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Olfactory identification dysfunction, aggression and impulsivity in war veterans with post-traumatic stress disorder

Published online by Cambridge University Press:  01 October 2007

J. F. Dileo
Affiliation:
Department of Psychology, University of Melbourne, Australia
W. J. Brewer*
Affiliation:
ORYGEN Research Centre, Department of Psychiatry, University of Melbourne, Australia
M. Hopwood
Affiliation:
Veterans Psychiatry Unit, Austin Health, University of Melbourne, Australia
V. Anderson
Affiliation:
Murdoch Children's Research Institute, Melbourne, Australia
M. Creamer
Affiliation:
Australian Centre for Posttraumatic Mental Health, University of Melbourne, Australia
*
*Address for correspondence: Associate Professor W. Brewer, ORYGEN Research Centre (Locked bag 10), Parkville, Victoria, 3052, Australia. (Email: w.brewer@unimelb.edu.au)

Abstract

Background

Due to neuropsychological conceptualizations of orbitoprefrontal cortex (OFC) dysfunction underpinning impulsive aggression and the incidence of such behaviour in post-traumatic stress disorder (PTSD), this study aimed to explore olfactory identification (OI) ability in war veterans with PTSD as a probe of putative OFC dysfunction; and to explore the utility of OI ability in predicting aggressive and impulsive behavior in this clinical population.

Method

Participants comprised 31 out-patient male war veterans with PTSD (mean=58.23 years, s.d.=2.56) recruited from a Melbourne Veterans Psychiatry Unit, and 31 healthy age- and gender-matched controls (mean=56.84 years, s.d.=7.24). All participants were assessed on clinical measures of PTSD, depression, anxiety, and alcohol misuse; olfactory identification; neurocognitive measures of dorsolateral prefrontal, lateral prefrontal and mesial temporal functioning; and self-report measures of aggression and impulsivity.

Results

War veterans with PTSD exhibited significant OI deficits (OIDs) compared to controls, despite uncompromised performance on cognitive measures. OIDs remained after covaring for IQ, anxiety, depression and alcohol misuse, and were significant predictors of aggression and impulsivity.

Conclusions

This research contributes to emerging evidence of orbitoprefrontal dysfunction in the pathophysiology underlying PTSD. This is the first study to report OIDs as a predictor of aggression and impulsivity in this clinical population. It prompts further exploration of the potential diagnostic utility of OIDs in the assessment of PTSD. Such measures may help delineate the clinical complexity of PTSD, and support more targeted interventions for individuals with a greater susceptibility to aggressive and impulsive behaviors.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2007

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References

Anderson, AK, Christoff, K, Stappen, I, Panitz, D, Ghahremani, DG, Glover, G, Gabrieli, JD, Sobel, N (2003). Dissociated neural representations of intensity and valence in human olfaction. Nature and Neuroscience 6, 196202.CrossRefGoogle ScholarPubMed
Babor, T, Fuente, J, Saunders, J, Grant, M (1989). The Alcohol Use Disorder Identification Test: Guidelines for Use in Primary Health Care. World Health Organisation, Division of Mental Health: Geneva.Google Scholar
Begic, D, Jokic-Begic, N (2001). Aggressive behavior in combat veterans with post-traumatic stress disorder. Military Medicine 166, 671676.CrossRefGoogle ScholarPubMed
Bennett-Levy, J (1984). Determinants of performance on the Rey-Osterrieth Complex Figure Test: an analysis, and a new technique for single-case assessment. British Journal of Clinical Psychology 23, 109119.CrossRefGoogle Scholar
Best, M, Williams, JM, Coccaro, EF (2002). Evidence for a dysfunctional prefrontal circuit in patients with an impulsive aggressive disorder. Proceedings of the National Academy of Sciences USA 99, 84488453.CrossRefGoogle ScholarPubMed
Blair, RJ (2004). The roles of orbital frontal cortex in the modulation of antisocial behavior. Brain & Cognition 55, 198208.CrossRefGoogle ScholarPubMed
Borkowoski, JG, Benton, AL, Spreen, O (1967). Verbal fluency and brain damage. Neuropsychologia 5, 135140.CrossRefGoogle Scholar
Brewer, WJ, Wood, SJ, DeLuca, C, Pantelis, C (2006). Models of olfaction for exploring neurodevelopment. In Olfaction and the Brain (ed. Brewer, W. J., Castle, D. and Pantelis, C.). Cambridge University Press: New York.CrossRefGoogle Scholar
Buss, AH, Perry, M (1992). The Aggression Questionnaire. Journal of Personality & Social Psychology 63, 452459.CrossRefGoogle ScholarPubMed
Chemtob, CM, Hamada, RS, Roitblat, HL, Muraoka, MY (1994). Anger, impulsivity, and anger control in combat-related posttraumatic stress disorder. Journal of Consulting & Clinical Psychology 62, 827832.CrossRefGoogle ScholarPubMed
Cohen, J (1988). Statistical Power Analysis for the Behavioral Sciences, 2nd edn. Lawrence Earlbaum Associates: Hillsdale, NJ.Google Scholar
Critchley, HD, Rolls, ET (1996). Olfactory neuronal responses in the primate orbitofrontal cortex: Analysis in an olfactory discrimination task. Journal of Neurophysiology 75, 16591672.CrossRefGoogle Scholar
Davidson, RJ, Putnam, KM, Larson, CL (2000). Dysfunction in the neural circuitry of emotion regulation – a possible prelude to violence. Science 289, 591594.CrossRefGoogle ScholarPubMed
de Araujo, IET, Rolls, ET, Kringelbach, ML, McGlone, F, Phillips, N (2003). Taste-olfactory convergence, and the representation of the pleasantness of flavour, in the human brain. European Journal of Neuroscience 18, 20592068.CrossRefGoogle ScholarPubMed
Doty, RL, Shaman, P, Dann, M (1984). Development of the University of Pennsylvania Smell Identification Test: a standardized microencapsulated test of olfactory function. Physiology & Behavior 32, 489502.CrossRefGoogle Scholar
Eysenck, SB, Pearson, PR, Easting, G, Allsopp, J (1985). Age norms for impulsiveness, venturesomeness and empathy in adults. Personality and Individual Differences 6, 613–610.CrossRefGoogle Scholar
Hamann, S (2003). Nosing in on the emotional brain. Nature Neuroscience 6, 106108.CrossRefGoogle Scholar
Joseph, S, Dalgleish, T, Thrasher, S, Yule, W (1997). Impulsivity and post-traumatic stress. Personality & Individual Differences 22, 279281.CrossRefGoogle Scholar
Kessler, RC, Sonnega, A, Bromet, E, Hughes, M, Nelson, CB (1995). Posttraumatic stress disorder in the National Comorbidity Survey. Archives of General Psychiatry 52, 10481060.CrossRefGoogle ScholarPubMed
Kline, NA, Rausch, JL (1985). Olfactory precipitants of flashbacks in posttraumatic stress disorder. Journal of Clinical Psychiatry 46, 383384.Google ScholarPubMed
Kotler, M, Iancu, I, Efroni, R, Amir, M (2001). Anger, impulsivity, social support, and suicide risk in patients with posttraumatic stress disorder. Journal of Nervous & Mental Disease 189, 162167.CrossRefGoogle ScholarPubMed
Luria, AR (ed.) (1969). Frontal Lobe Syndromes. Elsevier: New York.Google Scholar
Mackay-Sim, A, Doty, RL (2001). The University of Pennsylvania smell identification test: Normative adjustment for Australian subjects. Australian Journal of Oto-Laryngology 4, 174.Google Scholar
Martzke, JS, Kopala, LC, Good, KP (1997). Olfactory dysfunction in neuropsychological disorders: review and methodological considerations. Biolological Psychiatry 42, 721732.CrossRefGoogle Scholar
Nelson, HE, O'Donnell, A (1978). Dementia: the estimation of premorbid intelligence levels using the National Adult Reading Test. Cortex 14, 234244.CrossRefGoogle Scholar
O'Donnell, ML, Creamer, M, Pattison, P (2004). Posttraumatic stress disorder and depression following trauma: Understanding comorbidity. American Journal of Psychiatry 161, 13901396.CrossRefGoogle ScholarPubMed
Oozthuizen, F, Wegener, G, Harvey, BH (2005). Nitric oxide as inflammatory mediator in posttraumatic stress disorder (PTSD): evidence from an animal model. Neuropsychiatric Disease and Treatment 1, 109123.Google Scholar
Page, MC, Braver, SL, MacKinnon, DP (2003). Levine's Guide to SPSS for analysis of variance, 2nd edn. Erlbaum: Mahwah, NJ.Google Scholar
Pietrini, P, Guazzelli, M, Basso, G, Jaffe, K, Grafman, J (2000). Neural correlates of imaginal aggressive behavior assessed by positron emission tomography in healthy subjects. American Journal of Psychiatry 157, 17721781.CrossRefGoogle ScholarPubMed
Rey, A (1941). L'examen psychologique dans les cas d'encephalopathie traumatique. Archives de Psychologie 28.Google Scholar
Rolls, ET (1998). The Orbitofrontal Cortex. Oxford University Press: London.Google Scholar
Rolls, ET (2000). The orbitofrontal cortex and reward. Cerebral Cortex (Special: The Mysterious Orbitofrontal Cortex) 10, 284294.CrossRefGoogle ScholarPubMed
Rolls, ET, Kringelbach, ML, de Araujo, IET (2003). Different representations of pleasant and unpleasant odours in the human brain. European Journal of Neuroscience 18, 695703.CrossRefGoogle ScholarPubMed
Seguin, JR (2004). Neurocognitive elements of antisocial behavior: relevance of an orbitofrontal cortex account. Brain & Cognition 55, 185197.CrossRefGoogle ScholarPubMed
Stanley, B, Molcho, A, Stanley, M, Winchel, R, Gameroff, MJ, Parsons, B, Mann, JJ (2000). Association of aggressive behavior with altered serotonergic function in patients who are not suicidal [see comment]. American Journal of Psychiatry 157, 609614.CrossRefGoogle Scholar
Taylor, EM (1959). Psychological Appraisal of Children with Cerebral Deficits. Harvard University Press: Cambridge, MA.CrossRefGoogle Scholar
Turner, SM, Beidel, DC, Frueh, BC (2005). Multicomponent behavioral treatment for chronic combat-related posttraumatic stress disorder: trauma management therapy. Behavior Modification. Special: Beyond Exposure for Posttraumatic Stress Disorder Symptoms: Broad-Spectrum PTSD Treatment Strategies 29, 3969.Google ScholarPubMed
Vasterling, JJ, Brailey, K, Sutker, PB (2000). Olfactory identification in combat-related posttraumatic stress disorder. Journal of Traumatic Stress 13, 241253.CrossRefGoogle ScholarPubMed
Vasterling, JJ, Brailey, K, Tomlin, H, Rice, J, Sutker, PB (2003). Olfactory functioning in Gulf War-era veterans: relationships to war-zone duty, self-reported hazards exposures, and psychological distress. Journal of the International Neuropsychological Society 9, 407418.CrossRefGoogle ScholarPubMed
Vermetten, E, Bremner, JD (2002). Circuits and systems in stress. I. Preclinical studies. Depression & Anxiety 15, 126147.CrossRefGoogle ScholarPubMed
Vermetten, E, Bremner, JD (2003). Olfaction as a traumatic reminder in posttraumatic stress disorder: Case reports and review. Journal of Clinical Psychiatry 64, 202207.CrossRefGoogle Scholar
Weathers, FW, Litz, B, Herman, D, Huska, J, Keane, T (1993). >The PTSD Checklist (PCL): Reliability, Validity, and Diagnostic Utility. Paper presented at the Annual Convention of the International Society for Traumatic Stress Studies, San Antonio, TX, USA.The+PTSD+Checklist+(PCL):+Reliability,+Validity,+and+Diagnostic+Utility.+Paper+presented+at+the+Annual+Convention+of+the+International+Society+for+Traumatic+Stress+Studies,+San+Antonio,+TX,+USA.>Google Scholar
Wechsler, D (1987). Wechsler Memory Scale – Revised Manuel. The Psychological Corporation: San Antonio.Google Scholar
Zatorre, RJ, Jones-Gotman, M, Evans, AC, Meyer, E (1992). Functional localization and lateralization of human olfactory cortex. Nature 360, 339340.CrossRefGoogle ScholarPubMed
Zatorre, RJ, Jones-Gotman, M, Rouby, C (2000). Neural mechanisms involved in odor pleasantness and intensity judgments. Neuroreport 11, 27112716.Google Scholar
Zigmond, AS, Snaith, RP (1983). The Hospital Anxiety and Depression Scale. Acta Psychiatrica Scandinavica 67, 361370.Google Scholar