|Ahead of print publication
Mirtazapine-associated movement disorders: A literature review
Jamir Pitton Rissardo, Ana Leticia Fornari Caprara
Department of Medicine, Federal University of Santa Maria, Santa Maria, Brazil
|Date of Submission||21-Jan-2020|
|Date of Acceptance||04-Mar-2020|
|Date of Web Publication||13-Jul-2020|
Jamir Pitton Rissardo,
Department of Medicine, Federal University of Santa Maria, Santa Maria 97105110 Rio Grande do Sul
Source of Support: None, Conflict of Interest: None
Mirtazapine (MTZ) is an atypical antidepressant approved by the FDA, which mechanism of action involves the antagonism of alpha-2, H1, 5-HT2A, 5-HT2C, and 5-HT3 receptors. In this context, the aim of this literature review is to evaluate the clinical epidemiological profile, pathological mechanisms, and management of MTZ-associated movement disorders (MDs). Relevant reports of six databases were identified and assessed by two reviewers without language restriction. Fifty-two reports containing 179 cases from 20 countries were assessed. The mean age was 57 year (range, 17–85). The majority of the individuals were female (60%) and of European origin. The mean time from MTZ start to symptom onset was 7.54 days; the time from management to MD improvement was within one week in 82.60% of the individuals. The MDs associated with MTZ were 69 restless legs syndrome (RLS), 35 tremors, 10 akathisia (AKT), 9 periodic limb MD, 6 dystonia, 4 rapid eye movement sleep behavior disorders, 3 dyskinesia, 2 parkinsonism, and 1 tic, and in the group not clearly identified, 18 restlessness, 15 hyperkinesis, and 1 extrapyramidal symptom. In the literature, the majority of the reports lack important information about the neurological examination. The management should be the MTZ withdrawal, except in RLS that other options are possible. In AKT, the MTZ should not be rechallenge, and if available, the prescription of a benzodiazepine may reduce recovery time.
Keywords: Drug-induced, Mirtazapine, Movement disorder, Org 3770, Review
| Introduction|| |
Adverse events or unintended pharmacologic effects that occur when a medication is administered are stressful situations for patients and, in some cases, can be a challenge for the physicians. In this context, movement disorders (MDs) associated with drugs are even more difficult to describe or give a clear diagnosis because the clinical manifestations could overlap and provide a mixture of disorders in the same individuals, also every movement type can be induced by some drug or toxin. The most frequent causes of drug-induced MDs are dopamine receptor blocking drugs, including antipsychotics and antiemetics.
Mirtazapine (MTZ) is an atypical antidepressant, which first clinical studies started at the end of the 1980s. In 1994, this medication was primarily approved for the management of major depressive disorder (MDD) in the Netherlands. About three years later, MTZ was approved by the Food and Drug Administration for the treatment of moderate-to-severe depression. A recent systematic review comparing the efficacy of more than twenty different antidepressants revealed that MTZ is one of the most effective antidepressants when compared to other antidepressants. It also demonstrated a statistical advantage over current selective serotonin reuptake inhibitors (SSRIs). However, currently, guidelines such as the National Institute for Health and Care Excellence in the United Kingdom 2010 still recommended generic SSRIs as the first-line treatment for depression.
The mechanisms of action involved with MTZ are the antagonism of central presynaptic adrenergic (α2), histamine (H1), and serotonin (SER) (5-HT2A, 2C, and 3) receptors [Figure 1]. In addition, it has moderate antagonist effects on peripheral alpha-1 adrenergic and muscarinic receptors. The interference in these receptors explains the several significant side effects related to MTZ. The adverse events that affect more than ten percent of users are drowsiness, weight gain, and xerostomia.
|Figure 1: Skeletal formula and pharmacodynamic of mirtazapine. The size of the arrow is inversely proportionally to the Ki (smaller the value stronger is the drug binds to the site). Mirtazapine acts as antagonism of serotoninergic (5-HT2A, 5-HT2C, and 5-HT3), noradrenergic (a-2), and histaminergic (H1) receptors|
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MTZ was only approved by the FDA for the treatment of MDD. However, this drug is used off-label for the management of posttraumatic stress disorder, hot flushes, insomnia, panic disorder, obsessive–compulsive disorder, generalized anxiety disorder, and headaches,.
