Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Apr;51:30-6.
doi: 10.1016/j.jpsychires.2013.12.012. Epub 2013 Dec 28.

Plasma Oxytocin Concentrations Are Lower in Depressed vs. Healthy Control Women and Are Independent of Cortisol

Affiliations
Free PMC article

Plasma Oxytocin Concentrations Are Lower in Depressed vs. Healthy Control Women and Are Independent of Cortisol

Kaeli W Yuen et al. J Psychiatr Res. .
Free PMC article

Abstract

The neuropeptide oxytocin (OT) promotes social behavior and attenuates stress responsivity in mammals. Recent clinical evidence suggests OT concentrations may be dysregulated in major depression. This study extends previous research by testing whether: 1) OT concentrations vary systematically in depressive disorders with and without hypercortisolemia, 2) gender differences in OT concentrations are observed in depressed vs. healthy control participants, and 3) OT concentrations are predictive of clinical phenotypes. Plasma OT concentrations of psychotic major depressive (PMD; n = 14: 10 female, 4 male), non-psychotic major depressive (NPMD; n = 17: 12 female, 5 male), and non-depressed, healthy control (n = 19: 11 female, 8 male) participants were assayed at 2000, 2400, 0400, and 0800 h. Plasma cortisol concentrations were quantified at 2300 h, and clinical phenotypes were determined. As expected, PMD participants, compared to NPMD and healthy control participants, showed higher plasma cortisol concentrations. Although both depressed groups showed similar OT concentrations, a significant interaction effect between group and gender was observed. Specifically, depressed females exhibited lower mean OT concentrations than depressed males. Further, depressed vs. healthy control female participants exhibited lower mean OT concentrations, whereas depressed vs. healthy control male participants showed a trend in the opposite direction. OT concentrations were also predictive of desirability, drug dependence, and compulsivity scores as measured by the Million Clinical Multiaxial Inventory-III. All findings were independent of cortisol. These data suggest that OT signaling may provide a mechanism by which to better understand female-biased risk to develop depressive disorders and that plasma OT concentrations may be a useful biomarker of certain clinical phenotypes.

Keywords: Clinical phenotypes; Cortisol; Gender; Major depression; Plasma oxytocin; Psychotic major depression.

Conflict of interest statement

Conflict of Interest

Ms. Yuen, Dr. Garner, Dr. Carson, Dr. Keller, Dr. Lembke, Ms. Hyde, Ms. Kenna, Dr. Tennakoon, Dr. Schatzberg, and Dr. Parker report no biomedical financial interests or potential conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Mean plasma oxytocin (OT) concentrations differ by group and sex. Post-hoc tests revealed that depressed females have lower OT concentrations than healthy control females, and depressed females have lower OT concentrations than depressed males. Data show fitted means and standard errors. * indicates a significant finding after correction for multiple comparisons (p < 0.025). HC, healthy control; NPMD, non-psychotic major depression; PMD, psychotic major depression.
Fig. 2.
Fig. 2.
Mean plasma OT concentrations: positively predict MCMI Desirability scores in depressed participants (Panel A), negatively predict MCMI Drug Dependence Base Rate scores in depressed participants (Panel B), and positively predict MCMI Compulsivity Base Rate scores in PMD, but not NPMD, participants (Panel C). To correct for skew, mean plasma OT concentration is calculated as the mean of logged titers. To correct for the controlling variables in the analysis, the regression line is partialed (controlled) for other variables in the analysis, and calculated at the mean value of those variables. Similarly, data are shown as residuals from this mean regression line. NPMD, non-psychotic major depression; PMD, psychotic major depression.

Similar articles

See all similar articles

Cited by 23 articles

See all "Cited by" articles

Publication types

Feedback