TY - JOUR
T1 - Sleep disturbance may impact treatment outcome in bipolar disorder
T2 - A preliminary investigation in the context of a large comparative effectiveness trial
AU - Sylvia, Louisa G.
AU - Chang, Weilynn C.
AU - Kamali, Masoud
AU - Tohen, Mauricio
AU - Kinrys, Gustavo
AU - Deckersbach, Thilo
AU - Calabrese, Joseph R.
AU - Thase, Michael E.
AU - Reilly-Harrington, Noreen
AU - Bobo, William V.
AU - Kocsis, James H.
AU - McInnis, Melvin G.
AU - Bowden, Charles L.
AU - Ketter, Terence A.
AU - Friedman, Edward S.
AU - Shelton, Richard C.
AU - McElroy, Susan L.
AU - Gao, Keming
AU - Rabideau, Dustin J.
AU - Nierenberg, Andrew A.
N1 - Funding Information:
Funding: This work was supported by the Agency for Healthcare Research and Quality [grant number 1 R01 HS019371-01 ]. We have no other acknowledgements.
Funding Information:
Funding: This work was supported by the Agency for Healthcare Research and Quality [grant number 1 R01 HS019371-01]. We have no other acknowledgements.
Publisher Copyright:
© 2017 Elsevier B.V.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Background Bipolar patients experience sleep disturbances during and between mood episodes. Yet the impact of sleep on treatment with different medications has not been fully explored. The purpose of this paper is to explore the potential impact of poor sleep at baseline on outcomes in a randomized effectiveness trial of quetiapine and lithium. Methods The Bipolar CHOICE study was a 6-month, parallel group, multisite randomized controlled trial. Participants with bipolar disorder (N = 482; 59% female and age 18–70 years) received quetiapine or lithium. Patients were allowed to also receive adjunctive personalized treatments, which were guideline-informed, empirically-based medications added to treatment as needed. Medication changes were recorded as necessary clinical adjustments (NCA). Fisher's exact tests, mixed-regression models, and Mann-Whitney U tests were used to assess demographic and clinical characteristics as well as whether sleep disturbance would predict outcomes. Results 63% of patients had baseline sleep disturbance. Individuals with sleep disturbance had worse bipolar illness severity, greater severity of depression, mania, anxiety, irritability, and psychosis, were less likely to have sustained response (17% vs. 29%; adjusted RR: 0.55, 95% CI: 0.38–0.78, p = 0.0006) and had more NCAs (median 0.71 vs. 0.59, p = 0.03). Limitations Our findings were limited by how we defined sleep disturbance, and by how severity of sleep disturbance was assessed with one item with a non-sleep specific measure. Conclusions Baseline sleep disturbance was associated with more severe bipolar symptoms and worse 6-month outcomes. Further research is warranted on improving sleep in bipolar disorder, especially the role of psychosocial interventions.
AB - Background Bipolar patients experience sleep disturbances during and between mood episodes. Yet the impact of sleep on treatment with different medications has not been fully explored. The purpose of this paper is to explore the potential impact of poor sleep at baseline on outcomes in a randomized effectiveness trial of quetiapine and lithium. Methods The Bipolar CHOICE study was a 6-month, parallel group, multisite randomized controlled trial. Participants with bipolar disorder (N = 482; 59% female and age 18–70 years) received quetiapine or lithium. Patients were allowed to also receive adjunctive personalized treatments, which were guideline-informed, empirically-based medications added to treatment as needed. Medication changes were recorded as necessary clinical adjustments (NCA). Fisher's exact tests, mixed-regression models, and Mann-Whitney U tests were used to assess demographic and clinical characteristics as well as whether sleep disturbance would predict outcomes. Results 63% of patients had baseline sleep disturbance. Individuals with sleep disturbance had worse bipolar illness severity, greater severity of depression, mania, anxiety, irritability, and psychosis, were less likely to have sustained response (17% vs. 29%; adjusted RR: 0.55, 95% CI: 0.38–0.78, p = 0.0006) and had more NCAs (median 0.71 vs. 0.59, p = 0.03). Limitations Our findings were limited by how we defined sleep disturbance, and by how severity of sleep disturbance was assessed with one item with a non-sleep specific measure. Conclusions Baseline sleep disturbance was associated with more severe bipolar symptoms and worse 6-month outcomes. Further research is warranted on improving sleep in bipolar disorder, especially the role of psychosocial interventions.
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U2 - 10.1016/j.jad.2017.08.056
DO - 10.1016/j.jad.2017.08.056
M3 - Article
C2 - 28881294
AN - SCOPUS:85028713880
SN - 0165-0327
VL - 225
SP - 563
EP - 568
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -