Adverse Consequences of Glucocorticoid Medication: Psychological, Cognitive, and Behavioral Effects
This article has been corrected.
VIEW CORRECTIONPublication: American Journal of Psychiatry
Abstract
Glucocorticoids are the most commonly prescribed anti-inflammatory/immunosuppressant medications worldwide. This article highlights the risk of clinically significant and sometimes severe psychological, cognitive, and behavioral disturbances that may be associated with glucocorticoid use, as well as ways to prevent and treat these disturbances. An illustrative case vignette is presented describing a patient’s experience of cycles of manic-like behavior and depression while on high-dosage prednisone, with long-term cognitive disorganization, vulnerability to stress, and personality changes. Severe neuropsychiatric consequences (including suicide, suicide attempt, psychosis, mania, depression, panic disorder, and delirium, confusion, or disorientation) have been reported to occur in 15.7 per 100 person-years at risk for all glucocorticoid courses, and 22.2 per 100 person-years at risk for first courses. The majority of patients experience less severe but distressing and possibly persistent changes in mood, cognition, memory, or behavior during glucocorticoid treatment or withdrawal. Although prediction of such effects is difficult, risks vary with age, gender, dosage, prior psychiatric history, and several biological markers. Key mechanisms thought to underlie these risk factors are briefly described. Recommendations are given for identifying individual risk factors and for monitoring and managing adverse neuropsychiatric effects of glucocorticoids.
Glucocorticoids are a commonly prescribed class of medication used to suppress the immune system and decrease inflammation. Since their introduction in the 1950s, they have come into use as an effective treatment for a wide range of medical conditions, including back pain, allergies, rheumatic diseases, gastrointestinal disorders, ophthalmic conditions, dermatological conditions, asthma, chronic obstructive pulmonary disease, systemic lupus erythematosus, and cancer, as well as to prevent transplant rejection. In the United States alone, 44.3 million prescriptions for oral glucocorticoids are written annually (1).
Use of Glucocorticoids and Prevalence of Severe Neuropsychiatric Events in Adults
In the United Kingdom, the Health Improvement Network (THIN) database contains electronic medical records from over 400 general practices. In this large patient population, Fardet et al. (2) found that 8.5% of patients age 18 or older who were in the system from 1989 through 2008 received any oral glucocorticoid prescription, including 2.3% who received long-term glucocorticoid treatment (lasting ≥3 months). Between 1989 and 2008, the prevalence of long-term oral glucocorticoid prescriptions at any given time rose 34%, from 0.59% to 0.79%.
Recent reviews of neuropsychiatric effects of glucocorticoids in clinical populations have been based largely on individual case or case-series reports (3, 4). In a case-series study of 80 consecutive patients completing their first lifetime glucocorticoid therapy (at a mean of 42 mg/day of prednisone for 3 months), 52.5% of patients developed one or more mood-related conditions (5). These included irritability (25.0%), euphoric hyperactivity (12.5%), anxiety or depression (11.3%), or a manic episode (3.8%). A major psychiatric disorder occurred soon after initiation of glucocorticoid therapy in six patients, five of whom required hospitalization. Fardet et al. (6) used the THIN database to analyze the incidence of five serious neuropsychiatric outcomes (depression, mania, panic disorder, suicide or suicide attempt, and delirium, confusion, or disorientation) during the first 3 months of a course of oral glucocorticoid treatment in 261,272 patients compared with an age- and gender-matched group with the same underlying medical condition but no glucocorticoid therapy. The overall incidence of these five outcomes was 15.7 per 100 person-years of glucocorticoid exposure for all glucocorticoid courses, with an incidence of 22.2 per 100 person-years at risk for first courses, 14.0 for second courses, and 11.7 for third or later courses. Table 1 presents the hazard ratio for onset of specific neuropsychiatric disorders for patients taking a first course of glucocorticoid compared with the matched unexposed population. Glucocorticoid treatment was associated with a sevenfold higher risk of suicide or serious suicide attempt and with markedly higher risks of the other severe neuropsychiatric conditions examined.
| Neuropsychiatric Outcome | Adjusted Hazard Ratio | 95% CI |
|---|---|---|
| Suicide or suicide attempt | 6.89 | 4.52, 10.50 |
| Delirium, confusion, or disorientation | 5.14 | 4.54, 5.82 |
| Mania (nonpsychotic) | 4.35 | 3.67, 5.16 |
| Depression (nonpsychotic) | 1.83 | 1.72, 1.94 |
| Panic disorder | 1.45 | 1.15, 1.85 |
| >5 neuropsychiatric outcomes | 2.26 | 2.15, 2.37 |
a
Data From Fardet et al. (6), analysis of records for adult patients in the U.K. Health Improvement Network (THIN) medical database for the period 1989–2008. The overall estimates of incidence rates of five severe neuropsychiatric outcomes of oral glucocorticoid therapy are low because the authors did not analyze psychotic bipolar disorder or depression, generalized anxiety disorder, or other severe neuropsychiatric outcomes.
