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Year : 2013  |  Volume : 22  |  Issue : 2  |  Page : 149-152  Table of Contents     

An open-label trial of memantine in treatment-resistant obsessive-compulsive disorder

1 Department of Psychiatry, Ranchi Institute of Neuropsychiatry and Allied Sciences, Kanke, Ranchi, Jharkhand, India
2 Ranchi Institute of Neuropsychiatry and Allied Sciences, Kanke, Ranchi, Jharkhand, India
3 Institute of Psychiatry, Kolkata, West Bengal, India
4 Department of Psychiatry, Pravara Institute of Medical Sciences (Deemed University), Rural Medical College, Loni, Maharashtra, India

Date of Web Publication21-May-2014

Correspondence Address:
Suprakash Chaudhury
Department of Psychiatry, Pravara Institute of Medical Sciences (Deemed University), Rural Medical College, Loni - 413 736, Maharashtra
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0972-6748.132930

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Background: Obsessive-compulsive disorder (OCD) is often refractory to treatment. Glutamatergic neurotransmission modulating agents like memantine, an N-methyl-D-aspartate receptor open channel blocker (antagonist), has been reported to be beneficial in OCD. Materials and Methods: Twelve subjects of OCD who had been on various medications for over 5 years, but were poor responders, were enrolled for a 12-week open-label trial with fixed dose trial of memantine as an augmenting agent. The OCD symptoms and adverse effects of the drug were monitored. Results: Out of 12 subjects, eight had clear benefit, with reduction of 25% or more on Yale-Brown Obsessive-Compulsive Scale, and there were no side-effects with the medication, Conclusion: Memantine may be beneficial for treatment-resistant OCD as an augmenting agent.

Keywords: Glutamatergic modulation, memantine, obsessive compulsive disorder

How to cite this article:
Bakhla AK, Verma V, Soren S, Sarkhel S, Chaudhury S. An open-label trial of memantine in treatment-resistant obsessive-compulsive disorder. Ind Psychiatry J 2013;22:149-52

How to cite this URL:
Bakhla AK, Verma V, Soren S, Sarkhel S, Chaudhury S. An open-label trial of memantine in treatment-resistant obsessive-compulsive disorder. Ind Psychiatry J [serial online] 2013 [cited 2022 Aug 20];22:149-52. Available from: https://www.industrialpsychiatry.org/text.asp?2013/22/2/149/132930

Recent literature strongly implicate disrupted neurotransmission of glutamate within the cortico-striato-thalamocortical circuitry in the pathogenesis of obsessive-compulsive disorder (OCD). [1],[2] Based on this, drugs modulating glutaminergic neurotransmission like Riluzole [3] - a glutamatergic neurotransmission modulating agent and memantine [4],[5],[6],[7],[8] are being used in treatment of OCD. These case reports and open-label studies have shown the beneficial effect of memantine in case of OCD even in refractory and pediatric OCD. In view of available literature, we planned this open-label trial using fixed dose memantine in few OCD patients as augmenting agent, who were not responding to standard routine pharmacotherapy.

   Materials and methods Top

The study was conducted at Ranchi Institute of Neuropsychiatry and Allied Sciences, Ranchi. The Institutional Review Board of the institute approved the protocol. The sample consisted of a total of 13 patients, who gave informed consent for participation in the study. All subjects had at least moderately severe symptoms of OCD with Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) [9] scores above 25. There was persistence of symptoms for at least 5 years, despite having been put on at least two adequate trials (both in terms of dose and duration) of different Serotonin Reuptake Inhibitors or anti-obsessional medications with or without augmentation by any antipsychotic medications or exposure and response prevention therapy. The exclusion criteria were presence of any medical or psychiatric co-morbid conditions. Memantine was started at 5 mg/day, hiked up to 10 mg/day at the end of 4 weeks and this dose was kept constant throughout the study period [Table 1]. The subjects continued previously prescribed medications throughout the study period, but did not initiate new medications, nor did they engage in any new psychotherapy. The severity of OCD was assessed with Y-BOCS at baseline and after that every week until completion of 12 weeks of memantine use. Subjects were also assessed weekly for adverse effects with the Udvalg for Kliniske Undersøgelser (UKU) side-effect rating scale. Memantine was continued after the end of the 12 weeks if desired by subjects.
Table 1: Demographic characteristics Y‑BOCS scores of treatment resistant obsessive‑compulsive disorder patients

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Data were analyzed using SPSS version 16.0. Normality of distribution of the data was assessed using Shapiro Wilk test, which revealed that the data were normally distributed. Descriptive statistics was used for socio-demographic and clinical variables. Independent samples t-test was used to compare treatment responders with non-responders across various socio-demographic and clinical variables. Wilcoxon signed-rank test was used to compare the Y-BOCS scores at baseline and 12 weeks after treatment.

   Results Top

One patient was dropped from the study for stopping her medications in between; rest 12 patients participated in the augmentation for 12 weeks. Mean age of the sample was 30.33 years (SD = 6.84) and the mean duration of illness was 94.5 months (SD = 22.17). Response was defined as 25% or more reduction in Y-BOCS scores within 12 weeks. There were eight responders and four non-responders. Among responders, mean baseline Y-BOCS score was 29.25 (SD = 3.37), which reduced to a mean of 16.37(SD = 3.07) at the end of 12 weeks, i.e., 44% improvement from baseline. When the responder group was compared with the non-responder group in terms of age, duration of illness and baseline Y-BOCS scores, no significant difference was found between the two groups (P>0.05).

