You are in: eMedicine Specialties > Psychiatry > Adult Menopause and Mood DisordersArticle Last Updated: Jan 7, 2008AUTHOR AND EDITOR INFORMATIONAuthor: Sarah Guzofski, MD, Staff Physician, Department of Psychiatry, University of Massachusetts Medical School Sarah Guzofski is a member of the following medical societies: American Medical Association, American Psychiatric Association, and Massachusetts Medical Society Coauthor(s): Rebecca S Lundquist, MD, Consulting Staff, Department of Psychiatry, UMass Memorial Medical Center Editors: Mohammed A Memon, MD, Medical Director of Geriatric Psychiatry, Department of Psychiatry, Spartanburg Regional Hospital System; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Iqbal Ahmed, MBBS, Professor, Department of Psychiatry, John A Burns School of Medicine, University of Hawaii; Harold H Harsch, MD, Program Director of Geropsychiatry, Department of Geriatrics/Gerontology, Associate Professor, Department of Psychiatry and Department of Medicine, Froedtert Hospital, Medical College of Wisconsin; Stephen Soreff, MD, President of Education Initiatives, Nottingham, NH; Faculty, Metropolitan College of Boston University, Boston, MA Author and Editor Disclosure Synonyms and related keywords: menstruation, menstruation disorders, menstrual cycle, menses, perimenopause, perimenopausal, postmenopause, postmenopausal, premenopause, premenopausal, menopause, menopausal transition, amenorrhea, climacteric syndrome, climacterium, hot flashes, hot flushes, irregular menses, menarche, change of life, midlife change OCD, obsessive-compulsive disorder, depression, antidepressants, anxiety, anxiety disorders, insomnia, sleep disorders, panic disorder, estrogen-related sleep disturbance, weight gain, mood changes, lability FSH, follicle-stimulating hormone, luteinizing hormone, LH, estrogen, androstenedione, gonadotropin-releasing hormone, GnRH, hormone replacement therapy, HRT, estrogen replacement therapy, ERT INTRODUCTIONBackgroundMenopause is considered to occur when 12 menstrual cycles are missed.1, 2 Perimenopause, or menopausal transition, is defined as the time from the onset of the climacteric through the first year after last menses.3 Perimenopause is characterized by menstrual irregularities, prolonged and heavy menstruation intermixed with episodes of amenorrhea, decreased fertility, vasomotor symptoms, and insomnia. Some of these symptoms may emerge 4 years before menses cease, with a mean age of onset of perimenopause of 47.5 years.4 During the menopausal transition, estrogen levels decline, and levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) increase. Depression during menopause In the United States, 1.3 million women reach menopause annually. Although most women transition to menopause without experiencing psychiatric problems, an estimated 20% have depression at some point during menopause.5 Studies of mood during menopause have generally revealed an increased risk of depression during perimenopause. In a cross-sectional population survey from the Netherlands, 2103 women were asked to rate their symptoms of depression before menopause and 3.5 years later, during the menopausal transition. The women experienced most symptoms of depression during the menopausal transition. In the United States, a study of a community sample of women undergoing natural menopause also demonstrated an increase in depressive symptoms during perimenopause.6 Investigators from the Harvard Study of Moods and Cycles recruited premenopausal women aged 36-44 years with no history of major depression and followed up these women for 9 years to detect new onsets of major depression. Women who entered perimenopause were twice as likely as women who had not yet made the menopausal transition to have clinically significant depressive symptoms.7 Problems with sleep during menopause Insomnia occurs in 40-50% of women during the menopausal transition, and problems with sleep may or may not be connected to mood disorders.8 Women with insomnia are more likely than others to report problems such as anxiety, stress, tension, and depressive symptoms. Whether the sleep problems are associated with age-related changes in sleep architecture, hormonal status, or other symptoms of menopause (eg, vasomotor symptoms) is unclear. Many authors have suggested that hot flashes are to blame for patients' sleep problems; however, results