2022
DOI: 10.1016/j.bbih.2022.100516
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Examining the relationships between adverse childhood experiences (ACEs), cortisol, and inflammation among young adults

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Cited by 9 publications
(4 citation statements)
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“…ACEs is a persistent stressor that leads to dysregulation of the hypothalamic‐pituitary‐adrenal axis response (Clemens et al, 2020), which might lead to problems in the endocrine, neurological, and immune systems (Boullier & Blair, 2018). Thus, chronic inflammation and abnormal cortisol level are results of ACEs (Wong et al, 2022). Different brain areas (e.g., prefrontal cortex and hippocampus) might be impacted by ACEs' toxic stress leading to various issues such as poor executive function and concentration (Boullier & Blair, 2018).…”
Section: Discussionmentioning
confidence: 99%
“…ACEs is a persistent stressor that leads to dysregulation of the hypothalamic‐pituitary‐adrenal axis response (Clemens et al, 2020), which might lead to problems in the endocrine, neurological, and immune systems (Boullier & Blair, 2018). Thus, chronic inflammation and abnormal cortisol level are results of ACEs (Wong et al, 2022). Different brain areas (e.g., prefrontal cortex and hippocampus) might be impacted by ACEs' toxic stress leading to various issues such as poor executive function and concentration (Boullier & Blair, 2018).…”
Section: Discussionmentioning
confidence: 99%
“…24 Multiple studies indicate that exposure to trauma is associated with dysregulation of several physiological systems that have been shown to influence BP. [25][26][27][28] For instance, report of childhood trauma is associated with increased concentrations of circulating catecholamines and pro-inflammatory markers (eg, C-reactive protein, interleukin-6 [IL-6]) 18,[29][30][31][32] as well as epigenetic modifications (eg, DNA methylation [DNAm]). 33 DNAm has been implicated in the development of chronic conditions among adults, such as hypertension, CVD, and diabetes.…”
Section: Epigenetics Insightsmentioning
confidence: 99%
“…Common origins for both preeclampsia and mood disorders may be developmental and rely on conserved pathoetiologic mechanisms including stress reactivity and proinflammation [11][12][13]. ACEs, which developmentally precede pregnancy-onset disease and mood disorders, are known drivers of stress reactivity and inflammatory dysregulation and may serve as a modifiable risk factor in psycho-obstetric disease pathogenesis [14][15][16][17]. Despite this, few previous reports have evaluated the potential links between ACEs and perinatal health, leaving the early-life origins of and interactions with depression, anxiety, and cardiovascular disease risk in the perinatal period largely unexplored.…”
Section: Introductionmentioning
confidence: 99%