Neural - hormonal responses to negative affective stimuli: Impact of dysphoric mood and sex

被引:21
|
作者
Mareckova, K. [1 ,2 ,3 ]
Holsen, L. [1 ,2 ]
Admon, R. [4 ]
Whitfield-Gabrieli, S. [5 ]
Seidman, L. J. [6 ,7 ]
Buka, S. L. [8 ]
Klibanski, A. [9 ,10 ]
Goldstein, J. M. [1 ,2 ,11 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Connors Ctr Womens Hlth & Gender Biol, One Brigham Circle,3rd Flr 1620 Tremont St, Boston, MA 02120 USA
[2] Harvard Med Sch HMS, Dept Psychiat, Boston, MA USA
[3] Masaryk Univ, CEITEC, Brno, Czech Republic
[4] McLean Hosp, Dept Psychiat, HMS, Boston, MA USA
[5] MIT, Dept Brain & Cognit Sci, E25-618, Cambridge, MA 02139 USA
[6] Massachusetts Mental Hlth Ctr, Beth Israel Deaconess Med Ctr, Div Publ Psychiat, Boston, MA USA
[7] HMS, Dept Psychiat, Boston, MA USA
[8] Brown Univ, Dept Community Hlth, Providence, RI 02912 USA
[9] Massachusetts Gen Hosp, Dept Med, Neuroendocrine Unit, Boston, MA 02114 USA
[10] HMS, Dept Med, Boston, MA USA
[11] Harvard Med Sch, Dept Psychiat & Med, Boston, MA USA
关键词
Negative affect; Dysphoric mood; RDoC; FMRI; Sex differences; Cortisol response; ACUTE PSYCHOSOCIAL STRESS; PITUITARY-ADRENAL AXIS; ADULT HUMAN BRAIN; HPA-AXIS; CORTISOL RESPONSES; PREFRONTAL CORTEX; MAJOR DEPRESSION; PARAVENTRICULAR NUCLEUS; ENDOGENOUS CORTISOL; HIPPOCAMPAL VOLUME;
D O I
10.1016/j.jad.2017.06.050
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Maladaptive responses to negative affective stimuli are pervasive, including clinically ill and healthy people, and men and women respond differently at neural and hormonal levels. Inspired by the Research Domain Criteria initiative, we used a transdiagnostic approach to investigate the impact of sex and dysphoric mood on neural-hormonal responses to negative affective stimuli. Methods: Participants included 99 individuals with major depressive disorder, psychosis and healthy controls. Functional magnetic resonance imaging (fMRI) was complemented with real-time acquisition of hypothalamo-pituitary-adrenal (HPA) and -gonadal (HPG) hormones. fMRI data were analyzed in SPM8 and task-related connectivity was assessed using generalized psychophysiological interaction. Results: Across all participants, elevated cortisol response predicted lower brain activity in orbitofrontal cortex and hypothalamus-amygdala connectivity. In those with worse dysphoric mood, elevated cortisol response predicted lower activity in hypothalamus and hippocampus. In women, elevated cortisol response was associated with lower activity in medial prefrontal cortex and low hypothalamo-hippocampal connectivity. In women with high dysphoric mood, elevated cortisol response was associated with low hypothalamo-hippocampal connectivity. There were no interactions with diagnosis or medication. Limitations: There was limited power to correct for multiple comparisons across total number of ROIs and connectivity targets; cortisol responses were relatively low. Conclusions: We conclude that the pathophysiology in neural-hormonal responses to negative affective stimuli is shared across healthy and clinical populations and varies as a function of sex and dysphoric mood. Our findings may contribute to the development of hormonal adjunctive therapeutics that are sex-dependent, underscoring the importance of one's sex to precision medicine.
引用
收藏
页码:88 / 97
页数:10
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