Imbalanced Neural Responsivity to Risk and Reward Indicates Stress Vulnerability in Humans
Abstract
Trauma-related psychopathology has been associated with an intense emotional reaction to stressful event. Emotional responses have evolved to signal the presence of risks to be avoided or of rewards to be approached in the environment. Thus, individuals' sensitivity to signals of risk and reward may affect the level of stress vulnerability. Stress, however, can modify these sensitivities as well. In the current functional magnetic resonance imaging (fMRI) study, we prospectively probed the neural correlates of such sensitivities in 24 healthy soldiers by using an interactive game that encompasses risky and rewarding intervals both pre-exposure and post-exposure to stressful military service. As expected, risky and rewarding intervals elicited selective responses in the amygdala and nucleus accumbens (Nacc), respectively. Furthermore, increased post-traumatic stress disorder symptoms post-exposure (i.e., stress vulnerability) corresponded to greater amygdala's response to risk both pre-exposure and post-exposure and to decreased NAcc response to reward only post-exposure. By combining these regional responsivities post-exposure, we accurately identified all the most vulnerable soldiers. Imbalanced neural responsivity to risk and reward following exposure to stress may therefore constitute a marker for stress vulnerability. Such identification of vulnerability biomarkers can aid future diagnostic and therapeutic efforts by allowing early detection of vulnerability as well as follow up on patient's treatment progression.
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Increased risk of PTSD development is associated with dysregulations of central fear responses prior to and shortly after trauma exposure.
“An increased risk of PTSD development is associated with pre-existing dysregulations of (para)sympathetic [17,18] and hypothalamic-pituitary-adrenal axes [20,21], as well as dysregulations of central fear responses prior to [22] and shortly after trauma exposure [23,24].”
From Efficacy of oxytocin administration early after psychotrauma in preventing the development of PTSD: study protocol of a randomized controlled trial (2014) · cites this paper as [22]
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Szeszko, P. R., & Yehuda, R. (2019) · Psychiatry Research · doi:10.1016/j.psychres.2019.02.005 · Cited by 58 · see citing works
Building Resilience: The Stress Response as a Driving Force for Neuroplasticity and Adaptation
Hermans, E. J., Hendler, T., & Kalisch, R. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.10.016 · Cited by 60 · see citing works
Self-citationThe Role of BDNF-TrkB Signaling in the Pathogenesis of PTSD
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“In two prospective studies of military personnel, increased activity in the amygdala in response to emotional stimuli was associated with a greater vulnerability to developing PTSD symptoms [24,61].”
BackgroundRamikie, T. S., & Ressler, K. J. (2016) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2016.18.4/kressler · Cited by 53 · see citing works
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“…same research group, the authors found that greater amygdala activation in response to risk anticipation at pre-and post-trauma was related to more PTSD symptoms post-trauma [132] and reduced nucleus accumbens activation to reward post-trauma was related to greater PTSD symptoms post-trauma [132].”
BackgroundStriatal Dopamine Release and Genetic Variation of the Serotonin 2C Receptor in Humans
Mickey, B. J., Sanford, B., Love, T., Shen, P., Hodgkinson, C. A., Stohler, C. S., Goldman, D. A., & Zubieta, J.-K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1260-12.2012 · Cited by 47 · see citing works
Distinct Processing of Aversive Experience in Amygdala Subregions
Michely, J., Rigoli, F., Rutledge, R. B., Hauser, T. U., & Dolan, R. J. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.07.008 · Cited by 46 · see citing works
“This finding demonstrates that trait-anxious indivi uals display a failure to regulate BLA activity adequately in response to objectively different threat levels, supporting the notion that anxiety is associated with elevated and u ifferentiated amygdala activity, potentially due to a failure to adequately modulate it…”
BackgroundReward processing and future life stress: Stress generation pathway to depression.
Mackin, D. M., Kotov, R., Perlman, G., Nelson, B. D., Goldstein, B. L., Hajcak, G., & Klein, D. N. (2019) · Journal of Abnormal Psychology · doi:10.1037/abn0000427 · Cited by 43 · see citing works
“Life stress, including early childhood maltreatment, disrupts neural processing of reward (Admon et al., 2013; Auerbach, Admon, & Pizzagalli, 2014; Casement et al., 2014; McCrory, Gerin, & Viding, 2017; Novick et al., 2018), and these neurodevelopmental changes in reward processing influence later…”
BackgroundStress-resilience impacts psychological wellbeing as evidenced by brain–gut microbiome interactions
An, E., Delgadillo, D. R., Yang, J., Agarwal, R., Labus, J. S., Pawar, S., Leitman, M., Kilpatrick, L. A., Bhatt, R. R., Vora, P. P., et al. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00266-6 · Cited by 45 · see citing works
“Lower activity within the salience network 53 , but increased connectivity within the sensorimotor network 54,55 as well as greater responses in reward circuits (basal ganglia) 56 have been linked to resilience.”
