Mood Stabilizers of  First and Second Generation: History
View Latest Version
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor:
Janusz K. Rybakowski

Mood stabilizers can be classified into two generations based on the chronology of their introduction into the psychiatric armamentarium. First-generation mood stabilizers (FGMS) such as lithium, valproates and carbamazepine were introduced in the years 1960-1970s. Second-generation mood stabilizers (SGMS) started in 1995, with a discovery of the mood-stabilizing properties of clozapine. The SGMS include atypical antipsychotics such as clozapine, olanzapine, quetiapine, aripiprazole, and risperidone as well as a new anticonvulsant drug, lamotrigine. Recently as a candidate for SGMS, a novel antipsychotic, lurasidone, has been suggested. Several other atypical antipsychotics and anticonvulsants, as well as memantine showed some usefulness in the treatment and prophylaxis of bipolar disorder; however, they have not fully met the author’s criteria for mood stabilizers. 

  • mood stabilizer
  • bipolar disorder
  • first generation
  • second generation
  • mania
  • depression
  • prophylaxis

1. Introduction

Author proposes a definition that considers a role of a drug in the acute and long-term treatment of the bipolar disorder. The first aspect of such a definition contains a therapeutic effect on manic and/or depressive symptoms during an acute episode. The second aspect, which seems the most essential, requires the prevention of manic and/or depressive recurrences during long-term administration when a drug is given as monotherapy and a trial is performed for at least one year. The third important aspect is that the drug should not induce or worsen manic or depressive episodes or mixed states. Such criterion is therefore not met by typical antipsychotic medications which may cause depression and by antidepressants that can induce mania [1].

Having such a definition in mind, author suggested in 2007 a classification of mood stabilizers based on the chronology of their introduction into the psychiatric armamentarium [2]. The first generation of mood stabilizers (FGMS) such as lithium, valproates, and carbamazepine came in the 1960s and 1970s. It was not until 1995 that the mood-stabilizing property of clozapine was discovered [3] which started the second generation of mood stabilizers (SGMS). 

2. First Generation of Mood Stabilizers

2.1. Lithium

This year, researchers

observe sixty’s anniversary of the article, demonstrating, for the first time, the possibility of preventing recurrences in mood disorders by using lithium salts. The author of the paper was a British psychiatrist, Geoffrey Philip Hartigan (1917-1968), known as „Toby”, working in St. Augustine’s Hospital in Chartham Down [4]. Among 45 patients receiving lithium carbonate in this institution during the last six years, he presented his observations on long-term lithium administration (≥ three years) in seven patients with bipolar mood disorders (BD) and eight patients with recurrent depression. It transpired that there were no recurrences of the illness in six persons from the first group and six from the second group. This publication appeared 14 years after the article of an Australian psychiatrist, John Cade, showing the therapeutic effect of lithium in manic states [5]. The following year after Hartigan’s paper, a Danish psychiatrist, Poul Christian Baastrup, established the „prophylactic” effect of lithium in 11 BD patients receiving the drug for three years [6].

The pioneering idea of Hartigan was to point out the possibility of the favorable effect of lithium administration on the long-term course of mood disorders, both BD and recurrent depression. He referred to the terms „normothymotics” and „mood-normalizers” proposed by a Danish psychiatrist, Mogens Schou, in the article published in the same issue of the British Journal of Psychiatry, which included Hartigan’s paper. The names were suggested for lithium and imipramine, as the drugs normalizing moods, in BD and periodic depression, respectively [7]. Hartigan demonstarted the preventive action against manic and depressive recurrences what justified naming lithium a drug normalizing (stabilizing) mood. For such drugs, the name „mood stabilizers” became increasingly used and has been established nowadays. Whereas, in Polish and Russian psychiatric literature, the term „normothymic drugs” has been employed.

In 1967, a paper by Danish psychiatrists already mentioned (Poul Baastrup and Mogens Schou) appeared, summarizing the experiences of 88 patients treated in Glostrup psychiatric hospital with bipolar and unipolar mood disorders, receiving lithium for an average of six years. The authors compared the periods of disturbed mood (mania or depression) per year. The results showed that the mean duration of disturbed mood during lithium administration was more than six-fold shorter than in the period before lithium. This indicated a high probability of a favorable prophylactic effect of lithium on the course of mood disorders [8]. However, in the next year, a highly critical article against the Danish research showing a possibility of lithium prophylaxis appeared. It was published in the prestigious journal „Lancet”, authored by the British psychiatrists Barry Blackwell and Michael Shepherd, and titled: „Prophylactic lithium: another therapeutic myth?” The authors voiced strong doubts about the results of Danish researchers and postulated performing double-blind studies to verify the issue [9]. As it were in response to the recommendation of the Britons, in 1970-1973, the results of eight placebo-controlled studies carried out in Europe (Denmark and UK) and the USA, assessing the prophylactic efficacy of lithium were published. The patients participating in the trials had at least two episodes of the illness in the last two years. In the majority of studies, the comparison was made between patients in which a placebo replaced lithium and those continuing lithium (so-called “discontinuation design”). The recurrence of the illness was defined as a condition requiring psychiatric hospitalization or antidepressant/antimanic treatment. The overall analysis revealed that the percentage of patients with recurrences of depression or mania was significantly lower during lithium administration (mean 30%) than during placebo (average 70%) [10].

Lithium has become an established mood stabilizer in subsequent years, and its use has significantly increased. In the meantime, the antidepressant effect of lithium in acute depressive episodes [11][12], and augmentation of antidepressants by lithium [13] were noted. In 1999, making half a century following lithium’s introduction into contemporary psychiatry [5] and 36 years after Hartigan's article [4], a Canadian psychiatrist of Czechoslovakian origin, Paul Grof, presented a concept of „excellent lithium responders” (ELR) as a BD patients, in whom lithium monotherapy results in total elimination of the illness' recurrences [14]. At Poznań center, the assessment of the percentage of ELR was performed, showing that about one-third of BD patients were free of recurrences during ten years of lithium administration [15]. Several clinical factors have been indicated connected with good prophylactic efficacy of lithium, such as among others, moderate number of affective episodes with distinct periods of remission, the episode sequence mania-depression-remission, the absence of rapid cycling and psychiatric comorbidity [16].

In the 21st century, prophylactic lithium efficacy in BD was amply evidenced in three meta-analyses. They showed the superiority of lithium over placebo for preventing all kinds of recurrences, especially manic but also depressive ones [17][18][19]. In 2018, Kessing et al. [20] indicated that lithium monotherapy was prophylactically more effective in the BD population than monotherapy with any other MS. A meta-analysis performed in 2000 confirmed the therapeutic efficacy of lithium in mania [21]. Additionally, lithium augmentation of antidepressants in treatment-resistant depression became an established procedure [22] and was even suggested as the second indication for lithium in psychiatry after BD prophylaxis [16]. Therefore, lithium can meet the most demanding 2 × 2 criteria for MS, indicated by Bauer and Mischner as being therapeutically and prophylactically effective in both mania and depression [23]. Among mood-stabilizing drugs, lithium proved the most efficacious anti-suicidal agent [24]. Lithium also became a unique drug, with which ultra-long-term mood stabilization was experienced. For example, recently, in the Poznań center, researchers presented the case of a female patient receiving lithium for 50 years, with excellent results in most areas of health and social functioning [25].

2.2. Valproate

At the beginning of the 1970s, clinical observations showed that some anticonvulsant drugs may have the mood-stabilizing properties. French researchers led by Pierre Lambert, working at Bassens Hospital in Rhône-Alpe, found that valproic acid amide may exert an antimanic and prophylactic effect in BD. In patients with mood disorders, the drug produced a significant fall in manic episodes as well as a decrease in the duration of hospitalizations. They coined for such a pharmacological activity the French term „thymorégulatrice”, which can allude to such names as “mood-normalizing” or “normothymic” [26]. Intensive studies on valproates came in the USA in the 1990s, the instrumental in this respect was eminent BD specialist Charles Bowden. Valproic acid amide was not used here, but the equimolar combination of sodium valproate and valproic acid named „divalproex”. It transpired that besides the solid antimanic activity of this drug, its prophylactic effect preventing BD recurrences was demonstrated, similar to that of lithium [27]. This paved the way for the wide use of valproates as mood stabilizers in the treatment of mania and the prophylaxis of BD. However, due to the intensive promotion by pharmacological companies, at the beginning of the 21st century, the increasing use of valproate resulted, among others, in a decrease in lithium administration. Such a situation imposed the attempts to verify the real efficacy of both drugs, reflected by the project having the acronym BALANCE (Bipolar Affective disorder Lithium/ ANtiConvulsant Evaluation). This research assessed the prophylactic efficacy of divalproex monotherapy, lithium monotherapy, and the combination of both drugs for two years in 330 BD patients (110 in each group). Better prophylactic efficacy of lithium monotherapy compared with divalproex monotherapy, and the best preventive quality for the combination was found [28]. However, a recent paper did not find significant differences between valproate and lithium when used as monotherapy or combined with atypical psychotic in one-year maintenance administration [29].

2.3. Carbamazepine

Carbamazepine has appeared as another anticonvulsant with potential mood-stabilizing properties. The merit for demonstrating the mood-stabilizing action of this drug should be given to Japanese researchers led by excellent psychopharmacologist Teruo Okuma (1926-2010). In their paper of 1973, the antimanic effect of carbamazepine was observed in 52% of patients, and the prophylactic activity against manic and depressive episodes was noticed in 74% and 52% of patients, respectively [30]. In 1980-1990, the research on the therapeutic and prophylactic effects of carbamazepine in mood disorders was carried out mainly by American psychiatrists under the leadership of Robert Post. The prophylactic effect of carbamazepine in BD was confirmed [31], as well as the antimanic [32] and possible antidepressant action of the drug [33], which justified treating carbamazepine as “mood stabilizer”. The drug became popular in Europe, and in the 1990s, carbamazepine became the second medication after lithium used for the prophylaxis of mood disorders. In the late 1990s, German psychiatrists attempted to compare the prophylactic efficacy of carbamazepine and lithium within a study having the acronym MAP (Multicenter study of long-term treatment of Affective or schizoaffective Psychoses), where they assessed an efficacy during 2.5 years. They found that lithium was more efficacious in „classic” forms of BD, while carbamazepine – in atypical ones e.g., with psychiatric comorbidity or mood-incongruent delusions [34].

The introduction in the 1990s of carbamazepine derivative oxcarbazepine into psychiatric treatment, should also be mentioned. The antimanic and prophylactic efficacy of oxcarbazepine in BD was demonstrated, indicating that some pharmacokinetic and side-effect properties of this drug can be more favorable than those of carbamazepine [35].

3. Second generation of mood stabilizers

3.1. Clozapine

More than three decades passed from Hartigan’s paper when American psychiatrists observing the effects of clozapine, the drug introduced to the USA several years earlier, suggested that it can possess mood-stabilizing properties. In 1995, a paper appeared with Carlos Zarate as the first author [3], where 17 patients receiving clozapine for the treatment of mania successfully were followed up for 16 ± 6 months. Eleven of them (65%), during the administration of clozapine, had no recurrences or hospitalizations. Previously, the antimanic effect of clozapine had been widely observed. In the Poznan center, such an effect had been noted in the early 1980s [36]. A systematic review and meta-analysis performed in 2020 found the therapeutic effect of clozapine in mania equal to other antipsychotics and even better among treatment-resistant patients [37]. Employing clozapine in treatment-resistant mania was also suggested by major bipolar disorder specialists [38].

Thus, clozapine initiated the second generation of mood stabilizers (SGMSs) [2]. In 2015, Chinese authors performed a meta-analysis on long-term treatment with clozapine, where fifteen papers were covered, including more than 1000 patients. In the article, the long-term efficacy of clozapine, both therapeutic and prophylactic, was confirmed. It was shown that the drug used either as monotherapy or combined with other MSs produced a significant amelioration in mania, depression, psychosis, and rapid cycling. A substantial number of the patients significantly improved or achieved remission [39].

Therefore, clozapine can be helpful for preventing recurrences in severe and drug-resistant BD. In the recent Polish standards, the longitudinal administration of clozapine is suggested for treatment-resistant bipolar patients, providing sufficient hematological monitoring. Combination with lithium can augment its efficacy and diminish the risk of leukopenia. The predictive factor for the good prophylactic efficacy of clozapine in bipolar affective disorder is severe manic episodes with psychotic symptoms and substantial agitation [40].

3.2. Olanzapine

The next atypical antipsychotic meeting the above criteria for MS is olanzapine, which is structurally related to clozapine. Olanzapine, in doses of 10–20 mg/day, demonstrated excellent clinical efficacy and good tolerance in treating mania [41]. According to a comparative analysis, olanzapine exhibits the best profile of efficacy and tolerability among antimanic drugs [42]. In bipolar depression, olanzapine exerted a significant therapeutic effect when combined with fluoxetine. The effectiveness of composite olanzapine–fluoxetine treatment of drug-resistant depression and psychotic depression in bipolar and unipolar mood disorder has also been demonstrated [43]. Olanzapine can also serve to augment antidepressant drugs in treatment-resistant depression [44].

