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1.
Acta Psychiatr Scand ; 139(5): 464-471, 2019 05.
Article in English | MEDLINE | ID: mdl-30848483

ABSTRACT

OBJECTIVE: Associations between suicidality and lipid dysregulation are documented in mental illness, but the potential role of leptin remains unclear. We examined the association between leptin and suicidal behaviour in schizophrenia, together with the influence of other clinical and biological indices. METHOD: We recruited a sample of 270 participants with schizophrenia spectrum diagnoses. Blood samples were analysed for leptin, while symptom severity was assessed by Positive and Negative Syndrome Scale (PANSS) and Inventory of Depressive Symptomatology (IDS-C). Patients' history of suicidal behaviour was categorized into three subgroups based on IDS-C suicide subscale: No suicidal behaviour, mild/moderate suicidal behaviour and severe suicidal behaviour with/without attempts. RESULTS: Mild/moderate suicidal behaviour was present in 17.4% and severe suicidal behaviour in 34.8%. Both groups were significantly associated with female gender (OR = 6.0, P = 0.004; OR = 5.9, P = 0.001), lower leptin levels (OR = 0.4, P = 0.008; OR = 0.5, P = 0.008) and more severe depression (OR = 1.2, P < 0.001; OR = 1.1, P < 0.001) respectively. Smoking (OR = 2.6, P = 0.004), younger age of onset (OR = 0.9, P = 0.003) and less use of leptin-increasing medications (OR = 0.5, P = 0.031) were associated with severe/attempts group, while higher C-reactive protein CRP (OR = 1.3, P = 0.008) was associated with mild/moderate group. CONCLUSION: Lower leptin levels were associated with higher severity of suicidal behaviour in schizophrenia.


Subject(s)
Leptin/metabolism , Schizophrenia/blood , Suicide/psychology , Adult , Age of Onset , C-Reactive Protein/analysis , Cross-Sectional Studies , Depressive Disorder/complications , Depressive Disorder/psychology , Female , Humans , Male , Psychotropic Drugs/adverse effects , Risk Factors , Schizophrenia/complications , Schizophrenia/diagnosis , Schizophrenic Psychology , Severity of Illness Index , Smoking/epidemiology , Smoking/psychology , Suicidal Ideation , Suicide/trends
2.
Acta Psychiatr Scand ; 139(4): 348-360, 2019 04.
Article in English | MEDLINE | ID: mdl-30697685

ABSTRACT

OBJECTIVE: While CVD risk has decreased in the general population during the last decade, the situation in patients with schizophrenia (SCZ) and bipolar disorder (BD) is unknown. METHODS: We compared CVD risk factors in patients with SCZ and BD recruited from 2002-2005 (2005 sample, N = 270) with patients recruited from 2006-2017 (2017 sample, N = 1011) from the same catchment area in Norway. The 2017 sample was also compared with healthy controls (N = 922) and the general population (N range = 1285-4587, Statistics Norway) from the same area and period. RESULTS: Patients with SCZ and BD in the 2017 sample had significantly higher level of most CVD risk factors compared to healthy controls and the general population. There was no significant difference in the prevalence of CVD risk factors in SCZ between the 2005 and 2017 samples except a small increase in glucose in the 2017 sample. There were small-to-moderate reductions in hypertension, obesity, total cholesterol, low-density lipoprotein, systolic and diastolic blood pressure in the BD 2017 sample compared to the 2005 sample. CONCLUSION: Despite major advances in health promotion during the past decade, there has been no reduction in the level of CVD risk factors in patients with SCZ and modest improvement in BD.


Subject(s)
Bipolar Disorder/epidemiology , Cardiovascular Diseases/epidemiology , Schizophrenia/epidemiology , Adult , Comorbidity , Female , Humans , Male , Middle Aged , Norway/epidemiology , Risk Factors , Young Adult
3.
Psychol Med ; 47(4): 669-679, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27834153

ABSTRACT

BACKGROUND: Childhood trauma increases risk of a range of mental disorders including psychosis. Whereas the mechanisms are unclear, previous evidence has implicated atypical processing of emotions among the core cognitive models, in particular suggesting altered attentional allocation towards negative stimuli and increased negativity bias. Here, we tested the association between childhood trauma and brain activation during emotional face processing in patients diagnosed with psychosis continuum disorders. In particular, we tested if childhood trauma was associated with the differentiation in brain responses between negative and positive face stimuli. We also tested if trauma was associated with emotional ratings of negative and positive faces. METHOD: We included 101 patients with a Diagnostic and Statistical Manual of Mental Disorders (DSM) schizophrenia spectrum or bipolar spectrum diagnosis. History of childhood trauma was obtained using the Childhood Trauma Questionnaire. Brain activation was measured with functional magnetic resonance imaging during presentation of faces with negative or positive emotional expressions. After the scanner session, patients performed emotional ratings of the same faces. RESULTS: Higher levels of total childhood trauma were associated with stronger differentiation in brain responses to negative compared with positive faces in clusters comprising the right angular gyrus, supramarginal gyrus, middle temporal gyrus and the lateral occipital cortex (Cohen's d = 0.72-0.77). In patients with schizophrenia, childhood trauma was associated with reporting negative faces as more negative, and positive faces as less positive (Cohen's d > 0.8). CONCLUSIONS: Along with the observed negativity bias in the assessment of emotional valence of faces, our data suggest stronger differentiation in brain responses between negative and positive faces with higher levels of trauma.


Subject(s)
Adult Survivors of Child Adverse Events , Bipolar Disorder/physiopathology , Cerebral Cortex/physiopathology , Emotions/physiology , Facial Expression , Facial Recognition/physiology , Psychotic Disorders/physiopathology , Schizophrenia/physiopathology , Social Perception , Adult , Adult Survivors of Child Adverse Events/psychology , Bipolar Disorder/diagnostic imaging , Cerebral Cortex/diagnostic imaging , Female , Humans , Male , Psychotic Disorders/diagnostic imaging , Schizophrenia/diagnostic imaging , Young Adult
4.
Acta Psychiatr Scand ; 133(1): 44-52, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26371411

ABSTRACT

OBJECTIVE: Despite current diagnostic systems distinguishing schizophrenia (SZ) and bipolar disorder (BD) as separate diseases, emerging evidence suggests they share a number of clinical and epidemiological features, such as increased cardiovascular disease (CVD) risk. It is not well understood if poor cardiac autonomic nervous system regulation, which can be indexed non-invasively by the calculation of heart rate variability (HRV), contributes to these common CVD risk factors in both diseases. METHOD: We calculated HRV in 47 patients with SZ, 33 patients with BD and 212 healthy controls. Measures of symptom severity were also collected from the patient groups. RESULTS: Heart rate variability was significantly reduced in both these disorders in comparison with the healthy participants; however, there were no HRV differences between disorders. Importantly, these reductions were independent of the medication, age or body mass index effects. There was also preliminary evidence that patients with reduced HRV had increased overall and negative psychosis symptom severity regardless of SZ or BD diagnosis. CONCLUSION: We suggest that HRV may provide a possible biomarker of CVD risk and symptom severity in severe mental illness. Thus, our results highlight the importance of cardiometabolic screening across SZ and bipolar spectrum disorders.


Subject(s)
Bipolar Disorder/physiopathology , Cardiovascular Diseases/psychology , Heart Rate/physiology , Heart/physiopathology , Schizophrenia/physiopathology , Adult , Autonomic Nervous System/physiopathology , Cardiovascular Diseases/physiopathology , Case-Control Studies , Female , Humans , Male , Risk Factors , Severity of Illness Index
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