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1.
Psychol Med ; 49(13): 2256-2266, 2019 10.
Article in English | MEDLINE | ID: mdl-30392491

ABSTRACT

BACKGROUND: Jumping to conclusions (JTC), which is the proneness to require less information before forming beliefs or making a decision, has been related to formation and maintenance of delusions. Using data from the National Institute of Health Research Biomedical Research Centre Genetics and Psychosis (GAP) case-control study of first-episode psychosis (FEP), we set out to test whether the presence of JTC would predict poor clinical outcome at 4 years. METHODS: One-hundred and twenty-three FEP patients were assessed with the Positive and Negative Syndrome Scale (PANSS), Global Assessment of Functioning (GAF) and the probabilistic reasoning 'Beads' Task at the time of recruitment. The sample was split into two groups based on the presence of JTC bias. Follow-up data over an average of 4 years were obtained concerning clinical course and outcomes (remission, intervention of police, use of involuntary treatment - the Mental Health Act (MHA) - and inpatient days). RESULTS: FEP who presented JTC at baseline were more likely during the follow-up period to be detained under the MHA [adjusted OR 15.62, 95% confidence interval (CI) 2.92-83.54, p = 0.001], require intervention by the police (adjusted OR 14.95, 95% CI 2.68-83.34, p = 0.002) and have longer admissions (adjusted IRR = 5.03, 95% CI 1.91-13.24, p = 0.001). These associations were not accounted for by socio-demographic variables, IQ and symptom dimensions. CONCLUSIONS: JTC in FEP is associated with poorer outcome as indicated and defined by more compulsion police intervention and longer periods of admission. Our findings raise the question of whether the implementation of specific interventions to reduce JTC, such as Metacognition Training, may be a useful addition in early psychosis intervention programmes.


Subject(s)
Commitment of Mentally Ill/statistics & numerical data , Psychotic Disorders/therapy , Adolescent , Adult , Aged , Case-Control Studies , Decision Making , Delusions , Female , Humans , Male , Middle Aged , Patient Admission , Police , Psychiatric Status Rating Scales , United Kingdom , Young Adult
2.
Schizophr Res ; 195: 306-317, 2018 05.
Article in English | MEDLINE | ID: mdl-28982554

ABSTRACT

BACKGROUND: Schizophrenia has a large genetic component, and the pathways from genes to illness manifestation are beginning to be identified. The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) Consortium aims to clarify the role of genetic variation in brain abnormalities underlying schizophrenia. This article describes the GENUS Consortium sample collection. METHODS: We identified existing samples collected for schizophrenia studies consisting of patients, controls, and/or individuals at familial high-risk (FHR) for schizophrenia. Samples had single nucleotide polymorphism (SNP) array data or genomic DNA, clinical and demographic data, and neuropsychological and/or brain magnetic resonance imaging (MRI) data. Data were subjected to quality control procedures at a central site. RESULTS: Sixteen research groups contributed data from 5199 psychosis patients, 4877 controls, and 725 FHR individuals. All participants have relevant demographic data and all patients have relevant clinical data. The sex ratio is 56.5% male and 43.5% female. Significant differences exist between diagnostic groups for premorbid and current IQ (both p<1×10-10). Data from a diversity of neuropsychological tests are available for 92% of participants, and 30% have structural MRI scans (half also have diffusion-weighted MRI scans). SNP data are available for 76% of participants. The ancestry composition is 70% European, 20% East Asian, 7% African, and 3% other. CONCLUSIONS: The Consortium is investigating the genetic contribution to brain phenotypes in a schizophrenia sample collection of >10,000 participants. The breadth of data across clinical, genetic, neuropsychological, and MRI modalities provides an important opportunity for elucidating the genetic basis of neural processes underlying schizophrenia.


