TY - JOUR
T1 - Cumulative Adversity sensitizes neural response to acute stress
T2 - Association with health symptoms
AU - Seo, Dongju
AU - Tsou, Kristen A.
AU - Ansell, Emily B.
AU - Potenza, Marc N.
AU - Sinha, Rajita
N1 - Funding Information:
This research was supported by grants from the NIH Roadmap for Medical Research Common Fund and the National Institutes of Drug Abuse (NIDA) and the National Institute of Alcohol Abuse and Alcoholism (NIAAA): UL1-DE019586 (RS), R01-AA13892 (RS), PL1-DA024859 (RS), RL1-AA017539 (MP), and K08-DA029641 (EA). Dr Sinha is on the Scientific Advisory Board for Embera Neurotherapeutics. Dr Potenza has consulted for and advised Boehringer Ingelheim, Lundbeck and Ironwood; has received research support from the National Institutes of Health, Veteran’s Administration, Mohegan Sun Casino, the National Center for Responsible Gaming, and Forest Laboratories and Psyadon Pharmaceuticals; has participated in surveys, mailings, or telephone consultations related to drug addiction, impulse-control disorders, or other health topics; has consulted for law offices and gambling entities on issues related to addictions or impulse-control disorders; has provided clinical care in the Connecticut Department of Mental Health and Addiction Services Problem Gambling Services Program; has performed grant reviews for the National Institutes of Health and other agencies; has guest-edited journal sections; has given academic lectures in grand rounds, CME events and other clinical or scientific venues; and has generated books or book chapters for publishers of mental health texts.
PY - 2014/2
Y1 - 2014/2
N2 - Cumulative adversity (CA) increases stress sensitivity and risk of adverse health outcomes. However, neural mechanisms underlying these associations in humans remain unclear. To understand neural responses underlying the link between CA and adverse health symptoms, the current study assessed brain activity during stress and neutral-relaxing states in 75 demographically matched, healthy individuals with high, mid, and low CA (25 in each group), and their health symptoms using the Cornell Medical Index. CA was significantly associated with greater adverse health symptoms (P=0.01) in all participants. Functional magnetic resonance imaging results indicated significant associations between CA scores and increased stress-induced activity in the lateral prefrontal cortex, insula, striatum, right amygdala, hippocampus, and temporal regions in all 75 participants (p<0.05, whole-brain corrected). In addition to these regions, the high vs low CA group comparison revealed decreased stress-induced activity in the medial orbitofrontal cortex (OFC) in the high CA group (p<0.01, whole-brain corrected). Specifically, hypoactive medial OFC and hyperactive right hippocampus responses to stress were each significantly associated with greater adverse health symptoms (p<0.01). Furthermore, an inverse correlation was found between activity in the medial OFC and right hippocampus (p=0.01). These results indicate that high CA sensitizes limbic-striatal responses to acute stress and also identifies an important role for stress-related medial OFC and hippocampus responses in the effects of CA on increasing vulnerability to adverse health consequences.
AB - Cumulative adversity (CA) increases stress sensitivity and risk of adverse health outcomes. However, neural mechanisms underlying these associations in humans remain unclear. To understand neural responses underlying the link between CA and adverse health symptoms, the current study assessed brain activity during stress and neutral-relaxing states in 75 demographically matched, healthy individuals with high, mid, and low CA (25 in each group), and their health symptoms using the Cornell Medical Index. CA was significantly associated with greater adverse health symptoms (P=0.01) in all participants. Functional magnetic resonance imaging results indicated significant associations between CA scores and increased stress-induced activity in the lateral prefrontal cortex, insula, striatum, right amygdala, hippocampus, and temporal regions in all 75 participants (p<0.05, whole-brain corrected). In addition to these regions, the high vs low CA group comparison revealed decreased stress-induced activity in the medial orbitofrontal cortex (OFC) in the high CA group (p<0.01, whole-brain corrected). Specifically, hypoactive medial OFC and hyperactive right hippocampus responses to stress were each significantly associated with greater adverse health symptoms (p<0.01). Furthermore, an inverse correlation was found between activity in the medial OFC and right hippocampus (p=0.01). These results indicate that high CA sensitizes limbic-striatal responses to acute stress and also identifies an important role for stress-related medial OFC and hippocampus responses in the effects of CA on increasing vulnerability to adverse health consequences.
KW - cumulative adversity
KW - health problems
KW - hippocampus
KW - orbitofrontal cortex
UR - http://www.scopus.com/inward/record.url?scp=84892679151&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84892679151&partnerID=8YFLogxK
U2 - 10.1038/npp.2013.250
DO - 10.1038/npp.2013.250
M3 - Article
C2 - 24051900
AN - SCOPUS:84892679151
SN - 0893-133X
VL - 39
SP - 670
EP - 680
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 3
ER -