MDs are uncommonly related to MTZ. In the label of REMERON® (MTZ) tablets, in one of the clinical experiences in short-term United States control studies, nine individuals of more than four hundred taking MTZ had tremors, and this was the only MD found in more than one percent of the participants. Moreover, other postmarketing studies done throughout the last decades including hundreds of individuals did not report any MTZ-induced movement. A recent literature review of only the PubMed database from 1990 to June 2017 focused on hyperkinetic movements related to MTZ found twelve cases already reported, which were in descending order of frequency, akathisias (AKTs) (5), dystonia (DTN) (4), dyskinesias (DKNs) (2), and periodic limb MD (PLMD) (1). Their results conclude that these adverse effects were more common in older individuals, and the best treatment is the cessation of the medication. The aim of this literature review is to evaluate the clinical epidemiological profile, pathological mechanisms, and management of MTZ-associated MDs.
| Materials and Methods|| |
We searched six databases in an attempt to locate any and all existing reports on movement disorders secondary to mirtazapine published from 1990 to 2019 in electronic form. Excerpta Medica (Embase), Google Scholar, Latin American and Caribbean Health Sciences Literature (Lilacs), Medline, Scientific Electronic Library Online (Scielo), and ScienceDirect were searched. Search terms were “dystonia, restless legs syndrome, periodic limb movement disorder, akathisia, dyskinesia, tremor, stuttering, parkinsonism, tic, chorea, restlessness, ataxia, hyperkinetic, hypokinetic, bradykinesia, movement disorder, myoclonus, ballism.” These terms were combined with “mirtazapine, Org 3770” [Supplementary Material 1].
Inclusion and exclusion criteria
Original articles, case reports, case series, letters to editors, bulletins, and poster presentations published from 1990 to 2019 were included in this review with no language restriction. The two authors independently screened the titles and abstracts of all papers found from the initial search. Disagreements between the authors were resolved through discussion.
Cases where the cause of MD was already known and either motor symptoms did not worsen or were not related to MTZ were excluded. Furthermore, cases that were not accessible by electronic methods including after a formal request to the authors (by email) were excluded. Cases that had more than one contributing factor to the MD were evaluated based on the Naranjo algorithm to estimate the probability of the event occurring.
A total of 3794 papers were found; 3444 were irrelevant and 298 were unrelated to the complication, duplicate, inaccessible electronically, or provided insufficient data [Figure 2]. Data abstraction was done. When provided, we extracted from the articles: authors' name, authors' department, year of publication, country of occurrence, number of patients affected, MTZ indication including off-label uses, time from first MTZ-dose until MD onset, time from MTZ withdrawal to symptoms improvement, patient's status at the last follow-up, and important findings of clinical history and management. The majority of the reports did not provide sufficient information about the neurological examination and the time from drug withdrawal to the improvement of the symptoms. The data were extracted by two independent authors, double-checked to ensure matching, and organized by whether the MD was a side effect of the MTZ use.
Categorical variables were represented as proportions; continuous variables were represented as mean, standard deviations (SDs), median, and range.
The clinical characteristics and definitions of the MDs such as DTN, restless legs syndrome (RLS), PLMD, AKT, DKN, tremor, parkinsonism, tic, chorea, ballism, and myoclonus were obtained from the reference Jankovic and Tolosa. The clinical diagnosis for psychiatric disorders was obtained from the diagnostic and statistical manual of mental disorders (DSM-5®). The Naranjo algorithm was used for determining the likelihood of whether an adverse drug reaction was actually due to the drug rather than the result of other factors. In the cases where the non-English literature was beyond the authors' proficiency (English, Portuguese, Spanish, Italian, French, and German) and the English abstract did not provide enough data, such as Japanese, Korean, Chinese, Russian, and Dutch, Google Translate service was used.
| Results|| |
For 1990 and 2019, a total of 52 reports containing 179 individuals that developed a MD associated with MTZ were identified from 20 different countries [Table 1],1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,. 103 individuals were from European countries, 49 Asian, 17 Australian, 8 North American, and 2 South American. [Figure 3] shows the number of reports associated with MDs and MTZ over time. The MDs associated with MTZ encountered were 6 DTNs (isolated axial, isolated cervical, and axial + cervical), 69 RLS (induced and worsening RLS symptoms), 9 PLMD, 10 AKT, 3 DKN (chorea and choreoathetosis), 35 tremors (action and resting), 2 parkinsonism, 1 tic (complex motor facial without vocalization), 4 rapid eye movement sleep behavior disorders, and others not clearly identified cases such as 18 restlessness, 15 hyperkinesis, and 1 extrapyramidal symptoms.
|Table 1: Clinical reports presenting with mirtazapine-associated movement disorder from 1990 to 2019|
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|Figure 3: Graphic showing the number of clinical reports of mirtazapine.associated movement disorder from 1990 to 2019|
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The mean and median age was 57 (SD: 15.16) and 58 years (age range: 17–85). The female was the predominant sex in 60% (33/55) of the individuals. The most common indication of MTZ was MDD in 51% (21/41) of the cases, followed by MDD + insomnia (12), insomnia alone (3), hot flushes (1), major depressive episode (1), major depressive episode + insomnia (1), MDD + panic attacks (1), and mild depression + insomnia (1). The mean and median MTZ dose, when the MD occurred, was 24.68 (SD: 14.41) and 15 mg (MTZ dose range, 7.5–60). There were: 21 individuals with 15 mg of MTZ when the MD occurred, 19 with 30 mg, 7 with 7.5 mg, 4 with 45 mg, and 4 with 60 mg.
The mean and median time from MTZ start and the abnormal movement onset was 7.54 (SD: 15.53) and 2 days. The MD occurred within a week of the MTZ start in 78% (35/45) of the patients. The correlation between MTZ dose and the time from the drug start to the MD onset demonstrated a moderate linear correlation 0.367 when outliers were excluded.
Only two individuals did not have a complete recovery after the management. The time from drug withdrawal and the improvement of symptoms was specifically reported by 23 cases. In 19 cases, the recovery occurred within one week of the management.
In 82% (45/55) of the individuals, the management was the withdrawal of the offending drug. Other options were more commonly attempted on the MTZ-induced RLS, in which the management involved the inclusion of a new drug (clonazepam, ropinirole, pramipexole, or gabapentin) to improve the symptoms. In the AKT group, other choices to alleviate restlessness were attempted such as starting concurrent propranolol needed-basis, and as using every three days MTZ. By the way, in one individual with DKN, MTZ was not discontinued, and the symptoms improved over time.
| Discussion|| |
An important topic to discuss is the few numbers of clinical reports already reported in the literature of MTZ-induced MD. In this context, we believe that probably only were reported moderate to severe cases; on the other hand, those mild cases were only addressed by drug withdrawal without a report to the literature. Some findings supporting this assumption are a large number of reports with thousands of cases about MTZ and MDs adverse effects on the FDA Adverse Event Reporting System. In addition, more than eighty percent of the cases were diagnosed without the examination of a MD specialist. Thus, we presupposed that only the most severe cases with clear abnormal movements were published; also, it is worth mention that most cases did not clearly describe and lack significant features about the patients' neurological examination.
Herein, we would like to discuss some of the MDs in subtopics to give a better comprehension of the data. [Figure 4] shows a resume of the hypothesized pathophysiological mechanisms that we proposed for the development of MDs following the use of MTZ.
|Figure 4: Schematic diagram showing the pathophysiological mechanism of mirtazapine-associated movement disorders. (A) Receptors that are significantly antagonized by mirtazapine, which include H1, 5HT2A, HT2C, and α-2. (B) Dystonia mechanism associated with 5HT2A; mirtazapine? Represents that probably mirtazapine has some indirect action in the pathway between the frontal cortex and substantia nigra compact. D: Direct pathway, I: Indirect pathway. (C) Akathisia mechanism associated with 5HT2A and α-2; NAc: Nucleus accumbens, NE: Norepinephrine. (D) Restless legs syndrome mechanism associated with 5HT2A, HT2C, and α-2; IML: Intermediolateral cell column. (E) Acute dyskinesia mechanism related to H1, 5HT2C, 5HT2A, and α-2. (F) Tardive dyskinesia associated with serotonin receptors and H1 antagonism that lead to abnormal adaptation of striatal organization|
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In the cases related to DTN is observed the predominance of an elderly population, which could be explained by the reduced clearance of the drug that may increase the MTZ plasma levels and consequently the sensibility to the drug in this group of individuals. In addition, most of the early studies about the efficacy of MTZ showed a higher percentage of side effects in the elderly population when compared to a younger population, even though only a small percentage of the total individuals belonged to this group. Therefore, the initiation of MTZ in patients of sixty-five years or older should be at a low dose (7.5 mg or 15 mg) followed by a close follow-up.
