Published online Feb 22, 2012. doi: 10.5498/wjp.v2.i1.13
Revised: October 24, 2011
Accepted: January 21, 2012
Published online: February 22, 2012
Anxiety disorders are among the most common of all mental disorders and their pathogenesis is a major topic in psychiatry, both for prevention and treatment. Early stressful life events and alterations of hypothalamic pituitary adrenal (HPA) axis function seem to have a significant role in the onset of anxiety. Existing data appear to support the mediating effect of the HPA axis between childhood traumata and posttraumatic stress disorder. Findings on the HPA axis activity at baseline and after stimuli in panic disordered patients are inconclusive, even if stressful life events may have a triggering function in the development of this disorder. Data on the relationship between stress, HPA axis functioning and obsessive-compulsive disorder (OCD) are scarce and discordant, but an increased activity of the HPA axis is reported in OCD patients. Moreover, normal basal cortisol levels and hyper-responsiveness of the adrenal cortex during a psychosocial stressor are observed in social phobics. Finally, abnormal HPA axis activity has also been observed in generalized anxiety disordered patients. While several hypothesis have attempted to explain these findings over time, currently the most widely accepted theory is that early stressful life events may provoke alterations of the stress response and thus of the HPA axis, that can endure during adulthood, predisposing individuals to develop psychopathology. All theories are reviewed and the authors conclude that childhood life events and HPA abnormalities may be specifically and transnosographically related to all anxiety disorders, as well as, more broadly, to all psychiatric disorders.
- Citation: Faravelli C, Lo Sauro C, Godini L, Lelli L, Benni L, Pietrini F, Lazzeretti L, Talamba GA, Fioravanti G, Ricca V. Childhood stressful events, HPA axis and anxiety disorders. World J Psychiatr 2012; 2(1): 13-25
- URL: https://www.wjgnet.com/2220-3206/full/v2/i1/13.htm
- DOI: https://dx.doi.org/10.5498/wjp.v2.i1.13
Anxiety disorders are among the most common of all mental disorders[1]. The diagnostic and statistical manual of mental disorders (DSM-IV-TR)[2] includes generalized anxiety disorder (GAD; a chronic form of anxiety characterized by excessive, uncontrollable worry), panic disorder (PD; with recurrent, unexpected paroxysms of anxiety, somatic and autonomic symptoms and fear), phobic disorders [e.g., specific phobias, agoraphobia, social phobia (SP)], posttraumatic stress disorder (PTSD; characterized by unwanted, intrusive remembrances - as daytime thoughts and night-time dreams and nightmares - and avoidance of activities and other cues associated with prior life-threatening trauma) and obsessive-compulsive disorder (OCD; with recurrent obsessions and compulsions) in this category.
Exposure to stressors (i.e., early stressful life events) and sensitivity to stress have been strongly implicated in the manifestation or exacerbation of these syndromes[3-11]. Accordingly, the available literature reports that adults with an history of adverse childhood experiences develop anxiety disorders more frequently than adults without early stress[3-5,12].
However, studies about early life stress have investigated different periods of childhood and different adverse experiences. In the present review, the authors will consider the following early stressful life events, or adverse experiences: parental neglect; physical, emotional and sexual abuse; separation or death of a parent; and living with a mentally ill parent likely to be unable to provide continuous parental care. Frequency and duration of abuse, abuse involving penetration, force or violence, and a close relationship to the perpetrator, as well as early parental loss, appear to be the most harmful factors in terms of long-lasting effects on the child[4,6,7,10]. Usually, stressful events will be considered traumatic when they involve actual or threatened death or serious injury to oneself, or another threat to one’s physical integrity, to which the subjects respond with intense fear, helplessness or horror (or in children, the response must involve disorganized or agitated behavior)[2].
Preclinical studies in animals and humans suggest that an early-life stressor (e.g., maternal separation during infancy, childhood abuse and neglect) is associated with marked long-term changes in brain circuitry regulating stress reactivity, mood and behavior (e.g., corticotropin releasing factor-containing neurons)[3].
Several clinical models suggest that early stressful life events may provoke dysfunctions in the central nervous system[13] and alterations of the stress response that can endure during adulthood[14-16]. In fact, physical and psychological stress experiences activate the hypothalamic pituitary adrenal (HPA) axis[17] through the secretion of corticotropin releasing hormone (CRH) and arginine vasopressin (AVP) by the parvocellular neurons of the paraventricular nucleus of the hypothalamus. These neuropeptides activate the synthesis and the release of adrenocorticotropin hormone (ACTH) from the anterior pituitary, which successively stimulates the adrenal cortex to synthesize glucocorticoids, i.e., cortisol in humans. Cortisol influences several physiological processes and the synthesis of neurotrophic factors, with effects on mood and behavior[18,19].
