TY - JOUR
T1 - Distinct trajectories of cortisol response to prolonged acute stress are linked to affective responses and hippocampal gray matter volume in healthy females
AU - Admon, Roee
AU - Treadway, Michael T.
AU - Valeri, Linda
AU - Mehta, Malavika
AU - Douglas, Samuel
AU - Pizzagalli, Diego A.
N1 - Publisher Copyright:
© 2017 the authors.
PY - 2017/8/16
Y1 - 2017/8/16
N2 - The development of robust laboratory procedures for acute stress induction over the last decades has greatly advanced our understanding of stress responses in humans and their underlying neurobiological mechanisms. Nevertheless, attempts to uncover linear relationships among endocrine, neural, and affective responses to stress have generally yielded inconsistent results. Here, 79 healthy females completed a well established laboratory procedure of acute stress induction that was modified to prolong its effect. Endocrinological and subjective affect assessments revealed stress-induced increases in cortisol release and negative affect that persisted 65 and 100 min after stress onset, respectively, confirming a relatively prolonged acute stress induction. Applying latent class linear mixed modeling on individuals’ patterns of cortisol responses identified three distinct trajectories of cortisol response: the hyper-response (n = 10), moderate-response (n=21), and mild-response (n=48) groups. Notably, whereas all three groups exhibited a significant stress-induced increase in cortisol release and negative affect, the hyper-response and mild-response groups both reported more negative affect relative to the moderate-response group. Structural MRI revealed no group differences in hippocampal and amygdala volumes, yet a continuous measure of cortisol response (area under the curve) showed that high and low levels of stress-induced cortisol release were associated with less hippocampal gray matter volume compared with moderate cortisol release. Together, these results suggest that distinct trajectories of cortisol responsetoprolongedacute stressamonghealthy femalesmaynotbecapturedbyconventional linear analyses; instead, quadratic relationsmay better describe links between cortisol response to stress and affective responses, as well as hippocampal structural variability.
AB - The development of robust laboratory procedures for acute stress induction over the last decades has greatly advanced our understanding of stress responses in humans and their underlying neurobiological mechanisms. Nevertheless, attempts to uncover linear relationships among endocrine, neural, and affective responses to stress have generally yielded inconsistent results. Here, 79 healthy females completed a well established laboratory procedure of acute stress induction that was modified to prolong its effect. Endocrinological and subjective affect assessments revealed stress-induced increases in cortisol release and negative affect that persisted 65 and 100 min after stress onset, respectively, confirming a relatively prolonged acute stress induction. Applying latent class linear mixed modeling on individuals’ patterns of cortisol responses identified three distinct trajectories of cortisol response: the hyper-response (n = 10), moderate-response (n=21), and mild-response (n=48) groups. Notably, whereas all three groups exhibited a significant stress-induced increase in cortisol release and negative affect, the hyper-response and mild-response groups both reported more negative affect relative to the moderate-response group. Structural MRI revealed no group differences in hippocampal and amygdala volumes, yet a continuous measure of cortisol response (area under the curve) showed that high and low levels of stress-induced cortisol release were associated with less hippocampal gray matter volume compared with moderate cortisol release. Together, these results suggest that distinct trajectories of cortisol responsetoprolongedacute stressamonghealthy femalesmaynotbecapturedbyconventional linear analyses; instead, quadratic relationsmay better describe links between cortisol response to stress and affective responses, as well as hippocampal structural variability.
KW - Cortisol
KW - HPA
KW - Hippocampus
KW - Mood
KW - Stress
UR - http://www.scopus.com/inward/record.url?scp=85028015915&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.1175-17.2017
DO - 10.1523/JNEUROSCI.1175-17.2017
M3 - Article
C2 - 28739584
AN - SCOPUS:85028015915
SN - 0270-6474
VL - 37
SP - 7994
EP - 8002
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 33
ER -