Effects of acute glucocorticoid treatment on mood have also been reported in smaller prospective studies of changes within patients (7, 8) or healthy volunteers (9), while effects of long-term glucocorticoid treatment on mood have emerged from studies of changes within patients (10) and between treated and untreated patients with comparable illness severity (11). Numerous case studies have focused on the effects of acute glucocorticoid treatment on cognition, including difficulty with concentration, declarative memory, working memory, abstraction, and analysis (12, 13). Although generally thought to remit fully and quickly after glucocorticoid discontinuation (14), severe cognitive disturbances have occasionally been reported to persist for an extended period afterward (15). Cognitive impairments in patients have also been found in prospective studies of change associated with acute glucocorticoid treatment in children (16) and adults (7) and in longer-term treatment in adults (10), as well as studies of acutely (17) and chronically (18–20) treated patients compared with untreated patients with similar underlying illness severity. Cognitive effects of acute glucocorticoid treatment have been studied in medically and psychiatrically healthy adults (21), including in small double-blind placebo-controlled studies (22–27).
Neuropsychiatric effects during glucocorticoid discontinuation have also been reported from case studies (28). Again using THIN data, Fardet et al. (29) analyzed the incidence of five severe neuropsychiatric outcomes among 21,995 adult patients during withdrawal from 1 to 3 years of oral glucocorticoid therapy, counting only new episodes present during but not prior to withdrawal. Incidence rates per 100 person-years at risk during the withdrawal period were 11.1 (95% CI=10.0, 12.3) for depression; 3.9 (95% CI=3.3, 4.6) for delirium, confusion, or disorientation; 0.4 (95% CI=0.2, 0.7) for mania; 0.4 (95% CI=0.3, 0.7) for panic disorders; and 0.03 (95% CI=0.01, 0.20) for suicide or serious suicide attempt.
Risk Factors for Severe Neuropsychiatric Outcomes of Glucocorticoid Therapy
Fardet et al. (6) found that women were more likely than men to develop depression during initiation of oral glucocorticoid treatment, while men were more likely to develop mania or delirium, confusion, or disorientation. The risk of depression, mania, and delirium, confusion, or disorientation increased with age. Patients ages 18 to 50 had the highest risk of suicidal behavior, and those from 18 to 30 had the highest risk of panic disorder. Risk for depression, mania, panic disorder, or suicide attempt during glucocorticoid treatment increased for patients with past histories of these conditions, contrary to findings from some earlier studies (30). Experiencing a specific psychiatric disorder during glucocorticoid therapy increased the risk of recurrence of that disorder during subsequent glucocorticoid exposure. The risk for each of these disorders increased with the magnitude of the initial daily dose (in prednisone equivalents). This is consistent with an early case-series study of 676 patients showing an incidence of acute psychiatric reactions of 1.3% for patients receiving a daily equivalent of <40 mg of prednisone (low dosage), 4.6% for those receiving 41–80 mg/day (high dosage), and 18.4% in those receiving >80 mg/day (very high dosage) (31). In a large U.S. managed care population, the incidence of mood-related problems with long-term glucocorticoid use was also found to vary with dosage (32). Risk varies with timing. Early during a course of glucocorticoid treatment, especially a first course, patients often experience an idiosyncratic and unpredictable set of labile and manic or hypomanic symptoms unrelated to the underlying illness, whereas depressive symptoms are more common during long-term glucocorticoid treatment and are sometimes severe even at relatively low dosages (30, 33). Other risk factors are not well established at this time.
Risk factors identified for five severe psychiatric outcomes during withdrawal from long-term glucocorticoid therapy in an analysis of the THIN database (29) included an elevated risk of delirium, confusion, or disorientation for patients age 80 or older. A past history of depression or of delirium, confusion, or disorientation significantly increased the risk of that condition during withdrawal from long-term glucocorticoid therapy. Compared with short-acting glucocorticoids (e.g., prednisone, prednisolone, methylprednisolone, deflazacort), long-acting glucocorticoids (e.g., dexamethasone, betamethasone, triamcinolone) significantly increased the risk for withdrawal-induced depression (hazard ratio=1.92; 95% CI=1.07, 3.46; p=0.03) and delirium, confusion, or disorientation (hazard ratio=4.96; 95% CI=2.60, 9.49; p<0.001).