Several methods evaluate HPA axis functioning through dosage of cortisol in a 24 h urine collection, in plasma/serum, in saliva or in cerebrospinal fluid (CSF), both in a basal condition and after stimuli. The main difference between these dosages is that less than 10% of plasmatic cortisol is free and thus biologically active, whereas salivary and urinary cortisol consists completely of the free (bioactive) fraction. On the other hand, the majority of plasmatic cortisol is bound to cortisol-binding globulin or to other proteins and is biologically inactive. As plasma free cortisol is in equilibrium with salivary cortisol, the latter is preferred as it is an easily obtainable biofluid and noninvasive source for evaluating the HPA axis.
Moreover, since cortisol has a circadian rhythm, with low values at awakening, followed by peak values 30 min after awakening and a steady decline during the rest of the day, several measures across the day explore HPA axis activity and the efficacy of the physiological evening downregulation.
Several stress tests can be applied: the most widely used method is the dexamethasone (Dex) suppression test (DST), which explores HPA axis functioning by measuring the suppression of cortisol levels induced by the administration of Dex; the Dex suppression CRH stimulation test (Dex/CRH test) explores pituitary and adrenal functioning by measuring ACTH and cortisol levels after a low-DST and subsequent stimulation with CRH; the combined administration of CRH and AVP (CRH/AVP test) helps investigate the activity of the HPA axis by measuring both the response of cortisol (adrenal) and ACTH (pituitary) to a stressor; and the ACTH stimulation test explores adrenal activity by measuring cortisol levels.
The relationship between stress, HPA axis hormones and psychopathology has been demonstrated in animal and human models.
Studies on rodents have shown that early social isolation provokes behavioral abnormalities similar to human depression and anxiety disorders, while environmental enrichment displays an antidepressive and anxiolytic effect in animal models of depression and anxiety[20].
Increased plasmatic ACTH and cortisol levels have been observed during behavioral despair in neonate non-human primates when separated from the mother[21,22].
Furthermore, when CRH is injected into the cerebral nervous system of laboratory animals, it produces effects reminiscent of stress, depression, fear and anxiety through actions on specific brain regions[4,23-25].
Breier et al[14] observed 90 subjects exposed to early parental loss in childhood and found higher plasma cortisol and ACTH concentrations in subjects who had obtained a lifetime psychiatric diagnosis, compared to those who did not receive a psychiatric diagnosis.
More recently, some authors observed that children who experienced permanent or long-term separations from parents, or parental death, show a hyperactive HPA axis, with increased basal salivary cortisol concentrations[26,27] and cortisol non-suppression after the DST[28], as well as the combined Dex/CRH test[29].
Moreover, alterations of the HPA axis have been widely reported in psychiatric disorders, including anxiety disorders[30-39]. For instance, Vreeburg et al[40] showed a modest but significantly higher 1 h cortisol awakening response among anxious patients, especially in those with PD with agoraphobia and those with comorbid depression. However, if the diagnosis of current anxiety disorder was associated with higher awakening cortisol levels, remitted anxiety only showed a trend toward higher morning cortisol and any association was observed between anxious status and evening cortisol level or cortisol suppression after Dex administration[40].
However, neither the excess of stressful events during childhood nor the abnormalities of the HPA axis seem to be specific to any diagnostic group[11,41,42]. Moreover, data concerning the HPA axis in all anxiety diagnostic subgroups are scarce and few studies have examined the role of the HPA axis as a mediating factor between childhood stressful life events and anxiety disorders[3,4,11].
The present paper aims at reviewing the data on HPA axis functioning in anxiety disorders and the relationship between childhood stressful life events and these neuroendocrine alterations. Moreover, a hypothesis attempting to explain these associations will be discussed.
PTSD is a chronic psychiatric condition that may develop in subjects who have been exposed to or have witnessed an event or events that involve actual or threatened death or serious injury, or a threat to the physical integrity of oneself or others, experiencing fear, helplessness or horror[2]. This psychiatric condition is frequent in subjects with a history of adverse childhood experiences[4,12,43-45].
Data about HPA axis functioning and its relationship with early life stress in PTSD are reported in Table 1.