Subject(s)
Cognition Disorders/etiology , Genetic Predisposition to Disease/genetics , Magnetic Resonance Imaging , Polymorphism, Single Nucleotide/genetics , Schizophrenia , Adolescent , Adult , Aged , Aged, 80 and over , Child , Cognition Disorders/diagnostic imaging , Endophenotypes , Female , Genotype , Humans , Image Processing, Computer-Assisted , Male , Middle Aged , Neuropsychological Tests , Schizophrenia/complications , Schizophrenia/diagnostic imaging , Schizophrenia/genetics , Statistics, Nonparametric , Young Adult
3.
J Interpers Violence ; 31(12): 2175-95, 2016 07.
Article in English | MEDLINE | ID: mdl-25724877

ABSTRACT

The attrition of rape cases from the criminal justice system (CJS) remains high and there is a paucity of research in relation to marginalized groups. Sex workers (SWs) are vulnerable to sexual violence due to the nature of their work. They are also unlikely to report such violence to police for a range of reasons. Two stages of research sought to describe the victim, perpetrator, and offense characteristics of SW rape and to examine the attrition of these cases. All rapes and attempted rapes (N = 1,146) reported to police in a large city in the South West of England over a 21-year period were examined; 67 cases involved SWs. Data were extracted from police files in line with the variables of interest. Secondary analysis of the total number of SW rapes (n = 67) resulted in a profile of these cases. A matched pairs study revealed significant differences in victim, perpetrator, and assault characteristics between SW (n = 62) and non-sex-worker (NSW) samples (n = 62). Although no significant difference was found in terms of attrition from the CJS, SW cases were observed to secure more convictions for rape than NSW cases. The implications of the findings for practice and future research are discussed.


Subject(s)
Crime Victims/legislation & jurisprudence , Rape/legislation & jurisprudence , Sex Workers/legislation & jurisprudence , Adolescent , Adult , Female , Humans , Middle Aged , Young Adult
4.
Schizophr Res ; 165(2-3): 243-6, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25956634

ABSTRACT

BACKGROUND: Cognitive biases may contribute to delusion persistence. We tested this in a longitudinal study of first episode psychosis (FEP). METHODS: 34 FEP patients completed assessments of delusions and Jumping to Conclusions (JTC) at baseline and 12-month follow-up. RESULTS: JTC was associated with baseline delusion severity (t(32)=2.7, p=0.01). Baseline delusions persisted at follow-up for 8/20 participants (40%), who all jumped to conclusions (8/8, 100%), compared to half of those with no or changeable delusions (14/26, 54%; χ(2) (df=1)=5.7, p=0.03; Phi=0.4). CONCLUSION: Findings implicate cognitive biases in delusion persistence, and support the potential to reduce delusions through reasoning-focused interventions.


Subject(s)
Awareness , Decision Making/physiology , Delusions/etiology , Delusions/psychology , Psychotic Disorders/complications , Adolescent , Adult , Female , Follow-Up Studies , Humans , Male , Middle Aged , Psychiatric Status Rating Scales , Severity of Illness Index , Young Adult
5.
Schizophr Bull ; 41(2): 411-8, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25053654

ABSTRACT

BACKGROUND: The "jumping to conclusions" (JTC) data-gathering bias is implicated in the development and maintenance of psychosis but has only recently been studied in first episode psychosis (FEP). In this study, we set out to establish the relationship of JTC in FEP with delusions and neuropsychological functioning. METHODS: One hundred and eight FEP patients and 101 age-matched controls completed assessments of delusions, general intelligence (IQ), working memory (WM), and JTC (the probabilistic reasoning "beads" task). RESULTS: Half the FEP participants jumped to conclusions on at least 1 task, compared with 25% of controls (OR range 2.1 to 3.9; 95% CI range 1.5 to 8.0, P values ≤ .02). JTC was associated with clinical, but not nonclinical delusion severity, and with neuropsychological functioning, irrespective of clinical status. Both IQ and delusion severity, but not WM, were independently associated with JTC in the FEP group. CONCLUSIONS: JTC is present in FEP. The specific association of JTC with clinical delusions supports a state, maintaining role for the bias. The associations of JTC with neuropsychological functioning indicate a separable, trait aspect to the bias, which may confer vulnerability to psychosis. The work has potential to inform emerging interventions targeting reasoning biases in early psychosis.