Koch, K., Wagner, G., Schachtzabel, C., Schultz, C. C., Güllmar, D., Reichenbach, J. R., Sauer, H., Zimmer, C., & Schlösser, R. G. M. (2014) · Human Brain Mapping · doi:10.1002/hbm.22284 · Cited by 42 · see citing works
“Amongst these, the nucleus accumbens (NAcc) constituting a major portion of the ventral striatum and receiving direct mesolimbic projections from the ventral tegmental area (VTA) has been proposed as the key brain structure in the regulation of reward-appetitive behavior [Admon et al., 2013; Camara et al., 2009; Cohen…”
BackgroundAnhedonia in Posttraumatic Stress Disorder: Prevalence, Phenotypes, and Neural Circuitry
Vinograd, M., Stout, D. M., & Risbrough, V. B. (2021) · Current topics in behavioral neurosciences · doi:10.1007/7854_2021_292 · Cited by 39 · see citing works
Does Anhedonia Presage Increased Risk of Posttraumatic Stress Disorder?
Risbrough, V. B., Glynn, L. M., Davis, E. P., Sandman, C. A., Obenaus, A., Stern, H. S., Keator, D. B., Yassa, M. A., Baram, T. Z., & Baker, D. G. (2018) · Current topics in behavioral neurosciences · doi:10.1007/7854_2018_51 · Cited by 37 · see citing works
Hyatt, C. J., Assaf, M., Muska, C. E., Rosen, R. I., Thomas, A. D., Johnson, M. R., Hylton, J. L., Andrews, M. M., Reynolds, B. A., Krystal, J. H., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034917 · Cited by 37 · see citing works
“The Domino fMRI task was originally introduced to examine the role of the amygdala in signaling prospective negative outcomes during risk-taking [39,40], but has also been shown to strongly activate the reward system, particularly the ventral striatum, as a result of gains during gameplay [40,41].”
Self-citationAltered reward processing following an acute social stressor in adolescents
Lincoln, S. H., Pisoni, A., Bondy, E., Kumar, P., Singleton, P., Hajcak, G., Pizzagalli, D. A., & Auerbach, R. P. (2019) · PLoS ONE · doi:10.1371/journal.pone.0209361 · Cited by 35 · see citing works
“, ventral striatum) activation during reward receipt [21].”
BackgroundRab, S. L., & Admon, R. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.09.007 · Cited by 34 · see citing works
Self-citationPichon, S., Lombard, E., Eryilmaz, H., & Vuilleumier, P. O. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu044 · Cited by 35 · see citing works
Sheynin, S., Wolf, L., Ben‐Zion, Z., Sheynin, J., Balter, S. R., Keynan, J. N., Admon, R., Shalev, A. Y., Hendler, T., & Liberzon, I. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118242 · Cited by 34 · see citing works
“The rest of the connectivities are related to the 477 nature of this dynamic task, as was shown in previous work [1, 84, 6].”
InfluentialSelf-citationReward Processing and Circuit Dysregulation in Posttraumatic Stress Disorder
Lokshina, Y., Nickelsen, T., & Liberzon, I. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.559401 · Cited by 35 · see citing works
“Reward Outcome Several studies have indicated that PTSD patients, compared to trauma-exposed controls, exhibit decreased ventral striatal and decreased medial prefrontal cortex (mPFC) activation to reward (relative to loss) (10, 90).”
BackgroundLong-Term Effects of Acute Stress on the Prefrontal-Limbic System in the Healthy Adult
Li, Y., Hou, X., Wei, D., Du, X., Zhang, Q., Liu, G., & Qiu, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0168315 · Cited by 34 · see citing works
Neural indicators of interpersonal anger as cause and consequence of combat training stress symptoms
Gilam, G., Lin, T., Fruchter, E., & Hendler, T. (2017) · Psychological Medicine · doi:10.1017/s0033291716003354 · Cited by 31 · see citing works
“We recently proposed a model which aimed to disentangle predisposing from acquired neural abnormalities of PTSD (Admon et al. 2013b), highlighting hyperactivity of the amygdala and dorsal anterior cingulate cortex as predisposing factors and vmPFC– hippocampus hypoconnectivity as an acquired…”
BackgroundInfluentialSelf-citationEthridge, P., Ali, N., Racine, S. E., Pruessner, J. C., & Weinberg, A. (2020) · Clinical Psychological Science · doi:10.1177/2167702620917463 · Cited by 32 · see citing works
A Possible Role of Anhedonia as Common Substrate for Depression and Anxiety
Grillo, L. (2016) · Depression Research and Treatment · doi:10.1155/2016/1598130 · Cited by 31 · see citing works
“depression and anxiety are both part of the same continuum of problems [25, 26] and that they have a common substrate [27–29] that some authors suggest might be anhedonia [22].”
