhu, X., Sullivan, G. M., Schneier, F., Neria, M., Shvil, E., Malaga Aragon, M. J., Markowitz, J. C., et al. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.10.007 · Cited by 121 · see citing works
Self-citationSchindler, A. G., Messinger, D. I., Smith, J. S., Shankar, H., Gustin, R. M., Schattauer, S. S., Lemos, J. C., Chavkin, N. W., Hagan, C. E., Neumaier, J. F., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3220-12.2012 · Cited by 119 · see citing works
Elton, A., Tripathi, S. P., Mletzko, T., Young, J., Cisler, J. M., James, G. A., & Kilts, C. D. (2014) · Human Brain Mapping · doi:10.1002/hbm.22280 · Cited by 119 · see citing works
Sex‐based differences in brain alterations across chronic pain conditions
Gupta, A., Mayer, E. A., Fling, C., Labus, J. S., Naliboff, B. D., Hong, J., & Kilpatrick, L. A. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23856 · Cited by 116 · see citing works
Abnormal Structure of Fear Circuitry in Pediatric Post-Traumatic Stress Disorder
Keding, T. J., & Herringa, R. J. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.239 · Cited by 115 · see citing works
Oswald, L. M., Wand, G. S., Kuwabara, H., Wong, D. F., Zhu, S., & Brasic, J. R. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3407-z · Cited by 114 · see citing works
Ferree, N. K., Kamat, R., & Cahill, L. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2011.02.003 · Cited by 114 · see citing works
Sex differences in extinction recall in posttraumatic stress disorder: A pilot fMRI study
Shvil, E., Sullivan, G. M., Schafer, S., Markowitz, J. C., Campeas, M., Wager, T. D., Milad, M. R., & Neria, Y. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.02.003 · Cited by 113 · see citing works
Self-citationBangasser, D. A. (2013) · Biology of Sex Differences · doi:10.1186/2042-6410-4-2 · Cited by 108 · see citing works
Padgett, D. K., Hawkins, R. L., Abrams, C. B., & Davis, A. C. (2006) · American Journal of Orthopsychiatry · doi:10.1037/1040-3590.76.4.461 · Cited by 107 · see citing works
Hwang, M. J., Zsido, R. G., Song, H., Pace-Schott, E. F., Miller, K. K., Lebrón‐Milad, K., Marin, M., & Milad, M. R. (2015) · BMC Psychiatry · doi:10.1186/s12888-015-0673-9 · Cited by 106 · see citing works
Developmental sex differences in resting state functional connectivity of amygdala sub-regions
Alarcón, G., Cservenka, A., Rudolph, M. D., Fair, D. A., & Nagel, B. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.013 · Cited by 105 · see citing works
Blair, K. S., Vythilingam, M., Crowe, S. L., McCaffrey, D., Ng, P., Wu, C.-C., Scaramozza, M., Mondillo, K., Pine, D. S., Charney, D. S., et al. (2012) · Psychological Medicine · doi:10.1017/s0033291712000840 · Cited by 102 · see citing works
Local brain connectivity and associations with gender and age
Lopez-Larson, M. P., Anderson, J. S., Ferguson, M. A., & Yurgelun-Todd, D. A. (2010) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2010.10.001 · Cited by 102 · see citing works
Oxytocin and stress-related disorders: neurobiological mechanisms and treatment opportunities
Sippel, L. M., Allington, C. E., Pietrzak, R. H., Harpaz-Rotem, I., Mayes, L. C., & Olff, M. (2017) · Chronic Stress · doi:10.1177/2470547016687996 · Cited by 99 · see citing works
Koch, S. B., van Zuiden, M., Nawijn, L., Frijling, J. L., Veltman, D. J., & Olff, M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.299 · Cited by 98 · see citing works
Lawson, G. M., Camins, J. S., Wisse, L. E. M., Wu, J., Duda, J., Cook, P. A., Gee, J. C., & Farah, M. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175690 · Cited by 96 · see citing works
Neuroactive steroids and PTSD treatment
Rasmusson, A. M., Marx, C. E., Pineles, S. L., Locci, A., Scioli, E. R., Nillni, Y. I., Liang, J. J., & Pinna, G. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.01.054 · Cited by 91 · see citing works
Zhu, X., Helpman, L., Papini, S., Schneier, F. R., Markowitz, J. C., Meter, P. E. V., Lindquist, M. A., Wager, T. D., & Neria, Y. (2016) · Depression and Anxiety · doi:10.1002/da.22594 · Cited by 90 · see citing works
Self-citationAmygdala subnuclei resting-state functional connectivity sex and estrogen differences
Engman, J., Linnman, C., Van Dijk, K. R. A., & Milad, M. R. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.09.012 · Cited by 89 · see citing works
Function of the hippocampus in memory formation: desperately seeking resolution
Riedel, G., & Micheau, J. (2001) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(01)00153-1 · Cited by 88 · see citing works
Disrupted insula-based neural circuit organization and conflict interference in trauma-exposed youth
Marusak, H. A., Etkin, A., & Thomason, M. E. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.04.007 · Cited by 88 · see citing works
Cumulative adversity sensitizes neural response to acute stress: association with health symptoms
Seo, D., Tsou, K. A., Ansell, E. B., Potenza, M. N., & Sinha, R. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.250 · Cited by 88 · see citing works
Genetics of glucocorticoid regulation and posttraumatic stress disorder -what do we know?
