Brief reportAutonomic and cortical reactivity in acute and chronic posttraumatic stress
Highlights
► Acute Stress Disorder (ASD) patients have increased autonomic arousal to neutral stimuli. ► ASD patients display greater P300 amplitude to neutral stimuli. ► PTSD patients do not display increased autonomic arousal to neutral stimuli. ► PTSD patients do not display increased P300 amplitudes to neutral stimuli. ► These effects are not accounted for by greater comorbid depression in the PTSD group.
Introduction
Deficits in attention are commonly reported in Posttraumatic Stress Disorder (PTSD: Vasterling and Proctor, 2011). The P300 component of the Event-related Potential (ERP) is thought to reflect the allocation of attentional resources (Polich and Kok, 1995). P3 amplitude is reduced to neutral target stimuli in PTSD (McFarlane et al., 1993, Felmingham et al., 2002), but increased to trauma-relevant or novel stimuli (Attias et al., 1996, Kimble et al., 2000, Karl et al., 2006). It has been suggested that reduced P3 amplitudes to neutral target stimuli may be related to trauma exposure rather than PTSD status (Karl et al., 2006, Kimble et al., 2010). Kimble et al. (2010) found that trauma exposure, but not PTSD symptom severity, predicted reduced P3 amplitude. However, many participants did not reach criteria for PTSD in their study. Kimble et al. (2010) noted that most ERP studies do not include trauma-exposed and non-trauma exposed controls and comorbidity is ignored.
Accordingly, research needs to examine P3 amplitude to neutral target stimuli in a PTSD group relative to non-trauma and trauma-exposed controls. It would be informative to compare patients with ASD and chronic PTSD to examine the effects of amount of exposure to ongoing trauma reminders. Finally, ERP studies need to examine the effects of comorbid disorders. The most prevalent comorbidity (up to 50%) in PTSD is major depression (Kessler et al., 1995). Although depression is associated with reduced P3 amplitude (Kemp et al., 2009), no ERP studies have examined the effect of comorbid depression on P3 amplitudes in PTSD.
This study examined the impact of PTSD status and the amount of trauma exposure on P300 amplitude by comparing participants with PTSD, ASD, trauma-exposed and non-trauma exposed controls. Secondly, to examine the effect of comorbid depression, analyses were repeated removing PTSD participants with comorbid depression. Finally, skin conductance (reflecting orienting) was recorded concurrently with P300.
Section snippets
Participants
25 participants had survived a physical assault or motor vehicle accident within the past four weeks; 12 fulfilled DSM-IV criteria for ASD and 13 did not trauma-exposed controls (TC). 17 additional patients met DSM-IV criteria for PTSD, and 17 were age and sex-matched non-trauma-exposed controls (NC). Clinical participants were recruited from the PTSD Unit, Westmead Hospital, and controls from the community. Participants were excluded if they were less than 18 or more than 60 years, had any
Participant characteristics
Table 1 presents participant characteristics. There were no significant differences in education level, trauma type or reaction time between the groups.
The ASD and TC groups were significantly younger than the PTSD and NC groups (F3,55 = 6.5, p < .01). The PTSD group showed higher levels of state anxiety than the ASD group (p < .01), TC (p < .01) and NC groups (p < .01). The TC and ASD groups had higher levels of alcohol use than the NC (p < .001). There were fewer females in the TC group and fewer
Discussion
This study reveals a differential pattern of autonomic and cortical reactivity in acute and chronic PTSD. The ASD group displayed significantly greater P3 and SCR amplitude to neutral target tones compared to the PTSD group and both control groups, whereas P3 and SCR amplitude in the PTSD group did not differ significantly from controls.
We failed to find P3 amplitude differences between PTSD and control groups, contradicting previous ERP studies (McFarlane et al., 1993, Felmingham et al., 2002
Acknowledgement
This project was funded by an NHMRC Program Grant (300304).
References (28)
- et al.
Event-related potentials in Post-traumatic Stress Disorder of combat origin
Biological Psychiatry
(1996) - et al.
Event-related potential dysfunction in posttraumatic stress disorder: the role of numbing
Psychiatry Research
(2002) - et al.
A new method for off-line removal of ocular artifact
Electroencephalography and Clinical Neurophysiology
(1983) - et al.
Meta-analytic review of event-related potential studies in posttraumatic stress disorder
Biological Psychology
(2006) - et al.
Stimulus novelty differentially affects attentional allocation in PTSD
Biological Psychiatry
(2000) - et al.
Attention to novel and target stimuli in trauma survivors
Psychiatry Research
(2010) - et al.
Decomposing skin conductance into tonic and phasic components
International Journal of Psychophysiology
(1997) - et al.
Abnormal stimulus processing in posttraumatic stress disorder
Biological Psychiatry
(1993) - et al.
Psychophysiologic assessment of aversive conditioning in Posttraumatic Stress Disorder
Biological Psychiatry
(2000) - et al.
Cognitive and biological determinants of P300: an integrative review
Biological Psychology
(1995)