Mechanisms of Neuropsychiatric Effects
The main endogenous glucocorticoid, cortisol, plays a vital role in regulating glucose metabolism, inflammation, immune activity, and a wide range of homeostatic functions linked to the stress response. It also has important effects on emotional arousal, memory, and cognition, as well as on essential aspects of fetal development and aging. Cortisol is the end product of the hypothalamic-pituitary-adrenal (HPA) axis: Stress causes hypothalamic secretion of corticotropin-releasing factor, which stimulates the release of corticotropin from the anterior pituitary and the subsequent release of cortisol (hydrocortisone) from the adrenal glands. Within cells, cortisol facilitates or inhibits the expression of genes, with a U-shaped dose relationship (34, 35), and also has rapid nongenomic effects, which in turn provide feedback to the hypothalamus (36–40). These actions are mediated by two distinct receptors, mineralocorticoid receptors (MRs) and glucocorticoid receptors (GRs). MRs are important for appraisal processes and the onset of the stress reaction, while GRs terminate the stress response and promote recovery, memory, and adaptation. A balance between GRs and MRs in the brain and body is crucial for homeostasis and health. Synthetic glucocorticoids used in clinical treatment preferentially activate pituitary GRs while causing profound suppression of adrenal cortisol secretion, depleting the body and brain of endogenous cortisol (12, 41, 42). Hence, synthetic glucocorticoids can still activate glucocorticoids in the brain while depleting cortisol from MRs. Extreme imbalance between GRs and MRs caused by exogenous glucocorticoids may underlie cognitive impairment, disturbed emotions, and other central dysregulation experienced by many individuals during glucocorticoid therapy (43).
At prolonged high dosages, glucocorticoids impair brain function in several ways. In animal models, glucocorticoids have been shown to decrease branching of dendrites and sprouting of axons in some brain regions, impairing recovery from various forms of neuronal damage (44–46). In addition, glucocorticoids decrease glucose availability in the hippocampus, decrease neurotrophic factors in the hippocampus and neocortex, significantly diminish postnatal neurogenesis (47–52), and attenuate the synaptic strengthening that is essential for memory formation (38).
Impact on Mood
Although widely studied, the exact nature of the relationship of cortisol to depression remains unclear (12). High levels of cortisol and glucocorticoid resistance at the level of the pituitary and brain GRs are commonly observed. High cortisol levels inhibit brain-derived neurotrophic factor (BDNF), which is important for maintaining neural architecture in key brain regions such as the hippocampus and prefrontal cortex. Low BDNF levels in these areas may contribute to the development of depression and anxiety (53).
Impact on Memory, Cognition, and Behavior
Glucocorticoid effects on concentration, recall, abstraction, and analysis (sometimes referred to as “steroid dementia” when extreme and protracted) may be due partly to dysfunction in neural circuits in the hippocampus and the prefrontal cortex (12, 54), both of which contain high concentrations of MRs and GRs (44). Working memory is dependent on the prefrontal cortex and is involved in temporary storage of information necessary to carry out cognitive tasks like learning and reasoning (55, 56). Declarative memory, which is involved in explicit recall of verbal information, facts, and events, is dependent on the hippocampus (57, 58). Deficits in these functions can be attributed to the effect of prolonged glucocorticoid exposure on GRs or MRs in the hippocampus, reduction of hippocampal volume (59), or elevated glutamate accumulation in that area (60). Declarative memory impairment has also been associated with reduced blood flow in the medial temporal lobe during glucocorticoid therapy (21).
In healthy subjects, acute glucocorticoid administration is associated with functional changes in several brain regions: decreased activity in the left hippocampus (61), reduced hippocampal glucose metabolism (48), and reduced cerebral blood flow in the posterior medial temporal lobe (21). In patients with asthma or arthritis, long-term glucocorticoid exposure is associated with smaller hippocampal volume and lower levels of temporal lobe N-acetylaspartate (a marker of neuronal viability) compared with patients with the same conditions but with minimal lifetime glucocorticoid exposure (19). Atrophy of the right amygdala, which is important for regulation of mood and anxiety, was correlated with duration of prednisone treatment in this sample (62).