Castro-Vale, I., van Rossum, E. F. C., Machado, J. C., Mota-Cardoso, R., & Carvalho, D. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.005 · Cited by 85 · see citing works
Kong, L., Chen, K., Womer, F., Jiang, W., Luo, X., Driesen, N., Liu, J., Blumberg, H., Tang, Y., Xu, K., et al. (2013) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2013.02.003 · Cited by 84 · see citing works
Sabihi, S., Dong, S. M., Maurer, S., Goodpaster, C. M., & Leuner, B. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.06.024 · Cited by 84 · see citing works
Selective serotonin reuptake inhibitors in post-traumatic stress disorder
Hidalgo, R. B., & Davidson, J. R. T. (2000) · Journal of Psychopharmacology · doi:10.1177/026988110001400110 · Cited by 83 · see citing works
Bell, C., Nicholson, H. D., Mulder, R., Luty, S. E., & Joyce, P. R. (2006) · Journal of Psychopharmacology · doi:10.1177/0269881106060512 · Cited by 82 · see citing works
Koch, S. B. J., van Zuiden, M., Nawijn, L., Frijling, J. L., Veltman, D. J., & Olff, M. (2017) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.160129 · Cited by 80 · see citing works
Sex differences in the neural correlates of autonomic arousal: a pilot PET study
Nugent, A. C., Bain, E. E., Thayer, J. F., Sollers, J. J., & Drevets, W. C. (2011) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2011.03.001 · Cited by 78 · see citing works
Sex differences in the functional connectivity of the amygdalae in association with cortisol
Kogler, L., Müller, V. I., Seidel, E.-M., Boubela, R., Kalcher, K., Moser, E., Habel, U., Gur, R. C., Eickhoff, S. B., & Derntl, B. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.064 · Cited by 78 · see citing works
Lu, S., Gao, W., Huang, M., Li, L., & Xu, Y. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.03.009 · Cited by 75 · see citing works
De Bellis, M. D., Hooper, S. R., Chen, S. D., Provenzale, J. M., Boyd, B. D., Glessner, C. E., MacFall, J. R., Payne, M. E., Rybczynski, R., & Woolley, D. P. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000942 · Cited by 75 · see citing works
Frijling, J. L., van Zuiden, M., Nawijn, L., Koch, S. B. J., Neumann, I. D., Veltman, D. J., & Olff, M. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12300 · Cited by 74 · see citing works
Long‐term course of probable PTSD after the 9/11 attacks: A study in urban primary care
Neria, Y., Olfson, M., Gameroff, M. J., DiGrande, L., Wickramaratne, P., Gross, R., Pilowsky, D. J., Neugebaur, R., Manetti‐Cusa, J., Lewis‐Fernandez, R., et al. (2010) · Journal of Traumatic Stress · doi:10.1002/jts.20544 · Cited by 71 · see citing works
Self-citationFarrell, M. R., Sengelaub, D. R., & Wellman, C. L. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.04.002 · Cited by 69 · see citing works
Fenton, G. E., Halliday, D. M., Mason, R., Bredy, T. W., & Stevenson, C. W. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.019 · Cited by 65 · see citing works
Frijling, J. L., van Zuiden, M., Koch, S. B. J., Nawijn, L., Veltman, D. J., & Olff, M. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv116 · Cited by 62 · see citing works
Helpman, L., Papini, S., Thapa-Chhetry, B., Shvil, E., Rubin, M., Sullivan, G. M., Markowitz, J. C., Mann, J. J., & Neria, Y. (2016) · Depression and Anxiety · doi:10.1002/da.22471 · Cited by 61 · see citing works
Self-citationSadacca, B. F., Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.04.017 · Cited by 59 · see citing works
Gupta, A., Mayer, E. A., Acosta, J. R., Hamadani, K., Torgerson, C., van Horn, J. D., Chang, L., Naliboff, B., Tillisch, K., & Labus, J. S. (2017) · Neurobiology of Stress · doi:10.1016/j.ynstr.2017.02.003 · Cited by 56 · see citing works