Author | Control group | Sample | Cortisol levels | ACTH levels | Suppression (DST) | Stress test | Correlations with childhood traumata and psychopathology |
Lemieux et al[46], 1995 | 9 non abused women; 8 abused women w/o PTSD | 11 abused women with PTSD | ↑ Basal urinary levels | - | - | - | ↑ Scores on Impact Event Scale related to cortisol levels in PTSD sample |
De Bellis et al[48], 1999 | 10 non-traumatized children; 24 healthy controls | 18 children with PTSD due to childhood maltreatment | ↑ Basal urinary levels | - | - | - | ↑ Psychopathology |
Bremner et al[66], 2003 | 18 HC | 23 patients with abuse-related PTSD | Salivary cortisol: 61% higher | - | - | Cognitive challenge | Neurohormonal response to stress in PTSD subjects is not impaired |
Waiting for test; 46% higher during test | |||||||
Luecken[52], 1998 | 31 HC | 30 students who lost one parent before age 16 | ↑ Salivary levels post task | - | - | Video clip depicting the death of a parent + speech task | Altered neurohormonal responses to stress in those who lost one parent |
Elzinga et al[53], 2003 | 12 abused women without PTSD | 12 abused women with PTSD | Salivary cortisol: 60% higher waiting for test; 122% higher during test; 69% higher during recovery | - | - | Personalized trauma scripts | Altered neurohormonal responses to stress in PTSD abused women |
Rasmusson et al[56], 2001 | 11 HC | 12 outpatients with PTSD | = Plasma basal levels; ↑ plasma and urinary post tests levels | = Basal levels; ↑ post CRF levels | - | CRF and ACTH stimulation tests | Altered neurohormonal responses to stress in PTSD subjects |
Santa Ana et al[57], 2006 | 31 HC | 58 subjects with PTSD (25 with childhood trauma) | ↓ Plasma basal and post | ↓ Post task | - | Cold Pressor Task | - |
Task, if childhood trauma | |||||||
De Bellis et al[58], 1994 | 13 HC girls | 13 sexually abused girls | = Plasma and salivary basal and post CRH | ↓ Basal and post CRH | - | CRH stimulation test | ↑ Adult psychopathology and altered hormonal responses to stress |
Stein et al[61], 1997 | 21 non abused women | 19 children and/or adolescent with sexual abuse | - | - | ↑ | Low dose DST (0.5 mg) | ↑ Adult psychopathology |
Yehuda et al[31], 2004 | 10 non traumatized subjects | 52 traumatized subjects | - | - | ↑ | Low dose DST (0.5 mg) | - |
Jovanovic et al[59], 2010 | 61 traumatized non PTSD subjects | 29 traumatized PTSD subjects | = Basal plasma levels; ↓ post Dex plasma levels | ↓ Post Dex | ↑ | Low dose DST (0.5 mg) | Abnormalities of HPA feedback and ↑ psychopathology |
Altemus et al[62], 2003 | 15 HC | 16 women with PTSD due to childhood abuse | = Basal plasma and salivary levels | - | - | - | - |
Lindley et al[47], 2004 | 17 HC | 17 subjects with PTSD (88% due to childhood trauma) | ↑ Basal salivary levels | - | = | Low dose DST (0.5 mg) | No correlations between cortisol, childhood abuse and psychopathology |
Preclinical evidence showed a long-term sensitization of the stress response after early life stress[14]. Other authors reported increased cortisol levels in women with PTSD who experienced a childhood abuse[46,47] and in prepubertal children with PTSD secondary to past childhood maltreatment experiences[48], compared to non traumatized subjects.
Recent studies have provided evidence for sustained increases in CRH activation in the CSF of PTSD patients[49-51].
According to these findings, even in anticipation of and during a stressful cognitive challenge, PTSD patients with childhood abuse showed higher mean cortisol levels compared to healthy subjects[52-54]. Moreover, after CRH and ACTH administration, PTSD patients with childhood trauma had greater ACTH and cortisol responses, as well as a later cortisol peak[55,56].
On the other hand, Santa Ana et al[57] found that adults with PTSD had a less robust ACTH response to a cold pressor task compared to controls, regardless of age of index trauma. Moreover, when trauma happened in childhood, cortisol at baseline and at all post-task measurements was lower and did not display the decrease in cortisol over the course of the 2 h monitoring period, which was observed in subjects with adult index trauma and controls.
Similarly, after a CRH stimulation test, De Bellis et al[58] and Bremner et al[54] reported that childhood abused women with PTSD exhibited a significantly smaller ACTH response and no difference in cortisol response, than the healthy control group. Moreover, an excessive suppression of cortisol in response to a low dose of Dex (0.5 mg) was reported in similar groups of patients, compared to controls[31,59-61].
In contrast, other studies found no difference between women with PTSD and healthy subjects in terms of circadian rhythm of cortisol, baseline cortisol and ACTH levels[56,62] and in cortisol levels after DST[47].
In summary, these data show high baseline CRH levels and low plasma cortisol levels in PTSD patients and seem to confirm the mediating effect of the HPA axis between childhood traumata and PTSD[14,55,63].