Recommendations for Glucocorticoid Prescribers and Patients
Although our focus here is on their adverse neuropsychiatric effects, glucocorticoids have revolutionized the treatment of many medical conditions, and they are sometimes the only effective treatment available for severe and life-threatening illnesses. It should be noted, too, that many patients experience none of the side effects described here. That said, glucocorticoids in any form—oral, topical, inhaled, or parenteral—have the potential to disrupt HPA axis function and should be prescribed only if there is no effective non-glucocorticoid treatment for the medical condition (63). In one study, HPA axis dysfunction occurred in two-thirds of 143 asthmatic children treated with inhaled corticosteroids; in one-third of those affected, adrenal suppression persisted after central function recovered (64). The more potent topical glucocorticoids can also suppress the HPA axis (65). If glucocorticoid treatment is required, the safest and most effective one should be used based on current evidence-based guidelines for the patient’s age group, medical condition, and risk factors. Some concomitant medications also impose special requirements (66).
Educating patients about possible side effects and the need to report them is essential (67). Patients have individual levels of susceptibility to severe neuropsychiatric effects of glucocorticoid therapy, which can vary over time and stem from genetic and background factors at all levels of glucocorticoid regulation. Patients under age 6 (34) and the elderly (18) appear to be at greater risk for cognitive and memory disturbances. The risk for adverse neuropsychiatric effects may be elevated based on an individual’s past psychiatric history or response to previous courses of glucocorticoid treatment (4, 29), although the data have not always supported such an association (30). While gender, age, dosage, and duration of treatment influence risk, it is not currently possible to predict which patients will experience adverse neuropsychiatric effects during a given course of glucocorticoid therapy. Therefore, all patients should be considered to be at risk and should be monitored during glucocorticoid treatment and withdrawal, and for some time afterward, for signs of changes in mood, memory, thinking, or behavior.
The most appropriate first-line treatment for severe glucocorticoid-induced neuropsychiatric adverse events is dosage reduction or discontinuation. Recommended taper schedules need to be followed, especially after long-term glucocorticoid treatment. Patients need to be closely monitored for signs of new or increased depression or delirium or confusion during this time. If these occur, the patient should be checked for adrenocortical insufficiency, which can be resolved by readministering or increasing the dosage of the glucocorticoid (29). When severe problems with mood, memory, cognition, or behavior occur during glucocorticoid treatment or withdrawal, the prescribing physician should consider consulting with or referring the patient to a knowledgeable psychiatrist or a psychiatrist experienced in treating patients with these problems.
Preliminary evidence about medications that may help prevent or treat glucocorticoid-induced neuropsychiatric symptoms comes from case studies, a limited number of clinical trials, and animal studies. These studies point to several recommendations.
Glucocorticoid-induced mania or mixed manic symptoms appear to respond to lithium carbonate (4), olanzapine (68), or phenytoin (69). Sodium valproate has been shown to reverse manic-like symptoms rapidly while allowing glucocorticoid treatment to continue (70). Glucocorticoid-induced depressive symptoms appear to improve with the use of selective serotonin reuptake inhibitors, such as sertraline, fluoxetine, venlafaxine, and low-dosage fluvoxamine, as well as with lithium alone (4), but not tricyclic antidepressants (71). With any indication of underlying bipolarity, mood stabilizers (e.g., lithium, valproate, carbamazepine, lamotrigine) should be used instead of antidepressants, to prevent switch into manic or mixed dysphoric states (72). Glucocorticoid-induced psychotic depression has been shown to be responsive to ECT (4). Glucocorticoid-induced psychosis may be prevented or resolved with atypical antipsychotics alone (4, 30) or with lithium (4, 73), while glucocorticoid-induced delirium appears to respond to haloperidol or atypical antipsychotics (4). Glucocorticoid-induced memory problems in patients have been reduced by prophylactic administration of lamotrigine (74, 75) and by the NMDA receptor antagonist memantine (76). The beta-blocker propranolol has been found to block glucocorticoid-induced memory retrieval deficits in healthy subjects (77).
Close monitoring should be an especially high priority, and evidence-based prophylactic treatment should be considered for patients with a recent history of mood or cognitive disorder. Prophylactic treatment should also be considered for patients with medical conditions such as systemic lupus erythematosus (3), multiple sclerosis (78), and other neurological disorders (79) that are frequently characterized by comorbid mood or cognitive disturbance, since these conditions may increase the risk for new onsets or exacerbations of such problems during glucocorticoid treatment or withdrawal.
Summary and Conclusions
While glucocorticoids are a valuable and sometimes life-saving treatment for many conditions, population data show that their use, particularly in large dosages or for extended periods, is accompanied by a substantial risk of severe adverse neuropsychiatric effects. In this article we have provided recent and compelling data on the prevalence of this risk during glucocorticoid initiation and withdrawal, and we have summarized the key mechanisms by which glucocorticoids are currently believed to be capable of altering mood, memory, cognition, and behavior. Prescribing physicians and their patients need to operate in close partnership to balance the risks and benefits of initiating glucocorticoid treatment and use the latest evidence-based strategies to minimize, recognize, and treat severe adverse neuropsychiatric effects of glucocorticoids.
