DSM-5 mixed specifier for manic episodes: evaluating the effect of depressive features on severity and treatment

R S McIntyre1, M Tohen, M Berk

  • 1Mood Disorders Psychopharmacology Unit, University Health Network, University of Toronto, ON, Canada M5T 2S8.

Abstract

Insights

Depressive features are common in bipolar I disorder patients experiencing manic episodes. Asenapine showed stable treatment outcomes across depressive symptom severities, unlike olanzapine and placebo.

Area of Science:

  • Psychiatry
  • Clinical Psychology
  • Neuroscience

Background:

  • The Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) introduced a mixed features specifier for manic episodes in bipolar I disorder.
  • Understanding the prevalence and impact of this specifier is crucial for accurate diagnosis and effective treatment.

Purpose of the Study:

  • To determine the frequency of the DSM-5 mixed features specifier in bipolar I patients with manic episodes.
  • To evaluate how this specifier influences symptom severity and treatment outcomes.

Main Methods:

  • A post-hoc analysis utilizing the Montgomery-Åsberg Depression Rating Scale (MADRS) and the Positive and Negative Syndrome Scale (PANSS) to identify proxies for the DSM-5 mixed features specifier.
  • Analysis of 960 bipolar I patients diagnosed with manic episodes.

Main Results:

  • 34% of patients exhibited mild depressive features, 18% moderate, and 4.3% severe, based on MADRS and PANSS scores.
  • Treatment outcomes, particularly remission rates (MADRS ≤12, YMRS ≤12), varied by depressive symptom severity and medication.
  • Asenapine demonstrated stable remission rates across all severity levels, whereas olanzapine and placebo showed decreased remission with increasing depressive symptom severity.

Conclusions:

  • The findings support the validity of the proposed DSM-5 mixed features specifier criteria.
  • Depressive features are indeed frequent in bipolar I patients during manic episodes.
  • Treatment with asenapine appears more robust than olanzapine or placebo in patients with co-occurring depressive features during mania.

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