Olanzapine monotherapy for the prevention of recurrences in BD was compared to placebo and first-generation mood stabilizers in multiple controlled studies. The high prophylactic efficacy of olanzapine monotherapy was confirmed, mostly against manic episodes and especially in patients in whom the drug was therapeutically effective during such an acute episode [45]. When comparing olanzapine with lithium, it was found that mania recurrences were notably less frequent with olanzapine [46]. Polish recommendations suggest olanzapine monotherapy as the first-line prophylactic treatment in type I BD showing a preponderance of manic episodes [40].

3.3. Quetiapine

Quetiapine, similar to lithium, meets the stringent criteria for an MS to be therapeutically and prophylactically effective in both psychopathological poles [24][47]. In the manic state, quetiapine monotherapy is effective at 400–800 mg/day doses, and its efficacy is similar to that of lithium [48]. In placebo-controlled studies, quetiapine, at an amount of 300 or 600 mg/day, was found to be effective in treating depression in the course of bipolar affective disorder type I or type II. Such an efficacy of quetiapine was shown to be even more significant than that of lithium [49]. Quetiapine monotherapy has been proposed for treating bipolar depression in most guidance [50]. The drug can also be used for enhancing the antidepressant medications’ efficacy in both bipolar and unipolar depression resistant to treatment [44].

The antipsychotics of the second generation primarily prevent manic recurrences, whereas quetiapine monotherapy is effective in preventing both manic and depressive episodes. For depressive recurrences, the drug’s monotherapy has been equally efficacious as that of lithium [51]. A four-year comparison of the prophylactic efficacy of quetiapine in monotherapy or combination with other MSs showed that the percentage of patients without recurrences on quetiapine monotherapy was 29.3%. However, when combining quetiapine with lithium, no recurrences occurred in 80%, and with valproate, in 78.3% of patients [52]. In Polish standards, quetiapine monotherapy is among the first-line treatments for long-term therapy in bipolar disorder with a predominance of depressive episodes [40].

3.4. Aripiprazole

Aripiprazole is an atypical antipsychotic that started the third generation of these drugs [53]. It joined the family of MSs meeting the criteria above in 2007, when a prophylactic effect of the drug’s monotherapy was demonstrated in a two-year study. In this, aripiprazole significantly prevented the recurrences of manic episodes but not the depressive ones [54]. In a recent study, such prevention was also demonstrated for long-acting injectable (LAI) aripiprazole [55]. Previously, aripiprazole at doses of 15–30 mg/day was found to exert a significant anti-manic effect [56]. Further studies showed that such therapeutic efficacy was similar to lithium [57]. Aripiprazole in smaller doses (5–10 mg/day) has been used to enhance antidepressants’ effectiveness in case of their suboptimal outcome and has been recommended for the augmentation of antidepressants in drug-resistant depression [58].

3.5. Risperidone

Risperidone qualified as an SGMS in 2010 when a two-year study indicated that the drug’s monotherapy in the form of LAI showed a significant prophylactic effect concerning recurrences of manic episodes in patients with type I bipolar affective disorder [59]. Such an impact of LAI risperidone was also confirmed in more recent observations [55]. Previously, it was found that risperidone at doses of 1–6 (average 3–4) mg/day was therapeutically effective in mania [60] and presented, second to olanzapine, the best efficacy and tolerance profile in the treatment of manic episodes [42]. Risperidone does not exert an antidepressant effect. However, low doses of the drug can be used to augment antidepressants in treatment-resistant depression [44].

3.6. Lamotrigine

In addition to atypical antipsychotic drugs, the SGMSs were supplemented by a new anticonvulsant drug, lamotrigine. Among all mood-stabilizing drugs, lamotrigine exerts the most potent antidepressant activity and is, thus, regarded as a “mood stabilizer from below”. Lamotrigine is effective in the treatment of bipolar depression [61]. The favorable effects of lamotrigine were also described in brief recurrent depression [62]. In the prophylaxis of BD, the drug prevents mainly depressive recurrences. In a 1.5-year comparative study of lithium and lamotrigine, lithium was significantly better in preventing manic episodes. In contrast, lamotrigine was superior in the prevention of depressive ones [63]. Promising effects of lamotrigine were also reported in the rapid cycling BD [64]. Predictive factors for the prophylactic efficacy of lamotrigine are different from those for lithium and clozapine. A good prophylactic effect of lamotrigine can be obtained in patients with chronic depressive episodes, rapid cycling, and comorbid anxiety conditions, e.g., panic disorder [65].

3.7. Lurasidone

In recent years, a candidate for an MS was a second-generation antipsychotic, lurasidone, on account of its therapeutic activity in bipolar depression and prophylactic effects in BD. In bipolar depression, lurasidone, employed as monotherapy or in combination with lithium or valproic acid, produced a substantial decrease in depressive symptoms [66], corroborated by meta-analyses and systematic reviews [67]. Furthermore, a trial of lurasidone, 20 to 120 mg daily, for up to two years, following its use in bipolar depression, in a large group of patients, showed its safety and prophylactic efficacy as monotherapy and in combination with lithium or valproate [68]. In a one-year study in Japan, including BD patients, the drug was used in the same doses as above, with or without lithium or valproate. It was shown that in previously treated patients with bipolar depression, the drug continued the betterment in depressive symptoms and also improved psychiatric conditions in patients with manic, hypomanic, or mixed episodes [69]. Therefore, it seems that lurasidone may successfully meet the criteria for becoming an SGMS.

4. “Insufficient” Mood Stabilizers

Several drugs have shown some therapeutic and prophylactic efficacy in bipolar disorder, however, they do not sufficiently meet the criteria for mood stabilizers listed at the beginning of the paper. Nevertheless, they may be helpful mainly as an add-on to established mood stabilizers to augment their efficacy and treat psychiatric and somatic comorbidity.

4.1. Atypical antipsychotics

4.1.1. Asenapine

Asenapine was found to be therapeutically effective in mania and probably depression. At doses of 10-20 mg/day, it showed good efficacy and tolerability in the treatment of mania. This was confirmed in a meta-analysis published in 2013 [70], and asenapine is considered one of the most important drugs for the treatment of manic episodes, according to the recent guidelines of the Canadian Network for Mood and Anxiety Treatments (CANMAT) [50]. A posthoc analysis found that asenapine reduced depressive symptoms in bipolar I patients treated for manic or mixed episodes [71], and a therapeutic effect of the drug was reported in a small number of patients with bipolar depression [72]. Szegedi et al. [73] investigated the long-term prophylactic efficacy of asenapine in a randomized, placebo-controlled study abd observed that the drug significantly prevented both manic and depressive episodes in patients with bipolar I disorder when started after an acute manic or mixed episode [73]. However, the trial lasted only half a year, what was insufficient to meet the second criterion for mood stabilizers requiring at least one-year of study [1].

4.1.2. Ziprasidone

Ziprasidone was found efficacious and had good tolerability in mania [74]. However, there is no study on ziprasidone monotherapy for the maintenance treatment of BD. The addition of ziprasidone to monotherapy with lithium or valproate improved their efficacy during 6-month follow-up [75].

4.1.3. Paliperidone

In a randomized, double-blind study, published in 2010, paliperidone extended-release (ER), 12 mg/day, was superior to a placebo in the treatment of mania [76]. A paper appearing two years later presented a randomized, long-term placebo-controlled study showing that paliperidone ER prevented manic but not depressive episodes in patients with bipolar I disorder when started after an acute manic or mixed episode [77]. However, the responder-enriched design of this study does not allow researchers to infer the conclusion for the whole group of bipolar patients.

4.1.4. Cariprazine

Cariprazine, another third-generation antipsychotic, was therapeutically effective in mania and bipolar depression. In a double-blind, placebo-controlled study, cariprazine, both in low (3-6 mg/day) and high (6-12 mg/day) doses, were efficacious in the treatment of acute and mixed mania [78]. The drug also proved effective and well-tolerated in bipolar depression when used in amounts of 1.5-3 mg/day, and in 2019, Food and Drug Administration approved cariprazine for treating bipolar depression, based on the results of three randomized, double-blind, placebo-controlled trials [79]. However, there have been no results on cariprazine monotherapy in the maintenance treatment of BD.

4.1.5. Brexpiprazole

The successor of aripiprazole, brexpiprazole, was tried in a placebo-controlled study for the acute treatment of bipolar mania. In the short-term treatment, there was nodifference between brexiprazole and placebo, however, the open-label extension demonstrated a gradual improvement of manic symptoms with the drug [80]. Another pilot study found some improvement after brexpiprazole treatment in bipolar depression [81]. No maintenance trial of brexpiprazole in BD has been performed so far.

4.1.6. Lumatoperone

Lumateperone, at 42 mg/day, significantly improved depression symptoms in patients with depression in the course of BD, both type I and II [82]. Whereas no trials with lumateperone were performed in mania and maintenance treatment of BD.

4.2. Anticonvulsants

4.2.1. Topiramate

Anticonvulsant topiramate seemed a promising drug for mood-stabilizing agents when reports of its antimanic action used as monotherapy or add-on treatment appeared [83][84]. However, Cochrane analysis in 2016 did not fully confirm these claims [85]. Apart from positive case reports [86], there were no long-term trials with topiramate monotherapy in the maintenance treatment of BD, whereas, in a one-year study, adjunctive topiramate significantly reduced new manic and depressive episodes [87]. However, despite not fulfilling the criteria for MSs, adjunctive topiramate could be helpful in some special conditions in BD. The first is a reduction in weight gain. A favorable effect in this respect was already evidenced in a 24-week study [88]. Topiramate also demonstrated therapeutic properties in alcohol addiction [89] and some anxiety disorders [90]. However, no drug trials in BD patients with these comorbidities have been performed so far.

4.2.2. Gabapentin

The attempts to use gabapentin in BD mostly concerned add-on therapy. In 1999, the possible effectiveness of adjunctive gabapentin was shown in patients with drug-resistant bipolar states, particularly concerning depressive symptomatology [91]. Several years later, the same authors, showing such an effect on a higher number of patients, suggested that the drug’s effectiveness may be due to a simultaneous impact on anxiety and alcohol abuse comorbidity [92]. In a one-year double-blind placebo-controlled study, Vieta et al. [93], demonstrated the prophylactic efficacy of adjunctive gabapentin with no emerging manic and depressive symptoms. Thus, although the recent meta-analyses question the effectiveness of gabapentin in BD [94][95], it seems that the adjunctive use of the drug may augment the therapeutic and prophylactic efficacy of the well-established MSs, probably mostly in patients with concomitant anxiety and alcohol misuse.

4.2.3. Pregabalin

Pregabalin is an active metabolite of gabapentin, and its introduction into psychiatry was connected to its therapeutic effect on generalized anxiety disorder. The pursuits of using the drug in BD are fewer than those of gabapentin and pertain primarily to adjunctive therapy. In 2009, a case report described the successful use of pregabalin as an add-on to quetiapine in treating acute mania [96]. In 2013, the promising results of an open trial of pregabalin as an acute and maintenance adjunctive treatment for 58 outpatients with treatment-resistant bipolar disorder were presented. There were neither serious side effects nor adverse drug interactions with other MSs [97], although, similar to gabapentin, pregabalin does not meet the criteria for an MS. However, its adjunctive use in the treatment and prophylaxis of BD can be considered, especially with patients with generalized anxiety comorbidity.

4.2.4. Memantine

Memantine is a pro-cognitive drug acting mainly through a glutamatergic NMDA receptor. Studies in recent decades have shown that the drug may also make an application as an adjunctive agent in the treatment and prophylaxis of mood disorders. Italian investigators in a one-year open trial of 40 treatment-resistant BD patients showed that adjunctive memantine was associated with a clinically substantial antimanic and mood-stabilizing effect, with an excellent safety and tolerability profile [98]. They further demonstrated that such an effect was sustained after three years [99]. In a recent case report, an antidepressant effect of adjunctive memantine in bipolar patients was described [100]. Therefore, like the anticonvulsant drugs above, memantine does not meet the criteria for an MS as monotherapy. However, its adjunctive use in the treatment and prophylaxis of BD can be considered. It may be hypothesized that it can be of particular benefit to patients with cognitive problems.