When we analyzed the data found in [Table 1] about all MDs, we can see that only in one patient MTZ-indication was not for a psychiatric disorder, which is important because it decreases the possibility of the MDs found in the literature be psychogenic disorders. The most effective management was MTZ withdrawal.
The mechanism of DTN is poorly understood; as a result, we have many hypotheses in the literature. [Figure 4]B shows the most common explanations for the MTZ-induced DTN found in the literature. One possible explanation for this association is an increased direct pathway stimulation by the frontal cortex in the substantia nigra compact due to the release of norepinephrine (NE) and SER from the 5HT2C antagonism in the raphe nucleus with cortical projections; this is supported by studies showing frontal cortex hypermetabolism after MTZ. Another theory could be the direct action in 5HT2A receptors in the thalamus, as was already found in animal models,, leading to an increase of the thalamocortical drive by increasing direct pathway stimulation or decreasing the inhibitory projections to the thalamus. Both hypotheses above have a common pathway that is the cortico–striato–pallido–thalamo–cortical loop, which was first characterized in DTN secondary to stroke,.
Restless legs syndrome
RLS is probably the most underestimated of all abnormal movements secondary to MTZ. A prospective German study found that nine percent of patients receiving second-generation antidepressants had RLS-symptoms. In the study, 53 individuals were in use of MTZ, and more than twenty-five percent of these reported RLS-symptoms. Thus, we believe that this study included individuals with mild symptoms of RLS rather than just moderate-severe reports like most of the data found in the literature. Furthermore, the use of specific questions during the appointments about RLS probably led the researches to increase the number of diagnoses. When evaluating depressed patients, another important feature that more commonly occurs with RLS than with other MDs is the mixture of the patients' symptoms, in which the RLS-symptoms go unnoticed or are ignored in the absence of a basic screening by the physician, and possibly occurs due to the various complaints from patients.
There are at least three hypotheses for the explanation of RLS. The first hypothesis would be the prolonged use of dopamine antagonists, but we discard this theory because MTZ does not directly inhibit dopamine release. Another hypothesis is related to the central nervous system iron homeostasis, which was probably not the main mechanism responsible for the induced RLS because a long term alteration of the iron kinetic would be necessary to lead to abnormalities in the brain metabolism. The last hypothesis is an increase of SER in the brainstem [Figure 4]D. In this context, the antagonism of 5HT2C and 5HT2A could lead to disinhibition of serotoninergic neurons, and consequently causing the release of SER,. The SER release can affect the intermediolateral column and nucleus and provoke postganglionic adrenal glands to release NE, which causes the discomfort sensation in the limbs. Another possible pathway co-occurring is an increased firing rate of the raphe nucleus leading to NE release. Furthermore, NE release in the brainstem provokes insomnia, which is a common symptom reported by RLS patients,.
It is worthy of mentioning that MTZ worsening RLS-symptoms of RLS symptoms is a common-sense association among MDs specialists. Hence, MTZ should be avoided in patients with a previous history of RLS. In more than eighty percent of the MTZ-induced MDs, the management was drug withdrawal. However, in RLS, due to the lower severity of possible complications compared to other MDs, we may have more options depending on the situation. These choices include starting a new drug in association with MTZ to decrease the RLS symptoms, MTZ dose decrease, or even the rechallenge after a period of time. In this context, the MTZ rechallenge was attempted in two patients and was successful without the development of new symptoms.
The clinical description of the patients that developed AKT after MTZ use was the most comprehensible after the DTN group. However, sometimes, it was difficult to distinguish AKT patients from the RLS individuals due to overlap of the clinical manifestations of both disorders, what we will call AKT/RLS. One possible explanation for this common association with MTZ is that this drug interferes in a variety of pathways at the same time due to similar Ki values; as a result, MTZ interacts with noradrenergic, serotoninergic, and histaminergic receptors at the same time.
An interesting fact in the AKT subgroup was that the majority of the individuals were middle-aged adults with a mean age of 48 years, which is almost ten years younger than the general findings associated with MTZ, and with Asian origin. These findings can support the hypothesis of a probable genetic predisposition in this subgroup of individuals.