References
1.
Hsiao CJ, Cherry DK, Beatty PC, Rechtsteiner EA: National Ambulatory Medical Care Survey: 2007 Summary. National Health Statistics Reports, No 27. Hyattsville, Md, National Center for Health Statistics, 2010
2.
Fardet L, Petersen I, Nazareth I: Prevalence of long-term oral glucocorticoid prescriptions in the UK over the past 20 years. Rheumatology (Oxford) 2011; 50:1982–1990
3.
Bhangle SD, Kramer N, Rosenstein ED: Corticosteroid-induced neuropsychiatric disorders: review and contrast with neuropsychiatric lupus. Rheumatol Int 2013; 33:1923–1932
4.
Kenna HA, Poon AW, de los Angeles CP, Koran LM: Psychiatric complications of treatment with corticosteroids: review with case report. Psychiatry Clin Neurosci 2011; 65:549–560
5.
Fardet L, Flahault A, Kettaneh A, Tiev KP, Généreau T, Tolédano C, Lebbé C, Cabane J: Corticosteroid-induced clinical adverse events: frequency, risk factors, and patient’s opinion. Br J Dermatol 2007; 157:142–148
6.
Fardet L, Petersen I, Nazareth I: Suicidal behavior and severe neuropsychiatric disorders following glucocorticoid therapy in primary care. Am J Psychiatry 2012; 169:491–497
7.
Naber D, Sand P, Heigl B: Psychopathological and neuropsychological effects of 8-days’ corticosteroid treatment: a prospective study. Psychoneuroendocrinology 1996; 21:25–31
8.
Brown ES, Suppes T, Khan DA, Carmody TJ: Mood changes during prednisone bursts in outpatients with asthma. J Clin Psychopharmacol 2002; 22:55–61
9.
Wolkowitz OM, Rubinow D, Doran AR, Breier A, Berrettini WH, Kling MA, Pickar D: Prednisone effects on neurochemistry and behavior: preliminary findings. Arch Gen Psychiatry 1990; 47:963–968
10.
Lieb K, Engelbrecht MA, Gut O, Fiebich BL, Bauer J, Janssen G, Schaefer M: Cognitive impairment in patients with chronic hepatitis treated with interferon alpha (IFNalpha): results from a prospective study. Eur Psychiatry 2006; 21:204–210
11.
Gift AG, Wood RM, Cahill CA: Depression, somatization, and steroid use in chronic obstructive pulmonary disease. Int J Nurs Stud 1989; 26:281–286
12.
Wolkowitz OM, Burke H, Epel ES, Reus VI: Glucocorticoids: mood, memory, and mechanisms. Ann N Y Acad Sci 2009; 1179:19–40
13.
Wolkowitz OM, Lupien SJ, Bigler E, Levin RB, Canick J: The “steroid dementia syndrome”: an unrecognized complication of glucocorticoid treatment. Ann N Y Acad Sci 2004; 1032:191–194
14.
Oliveri RL, Sibilia G, Valentino P, Russo C, Romeo N, Quattrone A: Pulsed methylprednisolone induces a reversible impairment of memory in patients with relapsing-remitting multiple sclerosis. Acta Neurol Scand 1998; 97:366–369
15.
Varney NR, Alexander B, MacIndoe JH: Reversible steroid dementia in patients without steroid psychosis. Am J Psychiatry 1984; 141:369–372
16.
Bender BG, Lerner JA, Kollasch E: Mood and memory changes in asthmatic children receiving corticosteroids. J Am Acad Child Adolesc Psychiatry 1988; 27:720–725
17.
Coluccia D, Wolf OT, Kollias S, Roozendaal B, Forster A, de Quervain DJ: Glucocorticoid therapy-induced memory deficits: acute versus chronic effects. J Neurosci 2008; 28:3474–3478
18.
Keenan PA, Jacobson MW, Soleymani RM, Mayes MD, Stress ME, Yaldoo DT: The effect on memory of chronic prednisone treatment in patients with systemic disease. Neurology 1996; 47:1396–1402
19.
Brown ES, J Woolston D, Frol A, Bobadilla L, Khan DA, Hanczyc M, Rush AJ, Fleckenstein J, Babcock E, Cullum CM: Hippocampal volume, spectroscopy, cognition, and mood in patients receiving corticosteroid therapy. Biol Psychiatry 2004; 55:538–545
20.