This entry is adapted from the peer-reviewed paper 10.3390/brainsci13050741

References

  1. Rybakowski, J.K. Meaningful aspects of the term ‘mood stabilizer’. Bipolar Disord. 2018, 20, 391–392.
  2. Rybakowski, J.K. Two generations of mood stabilizers. Int. J. Neuropsychopharmacol. 2007, 10, 709–711.
  3. Zarate, C.A., Jr.; Tohen, M.; Banov, M.D.; Weiss, M.K.; Cole, J.O. Is clozapine a mood stabilizer? J. Clin. Psychiatry 1995, 56, 108–112.
  4. Hartigan, G.P. The use of lithium salts in affective disorders. Br. J. Psychiatry 1963, 109, 810–814.
  5. Cade, J.F.K. Lithium salts in the treatment of psychotic excitement. Med. J. Aust. 1949, 36, 349–352.
  6. Baastrup, P.C. The use of lithium in manic-depressive psychoses. Compr. Psychiatry 1964, 5, 396–408.
  7. Schou, M. Normothymotics, “mood-normalizers”: Are lithium and the imipramine drugs specific for affective disorders? Br. J. Psychiatry 1963, 109, 803–809.
  8. Baastrup, P.C.; Schou, M. Lithium as a prophylactic agent. Its effect against recurrent depression and manic-depressive psychosis. Arch. Gen. Psychiatry 1967, 16, 162–172.
  9. Blackwell, B.; Shepherd, M. Prophylactic lithium: Another therapeutic myth? An examination of the evidence to date. Lancet 1968, 291, 968–971.
  10. Schou, M.; Thompsen, K. Lithium prophylaxis of recurrent endogenous affective disorders. In Lithium Research and Therapy; Johnson, F.N., Ed.; Academic Press: London, UK, 1975; pp. 63–84.
  11. Rybakowski, J.; Chłopocka, M.; Lisowska, J.; Czerwiński, A. Studies on the therapeutic efficacy of lithium in endogenous depressive syndromes (in Polish). Psychiatr. Pol. 1974, 8, 129–135.
  12. Mendels, J. Lithium in the treatment of depression. Am. J. Psychiatry 1976, 133, 373–378.
  13. De Montigny, C.; Grunberg, F.; Mayer, A.; Deschenes, J.P. Lithium induces rapid relief of depression in tricyclic antidepressant nonresponders. Br. J. Psychiatry 1981, 138, 252–256.
  14. Grof, P. Excellent lithium responders: People whose lives have been changed by lithium prophylaxis. In Lithium: 50 Years of Psychopharmacology, New Perspectives in Biomedical and Clinical Research; Birch, N.J., Gallicchio, V.S., Becker, R.W., Eds.; Weidner Publishing Group: Cheshire, Connecticut, 1999; pp. 36–51.
  15. Rybakowski, J.K.; Chłopocka-Woźniak, M.; Suwalska, A. The prophylactic effect of long-term lithium administration in bipolar patients entering treatment in the 1970s and 1980s. Bipolar Disord. 2001, 3, 63–67.
  16. Rybakowski, J.K.; Ferensztajn-Rochowiak, E. Updated perspectives on how and when lithium should be used in the treatment of mood disorders. Expert Rev. Neurother. 2023, 23, 157–167.
  17. Geddes, J.R.; Burgess, S.; Kawton, K.; Jamison, K.; Goodwin, G.M. Long-term lithium therapy for bipolar disorder: Systematic review and meta-analysis of randomized controlled trials. Am. J. Psychiatry 2004, 161, 217–222.
  18. Nivoli, A.M.A.; Murru, A.; Vieta, E. Lithium: Still a cornerstone in the long-term treatment in bipolar disorder? Neuropsychobiology 2010, 62, 27–35.
  19. Severus, E.; Taylor, M.J.; Sauer, C.; Pfennig, A.; Ritter, P.; Bauer, M.; Geddes, J.R. Lithium for prevention of mood episodes in bipolar disorders: Systematic review and meta-analysis. Int. J. Bipolar Disord. 2014, 2, 15.
  20. Kessing, L.V.; Bauer, M.; Nolen, W.A.; Severus, E.; Goodwin, G.M.; Geddes, J. Effectiveness of maintenance therapy of lithium vs. other mood stabilizers in monotherapy and in combinations: A systematic review of evidence from observational studies. Bipolar Disord. 2018, 20, 419–431.
  21. Poolsup, N.; Li Wan Po, A.; de Oliveira, I.R. Systematic overview of lithium treatment in acute mania. J. Clin. Pharm. Ther. 2000, 25, 139–156.
  22. Bauer, M.; Adli, M.; Ricken, R.; Severus, E.; Pilhatsch, M. Role of lithium augmentation in the management of major depressive disorder. CNS Drugs 2014, 28, 331–342.
  23. Bauer, M.S.; Mitchner, L. What is a “mood stabilizer”? An evidence-based response. Am. J. Psychiatry 2004, 161, 3–18.
  24. Smith, K.A.; Cipriani, A. Lithium and suicide in mood disorders: Updated meta-review of the scientific literature. Bipolar Disord. 2017, 19, 575–586.
  25. Ferensztajn-Rochowiak, E.; Chłopocka-Woźniak, M.; Rybakowski, J.K. Ultra-long-term lithium therapy: All-important matters and a case of successful 50-year lithium treatment. Braz. J. Psychiatry 2021, 43, 407–413.
  26. Lambert, P.A.; Borselli, S.; Marcou, G.; Bouchardy, M.; Cabrol, G. Action thymorégulatrice a long terme de Depamide dans la psychose maniaco-dépressive. Ann. Med. Psychol. 1971, 2, 442–447.
  27. Bowden, C.L.; Calabrese, J.R.; McElroy, S.L.; Gyulai, L.; Wassef, A.; Petty, F.; Pope, H.G., Jr.; Chou, J.C.; Keck, P.E., Jr.; Rhodes, L.J.; et al. A randomized, placebo-controlled 12-month trial of divalproex and lithium in treatment of outpatients with bipolar I disorder. Divalproex Maintenance Study Group. Arch. Gen. Psychiatry 2000, 57, 481–489.
  28. BALANCE Investigators and Collaborators; Geddes, J.R.; Goodwin, G.M.; Rendell, J.; Azorin, J.-M.; Cipriani, A.; Ostacher, M.J.; Morriss, R.; Alder, N.; Juszczak, E. Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): A randomized open-label trial. Lancet 2010, 375, 385–395.
  29. Kang, M.G.; Qian, H.; Keramatian, K.; Chakrabarty, T.; Saraf, G.; Lam, R.W.; Wong, H.; Yatham, L.N. Lithium vs. valproate in the maintenance treatment of bipolar I disorder: A post- hoc analysis of a randomized double-blind placebo-controlled trial. Aust. New Zealand J. Psychiatry 2020, 54, 298–307.
  30. Okuma, T.; Kishimoto, A.; Inue, K.; Hisashi, M.; Atsushi, O.; Toji, M.; Nakao, T.; Chikara, O. Anti-manic and prophylactic effect of carbamazepine (Tegretol) on manic depressive psychosis. Psychiatry Clin. Neurosci. 1973, 27, 283–297.
  31. Post, R.M.; Uhde, T.W.; Ballenger, J.C.; Squillace, K.M. Prophylactic efficacy of carbamazepine in manic-depressive illness. Am. J. Psychiatry 1983, 140, 1602–1604.
  32. Post, R.M.; Uhde, T.W.; Roy-Byrne, P.P.; Joffe, R.T. Correlates of antimanic response to carbamazepine. Psychiatry Res. 1987, 21, 71–83.
  33. Post, R.M.; Uhde, T.W.; Roy-Byrne, P.P.; Joffe, R.T. Antidepressant effects of carbamazepine. Am. J. Psychiatry 1986, 143, 29–34.
  34. Kleindienst, N.; Greil, W. Differential efficacy of lithium and carbamazepine in the prophylaxis of bipolar disorder: Results of the MAP study. Neuropsychobiology 2000, 42 (Suppl. 1), 2–10.
  35. Rybakowski, J. Oxcarbazepine in bipolar affective disorder. Pharmakoter Psychiatr. Neurol. 2018, 34, 131–138.
  36. Strzyzewski, W.; Rybakowski, J.; Chłopocka-Woźniak, M.; Czerwiński, A. Clozapine in the treatment of manic states (in Polish). Psychiatr. Pol. 1981, 15, 331–332.
  37. Delgado, A.; Velosa, J.; Zhang, J.; Dursun, S.M.; Kapczinski, F.; de Azevedo Cardoso, T. Clozapine in bipolar disorder: A systematic review and meta-analysis. J. Psychiatr. Res. 2020, 125, 21–27.
  38. Fornaro, M.; Carvalho, A.F.; Fusco, A.; Anastasia, A.; Solmi, M.; Berk, M.; Sim, K.; Vieta, E.; de Bartolomeis, A. The concept and management of acute episodes of treatment-resistant bipolar disorder: A systematic review and exploratory meta-analysis of randomized controlled trials. J. Affect. Disord. 2020, 276, 970–983.
  39. Li, X.B.; Tang, Y.L.; Wang, C.Y.; de Leon, J. Clozapine for treatment-resistant bipolar disorder: A systematic review. Bipolar Disord. 2015, 17, 235–237.
  40. Rybakowski, J. Farmakoterapia choroby afektywnej dwubiegunowej. In Standardy Leczenia Farmakologicznego Niektórych Zaburzeń Psychicznych (in Polish); Jarema, M., Ed.; Via Medica: Gdansk, Poland, 2022; pp. 93–127.
  41. Tohen, M.; Jacobs, T.G.; Grundy, S.L.; McElroy, S.L.; Banov, M.C.; Janicak, P.G.; Sanger, T.; Risser, R.; Zhang, F.; Toma, V.; et al. Efficacy of olanzapine in acute bipolar mania: A double-blind, placebo-controlled study. The Olanzapine HGGW Study Group. Arch. Gen. Psychiatry 2000, 57, 841–849.
  42. Cipriani, A.; Barbui, C.; Salanti, G.; Rendell, J.; Brown, R.; Stockton, S.; Purgato, M.; Spineli, L.M.; Goodwin, G.M.; Geddes, J.R. Comparative efficacy and acceptability of antimanic drugs in acute mania: A multiple-treatments meta-analysis. Lancet 2011, 378, 1306–1315.
  43. Citrome, L. Olanzapine-fluoxetine combination for the treatment of bipolar depression. Expert Opin. Pharmacother. 2011, 12, 2751–2758.
  44. Cantù, F.; Ciappolino, V.; Enrico, P.; Moltrasio, C.; Delvecchio, G.; Brambilla, P. Augmentation with atypical antipsychotics for treatment-resistant depression. J. Affect. Disord. 2021, 280, 45–53.
  45. Tohen, M.F.; Calabrese, J.R.; Sachs, G.S.; Banov, M.D.; Detke, H.; Risser, R.; Baker, R.W.; Chou, J.C.; Bowden, C.L. Randomized, placebo-controlled trial of olanzapine as maintenance therapy in patients with bipolar I disorder responding to acute treatment with olanzapine. Am. J. Psychiatry 2006, 163, 247–256.
  46. Tohen, M.; Greil, W.; Calabrese, J.R.; Sachs, G.S.; Yatham, L.N.; Oerlingahausen, B.M.; Koukopoulos, A.; Cassano, G.B.; Grunze, H.; Licht, R.W.; et al. Olanzapine versus lithium in the maintenance treatment of bipolar disorder: A 12-month randomized double-blind controlled clinical trial. Am. J. Psychiatry 2005, 162, 1281–1290.
  47. Ketter, T.A.; Miller, S.; Dell’Osso, B.; Wang, P.W. Treatment of bipolar disorder: Review of evidence regarding quetiapine and lithium. J. Affect. Disord. 2016, 191, 256–273.
  48. Ketter, T.A.; Jones, M.; Paulsson, B. Rates of remission/euthymia with quetiapine monotherapy compared with placebo in patients with acute mania. J. Affect. Disord. 2007, 100 (Suppl. 1), S45–S53.
  49. Young, A.H.; McElroy, S.L.; Bauer, M.; Philips, N.; Chang, W.; Olauson, B.; Paulsson, B.; Brecher, M.; EMBOLDEN I (Trial 001) Investigators. A double-blind, placebo controlled study of quetiapine and lithium monotherapy in adults in the acute phase of bipolar depression (EMBOLDEN I). J. Clin. Psychiatry 2010, 71, 150–162.
  50. Yatham, L.N.; Kennedy, S.H.; Parikh, S.V.; Schaffer, A.; Bond, D.J.; Frey, B.N.; Sharma, V.; Goldstein, B.I.; Rej, S.; Beaulieu, S.; et al. Canadian Network for Mood and Anxiety Treatments (CANMAT) and International Society for Bipolar Disorders (ISBD) 2018 guidelines for the management of patients with bipolar disorder. Bipolar Disord. 2018, 20, 97–170.
  51. Pini, S.; Abelli, M.; Cassano, G.B. The role of quetiapine in the treatment of bipolar disorder. Expert Opin. Pharmacother. 2006, 7, 929–940.
  52. Altamura, A.C.; Mundo, E.; Dell’Osso, B.; Tacchini, G.; Buoli, M.; Calabrese, J.R. Quetiapine and classical mood stabilizers in the long-term treatment of Bipolar Disorder: A 4-year follow-up naturalistic study. J. Affect. Disord. 2008, 110, 135–141.
  53. Keltner, N.L.; Johnson, V. Biological perspectives. Aripiprazole: A third generation of antipsychotics begins? Perspect. Psychiatr. Care 2002, 38, 157–159.
  54. Keck, P.E.; Calabrese, J.R.; McIntyre, R.S.; McQuade, R.D.; Carson, W.H.; Eudicone, J.M.; Carlson, B.X.; Marcus, R.N.; Sanchez, R.; Aripiprazole Study Group. Aripiprazole monotherapy for maintenance therapy in bipolar I disorder: A 100-week, double-blind study versus placebo. J. Clin. Psychiatry 2007, 88, 1480–1491.
