Pituitary volume in individuals at elevated risk for psychosis: A systematic review and meta-analysis

被引:20
作者
Saunders, Tyler S. [1 ]
Mondelli, Valeria [2 ,3 ,4 ]
Cullen, Alexis E. [1 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, London, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychol Med, London, England
[3] South London & Maudsley NHS Fdn Trust, Mental Hlth Biomed Res Ctr, NIHR, London, England
[4] Kings Coll London, London, England
基金
英国惠康基金;
关键词
Hypothalamic-pituitary-adrenal (HPA) axis; Stress; Schizophrenia; Prodrome; Cortisol; Review; ULTRA-HIGH-RISK; MINOR PHYSICAL ANOMALIES; BIPOLAR DISORDER; YOUNG-PEOPLE; ADRENAL AXIS; SCHIZOPHRENIA; STRESS; CORTISOL; ABNORMALITIES; TRANSITION;
D O I
10.1016/j.schres.2018.12.026
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Pituitary volume (PV) abnormalities, representing one of several markers of hypothalamic-pituitary-adrenal (HPA) axis dysregulation, have been observed in psychosis, with variable patterns across illness stages. Typically, enlargements characterise first-episode patients, with reductions observed in those with chronic illness relative to healthy controls. Findings in high-risk populations have been inconsistent, highlighting the need for an updated review of the evidence. Methods: We searched PubMed, PsycINFO, and EMBASE for studies examining PV in high-risk [clinical high-risk (CHR), family history of psychosis (FHx), schizotypal personality disorder (SPD), and psychotic-experiences (PEs)] and healthy individuals. Random effects models were used to examine group differences in PV (Hedges g) with stratified analyses and meta-regression employed to investigate the effect of high-risk category, transition status, age, sex, and antipsychotic medication. Results: Ten studies, yielding 11 effect sizes, were eligible for inclusion. Overall, high-risk individuals had significantly larger PV relative to healthy controls (g = 0.16 [95% CI: 0.01 to 0.32] p = 0.04), despite showing a reduction in whole brain volume (g = -0.17, [95% CI. -0.30 to -0.03] p = 0.020). Individual sub-group analyses for CHR and FHx groups showed no significant differences relative to controls; however, larger PV increases characterised those who later transitioned to psychosis (g = 0.55, [95% CI. 0.06 to 1.04] p = 0.028). Larger effect sizes were positively associated with the proportion of high-risk individuals receiving antipsychotic medication. Conclusions: PV enlargements characterise high-risk individuals and are more pronounced among those who later develop psychosis. We provide recommendations for future studies. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 31
页数:9
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