A possible explanation for this finding is that high cortisol levels reflect an initial sensitization to the persistent intrusive nature of the memories and the continued sense of threat experienced by these individuals[64], while the following blunted response may reflect a physiological adaptation of the HPA axis to chronic stress, with the downregulation of the pituitary CRH-receptors[65]. Thus, the hypothalamic CRH hypersecretion may be due to the early life stress[4].
According to these hypotheses, several studies have documented a reduced hippocampal volume in adult patients with PTSD related to childhood abuse[66], as if the long-term overexposure to glucocorticoids would lead to cell atrophy, loss or decreased neurogenesis[67].
Moreover, different activation of corticolimbic pathways may induce an “overcoming” negative feedback inhibition, which causes a blunted ACTH/cortisol response after a psychosocial and not chemical stressor[4].
Another hypothesis is that the higher availability of glucocorticoid receptors on pituitary cells of PTSD patients induces an enhanced negative feedback signal on cortisol production[68,69].
An insufficient pituitary and/or adrenal response to central stimulation, or a reduced sensitivity in response to low cortisol levels, may also explain HPA axis hypersuppression[69].
Furthermore, de Kloet et al[69] hypothesized that subjects with PTSD display an enhanced bioavailability of Dex or an inadequate vasopressin reaction to a low dose Dex administration.
Moreover, other factors can be involved in the altered stress regulation of PTSD patients: hormone binding proteins (e.g., CRH binding protein and corticosteroid binding globulin); the immune factors; sample differences (e.g., age, gender, inclusion and exclusion criteria, presence of a comorbidity like major depressive disorder, medication use); the diurnal rhythm and pulsatile secretion of adrenal hormones; the time passed since the traumatic event occurred; experienced stress during the assessment; the subjectivity of the perception of stressors; and alterations in the activity of the central nervous system and/or in hormone bioavailability and/or in hormone receptor function[69].
None of these hypotheses is considered completely exhaustive; thus more studies are needed in order to explain the altered functioning of the HPA axis in PTSD patients.
Findings on HPA axis abnormalities in patients suffering from PD are conflicting and inconsistent[36], but stressful life events are known to be contributing factors[6].
Several studies have investigated the relationship between anxiety, panic attacks (PAs) and the activation of the HPA axis. In fact, anxiety and panic seem to be qualitatively different: the former is an emotional state related to a potential threat, mostly activating HPA and the sympathoadrenal axes; the latter is an emotion evoked by the perception of an actual danger that causes major sympathetic activation with small effects on the HPA axis[70].
Several authors have reported no increased salivary or plasma cortisol levels during the PA[70,71] (Table 2), maybe due to a successful habituation to the repeated experiences of panic[72]. However, probably due to anticipatory anxiety, higher salivary cortisol levels have been reported at the beginning of the PA[73,74] (Table 2).
Author | Control group | Sample | Cortisol levels | ACTH levels | DST | Stress test |
Woods et al[71], 1987 | 13 HC | 18 drug-free agoraphobic patients | Plasma cortisol not increased during PA | - | - | Exposure to phobic situations |
Goldstein et al[76], 1987 | 61 HC; 38 outpatients with MDE | 24 outpatients PD | ↑ Basal plasma cortisol vs HC; = plasma cortisol vs MDE | - | = | Dex 1 mg |
Cameron et al[74],1987 | 4 HC | 8 PD patients | = In basal conditions; ↑ during spontaneous PA | - | - | - |
Kathol et al[77], 1988 | 37 HC | 65 PD subjects | ↑ Urinary cortisol | - | - | - |
Uhde et al[75], 1988 | 12 HC | 12 drug-free PD patients | = Basal cortisol | - | - | - |
Abelson et al[78], 1996 | 12 HC | 20 PD subjects | ↑ Overnight plasma cortisol; ↑ amplitude of ultradian secretory episodes | If low frequency of PA→↑ daytime ACTH levels and ↑ ACTH ultradian amplitude. If high frequency of PA→ shifted ACTH circadian cycles | - | - |
Schreiber et al[30], 1996 | 10 MDE subjects, 10 HC | 13 PD subjects wth agoraphobia | ↑ Plasma cortisol versus controls | = Levels in PD vs controls and MDE subjects | 92% non suppressors (higher than MDE subjects and controls) | 69% abnormal Dex-CRH test (more than controls, but lesser than MDE subjects) |
Bandelow et al[73], 2000 | 23 HC | 23 PD patients | ↑ Urinary and salivary cortisol | - | - | - |
Coryell et al[81], 1989 | 38 HC | 82 PD patients | - | - | 25.6% non suppressors | Dex 1 mg |
Coryell et al[80], 1991 | - | 72 PD patients | - | - | 36% non suppressors | |
Erhardt et al[33], 2006 | 30 HC | 30 PD subjects | ↑ Basal plasma levels | ↑ Basal | - | 17% hyperresponder to Dex-CRH |
Petrowski et al[82], 2010 | 34 HC | 34 PD subjects | = Basal salivary levels; abnormally absent cortisol awakening response | - | - | Absent cortisol response to Trier Social Stress Test |
Lieberman et al[79], 1983 | 22 MDE | 10 PD | ↑ Plasma cortisol | - | = | DST |
Furthermore, several findings indicated that real life PAs and selective panicogen stimuli (e.g., sodium lactate and carbon dioxide) do not activate the HPA axis, while non-selective agents (e.g., agonists of the colecholecystokinin receptor B) induce the release of stress hormones, regardless of the occurrence of the PA[70]. On the other hand, Flumazenil and benzodiazepine receptor antagonists seem not to activate the HPA axis or induce PAs[70]. Finally, other agents, like yohimbine, mCCP and Fenfluramine, increase anticipatory anxiety and the release of stress hormones, without inducing a true PA[70].