  55. Keramatian, K.; Chakrabarty, T.; Yatham, L.N. Long-acting injectable second-generation/atypical antipsychotics for the management of bipolar disorder: A systematic review. CNS Drugs 2019, 33, 431–456.
  56. Keck, P.E., Jr.; Marcus, R.; Tourkodimitris, S.; Ali, M.; Liebeskind, A.; Saha, A.; Ingenito, G.; Aripiprazole Study Group. A placebo-controlled, double-blind study of the efficacy and safety of aripiprazole in patients with acute bipolar mania. Am. J. Psychiatry 2003, 160, 1651–1658.
  57. Keck, P.E.; Orsulak, P.J.; Cutler, A.J.; Sanchez, R.; Torbeyns, A.; Marcus, R.N.; McQuade, R.D.; Carson, W.H.; CN138-135 Study Group. Aripiprazole monotherapy in the treatment of acute bipolar I mania: A randomized, double-blind, placebo- and lithium-controlled study. J. Affect. Disord. 2009, 112, 36–49.
  58. Nelson, J.C.; Thase, M.E.; Bellochchio, E.E.; Rollin, L.M.; Eudicone, J.M.; McQuade, R.C.; Marcus, R.N.; Berman, R.M.; Baker, R.A. Efficacy of adjunctive aripiprazole in patients with major depressive disorder who showed minimal response to initial antidepressant therapy. Int. Clin. Psychopharmacol. 2012, 27, 125–133.
  59. Quiroz, J.A.; Yatham, L.N.; Palumbo, J.M.; Karcher, K.; Kushner, S.; Kusumakar, V. Risperidone long-acting injectable monotherapy in the maintenence treatment of bipolar disorder. Biol. Psychiatry 2010, 68, 156–162.
  60. Fenton, C.; Scott, L.J. Risperidone: A review of its use in the treatment of bipolar mania. CNS Drugs 2005, 19, 429–444.
  61. Calabrese, J.R.; Bowden, C.L.; Sachs, G.S.; Ascher, J.A.; Monaghan, E.; Rudd, G.D. A double-blind placebo-controlled study of lamotrigine monotherapy in outpatients with bipolar I depression. J. Clin. Psychiatry 1999, 60, 79–88.
  62. Ravindran, L.N.; Ravindran, A.V. Lamotrigine in the treatment of recurrent brief depression. Int. Clin. Psychopharmacol. 2007, 22, 121–123.
  63. Goodwin, G.M.; Bowden, C.L.; Calabrese, J.R.; Grunze, H.; Kasper, S.; White, R. A pooled analysis of 2 placebo-controlled 18-month trials of lamotrigine and lithium maintenance in bipolar I disorder. J. Clin. Psychiatry 2004, 65, 432–441.
  64. Calabrese, J.R.; Suppes, T.; Bowden, C.L.; Sachs, G.S.; Swann, A.C.; McElroy, S.L.; Kusumakar, V.; Ascher, J.A.; Earl, N.L.; Greene, P.L. Monaghan ETA double-blind, placebo-controlled, prophylaxis study of lamotrigine in rapid-cycling bipolar disorder. Lamictal 614 Study Group. J. Clin. Psychiatry. 2000, 61, 841–850.
  65. Passmore, M.J.; Garnham, J.; Duffy, A.; MacDougall, M.; Munro, A.; Slaney, C.; Teehan, A.; Alda, M. Phenotypic spectra of bipolar disorder in responders to lithium versus lamotrigine. Bipolar Disord. 2003, 5, 110–114.
  66. Findlay, L.J.; El-Mallakh, P.; El-Mallakh, R.S. Management of bipolar I depression: Clinical utility of lurasidone. Ther. Clin. Risk Manag. 2015, 11, 75–81.
  67. Fornaro, M.; De Berardis, D.; Perna, G.; Solmi, M.; Veronese, N.; Orsolini, L.; Buonaguro, E.F.; Iasevoli, F.; Köhler, C.A.; Carvalho, A.F.; et al. Lurasidone in the treatment of bipolar depression: Systematic review of systematic reviews. Biomed Res. Int. 2017, 2017, 3084859.
  68. Pikalov, A.; Tsai, J.; Mao, Y.; Silva, R.; Cucchiaro, J.; Loebel, A. Long-term use of lurasidone in patients with bipolar disorder: Safety and effectiveness over 2 years of treatment. Int. J. Bipolar Disord. 2017, 5, 9.
  69. Higuchi, T.; Kato, T.; Miyajima, M.; Watabe, K.; Masuda, T.; Hagi, K.; Ishigooka, J. Lurasidone in the long-term treatment of Japanese patients with bipolar I disorder: A 52 week open label study. Int. J. Bipolar Disord. 2021, 9, 25.
  70. Vita, A.; De Peri, L.; Siracusano, A.; Sacchetti, E.; ATOM Group. Efficacy and tolerability of asenapine for acute mania in bipolar I disorder: Meta-analyses of randomized-controlled trials. Int. Clin. Psychopharmacol. 2013, 28, 219–227.
  71. Szegedi, A.; Zhao, J.; van Willigenburg, A.; Nations, K.R.; Mackle, M.; Panagides, J. Effects of asenapine on depressive symptoms in patients with bipolar I disorder experiencing acute manic or mixed episodes: A post hoc analysis of two 3-week clinical trials. BMC Psychiatry 2011, 11, 101.
  72. El-Mallakh, R.S.; Nuss, S.; Gao, D.; Gao, Y.; Ahmad, S.C.; Schrodt, C.; Adler, C. Asenapine in the treatment of bipolar depression. Psychopharmacol. Bull. 2020, 50, 8–18.
  73. Szegedi, A.; Durgam, S.; Mackle, M.; Yu, S.Y.; Wu, X.; Mathews, M.; Landbloom, R.P. Randomized, double-blind, placebo-controlled trial of asenapine maintenance therapy in adults with an acute manic or mixed episode associated with bipolar i disorder. Am. J. Psychiatry 2018, 175, 71–79.
  74. Potkin, S.G.; Keck, P.E., Jr.; Segal, S.; Ice, K.; English, P. Ziprasidone in acute bipolar mania: A 21-day randomized, double-blind, placebo-controlled replication trial. J. Clin. Psychopharmacol. 2005, 25, 301–310.
  75. Bowden, C.L. The role of ziprasidone in adjunctive use with lithium or valproate in maintenance treatment of bipolar disorder. Neuropsychiatr. Dis. Treat. 2011, 7, 87–92.
  76. Berwaerts, J.; Xu, H.; Nuamah, I.; Lim, P.; Hough, D. Evaluation of the efficacy and safety of paliperidone extended-release in the treatment of acute mania: A randomized, double-blind, dose-response study. J. Affect. Disord. 2012, 136, e51–e60.
  77. Berwaerts, J.; Melkote, R.; Nuamah, I.; Lim, P. A randomized, placebo- and active-controlled study of paliperidone extended-release as maintenance treatment in patients with bipolar I disorder after an acute manic or mixed episode. J. Affect. Disord. 2012, 138, 247–258.
