Childhood adversity and allostatic overload of the hypothalamic–pituitary–adrenal axis: A vulnerability model for depressive disorders

2011 ◽  
Vol 23 (4) ◽  
pp. 1017-1037 ◽  
Author(s):  
Paul O. Wilkinson ◽  
Ian M. Goodyer

AbstractChildhood adversity is associated with increased risk for onset of depressive episodes. This review will present evidence that allostatic overload of the hypothalamic–pituitary–adrenal axis (HPAA) partially mediates this association. The HPAA is the physiological system that regulates levels of the stress hormone cortisol. First, data from animals and humans has shown that early environmental adversity is associated with long-term dysregulation of the HPAA. This may occur due to permanent epigenetic modification of the glucocorticoid receptor. Second, data from humans has demonstrated that HPAA dysregulation is associated with increased risk of future depression onset in healthy individuals, and pharmacological correction of HPAA dysregulation reduces depressive symptoms. HPAA dysregulation may result in corticoid-mediated abnormalities in neurogenesis in early life and/or neurotoxicity on neural systems that subserve emotion and cognition.

2016 ◽  
Vol 74 ◽  
pp. 203-211 ◽  
Author(s):  
Corinna Reichl ◽  
Anne Heyer ◽  
Romuald Brunner ◽  
Peter Parzer ◽  
Julia Madeleine Völker ◽  
...  

2011 ◽  
Vol 23 (4) ◽  
pp. 975-999 ◽  
Author(s):  
Theodore P. Beauchaine ◽  
Emily Neuhaus ◽  
Maureen Zalewski ◽  
Sheila E. Crowell ◽  
Natalia Potapova

AbstractThe term allostasis, which is defined as stability through change, has been invoked repeatedly by developmental psychopathologists to describe long-lasting and in some cases permanent functional alterations in limbic–hypothalamic–pituitary–adrenal axis responding following recurrent and/or prolonged exposure to stress. Increasingly, allostatic load models have also been invoked to describe psychological sequelae of abuse, neglect, and other forms of maltreatment. In contrast, neural adaptations to stress, including those incurred by monoamine systems implicated in (a) mood and emotion regulation, (b) behavioral approach, and (c) social affiliation and attachment, are usually not included in models of allostasis. Rather, structural and functional alterations in these systems, which are exquisitely sensitive to prolonged stress exposure, are usually explained as stress mediators, neural plasticity, and/or programming effects. Considering these mechanisms as distinct from allostasis is somewhat artificial given overlapping functions and intricate coregulation of monoamines and the limbic–hypothalamic–pituitary–adrenal axis. It also fractionates literatures that should be mutually informative. In this article, we describe structural and functional alterations in serotonergic, dopaminergic, and noradrenergic neural systems following both acute and prolonged exposure to stress. Through increases in behavioral impulsivity, trait anxiety, mood and emotion dysregulation, and asociality, alterations in monoamine functioning have profound effects on personality, attachment relationships, and the emergence of psychopathology.


PLoS ONE ◽  
2015 ◽  
Vol 10 (7) ◽  
pp. e0133898 ◽  
Author(s):  
Karlijn Becking ◽  
Annet T. Spijker ◽  
Erik Hoencamp ◽  
Brenda W. J. H. Penninx ◽  
Robert A. Schoevers ◽  
...  

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