Frol AB, Vasquez A, Getahun Y, Pacheco M, Khan DA, Brown ES: A comparison of clinician-rated neuropsychological and self-rated cognitive assessments in patients with asthma and rheumatologic disorders. Allergy Asthma Proc 2013; 34:170–175
21.
de Quervain DJ, Henke K, Aerni A, Treyer V, McGaugh JL, Berthold T, Nitsch RM, Buck A, Roozendaal B, Hock C: Glucocorticoid-induced impairment of declarative memory retrieval is associated with reduced blood flow in the medial temporal lobe. Eur J Neurosci 2003; 17:1296–1302
22.
Wolkowitz OM, Reus VI, Weingartner H, Thompson K, Breier A, Doran A, Rubinow D, Pickar D: Cognitive effects of corticosteroids. Am J Psychiatry 1990; 147:1297–1303
23.
Wolkowitz OM: Prospective controlled studies of the behavioral and biological effects of exogenous corticosteroids. Psychoneuroendocrinology 1994; 19:233–255
24.
Schmidt LA, Fox NA, Goldberg MC, Smith CC, Schulkin J: Effects of acute prednisone administration on memory, attention, and emotion in healthy human adults. Psychoneuroendocrinology 1999; 24:461–483
25.
Newcomer JW, Craft S, Hershey T, Askins K, Bardgett ME: Glucocorticoid-induced impairment in declarative memory performance in adult humans. J Neurosci 1994; 14:2047–2053
26.
Newcomer JW, Selke G, Melson AK, Hershey T, Craft S, Richards K, Alderson AL: Decreased memory performance in healthy humans induced by stress-level cortisol treatment. Arch Gen Psychiatry 1999; 56:527–533
27.
Young AH, Sahakian BJ, Robbins TW, Cowen PJ: The effects of chronic administration of hydrocortisone on cognitive function in normal male volunteers. Psychopharmacology (Berl) 1999; 145:260–266
28.
Mercadante S, Villari P, Intravaia G: Withdrawal acute psychosis after corticosteroid discontinuation. J Pain Symptom Manage 2007; 34:118–119
29.
Fardet L, Nazareth I, Whitaker HJ, Petersen I: Severe neuropsychiatric outcomes following discontinuation of long-term glucocorticoid therapy: a cohort study. J Clin Psychiatry 2013; 74:e281–e286
30.
Warrington TP, Bostwick JM: Psychiatric adverse effects of corticosteroids. Mayo Clin Proc 2006; 81:1361–1367
31.
The Boston Collaborative Drug Surveillance Program: Acute adverse reactions to prednisone in relation to dosage. Clin Pharmacol Ther 1972; 13:694–698
32.
Curtis JR, Westfall AO, Allison J, Bijlsma JW, Freeman A, George V, Kovac SH, Spettell CM, Saag KG: Population-based assessment of adverse events associated with long-term glucocorticoid use. Arthritis Rheum 2006; 55:420–426
33.
Brown ES: Effects of glucocorticoids on mood, memory, and the hippocampus: treatment and preventive therapy. Ann N Y Acad Sci 2009; 1179:41–55
34.
Joëls M: Corticosteroid effects in the brain: U-shape it. Trends Pharmacol Sci 2006; 27:244–250
35.
Lupien SJ, McEwen BS: The acute effects of corticosteroids on cognition: integration of animal and human model studies. Brain Res Brain Res Rev 1997; 24:1–27
36.
Rhen T, Cidlowski JA: Antiinflammatory action of glucocorticoids: new mechanisms for old drugs. N Engl J Med 2005; 353:1711–1723
37.
McEwen BS: The ever-changing brain: cellular and molecular mechanisms for the effects of stressful experiences. Dev Neurobiol 2012; 72:878–890
38.
Joëls M, Sarabdjitsingh RA, Karst H: Unraveling the time domains of corticosteroid hormone influences on brain activity: rapid, slow, and chronic modes. Pharmacol Rev 2012; 64:901–938
39.
Popoli M, Yan Z, McEwen BS, Sanacora G: The stressed synapse: the impact of stress and glucocorticoids on glutamate transmission. Nat Rev Neurosci 2012; 13:22–37
40.
Karst H, Berger S, Turiault M, Tronche F, Schütz G, Joëls M: Mineralocorticoid receptors are indispensable for nongenomic modulation of hippocampal glutamate transmission by corticosterone. Proc Natl Acad Sci USA 2005; 102:19204–19207
41.
