The HPA axis in bipolar disorder: Systematic review and meta-analysis

被引:225
|
作者
Murri, Martino Belvederi [1 ,2 ]
Prestia, Davide [1 ]
Mondelli, Valeria [2 ]
Pariante, Carmine [2 ]
Patti, Sara [1 ]
Olivieri, Benedetta [1 ]
Arzani, Costanza [1 ]
Masotti, Mattia [1 ]
Respino, Matteo [1 ]
Antonioli, Marco [3 ]
Vassallo, Linda [1 ]
Serafini, Gianluca [1 ]
Perna, Giampaolo [4 ]
Pompili, Maurizio [5 ]
Amore, Mario [1 ]
机构
[1] Univ Genoa, Dept Neurosci Ophthalmol Genet & Infant Maternal, Sect Psychiat, I-16132 Genoa, Italy
[2] Kings Coll London, Dept Psychol Med, Inst Psychiat Psychol & Neurosci, London WC2R 2LS, England
[3] Univ Sassari, Dept Neurosci & Infant Maternal Sci, Sect Psychiat, I-07100 Sassari, Italy
[4] San Benedetto Hosp, Hermanas Hosp, Dept Clin Neurosci, Albese Con Cassano, Como, Italy
[5] Univ Roma La Sapienza, St Andrea Hosp, Suicide Prevent Ctr, Dept Neurosci Mental Hlth & Sensory Organs, Rome, Italy
关键词
Bipolar disorder; Mania; Depression; HPA Axis; Cortisol; Glucocorticoid receptor; PITUITARY-ADRENAL AXIS; CORTICOTROPIN-RELEASING HORMONE; DEXAMETHASONE-SUPPRESSION TEST; GLUCOCORTICOID-RECEPTOR GENE; CORTISOL AWAKENING RESPONSE; SALIVARY CORTISOL; MAJOR DEPRESSION; PLASMA-CORTISOL; CEREBROSPINAL-FLUID; PREFRONTAL CORTEX;
D O I
10.1016/j.psyneuen.2015.10.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To provide a quantitative and qualitative synthesis of the available evidence on the role of Hypothalamic Pituitary Adrenal (HPA) axis in the pathophysiology of Bipolar Disorder (BD). Methods: Meta-analysis and meta-regression of case-control studies examining the levels of cortisol, ACTH, CRH levels. Systematic review of stress reactivity, genetic, molecular and neuroimaging studies related to HPA axis activity in BD. Results: Forty-one studies were included in the meta-analyses. BD was associated with significantly increased levels of cortisol (basal and post-dexamethasone) and ACTH, but not of CRH. In the meta-regression, case-control differences in cortisol levels were positively associated with the manic phase (p = 0.005) and participants' age (p = 0.08), and negatively with antipsychotics use (p = 0.001). Reviewed studies suggest that BD is associated with abnormalities of stress-related molecular pathways in several brain areas. Variants of HPA axis-related genes seem not associated with a direct risk of developing BD, but with different clinical presentations. Also, studies on unaffected relatives suggest that HPA axis dysregulation is not an endophenotype of BD, but seems related to environmental risk factors, such as childhood trauma. Progressive HPA axis dysfunction is a putative mechanism that might underlie the clinical and cognitive deterioration of patients with BD. Conclusions: BD is associated with dysfunction of HPA axis activity, with important pathophysiological implications. Targeting HPA axis dysfunctions might be a novel strategy to improve the outcomes of BD. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:327 / 342
页数:16
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