BackgroundThe Role of Mesolimbic Circuitry in Buffering Election-Related Distress
Tashjian, S. M., & Galván, A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2470-17.2018 · Cited by 29 · see citing works
Ben‐Zion, Z., Fine, N. B., Keynan, J. N., Admon, R., Halpern, P., Liberzon, I., Hendler, T., & Shalev, A. Y. (2019) · European Journal of Psychotraumatology · doi:10.1080/20008198.2019.1683941 · Cited by 30 · see citing works
Self-citationBen‐Zion, Z., Shany, O., Admon, R., Keynan, J. N., Avisdris, N., Balter, S. R., Shalev, A. Y., Liberzon, I., & Hendler, T. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2021.09.001 · Cited by 28 · see citing works
Self-citationFarber, M. J., Kim, M. J., Knodt, A. R., & Hariri, A. R. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.100711 · Cited by 26 · see citing works
Rowland, J. A., Stapleton-Kotloski, J. R., Alberto, G. E., Rawley, J. A., Kotloski, R. J., Taber, K. H., & Godwin, D. W. (2016) · Brain Connectivity · doi:10.1089/brain.2015.0406 · Cited by 25 · see citing works
“…deployment or combat exposure demonstrated changes in brain structure, function, and functional connectivity following war zone deployment (Admon et al., 2009, 2013a,b; van Wingen et al., 2011, 2012), although not directly due to the development of PTSD. Exploratory analyses to evaluate…”
BackgroundKehyayan, A., Wright, P., Marks, J., Matura, J.-M., Axmacher, N., Herpertz, S., & Kessler, H. (2023) · European Journal of Psychotraumatology · doi:10.1080/20008066.2023.2172258 · Cited by 23 · see citing works
Norbury, A., Seeley, S. H., Pérez-Rodríguez, M. M., & Feder, A. (2023) · Psychological Medicine · doi:10.1017/s0033291723001162 · Cited by 22 · see citing works
“…combat-exposed paramedics, decreased reward response in the nucleus accumbens post-, but not pre-exposure, was found to be related to self-18 reported PTSD symptoms – suggesting that preserved reward responses may be a marker of resilience, rather than a prospective indicator (Admon et al., 2013).”
BackgroundBoukezzi, S. C., Baunez, C., Rousseau, P., Warrot, D., Silva, C., Guyon, V., Zendjidjian, X. Y., Nicolas, F., Guedj, É., Nazarian, B., et al. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.102073 · Cited by 22 · see citing works
“As compared with healthy controls, PTSD patients showed lower activation in key components of the reward system when obtaining rewards, namely the NAcc, the ventral and dorsal striatum and the mPFC (Elman et al., 2009; Admon et al., 2013).”
Lijffijt, M., Green, C. E., Balderston, N. L., Iqbal, T., Atkinson, M. E., Vo‐Le, B., Vo-Le, B., O’Brien, B., Grillon, C., Swann, A. C., et al. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00846 · Cited by 20 · see citing works
“In humans, enhanced reactivity of the amygdala could predispose to development of PTSD symptoms (51, 52) and is associated with less resilience to stressors of everyday life (53).”
BackgroundParadoxical associations between familial affective responsiveness, stress, and amygdala reactivity.
Farber, M. J., Romer, A. L., Kim, M. J., Knodt, A. R., Elsayed, N. M., Williamson, D. E., & Hariri, A. R. (2018) · Emotion · doi:10.1037/emo0000467 · Cited by 19 · see citing works
“…et al., 2015; Pechtel et al., 2014; Sheridan et al., 2012; Tottenham, 2012; Tottenham et al., 2010) but also represents a biomarker of future risk for stress-related depression and anxiety (Admon et al., 2013; Etkin & Wager, 2007; Schlund & Cataldo, 2010; Swartz, Knodt, Radtke, & Hariri, 2015).”