Decreased Premotor Cortex Volume in Victims of Urban Violence with Posttraumatic Stress Disorder
Rocha-Rego, V., Pereira, M. G., Oliveira, L., Mendlowicz, M. V., Fiszman, A., Marques-Portella, C., Berger, W., Chu, C., Joffily, M., Moll, J., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042560 · Cited by 55 · see citing works
Wang, L., Cao, C., Wang, R., Qing, Y., Zhang, J., & Zhang, X. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.01.010 · Cited by 55 · see citing works
Lissek, S. M., & Grillon, C. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195399066.013.0013 · Cited by 54 · see citing works
Sex-specific neural circuits of emotion regulation in the centromedial amygdala
Wu, Y. H., Li, H., Zhou, Y., Yu, J., Zhang, Y., Song, M., Qin, W., Yu, C., & Jiang, T. (2016) · Scientific Reports · doi:10.1038/srep23112 · Cited by 53 · see citing works
Ramikie, T. S., & Ressler, K. J. (2016) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2016.18.4/kressler · Cited by 53 · see citing works
Pohlack, S. T., Nees, F., Ruttorf, M., Cacciaglia, R., Winkelmann, T., Schad, L. R., Witt, S. H., Rietschel, M., & Flor, H. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.12.018 · Cited by 50 · see citing works
Adolescent neural response to reward is related to participant sex and task motivation
Alarcón, G., Cservenka, A., & Nagel, B. J. (2016) · Brain and Cognition · doi:10.1016/j.bandc.2016.10.003 · Cited by 47 · see citing works
Sex Differences in the Neural Correlates of Specific and General Autobiographical Memory
Compère, L., Sperduti, M., Gallarda, T., Anssens, A., Lion, S., Delhommeau, M., Martinelli, P., Devauchelle, A.-D., Oppenheim, C., & Piolino, P. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00285 · Cited by 39 · see citing works
The Role of the PACAP Signaling System in Depression
Pinhasov, A., Nesher, E., Gross, M., Turgeman, G., Kreinin, A., & Yadid, G. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211795589328 · Cited by 37 · see citing works
Relationship of recent stress to amygdala volume in depressed and healthy adults
Sublette, M. E., Galfalvy, H., Oquendo, M. A., Bart, C. P., Schneck, N., Arango, V., & Mann, J. J. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.05.036 · Cited by 31 · see citing works
Luo, Y., Shan, H., Liu, Y., Wu, L., Zhang, X., Ma, T., Zhu, W., Yang, Y., Wang, J., & Cao, Z. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.03.003 · Cited by 30 · see citing works
Sarubin, N., Hilbert, S., Naumann, F., Zill, P., Wimmer, A.-M., Nothdurfter, C., Rupprecht, R., Baghai, T. C., Bühner, M., & Schüle, C. (2016) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-016-0722-5 · Cited by 30 · see citing works
Neuroendocrine Underpinnings of Increased Risk for Posttraumatic Stress Disorder in Women
Briscione, M. A., Michopoulos, V., Jovanović, T., & Norrholm, S. D. (2016) · Vitamins and hormones · doi:10.1016/bs.vh.2016.08.003 · Cited by 25 · see citing works
The prefrontal cortex as a critical gate of negative affect and motivation in alcohol use disorder
Pahng, A. R., McGinn, M. A., Paulsen, R. I., & Edwards, S. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2016.11.004 · Cited by 24 · see citing works
Sunderland, M., Carragher, N., Chapman, C., Mills, K. L., Teesson, M., Lockwood, E., Forbes, D., & Slade, T. N. (2016) · Journal of Anxiety Disorders · doi:10.1016/j.janxdis.2016.02.001 · Cited by 21 · see citing works
Examining the utility of using genotype and functional biology in a clinical pharmacology trial
