TY - JOUR
T1 - Perceived life stress exposure modulates reward-related medial prefrontal cortex responses to acute stress in depression
AU - Kumar, Poornima
AU - Slavich, George M.
AU - Berghorst, Lisa H.
AU - Treadway, Michael T.
AU - Brooks, Nancy H.
AU - Dutra, Sunny J.
AU - Greve, Douglas N.
AU - O'Donovan, Aoife
AU - Bleil, Maria E.
AU - Maninger, Nicole
AU - Pizzagalli, Diego A.
N1 - Funding Information:
This work was supported by NIMH R01 MH068376 and a NARSAD Independent Investigator award to DAP. PK was supported by the John and Charlene Madison Cassidy Fellowship in Translational Neuroscience through McLean Hospital, a Livingston and a NARSAD Young Investigator award. LB was supported in part by the Sackler Fellowship in Psychobiology and an NRSA Predoctoral Training Grant in Advanced Multimodal Neuroimaging. GS was partially supported by NIMH K08 MH103443. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2015 Published by Elsevier B.V.
PY - 2015/7/15
Y1 - 2015/7/15
N2 - Introduction Major depressive disorder (MDD) is often precipitated by life stress and growing evidence suggests that stress-induced alterations in reward processing may contribute to such risk. However, no human imaging studies have examined how recent life stress exposure modulates the neural systems that underlie reward processing in depressed and healthy individuals. Methods In this proof-of-concept study, 12 MDD and 10 psychiatrically healthy individuals were interviewed using the Life Events and Difficulties Schedule (LEDS) to assess their perceived levels of recent acute and chronic life stress exposure. Additionally, each participant performed a monetary incentive delay task under baseline (no-stress) and stress (social-evaluative) conditions during functional MRI. Results Across groups, medial prefrontal cortex (mPFC) activation to reward feedback was greater during acute stress versus no-stress conditions in individuals with greater perceived stressor severity. Under acute stress, depressed individuals showed a positive correlation between perceived stressor severity levels and reward-related mPFC activation (r=0.79, p=0.004), whereas no effect was found in healthy controls. Moreover, for depressed (but not healthy) individuals, the correlations between the stress (r=0.79) and no-stress (r=-0.48) conditions were significantly different. Finally, relative to controls, depressed participants showed significantly reduced mPFC gray matter, but functional findings remained robust while accounting for structural differences. Limitation Small sample size, which warrants replication. Conclusion Depressed individuals experiencing greater recent life stress recruited the mPFC more under stress when processing rewards. Our results represent an initial step toward elucidating mechanisms underlying stress sensitization and recurrence in depression.
AB - Introduction Major depressive disorder (MDD) is often precipitated by life stress and growing evidence suggests that stress-induced alterations in reward processing may contribute to such risk. However, no human imaging studies have examined how recent life stress exposure modulates the neural systems that underlie reward processing in depressed and healthy individuals. Methods In this proof-of-concept study, 12 MDD and 10 psychiatrically healthy individuals were interviewed using the Life Events and Difficulties Schedule (LEDS) to assess their perceived levels of recent acute and chronic life stress exposure. Additionally, each participant performed a monetary incentive delay task under baseline (no-stress) and stress (social-evaluative) conditions during functional MRI. Results Across groups, medial prefrontal cortex (mPFC) activation to reward feedback was greater during acute stress versus no-stress conditions in individuals with greater perceived stressor severity. Under acute stress, depressed individuals showed a positive correlation between perceived stressor severity levels and reward-related mPFC activation (r=0.79, p=0.004), whereas no effect was found in healthy controls. Moreover, for depressed (but not healthy) individuals, the correlations between the stress (r=0.79) and no-stress (r=-0.48) conditions were significantly different. Finally, relative to controls, depressed participants showed significantly reduced mPFC gray matter, but functional findings remained robust while accounting for structural differences. Limitation Small sample size, which warrants replication. Conclusion Depressed individuals experiencing greater recent life stress recruited the mPFC more under stress when processing rewards. Our results represent an initial step toward elucidating mechanisms underlying stress sensitization and recurrence in depression.
KW - Anhedonia
KW - Life events
KW - Reward processing
KW - Stress Depression
KW - fMRI
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U2 - 10.1016/j.jad.2015.03.035
DO - 10.1016/j.jad.2015.03.035
M3 - Article
C2 - 25898329
AN - SCOPUS:84927704028
SN - 0165-0327
VL - 180
SP - 104
EP - 111
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -