Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability?
Background: Individuals with psychosis are characterised by increased exposure and reactivity to psychosocial stressors and abnormal hypothalamic-pituitary-adrenal (HPA) axis function [i.e., elevated cortisol levels, a blunted cortisol awakening response (CAR), and pituitary volume abnormalities]. T...
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ndltd-bl.uk-oai-ethos.bl.uk-6770332017-07-25T03:29:49ZIncreased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability?Cullen, Alexis ElizabethLaurens, Kristin Robyn ; Pariante, Carmine Maria2014Background: Individuals with psychosis are characterised by increased exposure and reactivity to psychosocial stressors and abnormal hypothalamic-pituitary-adrenal (HPA) axis function [i.e., elevated cortisol levels, a blunted cortisol awakening response (CAR), and pituitary volume abnormalities]. The extent to which these features are present among at-risk individuals, prior to illness onset, is currently unclear. Aims: To determine whether putatively at-risk children who present multiple antecedents of schizophrenia (ASz) or a family history of illness (FHx) show increased susceptibility to psychosocial stressors and HPA axis abnormalities relative to typically-developing (TD) children. An additional aim was to explore associations between these measures and neurocognitive function. Methods: ASz (n=35), FHx (n=25), and TD (n=44) children were identified at age 9-12 years using a novel community-screening procedure or as relatives of individuals with schizophrenia. Measures of psychosocial stress, salivary cortisol, pituitary volume, and neurocognitive function were obtained at age 11-14 years. Results: Relative to TD children, both ASz and FHx children reported greater exposure to psychosocial stressors and were more distressed by these exposures (d=0.55-1.02, p<0.05). Additionally, FHx children, but not ASz children, showed a blunted CAR compared to TD children (d=0.73, p=0.01), yet neither group were characterised by elevated diurnal cortisol levels or pituitary volume abnormalities. In exploratory analyses, more abnormal HPA axis function (i.e., higher diurnal cortisol levels and a more blunted CAR) was associated with greater neurocognitive deficits among FHx and ASz children, whilst experiences of psychosocial stress were associated with better neurocognitive performance.616.89King's College London (University of London)http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677033http://kclpure.kcl.ac.uk/portal/en/theses/increased-stress-susceptibility-and-hypothalamicpituitaryadrenal-axis-dysfunction(b602f1f0-1006-4491-a112-83d5156f8e13).htmlElectronic Thesis or Dissertation |
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616.89 Cullen, Alexis Elizabeth Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
description |
Background: Individuals with psychosis are characterised by increased exposure and reactivity to psychosocial stressors and abnormal hypothalamic-pituitary-adrenal (HPA) axis function [i.e., elevated cortisol levels, a blunted cortisol awakening response (CAR), and pituitary volume abnormalities]. The extent to which these features are present among at-risk individuals, prior to illness onset, is currently unclear. Aims: To determine whether putatively at-risk children who present multiple antecedents of schizophrenia (ASz) or a family history of illness (FHx) show increased susceptibility to psychosocial stressors and HPA axis abnormalities relative to typically-developing (TD) children. An additional aim was to explore associations between these measures and neurocognitive function. Methods: ASz (n=35), FHx (n=25), and TD (n=44) children were identified at age 9-12 years using a novel community-screening procedure or as relatives of individuals with schizophrenia. Measures of psychosocial stress, salivary cortisol, pituitary volume, and neurocognitive function were obtained at age 11-14 years. Results: Relative to TD children, both ASz and FHx children reported greater exposure to psychosocial stressors and were more distressed by these exposures (d=0.55-1.02, p<0.05). Additionally, FHx children, but not ASz children, showed a blunted CAR compared to TD children (d=0.73, p=0.01), yet neither group were characterised by elevated diurnal cortisol levels or pituitary volume abnormalities. In exploratory analyses, more abnormal HPA axis function (i.e., higher diurnal cortisol levels and a more blunted CAR) was associated with greater neurocognitive deficits among FHx and ASz children, whilst experiences of psychosocial stress were associated with better neurocognitive performance. |
author2 |
Laurens, Kristin Robyn ; Pariante, Carmine Maria |
author_facet |
Laurens, Kristin Robyn ; Pariante, Carmine Maria Cullen, Alexis Elizabeth |
author |
Cullen, Alexis Elizabeth |
author_sort |
Cullen, Alexis Elizabeth |
title |
Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
title_short |
Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
title_full |
Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
title_fullStr |
Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
title_full_unstemmed |
Increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
title_sort |
increased stress susceptibility and hypothalamic-pituitary-adrenal axis dysfunction : early markers of psychosis vulnerability? |
publisher |
King's College London (University of London) |
publishDate |
2014 |
url |
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677033 |
work_keys_str_mv |
AT cullenalexiselizabeth increasedstresssusceptibilityandhypothalamicpituitaryadrenalaxisdysfunctionearlymarkersofpsychosisvulnerability |
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1718505030131122176 |