Graham, D. P., Nielsen, D. A., Kosten, T. R., Davis, L. L., Hamner, M. B., Makotkine, I., & Yehuda, R. (2014) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000039 · Cited by 8 · see citing works
Polusny, M. A., Martyr, M. A., Erbes, C. R., Arbisi, P. A., Kramer, M. D., Gibson, E., & Oleson, H. (2015) · Springer eBooks · doi:10.1007/978-3-319-08359-9_129 · Cited by 8 · see citing works
Marusak, H. A., Etkin, A., & Thomason, M. E. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.02.004 · Cited by 5 · see citing works
Association of PACAP and PACAPR1 gene variants with unipolar depression and panic disorder
Erhardt, A., Lucae, S., Ising, M., et al. (2013) · Pharmacopsychiatry · doi:10.1055/s-0033-1353350 · Cited by 3 · see citing works
Thornley, E., & Frewen, P. (2016) · Personality and Individual Differences · doi:10.1016/j.paid.2016.05.323 · Cited by 1 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
More than a feeling: A unified view of stress measurement for population science
Epel, E. S., Crosswell, A. D., Mayer, S. E., Prather, A. A., Slavich, G. M., Puterman, E., & Mendes, W. B. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.03.001 · Cited by 1,077 · see citing works
“In terms of structural changes due to stress, childhood trauma may impact the hippocampal volume of males more than females (reviewed in Tiwari and Gonzalez, 2018) and may enlarge amygdala and decrease connectivity of salience hubs such as the dACC in females more than males (Helpman et al., 2017).”
BackgroundHerzog, J. I., & Schmahl, C. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00420 · Cited by 583 · see citing works
Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma
Jiang, S., Postovit, L., Cattaneo, A., Binder, E. B., & Aitchison, K. J. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00808 · Cited by 288 · see citing works
Cuoco, S., Nisticò, V., Cappiello, A., Scannapieco, S., Gambini, O., Barone, P., Erro, R., & Demartini, B. (2021) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2021.110539 · Cited by 22 · see citing works
- Authors
- Helpman, L., Zhu, X., Suarez-Jimenez, B., Lazarov, A., Monk, C., & Neria, Y.
- Affiliations
- Columbia University Irving Medical Center (US)
- Corresponding author
- Helpman, Liat
- Venue
- Current Psychiatry Reports
- Published
- 2017-11-08
- Volume
- 19
- Issue
- 12
- Pages
- 104-104
- ISSN
- 1523-3812 (ISSN-L)
- 1535-1645
- PMC
- PMC5737777
- OpenAlex
- W2767812342
- Cited by
- 82
- References
- 116
- Citations by year
- 2026: 15 · 2025: 11 · 2024: 11 · 2023: 10 · 2022: 8 · 2021: 14 · 2020: 3 · 2019: 7 · 2018: 3
- FWCI
- 0.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Psychiatry Reports (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (T32MH020004, R01MH072833, R01MH105355, T32MH096724, T32MH015144)
- Topics
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Social Sciences › Psychology › Clinical Psychology › Child Abuse and Trauma
- Social Sciences › Psychology › Clinical Psychology › Psychoanalysis and Psychopathology Research
- Keywords
- sex differences, trauma-related psychopathology, post-traumatic stress disorder, gray matter loss, limbic system, prefrontal cortex, amygdala, hippocampus, dorsal anterior cingulate cortex, neuronal connectivity, endocrine system, epigenetics, resilience factors
- MeSH terms
- Psychological Trauma, Amygdala, Female, Gyrus Cinguli, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Psychopathology, Sex Characteristics, Prefrontal Cortex, Epigenesis, Genetic, Resilience, Psychological, Neuroimaging
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