Findings on baseline HPA axis activity and its reactivity to some stressors in panic disordered patients seem to be inconclusive (Table 2). In fact, during a resting state, both normal[74,75] and elevated cortisol levels have been reported[76-78]. On the other hand, a clear escape or hypersuppression after Dex administration has not been demonstrated[76,79], but some DST abnormalities exist and predict risk of relapse and long term disability in panic disordered subjects[30,80,81].
Furthermore, Schreiber et al[30] and Erhardt et al[33] reported a hyperresponsivity of the HPA axis to Dex/CRH test in patients with PD (Table 2), unlike Petrowski et al[82] who showed a lack of cortisol responsivity to acute uncontrollable stress in PD patients (Table 2).
As far as stressful life events are concerned, only Safren et al[5] found higher rates of childhood abuse among women with PD, than among subjects with other anxiety disorders. In fact, in most of the literature, no significant differences were found in terms of early stressful life events between PD and GAD[83], SP[84] or depression[85].
In conclusion, stressful life events may have a triggering function but they are not a conditio sine qua non that supports the development of PD[6] and data concerning HPA axis functioning are discordant, as both normal and increased hormonal activity have been reported[70,73].
A large number of studies reported that the onset of OCD is often preceded by stressful events, like increased responsibility (e.g., job promotion, birth of a child), losses (e.g., death of a family member, dismissal from employment) and traumata, such as abuse or combat[86]. Moreover, it is well documented that OCD symptoms increase under stressful situations[87] and that patients with OCD suffer from daily life stress more than healthy controls[87,88].
However, data about the relationship between stress, HPA axis functioning and OCD are scarce and discordant[86], even if several studies have shown an increased activity of the HPA axis in OCD disordered patients[86,89-91] (Table 3).
Author | Control group | Sample | Cortisol levels | Other hormones levels | DST | Correlations with psychopathology |
Monteleone et al[91], 1994 | 13 HC | 13 drug-free OCD patients | ↑ Plasma cortisol cyrcadian rhythm | - | - | ↑ Severity of OCD symptoms |
Kluge et al[86], 2007 | 9 HC | 9 OCD inpatients w/o comorbid depression | ↑ Plasma levels | ↑ Plasma ACTH | - | - |
Catapano et al[89], 1990 | 20 HC | 18 OCD patients | - | - | 27.7% non-suppression | Correlated with sex (all non suppressors were males) and independently of depression |
Coryell et al[92], 1989 | 82 panic disordered patients | 20 OCD outpatients | - | - | = | - |
Altemus et al[90], 1992 | 25 HC | 12 OCD subjects | - | ↑ CSF CRH; ↑ plasma and CSF AVP | - | ↑ Psychopathology |
For instance, Kluge et al[86] demonstrated that nocturnal plasma cortisol and ACTH levels were significantly elevated in patients with OCD, compared to healthy controls. The circadian rhythm of cortisol was preserved in OCD patients, although at a higher level compared with normal controls and proportional to the severity of obsessive-compulsive symptoms[91]. Furthermore, CRH and AVP levels have been found significantly elevated in the CSF and plasma of these patients, compared to healthy controls[90] (Table 3). Catapano et al[89] observed that a subgroup of OCD patients, particularly males, may escape the DST independently from the coexistence of depressive features. On the other hand, Coryell et al[92] reported normal suppression after 1 mg Dex (Table 3).
Moreover, the role of the stress responsive neurohormone AVP in the onset and maintenance of compulsive behaviors (e.g., hand-washing, cleaning and trichotillomania) has been studied in rats. The intracerebroventricular administration of ACTH or CRH in rats prolongs the maintenance of conditioned behaviors acquired during a period of stress (i.e., induction of aversive stimuli, like shocks and loud noises), and promotes grooming, which is considered a behavioral model for OCD[86,93]. In humans, the intranasal administration of vasopressin seems to narrow the focus of attention and influence cognitive processes, similar to the focused-obsessive thoughts and compulsive rituals of obsessive-compulsive patients[90].