of polysomnographic studies have been inconclusive. Rates of sleep apnea increase with age, rising from 6.5% in women aged 30-39 years to 16% in women aged 50-60 years. The pathophysiology is not known, but theories include a relationship to postmenopausal weight gain or to decreased progesterone levels because progesterone stimulates respiration.9, 10 In addition to undergoing changes in estrogen and progesterone levels, postmenopausal women experience a decline in melatonin and growth hormone levels, both of which have effects on sleep.11 Schizophrenia during menopause In most cases, schizophrenia first manifests in young adulthood, with the rate of new cases declining in both male and female individuals after early adulthood. A second peak in the incidence of schizophrenia is noted among women aged 45-50 years; this second peak is not observed in men.12 Some researchers have observed a worsening of the course of schizophrenia in women during the menopausal transition. These observations may suggest that estrogen plays a modulatory role in the pathophysiology of schizophrenia.13 Panic disorder during menopause Panic disorder is common during perimenopause. New-onset panic disorder may occur during menopause, or preexisting panic disorder may worsen. Panic disorder may be most common in women with many physical symptoms of menopause.14 Obsessive-compulsive disorder during menopause New-onset obsessive-compulsive disorder (OCD), a relapse of OCD, or a change in OCD symptoms may occur during menopause. Fluctuations in OCD have been correlated with the menstrual cycle and with pregnancy, suggesting that hormone levels may contribute to the disorder.15 Bipolar disorder during menopause Exacerbation of mood symptoms during menopause has been noted in women with preexisting bipolar disorder—especially with a worsening of depression and, perhaps, an increase in rapid cycling during the menopausal transition.16, 17 PathophysiologyDepression during perimenopause is likely due to fluctuating and declining estrogen levels in part. Steroid hormones, such as estrogen, act in the CNS by means of various mechanisms. For instance, they stimulate the synthesis of neurotransmitters, the expression of receptors, and influence membrane permeability.18 Estrogen increases the effects of serotonin and norepinephrine, which are thought to be the neurotransmitters most related to the physiologic cause of depression. Among other mechanisms, estrogen decreases monoamine oxidase (MAO) activity in the CNS, hindering the break down of serotonin and norepinephrine are not broken down as readily.2 In addition, estrogen increases serotonin synthesis, upregulates 5-hydroxytryptamine (5-HT)-1 (5-HT1) receptors, and downregulates 5-HT2 receptors. Estrogen also increases norepinephrine activity in the brain, perhaps by decreasing reuptake and degradation due to inhibition of the enzymes MAO and catechol O-methyltransferase.19 Although the precise mechanisms are yet unknown, regulation or serotonin and norepinephrine may change as estrogen levels fluctuate and thus contribute to depression. Because estrogen facilitates the actions of serotonin and norepinephrine, a decline in estrogen concentrations may, in turn, decrease levels of these hormones.2, 18, 19 Changes in estrogen levels, perhaps due to mechanisms involving these neurotransmitters, may be related to depressive symptoms in the menopausal transition of some women. FrequencyUnited StatesEach year, 1.3 million women reach menopause. An estimated 20% of these women experience depression.5 Mortality/MorbidityAlthough morbidity and mortality secondary to perimenopausal depression has not been studied, depression is known to be a significant health problem in women. According to the World Health Organization's Global Burden of Disease Study, unipolar depression is the leading cause of disease-related disability in women.20 In the Global Burden of Disease Study, unipolar major depression was second to only ischemic heart disease in terms of associated morbidity and mortality.21 RaceThe racial distribution of perimenopausal depression is not known. However, in countries where older women are highly valued, women experience fewer symptoms overall during menopause. SexDepression is approximately twice as common in women as in men (21% vs 12.7%). Moreover, depressive are more recurrent, longer, worse, and more impairing for women and for men.22, 23 In addition, the prevalence of dysthymia and minor depression is increases among women. These differences have not been noted for mania. Sex-related differences emerge at the age of 11-15 years.20 AgeThe mean age of onset for the menopausal transition is 47.5 years.4 CLINICALHistory