Meijer OC, de Lange ECM, Breimer DD, de Boer AG, Workel JO, de Kloet ER: Penetration of dexamethasone into brain glucocorticoid targets is enhanced in mdr1A P-glycoprotein knockout mice. Endocrinology 1998; 139:1789–1793
42.
Karssen AM, Meijer OC, Berry A, Sanjuan Piñol R, de Kloet ER: Low doses of dexamethasone can produce a hypocorticosteroid state in the brain. Endocrinology 2005; 146:5587–5595
43.
de Kloet ER, Joëls M, Holsboer F: Stress and the brain: from adaptation to disease. Nat Rev Neurosci 2005; 6:463–475
44.
McEwen BS: Protective and damaging effects of stress mediators: central role of the brain. Dialogues Clin Neurosci 2006; 8:367–381
45.
McEwen BS, Magarinos AM: Stress and hippocampal plasticity: implications for the pathophysiology of affective disorders. Hum Psychopharmacol 2001; 16(S1):S7–S19
46.
Woolley CS, Gould E, McEwen BS: Exposure to excess glucocorticoids alters dendritic morphology of adult hippocampal pyramidal neurons. Brain Res 1990; 531:225–231
47.
de Leon MJ, McRae T, Rusinek H, Convit A, De Santi S, Tarshish C, Golomb J, Volkow N, Daisley K, Orentreich N, McEwen B: Cortisol reduces hippocampal glucose metabolism in normal elderly, but not in Alzheimer’s disease. J Clin Endocrinol Metab 1997; 82:3251–3259
48.
Grundy PL, Patel N, Harbuz MS, Lightman SL, Sharples PM: Glucocorticoids modulate BDNF mRNA expression in the rat hippocampus after traumatic brain injury. Neuroreport 2000; 11:3381–3384
49.
Hansson AC, Cintra A, Belluardo N, Sommer W, Bhatnagar M, Bader M, Ganten D, Fuxe K: Gluco- and mineralocorticoid receptor-mediated regulation of neurotrophic factor gene expression in the dorsal hippocampus and the neocortex of the rat. Eur J Neurosci 2000; 12:2918–2934
50.
Vellucci SV, Parrott RF, Mimmack ML: Down-regulation of BDNF mRNA, with no effect on trkB or glucocorticoid receptor m RNAs, in the porcine hippocampus after acute dexamethasone treatment. Res Vet Sci 2001; 70:157–162
51.
Duman RS, Heninger GR, Nestler EJ: A molecular and cellular theory of depression. Arch Gen Psychiatry 1997; 54:597–606
52.
Gould E, Tanapat P: Stress and hippocampal neurogenesis. Biol Psychiatry 1999; 46:1472–1479
53.
Duman RS, Monteggia LM: A neurotrophic model for stress-related mood disorders. Biol Psychiatry 2006; 59:1116–1127
54.
Weerda R, Muehlhan M, Wolf OT, Thiel CM: Effects of acute psychosocial stress on working memory related brain activity in men. Hum Brain Mapp 2010; 31:1418–1429
55.
Oei NY, Everaerd WT, Elzinga BM, van Well S, Bermond B: Psychosocial stress impairs working memory at high loads: an association with cortisol levels and memory retrieval. Stress 2006; 9:133–141
56.
Zobel AW, Schulze-Rauschenbach S, von Widdern OC, Metten M, Freymann N, Grasmäder K, Pfeiffer U, Schnell S, Wagner M, Maier W: Improvement of working but not declarative memory is correlated with HPA normalization during antidepressant treatment. J Psychiatr Res 2004; 38:377–383
57.
McEwen BS, Sapolsky RM: Stress and cognitive function. Curr Opin Neurobiol 1995; 5:205–216
58.
Eichenbaum H, Otto T, Cohen NJ: The hippocampus: what does it do? Behav Neural Biol 1992; 57:2–36
59.
Lupien SJ, de Leon M, de Santi S, Convit A, Tarshish C, Nair NP, Thakur M, McEwen BS, Hauger RL, Meaney MJ: Cortisol levels during human aging predict hippocampal atrophy and memory deficits. Nat Neurosci 1998; 1:69–73
60.
Aulakh R, Singh S: Strategies for minimizing corticosteroid toxicity: a review. Indian J Pediatr 2008; 75:1067–1073
61.
Ganguli R, Singh A, Brar J, Carter C, Mintun M: Hydrocortisone induced regional cerebral activity changes in schizophrenia: a PET scan study. Schizophr Res 2002; 56:241–247
62.
Brown ES, Woolston DJ, Frol AB: Amygdala volume in patients receiving chronic corticosteroid therapy. Biol Psychiatry 2008; 63:705–709
63.