The pathophysiological mechanism of MTZ-induced AKT is based on psychopharmacological studies with substance use disorder, mainly with addict users that had drug-seeking behavior [Figure 4]C. It was already shown in rat models that 5HT2A antagonism leads to a decrease of dopamine in the surroundings of the nucleus accumbens, which signs by projections to the brainstem for release NE,. This neurotransmitter promotes the release of dopamine in the orbitofrontal cortex, leading to D1 hyperactivation and inducing AKT symptoms,. Furthermore, in the same context, MTZ antagonist effects on the central presynaptic alpha-2 antagonists cause an increased release of SER and NE in the brainstem reinforcing the process.
This MD was the only to reappear in all individuals that the drug was reintroduced. Thus, the best management in these situations should be the MTZ withdrawal without rechallenge. Also, if available, the prescription of a benzodiazepine for a short period of time due to possible faster recovery.
In the literature there is a lot of explanation about DKN secondary to medications, and many mechanisms were already proposed. In [Figure 4], we divided the DKN in [Figure 4]E, which represents the acute DKN, and [Figure 4]F, which represents the tardive DKN. We explained the tardive DKN associated with MTZ based on findings with serotoninergic neurotransmission in rat models, where probably the effects on 5HT and MTZ metabolites lead to damage by inflammation and oxidative stress, which culminate in an abnormal adaptation of the striatal organization leading to direct pathway overactivation. Otherwise, the acute DKN is probably more associated with antagonism H1 due to the time for the occurrence of the process described above; it is well known that antihistaminic medication can lead to DKN. The histamine receptors are commonly found throughout the central nervous system, but an important structure with a lot of H1 is the tuberomammillary nucleus, which has many connections with the cerebral cortex, neostriatum, hypothalamus, hippocampus, and nucleus accumbens. In this way, we hypothesized that in susceptible individuals, the disturbance by MTZ antagonism effect in the H1 receptor, mainly localized, in the tuberomammillary nucleus may play a central role in the pathophysiological mechanism of the acute DKN.
Tremor, tics, and other movement disorders
Four patients were assumed to have a diagnosis of parkinsonism in the use of MTZ; only two were clinically reported as having secondary parkinsonism. Nevertheless, Yamada et al. and Uvais et al. did not clearly describe the neurological examination, and they lack information about the characterization of bradykinesia,. Therefore, even though the diagnosis of parkinsonism in those cases is possible, we believe that a diagnosis of an exacerbation of physiological tremor, which can be explained by the increase of NE release in a situation such as stress and anxiety, is more probable more probable. In this context, MTZ interference in the α2 receptor enhances the release of NE and SER in the central nervous system leading to tremors. Or even another possible pathway correlated with the RLS/AKT mechanisms can be suspected. One supporting feature of this theory is the fact that the general description of the patients' symptoms. Moreover, the PLMD may also be related in the same way as tremor and RLS/AKT overlap pathways.
Tics were only reported in one individual, and Liu et al. proposed that tics may result in a dopamine surge by the interaction between serotoninergic receptors and the dopaminergic system. They include that the hyperadrenergic status by the MTZ antagonism in the alpha-2 receptor could contribute to the development of the tics.
Other movements not clearly defined in some reports include the description of restlessness and hyperkinesis that are general terms. We believe that these cases were referring AKT, but the data about the specific symptoms and physical examination of the patients were not provided by the studies. In addition, Madhusoodanan et al. reviewed the literature and found one patient with extrapyramidal symptoms associated with MTZ, but they did not describe or give a reference for the study. As is in the majority of the cases, the management in these conditions was the drug withdrawal and the follow-up had good outcomes with fast and full recovery.
| Conclusion|| |
MTZ is associated with RLS, tremors, AKT, PLMD, DTN, rapid eye movement sleep behavior disorders, DKN, parkinsonism, and tic. In the literature, the number of reports about MTZ-associated MD is probably of only moderate–severe cases with lacking data about mild conditions. However, in general, this drug is probably uncommonly related to abnormal movements. The management should be the MTZ withdrawal, except in RLS cases that other options are possible. In AKT, the MTZ should not be rechallenge, and if available, the prescription of a benzodiazepine may reduce recovery time. Further reports of MTZ-associated MDs need to focus on the times of MD onset and recovery, as well as the long follow-up of the patient. These data should be provided for a future assessment of the significance of these abnormal movements to predict the development of MDs such as Parkinson's disease.
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Conflicts of interest
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