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Early antidepressant effect of memantine during augmentation of lamotrigine inadequate response in bipolar depression: a double‐blind, randomized, placebo‐controlled trial
Author(s) -
Anand Amit,
Gunn Abigail D,
Barkay Gavriel,
Karne Harish S,
Nurnberger John I,
Mathew Sanjay J,
Ghosh Samiran
Publication year - 2012
Publication title -
bipolar disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.285
H-Index - 129
eISSN - 1399-5618
pISSN - 1398-5647
DOI - 10.1111/j.1399-5618.2011.00971.x
Subject(s) - lamotrigine , memantine , antidepressant , depression (economics) , bipolar disorder , medicine , placebo , randomized controlled trial , psychiatry , psychology , pharmacology , anesthesia , lithium (medication) , nmda receptor , epilepsy , receptor , alternative medicine , pathology , anxiety , economics , macroeconomics
Anand A, Gunn AD, Barkay G, Karne HS, Nurnberger JI, Mathew SJ, Ghosh S. Early antidepressant effect of memantine during augmentation of lamotrigine inadequate response in bipolar depression: a double‐blind, randomized, placebo‐controlled trial.
Bipolar Disord 2012: 14: 64–70. © 2012 The Authors.
Journal compilation © 2012 John Wiley & Sons A/S. Background: Recent studies indicate that modulation of glutamate neurotransmission is associated with antidepressant response. Lamotrigine, an anticonvulsant which decreases presynaptic glutamate release, has been shown to be effective in the depressive phase of bipolar disorder (BD‐D); however, only 40–50% of patients have a full response. This pilot study investigated whether memantine, a low‐affinity N‐methyl‐D‐aspartate (NMDA) receptor antagonist approved for Alzheimer’s disease, can augment the effects of lamotrigine. Methods: BD‐D outpatients in a major depressive episode on a stable dose of lamotrigine (100 mg or more) were randomized to either memantine (starting dose of 5 mg increased up to 20 mg over four weeks, then 20 mg stable dose from four to eight weeks) or matching pill placebo for eight weeks. Patients were rated on the 17‐item Hamilton Depression Rating Scale (HDRS) and other behavioral measures weekly. Results: The eight‐week repeated‐measures mixed‐effect model for HDRS was not significant for memantine (n = 14) versus placebo (n = 15). Exploratory mixed‐effect analyses for the first four weeks, while the memantine dose was being titrated up every week, revealed a significant decrease in HDRS scores from baseline (p = 0.007). Conclusion: This proof‐of‐concept study failed to show a statistically significant benefit of memantine augmentation of lamotrigine for patients with BD‐D over eight weeks. However, memantine had an antidepressant effect early on in the treatment while its dose was being titrated up. Larger placebo‐controlled studies are needed to ascertain optimal timing and dosing for memantine augmentation of lamotrigine in BD‐D.