Wilcoxon signed-rank test revealed a significant difference in Y-BOCS total scores between baseline and week 12 (P<0.002). Similarly, the mean Y-BOCS obsession and Y-BOCS compulsion scores at baseline and at week 12, are showed a significant difference (P<0.003 and 0.002) [Table 2]. There were no significant side-effects reported for the study period as measured with UKU side-effects rating scale.
Table 2: Characteristics of non‑responders and responders to memantine augmentation and change
in Y‑BOCS ratings at 12 weeks compared to baseline

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   Discussion Top

The response to currently available treatments in OCD is about 40% to 60% in terms of reduction in Y-BOCS scores, [10] which remains a major concern for clinicians and morbidity for patients in our day-to-day clinical practice. Based on earlier reports about the mechanism and improvement reported by memantine, we carried out this open-label trial. This study, though of small sample size, supported the role of NMDA receptor and Glutamate in OCD and showed significant improvement with memantine. This is in accordance with a few previous studies. [4],[5],[6],[7],[8] We found good result in eight patients with mean Y-BOCS reduction of 44% in good responders as compared to 14% in non- responders and for the total sample, it was 37.4% improvement. This is in accordance to previously reported rates of 40.6% [6] and 27%. [5] Although the duration of 12 weeks was the same as of our study, previous studies used higher dose (20 mg/day) of memantine in comparison to 10 mg/day in our study [Table 3]. This may be attributable to specific profile of Indian population, and we also plan a higher dose up to 20 mg/day in non-responders of this study. There was no significant side-effect found in this study, which may again be attributed to a lower dose selection. Thus, if equal efficacy can be established in further studies with a lower dose of memantine, it would help in reducing the potential for adverse effects in the patient population.
Table 3: Comparison with earlier studies using memantine as augmenting agent in treatment‑resistant obsessive‑compulsive disorder patients

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One of the patients stopped all her previous medications on her own and continued with memantine alone, and she found good response at 5 th week, but her obsessive compulsive (OC) symptoms reappeared by 9 th week, we dropped this case from the final analysis. Almost all of the patients were satisfied with the inclusion of memantine and were willing to continue with it beyond the study period.

Future studies should involve randomized controlled trials for more definitive evidence of the efficacy of memantine as an adjunctive treatment in resistant OCD as well as looking for clinical predictors for response with adequate sample size.

   Conclusion Top

Memantine augmentation was beneficial in resistant OCD and was well-tolerated in this open-label trial.

   References Top

1.Wu K, Hanna GL, Rosenberg DR, Arnold PD. The role of glutamate signaling in the pathogenesis and treatment of obsessive-compulsive disorder. Pharmacol Biochem Behav 2012;100:726-35.  Back to cited text no. 1
2.Pittenger C, Krystal JH, Coric V. Glutamate-modulating drugs as novel pharmacotherapeutic agents in the treatment of obsessive-compulsive disorder. NeuroRx 2006;3:69-81.  Back to cited text no. 2
3.Coric V, Taskiran S, Pittenger C, Wasylink S, Mathalon DH, Valentine G, et al. Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: An open-label trial. Biol Psychiatry 2005;58:424-8.  Back to cited text no. 3
4.Pasquini M, Biondi M. Memantine augmentation for refractory obsessive-compulsive disorder. Prog Neuropsychopharmacol Biol Psychiatry 2006;30:1173-5.  Back to cited text no. 4
5.Stewart SE, Jenike EA, Hezel DM, Stack DE, Dodman NH, Shuster L, et al. A single-blinded case-control study of memantine in severe obsessive-compulsive disorder. J Clin Psychopharmacol 2010;30:34-9.  Back to cited text no. 5
6.Feusner JD, Kerwin L, Saxena S, Bystritsky A. Differential efficacy of memantine for obsessive-compulsive disorder vs. generalized anxiety disorder: An open-label trial. Psychopharmacol Bull 2009;42:81-93.  Back to cited text no. 6
7.Aboujaoude E, Barry JJ, Gamel N. Memantine augmentation in treatment-resistant obsessive-compulsive disorder: An open-label trial. J Clin Psychopharmacol 2009;29:51-5.  Back to cited text no. 7
8.Poyurovsky M, Weizman R, Weizman A, Koran L. Memantine for treatment-resistant OCD. Am J Psychiatry 2005;162:2191-2.  Back to cited text no. 8
9.Kim SW, Dysken MW, Pheley AM, Hoover KM. The Yale-Brown Obsessive-Compulsive Scale: Measures of internal consistency. Psychiatry Res 1994;51:203-11.  Back to cited text no. 9
10.Goodman WK, Ward HE, Kablinger AS, Murphy TK. Biological approaches to treatment-resistant obsessive-compulsive disorder. In: Goodman WK, Rudorfer MV, Maser JD, editors. Obsessive-Compulsive Disorder: Contemporary Issues in Management. London, UK: Lawrence Erlbaum Associates; 2000. p. 333-69.  Back to cited text no. 10


  [Table 1], [Table 2], [Table 3]

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