Modafinil's effects on cognition and sleep quality in affectively-stable patients with bipolar disorder: a pilot study

被引:2
作者
Lipschitz, Jessica M. [1 ,2 ]
Perez-Rodriguez, Mercedes [3 ]
Majd, Marzieh [1 ,2 ]
Larsen, Emmett [4 ]
Locascio, Joseph [5 ,6 ,7 ]
Pike, Chelsea K. [1 ]
Shanahan, Megan [1 ]
Burdick, Katherine E. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Dept Psychiat, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Psychiat, Boston, MA 02115 USA
[3] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY USA
[4] SUNY Stony Brook, Dept Psychol, Stony Brook, NY USA
[5] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[6] Harvard Med Sch, Dept Neurol, Boston, MA USA
[7] Harvard Med Sch, Harvard Catalyst Biostat Grp, Boston, MA USA
关键词
bipolar disorder; modafinil; cognitive functioning; sleep; daytime sleepiness; RATING-SCALE; DOUBLE-BLIND; DEPRESSION; RELIABILITY; IMPAIRMENT; SYMPTOMS; BATTERY; MEMORY; MANIA; TRIAL;
D O I
10.3389/fpsyt.2023.1246149
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
IntroductionDespite advances in the treatment of bipolar disorder (BD), most patients do not achieve complete inter-episode recovery and functional disability is common. During periods of relative remission, many patients continue to experience neurocognitive dysfunction, reduced daytime activity levels, and sleep disturbances. This 8-week, randomized, placebo-controlled pilot study evaluated the feasibility, safety and preliminary efficacy of the wake-promoting drug, modafinil (Provigil & REG;), on neurocognitive functioning, daytime sleepiness, and sleep quality in affectively-stable BD patients.MethodsTwelve individuals with affectively-stable BD were recruited and randomized to a flexible dose of modafinil (100 to 200 mg/day) or placebo, adjunctive to a therapeutic dose of a mood stabilizer. Weekly in-person visits tracked sleep quality and daytime sleepiness as well as side effects and mood symptoms. Neurocognitive functioning was assessed at baseline, week 4, and week 8.ResultsNo serious adverse events were reported. Newly emergent side effects in the modafinil group included heart palpitations, itching, fatigue, and decreased energy. Two patients discontinued modafinil owing to side effects and one of these patients withdrew from the study. One patient discontinued placebo and was withdrawn from the study. Preliminary evaluations of clinical efficacy showed a marginally significant interaction between treatment group and time in two cognitive domains (speed of processing and verbal learning), indicating greater improvement in the modafinil group versus placebo. Additionally, there was a marginally significant effect of treatment group on daytime sleepiness, suggesting lower daytime sleepiness in the modafinil group versus placebo. Counterintuitively, we found a significant treatment group by time interaction effect on sleep quality, suggesting greater improvement in sleep quality in the placebo group versus the modafinil group.DiscussionResults suggest that modafinil is a relatively safe medication for affectively-stable BD patients when given with adjunctive mood stabilizers. Results are suggestive of cognitive benefit and improved daytime sleepiness, but worse sleep quality in those patients prescribed modafinil. A fully powered clinical trial is warranted with specific attention to the characteristics of patients who are most likely to benefit from treatment with modafinil and other methodological lessons learned from this pilot.Clinical trial registrationClinicalTrials.gov, identifier NCT01965925.
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页数:10
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