PhysicalFindings of perimenopause include urogenital atrophy, as well as flushing and diaphoresis during hot flashes. CausesCauses of menopause-related mood disorders may include hormonal changes, life stressors, psychological or social conditions, and/or a preexisting tendency to develop depression. Hormonal changes Depression seems to be significantly linked to times of hormonal change in women. Several observations and study data support this theory. For example, the disparity between rates of depression in women and men begins at puberty. Also, hormonal changes are thought to be major contributors to premenstrual dysphoric disorder, as well as mood changes experienced in the postpartum period and at the menopausal transition.22, 23 Furthermore, estrogen affects both serotonin and norepinephrine, the 2 neurotransmitters thought to be most directly associated with depression. Of note, absolute levels of gonadal hormones are not correlated with depression. Estrogen and progesterone levels do not distinguish a woman with depression from one without depression. When hormone concentrations were measured in perimenopausal or postmenopausal women with depression, no abnormal levels were found.24 Rather, a certain subset of women seem to be predisposed to have mood disturbances triggered by hormonal fluctuations. This subset includes women with a history of mood disorders or of premenstrual and postpartum mood-related symptoms. The risk of depression appears to be higher during perimenopause, when hormone levels are changing, than during postmenopause, when estrogen and progesterone levels are low but stable.18, 25 Life stressors Societal roles and expectations may contribute to the heightened rate of depression in women. Women with particular types of stressors seem to be at increased risk for perimenopausal depression. Such stressors include the following5, 23:
Dysphoric mood during the early perimenopausal transition is most common in women with relatively low educational status. Therefore, low levels of education may be a marker for other stressors, such as ongoing low socioeconomic status.26 An Australian study of women transitioning to menopause revealed more depression in women with the following states27:
Other stressors that tend to correspond with perimenopause and that are postulated to relate to depression include the following:
Psychological or social conditions Numerous psychological and social theories have been proffered to explain why women may become depressed during perimenopause. Some of these are related to the following factors:
Preexisting tendency to develop depression A personal or family history of major depression, postpartum depression, or premenstrual dysphoric disorder seem to be a major risk factor for depression in the perimenopausal period.5 However, perimenopausal depressive syndrome is a risk even in women without a history of depression. DIFFERENTIALSAdjustment Disorders Anemia Depression Dysthymic Disorder Hypothyroidism
|
| Drug Name | Citalopram (Celexa) |
|---|---|
| Description | Enhances serotonin activity by selectively inhibiting reuptake at neuronal membrane. |
| Adult Dose | 20-60 mg PO qd; 10 mg/d initially, titrate by 10 mg/wk |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; concurrent therapy with an MAO inhibitor |
| Interactions | Azole antifungals, omeprazole, macrolides may potentiate effects; serotonin syndrome (myoclonus, rigidity, confusion, nausea, hyperthermia, autonomic instability, coma, eventual death) occurs with simultaneous use of other serotonergic agents (eg, anorectic agents, tramadol, buspirone, trazodone, clomipramine, nefazodone, tryptophan); discontinue other serotonergic agents before starting SSRIs |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in liver dysfunction, cardiovascular disease, history of seizures, suicidal tendency, history of mania or hypomania; sudden stoppage can lead to SSRI discontinuation syndrome with symptoms of dizziness, ataxia, mood lability, insomnia, irritability, and paresthesias including head shocks |