Subject(s)
Delusions/physiopathology , Intelligence/physiology , Memory, Short-Term/physiology , Psychotic Disorders/physiopathology , Schizophrenia/physiopathology , Thinking/physiology , Adolescent , Adult , Aged , Delusions/etiology , Female , Humans , Male , Middle Aged , Psychotic Disorders/complications , Schizophrenia/complications , Severity of Illness Index , Young Adult
6.
Schizophr Res ; 159(1): 56-61, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25171858

ABSTRACT

BACKGROUND: The Brain-derived Neurotrophic Factor (BDNF) modulates cognitive processes and is associated with increased risk of schizophrenia. Childhood trauma (CT) is frequent in patients with psychosis and severely affects course and outcome. AIMS: We investigated the hypothesis that BDNF is associated with both CT and cognitive deficits in a sample of first-episode psychosis (FEP) cases and unaffected controls. METHOD: Participants with FEP and healthy controls were recruited between August 2008 and July 2011 from South London, UK. Childhood traumatic events were detected using the Childhood Experience of Care and Abuse Questionnaire (CECA-Q). Neuropsychological data were also collected. BDNF plasma levels were measured from fasting blood samples. RESULTS: Data were available on 87 FEP patients and 152 controls. Our results showed a significant effect of separation (F=5.5; df=1,115; p=.02), physical (F=4.7; df=1, 118; p=.03) and sexual abuse (F=5.4; df=1,117; p=.02) on BDNF levels with lower levels among those who experienced the traumatic event compared to those who did not. Physical abuse predicted lower plasma levels of BDNF (ß=-.30; p=.03) whereas sexual and/or physical abuse showed a trend (ß=-.26; p=.06) in FEP patients but not in unaffected controls. No association between BDNF plasma levels and cognitive functions was found among patients with FEP and controls. CONCLUSION: Our findings suggest the possible involvement of BDNF in the onset of first-episode psychosis in individuals exposed to early trauma and propose BDNF as a potential clinical biomarker to detect the detrimental effects of CT on human brain plasticity.


Subject(s)
Brain-Derived Neurotrophic Factor/blood , Child Abuse , Cognition , Psychotic Disorders/blood , Psychotic Disorders/psychology , Adult , Blood Chemical Analysis , Case-Control Studies , Child , Female , Humans , London , Male , Neuropsychological Tests , Surveys and Questionnaires
7.
Psychopathology ; 47(2): 93-100, 2014.
Article in English | MEDLINE | ID: mdl-24021460

ABSTRACT

BACKGROUND: The insight into psychosis can be assessed reliably by clinicians from interviews with patients. However, patients may retain implicit awareness of illness while lacking explicit awareness. SAMPLING AND METHODS: In a sample of first-episode psychosis patients, we used a test of processing of mental illness-related and other negative words as a measure of implicit awareness to see how this varied in relation to insight. An emotional-counting Stroop task tested reaction times to words of three types: psychosis-related (e.g. 'crazy'), general negative (e.g. 'cancer') and neutral (e.g. 'oyster'). Data were available from 43 patients and 23 healthy controls. Patients' insight was assessed using the Schedule for the Assessment of Insight (SAI-E). RESULTS: Patients reacted slower than controls to words across all conditions, and both patients and controls reacted slower to salient and negative words than neutral words. There was a near significant interaction between word type and group (Wilks' lambda = 0.53, p = 0.055); patients experienced greater interference from negative rather than psychosis-related words (p = 0.003), and controls experienced greater interference from salient rather than negative words (p = 0.01). Within the patient group, there was a correlation between insight and interference on salient words (r = 0.33, p = 0.05), such that those with less insight experienced less interference on psychosis-related words. CONCLUSIONS: Psychosis-related words were less threatening and less self-relevant to psychosis patients with less insight. This suggests that the lack of awareness such patients have of their illness is genuine and more likely to be mediated by lower-level information processing mechanisms than strategies such as conscious, motivated denial.