  78. Calabrese, J.R.; Keck, P.E., Jr.; Starace, A.; Lu, K.; Ruth, A.; Laszlovszky, I.; Németh, G.; Durgam, S. Efficacy and safety of low- and high-dose cariprazine in acute and mixed mania associated with bipolar I disorder: A double-blind, placebo-controlled study. J. Clin. Psychiatry 2015, 76, 284–292.
  79. Tohen, M. Cariprazine as a treatment option for depressive episodes associated with bipolar 1 disorder in adults: An evidence-based review of recent data. Drug Des. Dev. Ther. 2021, 15, 2005–2012.
  80. Vieta, E.; Sachs, G.; Chang, D.; Hellsten, J.; Brewer, C.; Peters-Strickland, T.; Hefting, N. Two randomized, double-blind, placebo-controlled trials and one open-label, long-term trial of brexpiprazole for the acute treatment of bipolar mania. J. Psychopharmacol. 2021, 35, 971–982.
  81. Brown, E.S.; Khaleghi, N.; Van Enkevort, E.; Ivleva, E.; Nakamura, A.; Holmes, T.; Mason, B.L.; Escalante, C. A pilot study of brexpiprazole for bipolar depression. J. Affect. Disord. 2019, 249, 315–318.
  82. Calabrese, J.R.; Durgam, S.; Satlin, A.; Vanover, K.E.; Davis, R.E.; Chen, R.; Kozauer, S.G.; Mates, S.; Sachs, G.S. Efficacy and safety of lumateperone for major depressive episodes associated with bipolar I or bipolar II disorder: A phase 3 randomized placebo-controlled trial. Am. J. Psychiatry 2021, 178, 1098–1106.
  83. Grunze, H.C.; Normann, C.; Langosch, J.; Schaefer, M.; Amann, B.; Sterr, A.; Schloesser, S.; Kleindienst, N.; Walden, J. Antimanic efficacy of topiramate in 11 patients in an open trial with an on-off-on design. J. Clin. Psychiatry 2001, 62, 464–468.
  84. Chengappa, K.N.; Rathore, D.; Levine, J.; Atzert, R.; Solai, L.; Parepally, H.; Levin, H.; Moffa, N.; Delaney, J.; Brar, J.S. Topiramate as add-on treatment for patients with bipolar mania. Bipolar Disord. 1999, 1, 42–53.
  85. Pigott, K.; Galizia, I.; Vasudev, K.; Watson, S.; Geddes, J.; Young, A.H. Topiramate for acute affective episodes in bipolar disorder in adults. Cochrane Database Syst. Rev. 2016, 9, CD003384.
  86. Erfurth, A.; Kuhn, G. Topiramate monotherapy in the maintenance treatment of bipolar I disorder: Effects on mood, weight and serum lipids. Neuropsychobiology 2000, 42 (Suppl. 1), 50–51.
  87. Lykouras, L.; Hatzimanolis, J. Adjunctive topiramate in the maintenance treatment of bipolar disorders: An open-label study. Curr. Med. Res. Opin. 2004, 20, 843–847.
  88. McElroy, S.L.; Frye, M.A.; Altshuler, L.L.; Suppes, T.; Hellemann, G.; Black, D.; Mintz, J.; Kupka, R.; Nolen, W.; Leverich, G.S.; et al. A 24-week, randomized, controlled trial of adjunctive sibutramine versus topiramate in the treatment of weight gain in overweight or obese patients with bipolar disorders. Bipolar Disord. 2007, 9, 426–434.
  89. Fluyau, D.; Kailasam, V.K.; Pierre, C.G. A Bayesian meta-analysis of topiramate’s effectiveness for individuals with alcohol use disorder. J. Psychopharmacol. 2023, 37, 155–163.
  90. Van Ameringen, M.; Mancini, C.; Pipe, B.; Oakman, J.; Bennett, M. An open trial of topiramate in the treatment of generalized social phobia. J. Clin. Psychiatry 2004, 65, 1674–1678.
  91. Perugi, G.; Toni, C.; Ruffolo, G.; Sartini, S.; Simonini, E.; Akiskal, H. Clinical experience using adjunctive gabapentin in treatment-resistant bipolar mixed states. Pharmacopsychiatry 1999, 32, 136–141.
  92. Perugi, G.; Toni, C.; Frare, F.; Ruffolo, G.; Moretti, L.; Torti, C.; Akiskal, H.S. Effectiveness of adjunctive gabapentin in resistant bipolar disorder: Is it due to anxious-alcohol abuse comorbidity? J. Clin. Psychopharmacol. 2002, 22, 584–591.
  93. Vieta, E.; Manuel Goikolea, J.; Martínez-Arán, A.; Comes, M.; Verger, K.; Masramon, X.; Sanchez-Moreno, J.; Colom, F. A double-blind, randomized, placebo-controlled, prophylaxis study of adjunctive gabapentin for bipolar disorder. J. Clin. Psychiatry 2006, 67, 473–477.
  94. Ng, Q.X.; Han, M.X.; Teoh, S.E.; Yaow, C.Y.L.; Lim, Y.L.; Chee, K.T. A systematic review of the clinical use of gabapentin and pregabalin in bipolar disorder. Pharmaceuticals 2021, 14, 834.
  95. Hong, J.S.W.; Atkinson, L.Z.; Al-Juffali, N.; Awad, A.; Geddes, J.R.; Tunbridge, E.M.; Harrison, P.J.; Cipriani, A. Gabapentin and pregabalin in bipolar disorder, anxiety states, and insomnia: Systematic review, meta-analysis, and rationale. Mol. Psychiatry 2022, 27, 1339–1349.
  96. Oulis, P.; Florakis, A.A.; Tzanoulinos, G.; Papadimitriou, G.N. Adjunctive pregabalin to quetiapine in acute mania. Clin. Neuropharmacol. 2009, 32, 174.
  97. Schaffer, L.C.; Schaffer, C.B.; Miller, A.R.; Manley, J.L.; Piekut, J.A.; Nordahl, T.E. An open trial of pregabalin as an acute and maintenance adjunctive treatment for outpatients with treatment resistant bipolar disorder. J. Affect. Disord. 2013, 147, 407–410.
  98. Koukopoulos, A.; Serra, G.; Koukopoulos, A.E.; Reginaldi, D.; Serra, G. The sustained mood-stabilizing effect of memantine in the management of treatment resistant bipolar disorders: Findings from a 12-month naturalistic trial. J. Affect. Disord. 2012, 136, 163–166.
  99. Serra, G.; Koukopoulos, A.; De Chiara, L.; Koukopoulos, A.E.; Tondo, L.; Girardi, P.; Baldessarini, R.J.; Serra, G. Three-year, naturalistic, mirror-image assessment of adding memantine to the treatment of 30 treatment-resistant patients with bipolar disorder. J. Clin. Psychiatry 2015, 76, e91–e97.
  100. Krzystanek, M.; Surma, S.; Pałasz, A.; Romańczyk, M.; Krysta, K. Possible antidepressant effects of memantine-systematic review with a case study. Pharmaceuticals 2021, 14, 481.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
This entry is offline, you can click here to edit this entry!
ScholarVision Creations
Feedback