| Literature DB >> 32666403 |
Suzanne O' Brien1, Arjun Sethi1, Maria Gudbrandsen2, Laura Lennuyeux-Comnene1, Declan G M Murphy1, Michael C Craig3,4.
Abstract
Postnatal depression (PND) has an estimated prevalence of 6.5 to 12.9%. In addition to the direct consequences for women, PND also interferes with the maternal-infant interaction, contributing to long-term cognitive and emotional impairments in exposed offspring. It is unclear how PND differs from major depressive disorder (MDD) more generally, and if PND represents a distinct subtype of depression. We explored whether women with a history of PND have specific differences in brain activation associated with sex hormone changes during the late luteal phase of the menstrual cycle, compared to parous women with either a past history of MDD outside of the postnatal period, or an absent history of MDD ('never depressed'). Thirty mothers (history of PND (n = 10), history of MDD (n = 10), and 'never depressed' (n = 10)) underwent blood-oxygen-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) acquisition during an emotional faces task. Amygdala activity was analysed using a region of interest (small volume correction) approach. There was a significant reduction in BOLD response to positive emotional faces in the right amygdala in women with a history of PND compared to women with a history of MDD. A similar but non-significant trend was found in the left amygdala in women with a history of PND compared to 'never depressed' women. Our findings support the hypothesis that women with vulnerability to PND represent a distinct subgroup of women with a differential sensitivity to changes in sex hormones. Further, albeit highly tentative, they provide a putative biomarker that could assist in detection of women at-risk to PND.Entities:
Keywords: Amygdala; Functional magnetic resonance imaging (fMRI); Hormones; Major depressive disorder (MDD); Postnatal depression (PND); Postpartum depression
Mesh:
Year: 2020 PMID: 32666403 PMCID: PMC7979595 DOI: 10.1007/s00737-020-01051-x
Source DB: PubMed Journal: Arch Womens Ment Health ISSN: 1434-1816 Impact factor: 3.633