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Original Articles

A face a mother could love: Depression-related maternal neural responses to infant emotion faces

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Pages 228-239 | Received 22 Aug 2012, Published online: 21 Jan 2013
 

Abstract

Depressed mothers show negatively biased responses to their infants' emotional bids, perhaps due to faulty processing of infant cues. This study is the first to examine depression-related differences in mothers' neural response to their own infant's emotion faces, considering both effects of perinatal depression history and current depressive symptoms. Primiparous mothers (n = 22), half of whom had a history of major depressive episodes (with one episode occurring during pregnancy and/or postpartum), were exposed to images of their own and unfamiliar infants' joy and distress faces during functional neuroimaging. Group differences (depression vs. no-depression) and continuous effects of current depressive symptoms were tested in relation to neural response to own infant emotion faces. Compared to mothers with no psychiatric diagnoses, those with depression showed blunted responses to their own infant's distress faces in the dorsal anterior cingulate cortex. Mothers with higher levels of current symptomatology showed reduced responses to their own infant's joy faces in the orbitofrontal cortex and insula. Current symptomatology also predicted lower responses to own infant joy–distress in left-sided prefrontal and insula/striatal regions. These deficits in self-regulatory and motivational response circuits may help explain parenting difficulties in depressed mothers.

Acknowledgments

The authors thank the participants and research assistants who made this research possible. This study was supported by a National Institute of Mental Health postdoctoral fellowship (F32MH083462-02) to HL, a pilot grant from the University of Oregon Brain Biology Machine Initiative, and a grant from the National Science Foundation (0643393).

Notes

1In addition to primary tests of depression group and symptom effects, potential impacts of depression chronicity (number of episodes, age of onset) and comorbidities were probed. These tests yielded nonsignificant results but may have been underpowered (n = 11 for testing psychopathology-related effects). SES variables (i.e., household income, maternal education) were tested as controls in depression analyses; the only difference these made in results reported below was that the occipital cluster of nondepressed > depressed response to own > other infant distress faces disappeared.

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