Overview
Related Diseases & Conditions
Summary
Depressive disorders are characterized by persistent low mood, loss of interest and enjoyment, neurovegetative symptoms, and reduced energy, causing varying levels of social and occupational dysfunction. Depressive disorders are very common and are among the leading causes of disability worldwide.[2] The etiology of depression remains poorly understood. Integrative models, taking into account biologic and social variables, most effectively reflect the complex etiology. Depressive symptoms include depressed mood, anhedonia, weight changes, libido changes, sleep disturbance, psychomotor problems, low energy, excessive guilt, poor concentration, and suicidal ideation. In some cases the mood is not sad, but anxious or irritable or flat.[1] Key risk factors include older age; recent childbirth, stress, or trauma; coexisting medical conditions (diabetes mellitus, cancer, stroke, myocardial infarction, and obesity); personal or family history of depression; certain medications (e.g., corticosteroids) and female sex.Summary
Characterized by sad or irritable mood, anhedonia, decreased capacity to have fun, decreased self-esteem, sleep disturbance, social withdrawal or impaired social relationships, and impaired school performance. The presence of poverty has been associated with an increased risk of children requiring treatment for depression.[3] Childhood depression is likely to be caused by both genetic and environmental factors, and by their interactions. Life stress has been strongly associated with risk of depression, especially in girls.[4] Adolescent and preadolescent depressive disorders are clinical diagnoses, based on a comprehensive diagnostic evaluation of history and presenting symptoms. Key risk factors include positive family history of depression, other parental psychopathology, history of stressful life events or trauma, female sex, postpartum status, comorbid psychiatric disorders or chronic medical illnesses, and neighbourhood and social instability are important risk factors for depression.- Disruptive mood dysregulation disorder
Summary
Disruptive mood dysregulation disorder is a category of depressive disorders first diagnosed at 6-18 years of age, with age of onset before 10 years. It is characterized by the Diagnostic and Statistical Manual of Mental Disorders, fifth edition, text revision (DSM-5-TR) as severe and recurrent temper outbursts on average 3 or more times per week for at least 1 year, and a persistent irritable or angry mood for most of the day nearly every day between temper outburst.[1] Summary
Includes common forms of depression, but lasting longer than acute major depressive disorder. The DSM-5-TR modified its classification system to include all chronic forms of depression under the single category persistent depressive disorder, which includes both chronic major depressive disorder and the previous category of dysthymic disorder (dysthymia), or chronic low-grade depression. Chronic major depressive disorder may be more common than dysthymia. The etiology of the various subtypes of persistent depressive disorder, as well as other mood disorders, is unknown. It is likely that depressive disorders are heterogeneous in nature, and this may be particularly true for persistent depressive disorder, which has a wide range of presentations and varying severity.[5] The DSM-5-TR includes specifiers to identify different pathways to the diagnosis of persistent depressive disorder and various presentations based on severity and clinical characteristics.[1]Summary
Postpartum depression refers to the development of a depressive illness following childbirth and may form part of a bipolar or, more usually, a unipolar illness. Postpartum depression is not recognized by current classification systems as a condition in its own right, but the onset of a depressive episode within 4 weeks of childbirth can be recorded via the peripartum-onset specifier in the DSM-5-TR.[1] In common usage, depressive episodes occurring within 6-12 months of delivery may be considered to be postpartum depression. One large review of 143 studies from 40 countries reports a wide range in the prevalence of postpartum depression worldwide, ranging from 0% to 60%.[6] The etiology is poorly understood and clinical consensus is lacking; the development of postpartum depression is likely to involve an interaction between psychologic social, and biologic factors.[7]Characteristics of postpartum depression may include guilt about the depressive symptoms, ambivalent feelings toward the infant, impaired bonding, and obsessive ruminations, including intrusive thoughts about harming the infant. Postpartum depression should be distinguished from a minor mood disturbance (postpartum blues or "baby blues"), in which the symptoms generally resolve within 2 weeks.Summary
Premenstrual syndrome (PMS) is characterized by cyclical, physical, and behavioral symptoms occurring in the luteal phase of the normal menstrual cycle (the period between ovulation and onset of menstruation). Premenstrual dysphoric disorder (PMDD) is a more severe variant that includes at least one affective symptom. Depression may coexist with PMS or PMDD in up to 50% of cases. A diagnosis of PMS or PMDD may predate a diagnosis of depression.[8] PMS and PMDD are diagnoses of exclusion, confirmed by a prospective symptom diary that verifies their repetitive, cyclical nature. Physical exam and limited laboratory testing are typically normal. Key risk factors include postpubescent and premenopausal women, family history, and mood disorders.Summary
Seasonal affective disorder (SAD) is a subtype of major depression and bipolar disorder, occurring with seasonal change over at least a 2-year period. Atypical vegetative symptoms of depression are common, such as hypersomnia, hyperphagia, and weight gain. Most commonly presents with onset of depression in the autumn or winter, and full remission of symptoms over the spring or summer. Diminished light during winter months and increased light during summer months may contribute to risk for seasonal mood variations.[9] Lifetime estimates for depressive and bipolar disorders with a seasonal pattern average between 0.4% and 2.9% in US, Canadian, and UK community studies.[10] [11] [12] Some estimates may be as high 9.7%.[13] However, these differences are probably due to differences in the sampling and diagnostic criteria used. Assessment is based on self-report, clinical interview, and behavioral observation. Risk factors that are strongly associated with SAD include being a woman, an age of onset of 20-30 years, having a positive family history of the condition, and living in an area exposed to diminished light during winter and increased light during summer.Summary
