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Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder.

Publication ,  Journal Article
Madhoo, M; Keefe, RSE; Roth, RM; Sambunaris, A; Wu, J; Trivedi, MH; Anderson, CS; Lasser, R
Published in: Neuropsychopharmacology
May 2014

Evaluate lisdexamfetamine dimesylate (LDX) augmentation of antidepressant monotherapy for executive dysfunction in partially or fully remitted major depressive disorder (MDD). This randomized, placebo-controlled study (NCT00985725) enrolled 143 adults (18-55 years) with mild MDD (Montgomery-Åsberg Depression Rating Scale (MADRS) score ≤ 18) and executive dysfunction (Behavior Rating Inventory of Executive Function-Adult Version (BRIEF-A) Self-Report Global Executive Composite (GEC) T score ≥ 60) on stable antidepressant monotherapy for ≥ 8 weeks. After 2 weeks of screening, participants were randomized to 9 weeks of double-blind LDX (20-70 mg/day) or placebo augmentation, followed by 2 weeks of single-blind placebo. The primary end point was change from baseline to week 9/end of study (EOS) in BRIEF-A Self-Report GEC T score; secondary assessments included the BRIEF-A Informant Report, MADRS, and treatment-emergent adverse events (TEAEs). Of 143 randomized participants, 119 completed double-blind treatment (placebo, n=59; LDX, n=60). Mean ± standard deviation (SD) BRIEF-A GEC T scores decreased from baseline (placebo, 74.2 ± 8.88; LDX, 76.8 ± 9.66) to week 9/EOS (placebo, 61.4 ± 14.61; LDX, 55.2 ± 16.15); the LS mean (95% CI) treatment difference significantly favored LDX (-8.0 (-12.7, -3.3); P=0.0009). The LS mean (95% CI) treatment difference for MADRS total score also significantly favored LDX (-1.9 (-3.7, 0.0); P=0.0465). TEAE rates were 73.6% with placebo and 78.9% with LDX; serious TEAE rates were 4.2 and 2.8%. In this trial, LDX augmentation significantly improved executive dysfunction and depressive symptoms in participants with mild MDD. The safety profile of LDX was consistent with prior studies in adults with attention-deficit/hyperactivity disorder.

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Published In

Neuropsychopharmacology

DOI

EISSN

1740-634X

Publication Date

May 2014

Volume

39

Issue

6

Start / End Page

1388 / 1398

Location

England

Related Subject Headings

  • Treatment Outcome
  • Single-Blind Method
  • Remission Induction
  • Psychotropic Drugs
  • Psychiatry
  • Psychiatric Status Rating Scales
  • Male
  • Lisdexamfetamine Dimesylate
  • Humans
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
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Madhoo, M., Keefe, R. S. E., Roth, R. M., Sambunaris, A., Wu, J., Trivedi, M. H., … Lasser, R. (2014). Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder. Neuropsychopharmacology, 39(6), 1388–1398. https://doi.org/10.1038/npp.2013.334
Madhoo, Manisha, Richard S. E. Keefe, Robert M. Roth, Angelo Sambunaris, James Wu, Madhukar H. Trivedi, Colleen S. Anderson, and Robert Lasser. “Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder.Neuropsychopharmacology 39, no. 6 (May 2014): 1388–98. https://doi.org/10.1038/npp.2013.334.
Madhoo M, Keefe RSE, Roth RM, Sambunaris A, Wu J, Trivedi MH, et al. Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder. Neuropsychopharmacology. 2014 May;39(6):1388–98.
Madhoo, Manisha, et al. “Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder.Neuropsychopharmacology, vol. 39, no. 6, May 2014, pp. 1388–98. Pubmed, doi:10.1038/npp.2013.334.
Madhoo M, Keefe RSE, Roth RM, Sambunaris A, Wu J, Trivedi MH, Anderson CS, Lasser R. Lisdexamfetamine dimesylate augmentation in adults with persistent executive dysfunction after partial or full remission of major depressive disorder. Neuropsychopharmacology. 2014 May;39(6):1388–1398.

Published In

Neuropsychopharmacology

DOI

EISSN

1740-634X

Publication Date

May 2014

Volume

39

Issue

6

Start / End Page

1388 / 1398

Location

England

Related Subject Headings

  • Treatment Outcome
  • Single-Blind Method
  • Remission Induction
  • Psychotropic Drugs
  • Psychiatry
  • Psychiatric Status Rating Scales
  • Male
  • Lisdexamfetamine Dimesylate
  • Humans
  • Female