Finally, structural neuroimaging studies observed dysfunctioning in OCD patients’ anterior cingulated gyrus, which is known to be involved in the regulation of the HPA axis[94,95].
In conclusion, obsessive-compulsive disordered subjects show a hyperactivity of the HPA axis but the increased hormonal levels might be a consequence of stress[7] or, vice versa, they might be involved in the pathophysiology of OCD, sustaining clinical features like perseverative or grooming behaviors[86].
Several authors hypothesized that early stressful life events (including separation from parents, parents’ marital discord, sexual/physical/emotional abuse, familial violence, childhood diseases) and parental rearing styles (such as neglect and family history of psychiatric disorders, like anxiety disorders, depression and suicidality) have a role in the onset of SP and may increase the severity of social phobic symptoms[5,55,96-98].
Accordingly, sexual and/or physical abuse were most specifically associated with SP and childhood abuse seems to be an important risk factor for the development of this disorder[4,97,98].
Moreover, in line with the hypothesis that SP is a stress-related condition, HPA axis hyperactivity can represent the linkage between stressful events and the onset and development of this disorder[4,11].
Elzinga et al[99] found a significant association between a history of childhood abuse (emotional, physical or sexual abuse) and enhanced cortisol reactivity to a psychosocial stress task in patients with SP, although any difference in baseline cortisol levels has been reported between SP patients, PTSD patients and healthy controls (Table 4).
Author | Control group | Sample | Cortisol levels | CRH levels | Stress test | Correlations with childhood traumata and psychopathology |
Potts et al[100], 1991 | 15 HC | 10 SP | = Urinary | - | - | - |
Levin et al[103], 1993 | 14 HC | 36 (28 generalized SP + 8 specific SP) | = Plasma | - | Ten-minute talk | - |
Uhde et al[101], 1994 | - | 54-64 SP patients | = Plasma and urinary | - | = DST (Dex 1 mg) | - |
Martel et al[105], 1999 | 21 HC | 27 SP | = Salivary basal and task-related | - | Modified TSST | Correlated to anticipatory anxiety in both groups |
Furlan et al[104], 2001 | 17 HC | 18 SP | After speech task: ↑ 90% increase in salivary levels in 7 SP; ↓ 32% in salivary LE in 11 SP. After exercise task: = | - | Public speaking task and physical exercise task | - |
Condren et al[32], 2002 | 15 HC | 15 SP | ↑ Plasma cortisol after test; = plasma cortisol basal | = Basal and after test | Public mental arithmetic and short term memory test | - |
van West et al[106], 2008 | 25 HC | 25 SP | ↑ Salivary cortisol after test | - | Public speaking test | Correlated to trait but not state anxiety levels |
Roelofs et al[107], 2009 | 22 HC, 17 patients with PTSD | 18 SP | ↑ Salivary cortisol after test | - | Social approach-avoidance task in social stress condition (TSST) | Cortisol increase correlated to the social avoidance behavior |
Elzinga et al[99], 2010 | 16 SAD w/o CA, 16 HC, 16 PTSD with CA | 9 SAD with CA | ↑ Salivary cortisol after test; = salivary cortisol basal | - | TSST | CA is associated with ↑ cortisol reactivity to TSST |
Lanzenberger et al[102], 2010 | 18 HC | 12 subjects with SP | ↓ Plasma levels | - | - | Negative correlations with 5HT binding in brain regions and positive correlation with trait anxiety |
Moreover, several authors reported normal basal HPA axis functioning in adult social phobics[100,101] (Table 4). Mean basal morning plasma cortisol levels were significantly lower in patients with SP, than in healthy control subjects, and a significant correlation between cortisol plasma levels and trait but non state anxiety scores seems to exist[102] (Table 4).
Conflicting results are reported after a stress test (Table 4). Levin et al[103] found decreased plasma cortisol levels in response to a public speaking task, both in adult patients with SP and normal controls. Furlan et al[104] found that SP patients display a bimodal salivary cortisol response and a larger increase in salivary cortisol levels following a speech task, but any difference from normal subjects has been reported, under physical stress or basal conditions (Table 4).
Martel et al[105] observed similar salivary cortisol levels in social phobic adolescent girls and controls, in response to a modified trier social stress test (TSST), even if cortisol levels appeared to be a sensitive measure of anticipatory anxiety prior to the performance task in both groups (Table 4). On the other hand, van West et al[106] reported that prepubertal subjects with social anxiety show elevated salivary cortisol response to a psychosocial stressor (Table 4).
