Seasonality Patterns in Bipolar Disorder: Associations With Clinical Phenotypes and Treatment-Related Outcomes

  • Siralp Bostan
  • , Lindsay M. Melhuish Beaupre
  • , Mete Ercis
  • , Brandon J. Coombes
  • , Francisco Romo-Nava
  • , Miguel L. Prieto
  • , Alfredo B. Cuellar Barboza
  • , Susan L. McElroy
  • , Mark A. Frye
  • , Joanna M. Biernacka
  • , Aysegul Ozerdem*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Mood episodes in bipolar disorder (BD) follow a seasonal pattern in approximately 25% of patients. We aimed to examine the associations of specific seasonality patterns in BD with various clinical phenotypes and treatment-related outcomes. Methods: Patients from the Mayo Clinic Bipolar Disorder Biobank with available seasonality data were included in the study. Among those reporting any seasonality, participants were further categorized into four seasonality groups: fall/winter depression, spring/summer (hypo)mania, biphasic (fall/winter depression with spring/summer (hypo)mania), and equinoctial seasonality (any mood episode occurring in spring or fall). Regression models were used, treating seasonality patterns as the predictor of clinical phenotypes (BD subtype, early onset, history of psychosis, suicide attempt, rapid cycling), lifetime medication exposure (number of unique antidepressants, antipsychotics, and any psychotropics) and treatment response to mood stabilizers (Alda A score). Results: Among 1702 patients with BD (61.5% female, mean age = 41.43 ± 14.73 years), 44.6% reported seasonal mood episodes. Individuals with any seasonality were more likely to have BD-I (OR = 1.29, p = 0.024), early onset (OR = 1.29, p = 0.026), exposure to higher lifetime number of antipsychotics (IRR = 1.20, p < 0.001) and any psychotropics (IRR = 1.13, p < 0.001). Fall/winter depression was associated with a higher lifetime number of antidepressants (IRR = 1.18, p = 0.021), any psychotropics (IRR = 1.14, p = 0.013), worse response to lithium (β = −0.82, p = 0.029) and all mood stabilizers (β = −0.69, p = 0.014). Spring/summer (hypo)mania showed negative associations with rapid cycling (OR = 0.36, p < 0.001) and lifetime number of antidepressants (IRR = 0.70, p = 0.013). Equinoctial seasonality was linked to a history of psychosis (OR = 1.76, p = 0.004). Conclusion: Seasonality in BD is associated with distinct clinical features and treatment-related outcomes. Specific seasonality patterns, particularly fall/winter depression, may reflect a more complex and difficult-to-treat illness course. These findings highlight the need for research to better characterize seasonality subtypes beyond a binary “seasonal” vs. “non-seasonal” classification and to explore how these patterns influence the illness course and management of BD.

Original languageEnglish
JournalActa Psychiatrica Scandinavica
DOIs
StateAccepted/In press - 2025

Bibliographical note

Publisher Copyright:
© 2025 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Keywords

  • bipolar disorder
  • lithium
  • mood stabilizers
  • seasonal depression
  • seasonal mania
  • seasonality
  • treatment response

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