PMID- 20483885 OWN - NLM STAT- MEDLINE DCOM- 20100922 LR - 20211020 IS - 1477-0970 (Electronic) IS - 1352-4585 (Linking) VI - 16 IP - 6 DP - 2010 Jun TI - Memantine for cognitive impairment in multiple sclerosis: a randomized placebo-controlled trial. PG - 715-23 LID - 10.1177/1352458510367662 [doi] AB - BACKGROUND: Memantine, an NMDA antagonist, is effective for moderate to severe Alzheimer's disease. OBJECTIVE: Determine whether memantine improves cognitive performance (CP) among subjects with multiple sclerosis (MS) and cognitive impairment (CI). METHODS: This double-blind, randomized, placebo-controlled trial (Clinicaltrials.gov NCT00300716) compared memantine 10 mg twice a day (4 week titration followed by 12 weeks on the highest tolerated dose) with placebo. The primary outcome was the change from baseline to exit on the Paced Auditory Serial Addition Test (PASAT) and the California Verbal Learning Test-II (CVLT-II) Long Delay Free Recall (LDFR). Secondary outcomes included additional neuropsychological tests; self-report measures of quality of life, fatigue, and depression; and family/caregiver reports of subjects' CI and neuropsychiatric symptoms. RESULTS: The differences between the groups on the change on the PASAT (placebo-memantine = 0.0 correct responses, 95% CI 3.4, 3.4; p = 0.9) and on CVLT-II LDFR (placebo-memantine =-0.6 words, 95% CI -2.1, 0.8; p = 0.4) as well as on the other cognitive tests were not significant. Subjects on memantine had no serious adverse events (AEs) but had more fatigue and neurological AEs as well as, per family members' reports, less cognitive improvement and greater neuropsychiatric symptoms than subjects on placebo. CONCLUSION: Memantine 10 mg twice a day does not improve CP in subjects with MS, ages 18-65, without major depression, who have subjective cognitive complaints and perform worse than one SD below the mean on the PASAT or on the California Verbal Learning Test-II (total recall or delayed free recall). FAU - Lovera, J F AU - Lovera JF AD - Neurology, Louisiana State University Health Sciences Center, New Orleans, LA 70003, USA. jlover@lsuhsc.edu FAU - Frohman, E AU - Frohman E FAU - Brown, T R AU - Brown TR FAU - Bandari, D AU - Bandari D FAU - Nguyen, L AU - Nguyen L FAU - Yadav, V AU - Yadav V FAU - Stuve, O AU - Stuve O FAU - Karman, J AU - Karman J FAU - Bogardus, K AU - Bogardus K FAU - Heimburger, G AU - Heimburger G FAU - Cua, L AU - Cua L FAU - Remingon, G AU - Remingon G FAU - Fowler, J AU - Fowler J FAU - Monahan, T AU - Monahan T FAU - Kilcup, S AU - Kilcup S FAU - Courtney, Y AU - Courtney Y FAU - McAleenan, J AU - McAleenan J FAU - Butler, K AU - Butler K FAU - Wild, K AU - Wild K FAU - Whitham, R AU - Whitham R FAU - Bourdette, D AU - Bourdette D LA - eng SI - ClinicalTrials.gov/NCT00300716 GR - K23 AT004433/AT/NCCIH NIH HHS/United States PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20100518 PL - England TA - Mult Scler JT - Multiple sclerosis (Houndmills, Basingstoke, England) JID - 9509185 RN - W8O17SJF3T (Memantine) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Cognition Disorders/complications/*drug therapy/psychology MH - Depression/psychology MH - Double-Blind Method MH - Fatigue/psychology MH - Female MH - Humans MH - Male MH - Memantine/*therapeutic use MH - Middle Aged MH - Multiple Sclerosis/*complications/psychology MH - Neuropsychological Tests MH - Patient Selection MH - Quality of Life/psychology MH - Surveys and Questionnaires MH - Treatment Outcome EDAT- 2010/05/21 06:00 MHDA- 2010/09/24 06:00 CRDT- 2010/05/21 06:00 PHST- 2010/05/21 06:00 [entrez] PHST- 2010/05/21 06:00 [pubmed] PHST- 2010/09/24 06:00 [medline] AID - 1352458510367662 [pii] AID - 10.1177/1352458510367662 [doi] PST - ppublish SO - Mult Scler. 2010 Jun;16(6):715-23. doi: 10.1177/1352458510367662. Epub 2010 May 18.