The hyper-responsiveness of the adrenal cortex during the psychosocial stressor and the similar basal levels of cortisol with respect to controls were also confirmed by Condren et al[32] (Table 4).
Recently, Roelofs et al[107] provided the first evidence for a direct link between increased cortisol stress-responsiveness and social avoidance behavior in SP patients (Table 4). During a social approach avoidance task in a social stress condition (provided by the TSST), social phobics showed increased cortisol responses compared to healthy participants and PTSD patients. Moreover, social stress elicited increased avoidance tendencies towards social threat stimuli in SP patients and this behavior was predicted by cortisol responses[107].
Moreover, stating that shyness, separation anxiety disorder (SAD) and behavioral inhibition (BI) have been postulated to be precursors of SP[108], high cortisol levels have been reported in shy children and adults[29,109], in children suffering from SAD[110], and in children with BI[111]. Some authors have hypothesized that the increased CRH and cortisol levels of these children can exacerbate their fearfulness and predispose them to develop SP[109].
In conclusion, a hyper-responsiveness of the adrenal cortex has been reported in social phobics, mainly during a psychosocial stressor[32,104,106,107], while findings at baseline are similar to those of controls[32,107]. However, several authors have hypothesized that HPA axis hyperactivity may link early stressful events to the development of SP[11,40,99].
Few studies have examined HPA axis activity in GAD, even if the persistent excessive anxiety and uncontrollable worry about a variety of events and situations that characterize GAD patients[2] suggest that these subjects are exposed to repeated stressful experiences, which could consequently lead to an altered cortisol secretory pattern.
The first investigations on HPA axis functioning in GAD used the DST (Table 5). Non-suppression rates of 27% were reported[112,113], suggesting a reduced negative feedback sensitivity of the HPA axis.
Author | Control group | Sample | Cortisol levels | DST | Correlations with psychopathology |
Mantella et al[114], 2008 | 42 HC | 71 GAD subjects | ↑ Morning basal and peak salivary cortisol | - | ↑ Psychopathology |
Steudte et al[118], 2011 | 15 HC | 15 GAD patients | ↓ Cortisol in the first and second 3-cm hair segments; = salivary diurnal cortisol profiles | - | - |
Schweizer et al[112], 1986 | - | 79 GAD subjects | - | 27% non-suppression | - |
Tiller et al[113], 1988 | 13 HC | 30 GAD patients | - | 27% non-suppression | Normalization of HPAA suppression after successful non drug behavioral treatment |
Tafet et al[115], 2005 | 8 non treated GAD outpatients | 17 treated GAD outpatients | = Morning plasma cortisol; ↑ evening plasma cortisol | - | ↓ Evening plasma cortisol level after cognitive treatment |
Pomara et al[116], 2005 | 90 HC | 41 GAD patients | ↑ Plasma cortisol levels | - | ↓ Plasma cortisol after acute and chronic treatment with diazepam |
Rosenbaum et al[117], 1983 | 22 HC | 22 GAD subjects | = 24 h urinary cortisol levels | - | - |
More recently, Mantella et al[114] showed that elderly individuals with GAD exhibited a 40%-50% increase in basal salivary cortisol levels, with higher peak cortisol levels and larger areas under the curve, compared to matched control subjects (Table 5). Additionally, severity of GAD, as measured by psychometric instruments, was positively correlated with cortisol levels[114]. Also Tafet et al[115] and Pomara et al[116] observed that patients with GAD presented increased levels of circulating cortisol (Table 5). Tafet et al[115] reported that cognitive therapy (CT) was effective in improving distressful clinical symptoms of GAD and in recovering psychoneuroendocrinological functions of these subjects. In fact, after a maximum of 24 sessions of CT, a significant decrease in the Hamilton Anxiety Rating Scale and a significant decrease in previously increased levels of circulating cortisol were observed[115]. Pharmacological therapy also showed its efficacy in the treatment of GAD: reductions of anxiety symptoms and plasma cortisol levels were reported after acute and chronic diazepam treatment, even if independent of GAD status and drug dosage[116].
On the other hand, other studies failed to show aberrant adrenocortical activity in GAD: similar 24 h urinary cortisol levels[117] and plasma cortisol levels[118] were observed in GAD patients and healthy controls (Table 5).
Finally, Steudte et al[118] studied cortisol secretion using hair analysis, which provides a retrospective reflection of cortisol secretion for a period up to 6 mo. Results showed significantly lower (50%-60%) cortisol levels in the first and second 3 cm hair segments of GAD patients, compared to those of controls, while no group difference in salivary diurnal cortisol profiles was observed (Table 5). An attempt to explain this finding is that, under naturalistic conditions, GAD may be associated with hypocortisolism, similar to healthy individuals living under chronic stress conditions and to patients with several bodily disorders (like chronic fatigue syndrome, fibromyalgia, other somatoform disorders, rheumatoid arthritis and asthma)[119,120].