Scheeringa, M. S. (2020) · International Journal of Methods in Psychiatric Research · doi:10.1002/mpr.1864 · Cited by 19 · see citing works
Freeman, C. R., Panier, L. Y. X., Schaffer, J., & Weinberg, A. (2022) · Psychophysiology · doi:10.1111/psyp.14206 · Cited by 18 · see citing works
Can Understanding Reward Help Illuminate Anhedonia?
Kaya, S., & McCabe, C. (2019) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-019-00186-1 · Cited by 16 · see citing works
Simon, L., Levi, S., Shapira, S., & Admon, R. (2024) · SLEEP · doi:10.1093/sleep/zsae183 · Cited by 17 · see citing works
Self-citationProspective examination of pre-trauma anhedonia as a risk factor for post-traumatic stress symptoms
Acheson, D. T., Vinograd, M., Nievergelt, C. M., Yurgil, K. A., Moore, T. M., Risbrough, V. B., & Baker, D. G. (2022) · European Journal of Psychotraumatology · doi:10.1080/20008198.2021.2015949 · Cited by 17 · see citing works
“ventral striatum BOLD response) are also associated with more severe post-traumatic stress (PTS) symptoms or PTSD diagnosis (Admon et al., 2013; Admon, Milad, & Hendler, 2013; Elman et al., 2009; Sailer et al., 2008).”
BackgroundClockViz: Designing Public Visualization for Coping with Collective Stress in Teamwork
Xue, M., Liang, R.-H., Hu, J., & Feijs, L. M. G. (2017) · InTech eBooks · doi:10.5772/intechopen.71220 · Cited by 16 · see citing works
“can be created and adjusted through complete difficult tasks or challenging games, such as memory card game [13], domino game [14], soccer game [15], and first-person shooter game [16], which validity and practicability have been proven in the previous research [17].”
BackgroundGhaffarzadegan, R., Akhondzadeh, S., Nikasa, Z., Hajizamani, S., Mehrabanifar, S., Cheraghi, I., & Vaseghi, S. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04242-5 · Cited by 16 · see citing works
“In the NAc, research on soldiers found diminished coping in individuals with decreased BDNF-TrkB signal - ing and activity in the NAc, mediated by a combination of genetic vulnerability and traumatic experience [ 76 ].”
Dell’Acqua, C., Moretta, T., Bò, E. D., Benvenuti, S. M., & Palomba, D. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.02.027 · Cited by 16 · see citing works
de Voogd, L. D., Hashemi, M. M., Zhang, W., Kaldewaij, R., Koch, S. B. J., van Ast, V. A., Klumpers, F., & Karin Roelofs, A. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.02.894 · Cited by 15 · see citing works
Martin-Söelch, C., Guillod, M., Gaillard, C., Recabarren, R. E., Federspiel, A., Mueller‐Pfeiffer, C., Homan, P., Hasler, G., Schoebi, D., Horsch, A., et al. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.563475 · Cited by 14 · see citing works
“It has been hypothesized that an imbalance between stress and reward reactivity could be a predictor for the development of psychopathology in general (39, 40) and for MDD in particular (9).”
BackgroundWarhaftig, G., Zifman, N., Sokolik, C. M., Massart, R., Gabay, O., Sapozhnikov, D. M., Vaisheva, F., Lichtenstein, Y., Confortti, N., Ahdoot, H. L., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01178-y · Cited by 16 · see citing works
Thaler, A., Gonen, T., Mirelman, A., Helmich, R. C. G., Gurevich, T., Orr‐Urtreger, A., Bloem, B. R., Giladi, N., & Hendler, T. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-9920-2 · Cited by 15 · see citing works
Self-citationFrom Animal Model to Human Brain Networking: Dynamic Causal Modeling of Motivational Systems
Gonen, T., Admon, R., Podlipsky, I., & Hendler, T. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6188-11.2012 · Cited by 16 · see citing works
“To achieve this aim, we used an interactive game that included distinct expressions of relevant motivational states and that has been previously shown to elicit increased amygdala response to punishment and NAcc response to reward (Kahn et al., 2002; Assaf et al., 2009; Admon et al., 2012).”
