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1.
Epidemiol Psychiatr Sci ; 30: e18, 2021 Feb 26.
Article in English | MEDLINE | ID: mdl-33632368

ABSTRACT

AIMS: Refugees and asylum-seekers are typically exposed to multiple potentially traumatic events (PTEs) in the context of war, persecution and displacement, which confer elevated risk for psychopathology. There are significant limitations, however, in extant approaches to measuring these experiences in refugees. The current study aimed to identify profiles of PTE exposure, and the associations between these profiles and key demographics, contextual factors (including ongoing stressors, method of travel to Australia and separation from family), mental health and social outcomes, in a large sample of refugees resettled in Australia. METHODS: Participants were 1085 from Arabic, Farsi, Tamil and English-speaking refugee backgrounds who completed an online or pen-and-paper survey in their own language. Constructs measured included PTE exposure, demographics, pre-displacement factors, ongoing stressors, post-traumatic stress disorder symptoms, depression symptoms, anger reactions, plans of suicide and social engagement. RESULTS: Latent class analysis identified four profiles of PTE exposure, including the torture and pervasive trauma class, the violence exposure class, the deprivation exposure class and the low exposure class. Compared to the low exposure class, participants in the trauma-exposed classes were more likely to be male, highly educated, from Farsi and Tamil-speaking backgrounds, have travelled to Australia by boat, experience more ongoing stressors and report both greater psychological symptoms and social engagement. CONCLUSIONS: This study found evidence for four distinct profiles of PTE exposure in a large sample of resettled refugees, and that these were associated with different demographic, psychological and social characteristics. These findings suggest that person-centred approaches represent an important potential avenue for investigation of PTE exposure in refugees, particularly with respect to identifying subgroups of refugees who may benefit from different types or levels of intervention according to their pre-migration PTE experiences.


Subject(s)
Depression/psychology , Exposure to Violence , Refugees/psychology , Stress Disorders, Post-Traumatic/psychology , Adolescent , Adult , Anger , Australia , Female , Humans , Latent Class Analysis , Mental Health
2.
Epidemiol Psychiatr Sci ; 26(4): 403-413, 2017 08.
Article in English | MEDLINE | ID: mdl-27573421

ABSTRACT

AIMS: Grief symptoms and a sense of injustice may be interrelated responses amongst persons exposed to mass conflict and both reactions may contribute to post-traumatic stress disorder (PTSD) symptoms. As yet, however, there is a dearth of data examining these relationships. Our study examined the contributions of grief and a sense of injustice to a model of PTSD symptoms that included the established determinants of trauma events, ongoing adversity and severe psychological distress. The study involved a large population sample (n = 2964, response rate: 82.4%) surveyed in post-conflict Timor-Leste. METHODS: The survey sites included an urban administrative area (suco) in Dili, the capital of Timor-Leste and a rural village located an hour's drive away. Culturally adapted measures were applied to assess conflict related traumatic events (TEs), ongoing adversity, persisting preoccupations with injustice, symptoms of grief, psychological distress (including depressive symptoms) and PTSD symptoms. RESULTS: We tested a series of structural equation models, the final comprehensive model, which included indices of grief symptoms and injustice, producing a good fit. Locating grief symptoms as the endpoint of the model produced a non-converging model. In the final model, strong associations were evident between grief and injustice (ß = 0.34, s.e. = 0.02, p < 0.01) and grief and PTSD symptoms (ß = 0.14, s.e. = 0.02, p < 0.01). The sense of injustice exerted a considerable effect on PTSD symptoms (ß = 0.13, s.e. = 0.03, p < 0.01). In addition, multiple indirect paths were evident, most involving grief and a sense of injustice, attesting to the complex inter-relationship of these factors in contributing to PTSD symptoms. CONCLUSIONS: Our findings support an expanded model of PTSD symptoms relevant to post-conflict populations, in which grief symptoms and a sense of injustice play pivotal roles. The model supports the importance of a focus on loss, grief and a sense of injustice in conducting trauma-focused psychotherapies for PTSD amongst populations exposed to mass conflict and violence. Further research is needed to identify the precise mechanisms whereby grief symptoms and the sense of injustice impact on PTSD symptoms.