| Drug Name | Fluoxetine (Prozac) |
|---|---|
| Description | Enhances serotonin activity by selectively inhibiting reuptake at neuronal membrane; long half-life is advantage and drawback; if drug works well, occasional missed dose not a problem; if problems occur, eliminating all active metabolites takes a long time. |
| Adult Dose | 20 mg/d PO in am; after several wk, increase by 20 mg/d; not to exceed 80 mg/d If patient is taking 20 mg/d, may start once-weekly dosing with 90-mg delayed-release product 7 d after last daily dose of 20 mg |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; concurrent use of MAO inhibitors or use in past 2 wk; coadministration with thioridazine |
| Interactions | Increases toxicity of diazepam and trazodone by decreasing clearance; increases toxicity of MAO inhibitors and highly protein-bound drugs; serotonin syndrome (myoclonus, rigidity, confusion, nausea, hyperthermia, autonomic instability, coma, eventual death) occurs with simultaneous use of other serotonergic agents (eg, anorectic agents, tramadol, buspirone, trazodone, clomipramine, nefazodone, tryptophan); discontinue other serotonergic agents at least 2 wk before starting SSRIs |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in liver dysfunction, cardiovascular disease, history of seizures, suicidal tendencies, history of mania or hypomania |
| Drug Name | Paroxetine (Paxil) |
|---|---|
| Description | Potent selective inhibitor of neuronal serotonin reuptake; also has weak effect on norepinephrine and dopamine neuronal reuptake. |
| Adult Dose | Initial therapy: 10 mg/d PO, increase by 10-mg/d increments prn; dosage changes should occur at intervals of at least 1 wk; usual dosage range 10-60 mg/d, not to exceed 60 mg/d Paxil CR: 25 mg PO qd initially; may increase by 12.5 mg/d q1wk; not to exceed 62.5 mg/d |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; concurrent administration with MAO inhibitors or administration within 14 days of discontinuing MAO inhibitor; coadministration with thioridazine |
| Interactions | Inhibits CYP2D6; therefore, may increase toxicity of CYP2D6 substrates (eg, phenothiazines, propafenone, flecainide and encainide, other SSRIs, tricyclic antidepressants); phenobarbital and phenytoin decrease effects; alcohol, cimetidine, sertraline, phenothiazines, and warfarin increase toxicity; serotonin syndrome (myoclonus, rigidity, confusion, nausea, hyperthermia, autonomic instability, coma, eventual death) occurs with simultaneous use of other serotonergic agents (eg, anorectic agents, tramadol, buspirone, trazodone, clomipramine, nefazodone, tryptophan); discontinue other serotonergic agents before starting SSRIs |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Caution in liver dysfunction, cardiovascular disease, history of seizures, suicidal tendencies, history of mania or hypomania; dosage of controlled-release product should not exceed 50 mg/d for elderly, debilitated individuals or those with severe renal or hepatic impairment Sudden stoppage can lead to SSRI discontinuation syndrome with symptoms of dizziness, ataxia, mood lability, insomnia, irritability, and paresthesias including head shocks |
| Drug Name | Sertraline (Zoloft) |
|---|---|
| Description | Enhances serotonin activity by selectively inhibiting reuptake at neuronal membrane. |
| Adult Dose | 50 mg/d PO in am with 50-mg/d increments q2-3d to 100 mg/d, if tolerated; not to exceed 200 mg/d |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; do not use concurrently or within 2 wk of MAO inhibitors |
| Interactions | Inhibits CYP isoenzymes 3A3/4, 2C9, 2C19, and 2D6, possibly decreasing clearance of isoenzyme substrates (eg, metoprolol, thioridazine, imipramine, haloperidol, phenytoin, barbiturates, glyburide, warfarin); increases toxicity of MAO inhibitors, diazepam, tolbutamide, and warfarin; serotonin syndrome (myoclonus, rigidity, confusion, nausea, hyperthermia, autonomic instability, coma, eventual death) occurs with simultaneous use of other serotonergic agents (eg, anorectic agents, tramadol, buspirone, trazodone, clomipramine, nefazodone, tryptophan); discontinue other serotonergic agents before starting SSRIs |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in liver dysfunction, cardiovascular disease, history of seizures, suicidal tendencies, history of mania or hypomania; sudden stoppage can lead to SSRI discontinuation syndrome with symptoms of dizziness, ataxia, mood lability, insomnia, irritability, and paresthesias including head shocks |