Subject(s)
Awareness , Emotions , Psychotic Disorders/psychology , Stroop Test , Adolescent , Adult , Female , Humans , Male , Middle Aged , Reaction Time
8.
Biol Psychiatry ; 72(10): 811-6, 2012 Nov 15.
Article in English | MEDLINE | ID: mdl-22831980

ABSTRACT

BACKGROUND: Cannabis use is associated with an increased risk of psychosis. One study has suggested that genetic variation in the AKT1 gene might influence this effect. METHODS: In a case-control study of 489 first-episode psychosis patients and 278 control subjects, we investigated the interaction between variation at the AKT1 rs2494732 single nucleotide polymorphism and cannabis use in increasing the risk of psychosis. RESULTS: The rs2494732 locus was not associated with an increased risk of a psychotic disorder, with lifetime cannabis use, or with frequency of use. We did, however, find that the effect of lifetime cannabis use on risk of psychosis was significantly influenced by the rs2494732 locus (likelihood ratio statistic for the interaction = 8.54; p = .014). Carriers of the C/C genotype with a history of cannabis use showed a greater than twofold increased likelihood of a psychotic disorder (odds ratio = 2.18 [95% confidence interval: 1.12, 4.31]) when compared with users who were T/T carriers. Moreover, the interaction between the rs2494732 genotype and frequency of use was also significant at the 5% level (likelihood ratio = 13.39; p = .010). Among daily users, C/C carriers demonstrated a sevenfold increase in the odds of psychosis compared with T/T carriers (odds ratio = 7.23 [95% confidence interval: 1.37, 38.12]). CONCLUSIONS: Our findings provide strong support for the initial report that genetic variation at rs2494732 of AKT1 influences the risk of developing a psychotic disorder in cannabis users.


Subject(s)
Gene-Environment Interaction , Marijuana Abuse , Proto-Oncogene Proteins c-akt/genetics , Psychotic Disorders , Adult , Case-Control Studies , Confidence Intervals , Demography , Episode of Care , Female , Genetic Predisposition to Disease , Genetic Testing , Humans , International Classification of Diseases , London , Male , Marijuana Abuse/complications , Marijuana Abuse/genetics , Odds Ratio , Polymorphism, Single Nucleotide , Psychotic Disorders/diagnosis , Psychotic Disorders/etiology , Psychotic Disorders/genetics , Risk Assessment/methods , Risk Factors , Socioeconomic Factors
9.
Schizophr Res ; 137(1-3): 104-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22341899

ABSTRACT

Estimates of pre-morbid IQ are widely used to measure the trajectory of cognitive function and decline in people with schizophrenia. This study examined the usefulness of two indices of decline to identify cognitive subtypes in first episode psychosis, and to determine the specificity of non-IQ neuropsychological impairments in this population. Neuropsychological data were collected from 118 first episode psychosis patients and compared to 118 epidemiologically matched controls. The National Adult Reading Test (NART) and the Information subtest of the WAIS-III were compared as indicators of crystallised intelligence or 'pre-morbid IQ'. Measurement of NART minus current full scale IQ (FSIQ) (where 10 points discrepancy is the decline criterion) did not reveal a large group of individuals with 'deteriorating' IQ patterns. Using the Information subtest and the same decline criteria, a 'deteriorating' patient group emerged (36%) but was matched by a larger 'deteriorating' control group (45%). The 'deteriorating' patient group performed at a low IQ level for tasks that loaded highly on performance ability but a relatively high level for tasks measuring verbal skills. Verbal memory discriminated patients from controls better than IQ. Compared to controls, patients showed large selective impairments of verbal episodic memory (effect size, d=1.4) These data suggest that in first episode populations, caution should be exercised in inferring deterioration of IQ from discrepancies between reading-based and other IQ tests. Rather, sub-groups of patients and controls do show greater verbal aptitude in comparison to performance skills. Memory is generally impaired in first episode patients regardless of IQ.


Subject(s)
Cognition Disorders/etiology , Intellectual Disability/diagnosis , Intellectual Disability/etiology , Psychotic Disorders/complications , Adolescent , Adult , Aged , Analysis of Variance , Cognition Disorders/diagnosis , Executive Function , Female , Humans , Intelligence Tests , Male , Memory , Middle Aged , Neuropsychological Tests , Psychiatric Status Rating Scales , Psychotic Disorders/diagnosis , Reading , Regression Analysis , Retrospective Studies , Verbal Learning , Young Adult
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