4.6 Article

Clinical predictors of recurrences in bipolar disorders type 1 and 2: A FACE-BD longitudinal study

Journal

JOURNAL OF PSYCHIATRIC RESEARCH
Volume 134, Issue -, Pages 129-137

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpsychires.2020.12.041

Keywords

Bipolar disorder; Subtype; Recurrence; Prediction; Longitudinal study

Categories

Funding

  1. Foundation FondaMental, Institut National de la Sante et de la Recherche Medicale (INSERM), AP-HP
  2. Investissements d'Avenir program
  3. ANR [ANR-11-IDEX-0004-02, ANR-10-COHO-10-01]

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The study found that the time to first recurrence of any polarity was earlier in BD-II compared to BD-I, with first depressive recurrence occurring earlier in BD-II and first (hypo)manic recurrence occurring earlier in BD-I. In clinical terms, predictors of the time to a first mood recurrence in BD-I were associated with depressive symptoms, lifetime rapid cycling, global activation, and the number of psychotropic medications at baseline, while in BD-II, predictors were associated with a younger age at onset of BD and a higher number of lifetime mood episodes.
Objective: To examine which characteristics predict the time to a first mood recurrence at three years in Bipolar Disorder type I (BD-I) and type II (BD-II). Methods: Individuals with BD were followed up to 3 years. Turbull's extension of the Kaplan-Meier analysis for interval-censored data was used to estimate the cumulative probability of recurrence over time. Separate models were performed according to BD subtype to determine which baseline factors were predictive of recurrences and were adjusted for age, gender and educational level. Results: We included 630 individuals with BD-I and 505 with BD-II. The first recurrence of any polarity occurred earlier in BD-II (p = 0.03). The first depressive recurrence occurred earlier in BD-II (p < 0.0001), whereas the first (hypo)manic recurrence occurred earlier in BD-I (p = 0.0003). In BD-I, the clinical variables that were associated to the time to a first mood recurrence were depressive symptoms, lifetime rapid cycling, global activation and the number of psychotropic medications at baseline. In BD-II, the time to a first recurrence was associated with a younger age at onset of BD and a higher number of lifetime mood episodes. The Areas Under the Curve for both models were moderate. Conclusion: Predictors of recurrences showed few specificities to BD-I or BD-II. The ability to predict recurrences in BD based on socio-demographic and clinical variables remained too moderate for a transfer in daily practice. This study highlights the need for further studies that would include other types of predictors, such as molecular, cognitive or neuro-imaging ones, to achieve an accurate level of prediction of recurrences in BD.

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