MethodSelf-citationHinojosa, C. A., VanElzakker, M. B., Hughes, K. C., Offringa, R., Sangermano, L., Spaulding, I. G., Staples-Bradley, L. K., Whitman, E. T., Lasko, N. B., Rauch, S. L., et al. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.10.049 · Cited by 13 · see citing works
Bennett, M. M., Davis, K. E., & Fitzgerald, J. M. (2023) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2023.05.007 · Cited by 15 · see citing works
Nahum, M., Sinvani, R.-T., Afek, A., Ben-Avraham, R., Jordan, J. T., Ben‐Shachar, M. S., Yehuda, A. B., Cohen, N., Davidov, A., & Gilboa, Y. (2023) · Scientific Reports · doi:10.1038/s41598-023-40242-1 · Cited by 14 · see citing works
Pegg, S. L., & Kujawa, A. (2023) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-023-01143-y · Cited by 14 · see citing works
“…literature, exposure to stressors is associated with altered response in regions of the brain associated with reward processing, including the striatum (Admon et al., 2013; Born et al., 2010; Kruse et al., 2018; Kumar et al., 2014; Lincoln et al., 2019; Porcelli et al., 2012; Wei et al., 2013).”
InfluentialDefining the r factor for post-trauma resilience and its neural predictors
van Rooij, S. J. H., Santos, J. L., Hinojosa, C. A., Ely, T. D., Harnett, N. G., Murty, V. P., Lebois, L. A. M., Jovanović, T., House, S. L., Bruce, S. E., et al. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00242-0 · Cited by 16 · see citing works
“Few studies in the early aftermath of trauma have investigated rewardrelated processing 52–54 , and the current study shows the importance of studying neurobiological mechanisms of reward processing in addition to threat and inhibi tion.”
Iadipaolo, A. S., Marusak, H. A., Sala‐Hamrick, K., Crespo, L. M., Thomason, M. E., & Rabinak, C. A. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.06.039 · Cited by 14 · see citing works
“Links among BAS sensitivity, stress exposure, and onset of psychopathology are established in prior prospective studies [60], suggesting that potential mediating effects of BAS sensitivity, and/or associated DMN-sgACC rsFC may emerge over time, or later in life.”
BackgroundNeurophysiological Assessment of Anhedonia in Depression and Schizophrenia
Foti, D., Novak, K. D., Hill, K. E., & Oumeziane, B. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813693-5.00013-7 · Cited by 14 · see citing works
Eckstrand, K., Forbes, E. E., Bertocci, M. A., Chase, H. W., Greenberg, T., Lockovich, J., Stiffler, R., Aslam, H. A., Graur, S., Bebko, G. M., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.11.017 · Cited by 14 · see citing works
Eckstrand, K., Silk, J. S., Nance, M., Wallace, M. L., Buckley, N., Lindenmuth, M., Flores, L. E., Alarcón, G., Quevedo, K. M., Phillips, M. L., et al. (2022) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2022.08.009 · Cited by 14 · see citing works
Suarez‐Jimenez, B., Lazarov, A., Zhu, X., Pine, D. S., Bar‐Haim, Y., & Neria, Y. (2022) · Psychological Medicine · doi:10.1017/s003329172200157x · Cited by 13 · see citing works
“This exploratory finding corresponds with approaches viewing PTSD as an imbalance of the negative (fear-related) and positive (reward-related) valence systems, with the former attaining precedence over the latter (Admon et al., 2013; Stein & Paulus, 2009).”
- Authors
- Admon, R., Lubin, G., Rosenblatt, J. D., Stern, O., Kahn, I., Assaf, M., & Hendler, T.
- Affiliations
- Tel Aviv University (IL)
- Israel Defense Forces Medical Corps (IL)
- Technion – Israel Institute of Technology (IL)
- Hartford Hospital (US)
- Venue
- Cerebral Cortex
- Publisher
- Oxford University Press (OUP)
- Published
- 2012-01-30
- Volume
- 23
- Issue
- 1
- Pages
- 28-35
- ISSN
- 1047-3211 (ISSN-L)
- 1460-2199
- OpenAlex
- W2103498835
- Cited by
- 143
- References
- 41
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 10 · 2023: 9 · 2022: 10 · 2021: 11 · 2020: 15 · 2019: 13 · 2018: 6 · 2017: 10 · 2016: 14 · 2015: 10 · 2014: 8 · 2013: 9 · 2012: 8
- FWCI
- 12.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cerebral Cortex (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- stress vulnerability, risk sensitivity, reward sensitivity, amygdala, nucleus accumbens, post-traumatic stress disorder, military service, military personnel, emotional reactivity, stress exposure
- MeSH terms
- Adolescent, Cerebral Cortex, Cognitive Dissonance, Decision Making, Disease Susceptibility, Female, Games, Experimental, Humans, Male, Reward, Risk-Taking, Stress Disorders, Post-Traumatic, Stress, Psychological
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