| Drug Name | Escitalopram (Lexapro) |
|---|---|
| Description | Enhances serotonin activity by selectively inhibiting reuptake at neuronal membrane. S-enantiomer of citalopram. |
| Adult Dose | 10 mg PO qd initially; may increase to 20 mg/d after 1 wk prn |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; administration within 14 d of receiving MAO inhibitor |
| Interactions | Primarily metabolized by CYP3A4 and CYP2C19; coadministration with alcohol or other centrally acting drugs increases CNS depression |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in liver dysfunction, cardiovascular disease, history of seizures, suicidal tendencies, history of mania or hypomania; sudden stoppage can lead to SSRI discontinuation syndrome with symptoms of dizziness, ataxia, mood lability, insomnia, irritability, and paresthesias including head shocks |
In women with mild mood-disorder symptoms not meeting the criteria for depression, hormone replacement therapy may be considered. Hormone replacement therapy may also be an adjunctive treatment for women with perimenopausal depression and prominent vasomotor symptoms.
| Drug Name | Conjugated equine estrogen (CEE) and medroxyprogesterone (Premphase, Prempro) |
|---|---|
| Description | Hormone replacement therapy that induces synthesis of DNA, RNA, and various proteins in target tissues. Inhibits secretion of pituitary gonadotropins. |
| Adult Dose | 0.45-0.625 mg conjugated estrogen PO 1.5-5 mg medroxyprogesterone PO qd Combination CEE and progestin daily |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; known or suspected pregnancy; breast cancer; undiagnosed abnormal genital bleeding; active thrombophlebitis or thromboembolic disorders; history of thrombophlebitis, thrombosis, or thromboembolic disorders associated with previous estrogen use (except when used in treatment of breast malignancy); cerebral apoplexy; liver dysfunction |
| Interactions | May decrease effects of aminoglutethimide; may reduce hypoprothrombinemic effect of anticoagulants; coadministration of barbiturates, rifampin, and other agents that induce hepatic microsomal enzymes may reduce estrogen levels; pharmacologic and toxicologic effects of corticosteroids may occur as a result of estrogen-induced inactivation of hepatic CYP enzyme; loss of seizure control noted when administered concurrently with hydantoins |
| Pregnancy | X - Contraindicated; benefit does not outweigh risk |
| Precautions | Risk of endometrial cancer with unopposed estrogen; risk greatly reduced when progestin is given with estrogen; hormone replacement associated with small increased relative risk of breast cancer and increased relative risk of ovarian cancer; doubles rate of thromboembolic disease; doubles risk of gallbladder disease; increased risk of myocardial infarction and cerebrovascular accident Carefully weigh risks of estrogen treatment (eg, those revealed in Women's Health Initiative studies) When estrogen plus progestin was compared with placebo for primary prevention of cardiovascular events, risk of breast cancer, coronary heart disease, stroke, and venous thromboemboli increased in patients treated with hormones (Roussouw, 2002) When estrogen alone was compared with placebo, risk of stroke increased (Anderson, 2004) |
See the Medication section above.
Patients may benefit from learning that mood symptoms are not uncommon during menopause. Providing education about depressive symptoms can help women understand their experiences and recognize depression as a treatable illness. Family members may also benefit from learning about the symptoms of major depression and the association of its onset with the menopausal transition. This information may help them understand changes they observe in their family member.
Patients should be educated about emergency mental health services that are available in their area. They should be aware of how to access help if they have suicidal thoughts.
Listed below are some useful clinician and patient education resources, as well as sources of additional information and support:
Carefully weigh the risks of estrogen treatment (see Medication).
Menopause and Mood Disorders excerpt
Article Last Updated: Jan 7, 2008