A recurrent and often chronic mental illness, bipolar disorder is marked by episodes of hypomania or mania and depression, associated with a change or impairment in functioning. The long-term course of illness is characterized by a predominance of depression, although a history of at least one manic, hypomanic, or mixed episode is required to make the diagnosis of a bipolar disorder.Bipolar I disorder: at least one manic episode.Bipolar II disorder: has never had a full manic episode; at least one hypomanic episode and at least one major depressive episode.[1]Global prevalence of bipolar disorder is estimated to be approximately 2.5%.[14] The exact cause of bipolar disorder is unknown; in common with many psychiatric disorders, it is considered to be caused by the complex interaction of multiple genetic, cellular, and environmental factors.[15] Key risk factors include early age of mood disorder onset, family history of bipolar disorder or suicide, poor or limited response to traditional antidepressants, highly recurrent mood episodes, comorbid anxiety or substance misuse disorders, and a pattern of psychosocial instability.Summary
Bipolar disorder is an uncommon condition in children that becomes more frequent in teens, approaching the rate of frequency seen in adults.[16] [17] The adult criteria describe a disorder of fluctuating mood cycles, consisting of episodes of elevated mood and increased activity or energy (mania) lasting at least 1 week, and episodes of lowered mood and activity (depression); an episode of mania is necessary for a diagnosis to be made. The diagnosis can be controversial, as criteria overlap with other childhood conditions such as ADHD and comorbid oppositional defiant disorder.Summary
Suicide risk mitigation refers to the identification, assessment, intervention, and treatment of a person at risk of suicide. It is an ongoing process whether due to a mental illness or a life crisis. Suicide is an important cause of death globally and a significant public health concern. An estimated 800,000 people die by suicide each year; it is the second leading cause of death among people aged 15-29 years.[18] Suicide is associated with a constellation of psychologic, biologic, genetic, social, and environmental factors, but whether these factors are causative remains uncertain. Self-harm and suicidal thoughts should be taken seriously, and met with empathy, compassion, and understanding given that they are risk factors for suicide, particularly when associated with a history of a mental illness (most commonly major depressive disorder and substance misuse).
Citations
American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 5th ed., text revision (DSM-5-TR). Washington, DC: American Psychiatric Publishing; 2022.
1. American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 5th ed., text revision (DSM-5-TR). Washington, DC: American Psychiatric Publishing; 2022.
2. World Health Organization. Depression and other common mental disorders: global health estimates. 2017 [internet publication].[Full Text]
3. Ghandour RM, Sherman LJ, Vladutiu CJ, et al. Prevalence and treatment of depression, anxiety, and conduct problems in US children. J Pediatr. 2019 Mar;206:256-7.e3.[Abstract][Full Text]
4. Harkness KL, Alavi N, Monroe SM, et al. Gender differences in life events prior to onset of major depressive disorder: the moderating effect of age. J Abnorm Psychol. 2010 Nov;119(4):791-803.[Abstract][Full Text]
5. Peterson RE, Cai N, Dahl AW, et al. Molecular genetic analysis subdivided by adversity exposure suggests etiologic heterogeneity in major depression. Am J Psychiatry. 2018 Jun 1;175(6):545-54.[Abstract][Full Text]
6. Halbreich U, Karkun S. Cross-cultural and social diversity of prevalence of postpartum depression and depressive symptoms. J Affect Disord. 2006 Apr;91(2-3):97-111.[Abstract]
7. Yim IS, Tanner Stapleton LR, Guardino CM, et al. Biological and psychosocial predictors of postpartum depression: systematic review and call for integration. Annu Rev Clin Psychol. 2015;11:99-137.[Abstract][Full Text]
8. Beck LE, Gevirtz R, Mortola JF. The predictive role of psychosocial stress on symptom severity in premenstrual syndrome. Psychosom Med. 1990 Sep-Oct;52(5):536-43.[Abstract]
9. McClung CA. Circadian genes, rhythms and the biology of mood disorders. Pharmacol Ther. 2007 May;114(2):222-32.[Abstract][Full Text]
10. Levitt AJ, Boyle MH. The impact of latitude on the prevalence of seasonal depression. Can J Psychiatry. 2002 May;47(4):361-7.[Abstract][Full Text]
11. Levitt AJ, Boyle MH, Joffe RT, et al. Estimated prevalence of the seasonal subtype of major depression in a Canadian community sample. Can J Psychiatry. 2000 Sep;45(7):650-4.[Abstract][Full Text]
12. Blazer DG, Kessler RC, Swartz MS. Epidemiology of recurrent major and minor depression with a seasonal pattern: the National Comorbidity Survey. Br J Psychiatry. 1998 Feb;172:164-7.[Abstract]
13. Magnusson A, Axelsson J, Karlsson MM, et al. Lack of seasonal mood change in the Icelandic population: results of a cross-sectional study. Am J Psychiatry. 2000 Feb;157(2):234-8.[Abstract][Full Text]
14. McGrath JJ, Al-Hamzawi A, Alonso J, et al. Age of onset and cumulative risk of mental disorders: a cross-national analysis of population surveys from 29 countries. Lancet Psychiatry. 2023 Sep;10(9):668-81.[Abstract]
15. Kendler KS. From many to one to many-the search for causes of psychiatric illness. JAMA Psychiatry. 2019 Oct 1;76(10):1085-91.[Abstract]
16. Merikangas KR, Lamers F. The 'true' prevalence of bipolar II disorder. Curr Opin Psychiatry. 2012 Jan;25(1):19-23.[Abstract][Full Text]
17. Van Meter AR, Moreira AL, Youngstrom EA. Meta-analysis of epidemiologic studies of pediatric bipolar disorder. J Clin Psychiatry. 2011 Sep;72(9):1250-6.[Abstract][Full Text]
18. World Health Organization. Suicide in the world: Global Health Estimates. Sep 2019 [internet publication]. [Full Text]
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