Subject(s)
Grief , Social Justice/psychology , Stress Disorders, Post-Traumatic/psychology , Stress, Psychological/psychology , Survivors/psychology , Violence/psychology , Warfare , Adolescent , Adult , Aged , Anger , Bereavement , Female , Humans , Male , Middle Aged , Rural Population/statistics & numerical data , Social Justice/statistics & numerical data , Stress Disorders, Post-Traumatic/epidemiology , Stress, Psychological/epidemiology , Survivors/statistics & numerical data , Timor-Leste/epidemiology , Violence/statistics & numerical data , Young Adult
3.
Transl Psychiatry ; 6(10): e925, 2016 10 18.
Article in English | MEDLINE | ID: mdl-27754486

ABSTRACT

The FKBP5 polymorphism is a key regulator of the glucocorticoid system underpinning stress responsivity, and risk alleles can increase vulnerability for developing posttraumatic stress disorder. To delineate the specific role of FKBP5 risk alleles unencumbered by the confounds of psychopathology, this study investigated whether high-risk alleles of the FKBP5 polymorphism are characterized by distinctive neural activity during resting state. Thirty-seven healthy participants were selected on the basis of four SNPs in the FKBP5 gene region (rs3800373, rs9296158, rs1360780 and rs9470080) to determine participants who were carriers of the FKBP5 high- and low-risk alleles. Spatial maps, power spectra and connectivity in neural networks active during resting state were assessed with functional magnetic resonance imaging (fMRI). During resting-state fMRI, FKBP5 low-risk allele group displayed more power in the low frequency range (<0.1 Hz) than the high-risk allele group, who had significantly more power in higher frequency bins (>0.15 Hz). This difference was apparent only in a frontotemporoparietal network underpinning salience detection and emotion processing. This study provides initial evidence that the risk alleles of the FKBP5 polymorphism are associated with different resting-state activity in a frontotemporal-parietal network, and may point to mechanisms underpinning high-risk carriers' vulnerability to severe stress reactions.


Subject(s)
Alleles , Frontal Lobe/physiopathology , Magnetic Resonance Imaging , Nerve Net/physiopathology , Parietal Lobe/physiopathology , Polymorphism, Genetic/genetics , Stress Disorders, Post-Traumatic/genetics , Tacrolimus Binding Proteins/genetics , Temporal Lobe/physiopathology , Arousal/genetics , Arousal/physiology , Brain Mapping , Emotions/physiology , Female , Genetic Carrier Screening , Genotype , Humans , Hypothalamo-Hypophyseal System/physiopathology , Male , Pituitary-Adrenal System/physiopathology , Risk , Stress Disorders, Post-Traumatic/physiopathology , Young Adult
6.
Pharmacol Biochem Behav ; 20(2): 307-10, 1984 Feb.
Article in English | MEDLINE | ID: mdl-6144111

ABSTRACT

Four rats lever pressed for food on a two component multiple FR-VI schedule of reinforcement. In the FR component a brief electric shock coincided with the presentation of food. After level pressing stabilized in the presence of the shock, drugs were administered in two phases. In Phase 1, one of four doses of either gamma-butyrolactone or sodium pentobarbital was injected before sessions. Both drugs increased lever pressing rates during the shocked component of the schedule at doses which did not affect lever pressing rates during the unshocked component. In Phase 2, one of four doses of a mixture of the two compounds was injected. The drug mixture increased rates of punished lever-pressing to levels similar to those reached in Phase 1. These results confirm previous findings for sodium pentobarbital and indicate that gamma-butyrolactone warrants further investigation into its behavioral properties.


Subject(s)
4-Butyrolactone/pharmacology , Anti-Anxiety Agents/pharmacology , Conditioning, Operant/drug effects , Furans/pharmacology , Animals , Dose-Response Relationship, Drug , Male , Pentobarbital/pharmacology , Punishment , Rats
7.
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