Brown ES, Chandler PA: Mood and cognitive changes during systemic corticosteroid therapy. Prim Care Companion J Clin Psychiatry 2001; 3:17–21
64.
Zöllner EW, Lombard CJ, Galal U, Hough FS, Irusen EM, Weinberg E: Hypothalamic-pituitary-adrenal axis suppression in asthmatic school children. Pediatrics 2012; 130:e1512–e1519
65.
Hengge UR, Ruzicka T, Schwartz RA, Cork MJ: Adverse effects of topical glucocorticosteroids. J Am Acad Dermatol 2006; 54:1–15
66.
Liu D, Ahmet A, Ward L, Krishnamoorthy P, Mandelcorn ED, Leigh R, Brown JP, Cohen A, Kim H: A practical guide to the monitoring and management of the complications of systemic corticosteroid therapy. Allergy Asthma Clin Immunol 2013; 9:30
67.
Zukerman E, Ingelfinger JR: Coping With Prednisone (and Other Cortisone-Related Medicines): It May Work Miracles, But How Do You Handle the Side Effects? New York, St. Martin’s Griffin, 2007
68.
Brown ES, Chamberlain W, Dhanani N, Paranjpe P, Carmody TJ, Sargeant M: An open-label trial of olanzapine for corticosteroid-induced mood symptoms. J Affect Disord 2004; 83:277–281
69.
Brown ES, Stuard G, Liggin JD, Hukovic N, Frol A, Dhanani N, Khan DA, Jeffress J, Larkin GL, McEwen BS, Rosenblatt R, Mageto Y, Hanczyc M, Cullum CM: Effect of phenytoin on mood and declarative memory during prescription corticosteroid therapy. Biol Psychiatry 2005; 57:543–548
70.
Roxanas MG, Hunt GE: Rapid reversal of corticosteroid-induced mania with sodium valproate: a case series of 20 patients. Psychosomatics 2012; 53:575–581
71.
Brown CK, Meeker G, Brown ES: Examination of a possible interaction between prednisone and newer antidepressants. Prim Care Community Psychiatry 2005; 10:143–147
72.
Thase ME: Bipolar depression: diagnostic and treatment considerations. Dev Psychopathol 2006; 18:1213–1230
73.
Falk WE, Mahnke MW, Poskanzer DC: Lithium prophylaxis of corticotropin-induced psychosis. JAMA 1979; 241:1011–1012
74.
Brown ES, Wolfshohl J, Shad MU, Vazquez M, Osuji IJ: Attenuation of the effects of corticosteroids on declarative memory with lamotrigine. Neuropsychopharmacology 2008; 33:2376–2383
75.
Desai S, Khanani S, Shad MU, Brown ES: Attenuation of amygdala atrophy with lamotrigine in patients receiving corticosteroid therapy. J Clin Psychopharmacol 2009; 29:284–287
76.
Brown ES, Vazquez M, Nakamura A: Randomized, placebo-controlled, crossover trial of memantine for cognitive changes with corticosteroid therapy. Biol Psychiatry 2008; 64:727–729
77.
de Quervain DJF, Aerni A, Roozendaal B: Preventive effect of beta-adrenoceptor blockade on glucocorticoid-induced memory retrieval deficits. Am J Psychiatry 2007; 164:967–969
78.
Carta MG, Moro MF, Lorefice L, Trincas G, Cocco E, Giudice ED, Fenu G, Colom F, Marrosu MG: The risk of bipolar disorders in multiple sclerosis. J Affect Disord 2014; 155:255–260
79.
Thielscher C, Thielscher S, Kostev K: The risk of developing depression when suffering from neurological diseases. Ger Med Sci 2013; 11:Doc02
Information & Authors
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Published In
History
Received: 24 September 2013
Revision received: 7 February 2014
Accepted: 14 February 2014
Published online: 1 October 2014
Published in print: October 2014
Authors
Competing Interests
All but the last four authors are members of the Workgroup on Neuropsychiatric Sequelae of Glucocorticoid Treatment, which is funded by the Diana Padelford Binkley Foundation. Dr. Schettler received payment from the Diana Padelford Binkley Foundation for work related to the Workgroup and to this study. Dr. Brown has received research grants from Sunovion and Forest. Dr. de Kloet has served as a scientific adviser for Corcept Therapeutics and DynaCorts Therapeutics and owns stock in Corcept Therapeutics. Dr. Joëls has received a research grant from Corcept Pharmaceuticals and research support from the Netherlands Organization for Scientific Research. Dr. van Rossum is supported by the Netherlands Brain Foundation. The other authors report no financial relationships with commercial interests.
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