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Author Notes:

Correspondence should be addressed to either of the following: Roee Admon, Ph.D., Department of Psychology, University of Haifa, 199 Aba Khoushy Ave., Haifa, Israel 3498838, radmon@psy.haifa.ac.il; or Diego A. Pizzagalli, Ph.D., Center for Depression, Anxiety and Stress Research, McLean Hospital/Harvard Medical School, 115 Mill Street, McLean Hospital, Belmont, MA 02478, dap@mclean.harvard.edu

Author contributions: R.A., M.T.T., and D.A.P. designed research

R.A., M.T.T., M.M., and S.D. performed research

R.A., M.T.T., L.V., and M.M. analyzed data

R.A., M.T.T., L.V., M.M., S.D., and D.A.P. wrote the paper.

We thank Dr. Nicolas Rohleder and Dr. Jutta Wolf, directors of the Laboratory for Biological Health Psychology at Brandeis University, for performing endocrinological assays.

Over the past 3 years, D.A.P. has received consulting fees from Akili Interactive Labs, BlackThorn Therapeutics, Boehringer Ingelheim, Pfizer, and Posit Science for activities unrelated to the current research.

M.T.T. has served as a paid consultant to Avanir Pharmaceuticals and the Boston Consulting Group.

The remaining authors declare no competing financial interests.

Subjects:

Research Funding:

This work was support by the National Institutes of Mental Health–National Institutes of Health (Grants R01 and R37 MH068376, MH068376-09S1 to D.A.P.).

R.A. was supported by the Israeli Council for Higher Education (Alon Scholarship).

M.T.T. was supported by the National Institutes of Health (Grant K99 MH102355).

L.V. was supported by Harvard Catalyst Biostatistics Consulting for Harvard Medical School-affiliated researchers.

Keywords:

  • HPA
  • cortisol
  • hippocampus
  • mood
  • stress
  • Acute Disease
  • Cold Temperature
  • Female
  • Gray Matter
  • Hippocampus
  • Humans
  • Hydrocortisone
  • Magnetic Resonance Imaging
  • Organ Size
  • Saliva
  • Stress, Psychological
  • Time Factors

Distinct trajectories of cortisol response to prolonged acute stress are linked to affective responses and hippocampal gray matter volume in healthy females

Tools:

Journal Title:

Journal of Neuroscience Nursing

Volume:

Volume 37, Number 33

Publisher:

, Pages 7994-8002

Type of Work:

Article | Final Publisher PDF

Abstract:

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.

Copyright information:

© 2017 the authors.

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