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Clinical Synthesis
Published Online: 14 January 2016

Mood Disorders of Children and Adolescents

Depressed, irritable, or moody feelings are common symptoms of children and adolescents. At least 50% of youths endorse at least one of those symptoms as occurring to a significant degree and only slightly fewer of their parents do (1). Negative mood characterizes a number of mental health conditions, but depressive disorders are the most commonly associated. The co-occurrence of other symptoms (e.g., sadness, impatience, anger, or the inability to enjoy life or being with others) that last long enough to interfere with school or relationships or with sleep and appetite signals a major depressive episode. However, once the possibility of a depressive disorder is raised, it becomes important to consider other mood disorders as well.
The following three articles describe three of the most important conditions associated with mood disturbance of children and adolescents: major depressive disorder, bipolar disorder, and disruptive mood dysregulation disorder (DMDD), which is a new diagnosis in DSM-5. Although negative mood is a core or important feature of major depressive disorder and DMDD, it is also important in bipolar disorder, in which irritability/negative mood may co-occur with depression even during a manic episode. There are, of course, important differences. Although both major depressive disorder and bipolar disorder are episodic, by definition DMDD is characterized by chronic irritable mood. Comorbidity with attention-deficit hyperactivity disorder (ADHD) is common in all three conditions. There are genetic underpinnings in bipolar disorder, although they have a lesser role in major depressive disorder and are not yet well studied in DMDD. Neurocognitive findings are emerging and point to similarities and differences between these disorders. Treatment, however, is quite different.
Mood disorders of youths share depressive symptoms, frequent comorbidity, and the potential for significant and enduring impairment in social and academic function. Although overall heritability of major depression is approximately 35% (2) and increases with age of onset, genetic factors contributing to bipolar disorder are far greater, ranging from 60% to 93% (3). Heritability of DMDD, a less stable diagnosis that diminishes over time (4), is unknown, yet long-term follow-up suggests that future rates of anxiety and depression are high (5). Successful treatment of youths with major depression is more robust than for youths with bipolar disorder or DMDD. Selective serotonin reuptake inhibitor antidepressant and cognitive-behavioral therapy alone and/or in combination is efficacious for approximately two-thirds of youths with major depression (6), whereas second-generation antipsychotics appear to be more efficacious than either lithium or divalproex for youths with bipolar disorder (7). Until placebo-controlled treatment studies for DMDD have been completed (8), treating the known prominent comorbidities (e.g., ADHD and oppositional defiant disorder) is a sensible course of action. Finally, more efficacious treatments need to be developed for depression, bipolar disorder, and DMDD.

References

1.
Achenbach TM: Manual for the Child Behavior Checklist 6–18 Profile. Burlington, University of Vermont, Department of Psychiatry, 2001; 59 chapter 11 p. 159
2.
Uher R: Gene-environment interactions in severe mental illness. Front Psychiatry 2014; 5:48
3.
Althoff RR, Faraone SV, Rettew DC, et al: Family, twin, adoption, and molecular genetic studies of juvenile bipolar disorder. Bipolar Disord 2005; 7:598–609
4.
Deveney CM, Hommer RE, Reeves E, et al: A prospective study of severe irritability in youths: 2- and 4-year follow-up. Depress Anxiety 2015; 32:364–372
5.
Copeland WE, Angold A, Costello EJ, et al: Prevalence, comorbidity, and correlates of DSM-5 proposed disruptive mood dysregulation disorder. Am J Psychiatry 2013; 170:173–179
6.
March J, Silva S, Curry J, et al; The Treatment for Adolescents With Depression Study (TADS): outcomes over 1 year of naturalistic follow-up. Am J Psychiatry 2009; 166:1141–1149
7.
Geller B, Luby JL, Joshi P, et al: A randomized controlled trial of risperidone, lithium, or divalproex sodium for initial treatment of bipolar I disorder, manic or mixed phase, in children and adolescents. Arch Gen Psychiatry 2012; 69:515–528
8.
Axelson D, Findling RL, Fristad MA, et al: Examining the proposed disruptive mood dysregulation disorder diagnosis in children in the Longitudinal Assessment of Manic Symptoms study. J Clin Psychiatry 2012; 73:1342–1350

Information & Authors

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Published in print: Winter 2016
Published online: 14 January 2016

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Gabrielle A. Carlson, M.D.
Dr. Carlson is professor of Psychiatry and Pediatrics and director emerita in the Division of Child and Adolescent Psychiatry, Stony Brook University School of Medicine, Stony Brook, New York (e-mail: [email protected]). Dr. Pataki is clinical professor of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at University of California, Los Angeles.
Caroly Pataki, M.D.
Dr. Carlson is professor of Psychiatry and Pediatrics and director emerita in the Division of Child and Adolescent Psychiatry, Stony Brook University School of Medicine, Stony Brook, New York (e-mail: [email protected]). Dr. Pataki is clinical professor of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at University of California, Los Angeles.

Competing Interests

Dr. Carlson reports receipt of research funds from Pfizer Pharmaceuticals. Dr. Pataki reports no financial relationships with commercial interests.

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