In conclusion, different studies suggest that GAD is associated with hypercortisolism. A possible explanation of this finding is that chronic stress, along with the inadequacy to cope with it or the perceived loss of controllability, may lead to persistent HPA axis activation and the sustained increase of cortisol levels[121]. Moreover, the unremitting activation of the HPA axis is supposed to be mediated by changes in the sensitivity, or in the number, of CRH and/or glucocorticoid receptors of the hippocampus, limbic system and cortical levels (brain areas associated with anxiety disorders). Thus, it is possible that the autoregulatory feedback of GAD is not as efficient as in healthy subjects and cortisol hypersecretion is not downregulated[114].
Furthermore, GAD patients report a high rate of childhood physical or sexual abuse that can be associated with an alteration of the HPA axis and can contribute to the onset and maintenance of the disorder[5].
Data concerning the relationship between childhood stressful life events, HPA axis and anxiety disorders have been reviewed.
The vast majority of studies agreed on the hyperactivity of the HPA axis[40] and high rates of early stressful life events[3-5,12] in anxiety disorders. However, conflicting results on HPA axis functioning emerged from this review: patients with PTSD show baseline high CRH levels and low plasma cortisol levels; both normal and increased hormonal activity have been reported in PD patients[70,73]; OCD subjects show a hyperactivity of HPA axis[86,89-91]; a hyper-responsiveness of the adrenal cortex has been reported in social phobics after a psychosocial stressor[32,104,106,107], but normal levels have been observed at baseline[32,101]; and lastly, several studies suggest that GAD is associated with hypercortisolism[112-116].
Several hypotheses have been proposed in order to explain these discordant data. The first is the effect of comorbidity that might explain some of the differences in HPA axis activity among comorbid depressed patients[122].
Another explanation is based on the cognitive/emotional modulation, as some authors observed a normalization of the HPA axis of panic patients after treatment[36].
A third hypothesis develops from the habituation phenomena. In fact, individuals with high and persistent anxiety levels feel stressed regularly, showing a state of chronic adrenal stress hyper-reactivity and persistently elevated cortisol concentrations. These effects may influence HPA axis functioning, inducing a sort of counterregulative adaptation and thus downregulating HPA axis stress responsivity[8,16]. Hence, high and persistent levels of anxiety could be associated with low cortisol concentrations[123,124], reflecting resilience rather than a risk for psychopathology[8,16].
On the other hand, elevations in cortisol levels that persist across time could also tune HPA axis activity to a higher level and could result in damage of the hippocampal glucocorticoid receptors or even a loss of hippocampal neurons[66], reducing the negative feedback of CRH secretion and resulting in higher CRH and cortisol concentrations[124].
Furthermore, the link between childhood adverse experiences, HPA axis abnormalities and anxiety disorders has not been studied carefully. A well accepted hypothesis is that stressful life events, not being specific of any psychiatric disorder, can act as triggers on HPA axis dysregulation, predicting a general vulnerability to anxiety and mood disorders[4,5,11].
In line with these observations, some authors have hypothesized that the neuroendocrine alterations after an early stress can result in a biological ‘wound’ that increases the individual’s vulnerability to stressors later in life and, thus, predisposes an individual to develop mood or anxiety disorders that are known to manifest or worsen in relationship to acute or chronic life stress[3-5,7,11,96]. In fact, once the HPA axis is over-activated during the developmental processes, it remains permanently unstable, overdriven, vulnerable or dysfunctional[7,16,125], possibly due to transcriptional/epigenomic mechanisms[126,127].
However, a retrospective recall bias may influence the assessment of early events in several ways[11]. The poor reliability of the memories relevant to childhood[9,10], the “search for meaning”, by which the subjects tend to search for reasons for the present distress in their past experiences, and the attitude of the interviewer, who may or may not encourage the patient, all affect the accurate retrieval of past events[11].
In conclusion, the review of the available literature supports an alteration of the HPA axis in anxiety disordered patients but the relationship with early stressful life events is still to be elucidated. Authors conclude that childhood life events and HPA abnormalities may be aspecifically and transnosographically related, not only to all anxiety disorders, but broadly to all psychiatric disorders. Thus, studying the role of early stressful life events in the later development of anxiety disorders may help clinicians in the prevention and treatment of these disorders.
Peer reviewer: Eric Bui, MD, PhD, Laboratoire du Stress Traumatique (EA4560), Hopital Casselardit Psychiatrie, 170 avenue de Casselardit, 31059 Toulouse Cedex 9, France
S- Editor Lu YJ L- Editor Roemmele A E- Editor Zheng XM
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