Mirtazapine for fibromyalgia in adults Edited (no change to conclusions)

Abstract

Abstract Background

Fibromyalgia is a clinically defined chronic condition of unknown etiology characterised by chronic widespread pain, sleep disturbance, cognitive dysfunction, and fatigue. Many patients report high disability levels and poor quality of life. Drug therapy aims to reduce key symptoms, especially pain, and improve quality of life. The tetracyclic antidepressant, mirtazapine, may help by increasing serotonin and noradrenaline in the central nervous system (CNS).

Objectives

To assess the efficacy, tolerability and safety of the tetracyclic antidepressant, mirtazapine, compared with placebo or other active drug(s) in the treatment of fibromyalgia in adults.

Search methods

We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, SCOPUS, the US National Institutes of Health, and the World Health Organization (WHO) International Clinical Trials Registry Platform for published and ongoing trials, and examined reference lists of reviewed articles, to 9 July 2018.

Selection criteria

Randomised controlled trials (RCTs) of any formulation of mirtazapine against placebo, or any other active treatment of fibromyalgia, in adults.

Data collection and analysis

Two review authors independently extracted study characteristics, outcomes of efficacy, tolerability and safety, examined issues of study quality, and assessed risk of bias, resolving discrepancies by discussion. Primary outcomes were participant‐reported pain relief (at least 50% or 30% pain reduction), Patient Global Impression of Change (PGIC; much or very much improved), safety (serious adverse events), and tolerability (adverse event withdrawal). Other outcomes were health‐related quality of life (HRQoL) improved by 20% or more, fatigue, sleep problems, mean pain intensity, negative mood and particular adverse events. We used a random‐effects model to calculate risk difference (RD), standardised mean difference (SMD), and numbers needed to treat. We assessed the evidence using GRADE and created a 'Summary of findings' table.

Main results

Three studies with 606 participants compared mirtazapine with placebo (but not other drugs) over seven to 13 weeks. Two studies were at unclear or high risk of bias in six or seven of eight domains. We judged the evidence for all outcomes to be low‐ or very low‐quality because of poor study quality, indirectness, imprecision, risk of publication bias, and sometimes low numbers of events.

There was no difference between mirtazapine and placebo for any primary outcome: participant‐reported pain relief of 50% or greater (22% versus 16%; RD 0.05, 95% confidence interval (CI) ‐0.01 to 0.12; three studies with 591 participants; low‐quality evidence); no data available for PGIC; only a single serious adverse event for evaluation of safety (RD ‐0.00, 95% CI ‐0.01 to 0.02; three studies with 606 participants; very low‐quality evidence); and tolerability as frequency of dropouts due to adverse events (3% versus 2%; RD 0.00, 95% CI ‐0.02 to 0.03; three studies with 606 participants; low‐quality evidence).

Mirtazapine showed a clinically‐relevant benefit compared to placebo for some secondary outcomes: participant‐reported pain relief of 30% or greater (47% versus 34%; RD 0.13, 95% CI 0.05 to 0.21; number needed to treat for an additional beneficial outcome (NNTB) 8, 95% CI 5 to 20; three studies with 591 participants; low‐quality evidence); participant‐reported mean pain intensity (SMD ‐0.29, 95% CI ‐0.46 to ‐0.13; three studies with 591 participants; low‐quality evidence); and participant‐reported sleep problems (SMD ‐0.23, 95% CI ‐0.39 to ‐0.06; three studies with 573 participants; low‐quality evidence). There was no benefit for improvement of participant‐reported improvement of HRQoL of 20% or greater (58% versus 50%; RD 0.08, 95% CI ‐0.01 to 0.16; three studies with 586 participants; low‐quality evidence); participant‐reported fatigue (SMD ‐0.02, 95% CI ‐0.19 to 0.16; two studies with 533 participants; low‐quality evidence); participant‐reported negative mood (SMD ‐0.67, 95% CI ‐1.44 to 0.10; three studies with 588 participants; low‐quality evidence); or withdrawals due to lack of efficacy (1.5% versus 0.1%; RD 0.01, 95% CI ‐0.01 to 0.02; three studies with 605 participants; very low‐quality evidence).

There was no difference between mirtazapine and placebo for participants reporting any adverse event (76% versus 59%; RD 0.12, 95 CI ‐0.01 to 0.26; three studies with 606 participants; low‐quality evidence). There was a clinically‐relevant harm with mirtazapine compared to placebo: in the number of participants with somnolence (42% versus 14%; RD 0.24, 95% CI 0.18 to 0.30; number needed to treat for an additional harmful outcome (NNTH) 5, 95% CI 3 to 6; three studies with 606 participants; low‐quality evidence); weight gain (19% versus 1%; RD 0.17, 95% CI 0.11 to 0.23; NNTH 6, 95% CI 5 to 10; three studies with 606 participants; low‐quality evidence); and elevated alanine aminotransferase (13% versus 2%; RD 0.13, 95% CI 0.04 to 0.22; NNTH 8, 95% CI 5 to 25; two studies with 566 participants; low‐quality evidence).

Authors' conclusions

Studies demonstrated no benefit of mirtazapine over placebo for pain relief of 50% or greater, PGIC, improvement of HRQoL of 20% or greater, or reduction of fatigue or negative mood. Clinically‐relevant benefits were shown for pain relief of 30% or greater, reduction of mean pain intensity, and sleep problems. Somnolence, weight gain, and elevated alanine aminotransferase were more frequent with mirtazapine than placebo. The quality of evidence was low or very low, with two of three studies of questionable quality and issues over indirectness and risk of publication bias. On balance, any potential benefits of mirtazapine in fibromyalgia were outweighed by its potential harms, though, a small minority of people with fibromyalgia might experience substantial symptom relief without clinically‐relevant adverse events.

Author(s)

Patrick Welsch, Kathrin Bernardy, Sheena Derry, R Andrew Moore, Winfried Häuser

Abstract

Plain language summary

Mirtazapine for treating fibromyalgia in adults

Bottom line

Mirtazapine at 15 mg to 45 mg daily is unlikely to substantially reduce pain in people with fibromyalgia. Mirtazapine can cause drowsiness, weight gain, and liver damage. A small number of people may experience some improvement (moderate pain relief, better sleep) without side effects from mirtazapine, but that cannot be predicted. The off‐label use of mirtazapine can be considered, if established treatment options have failed.

Background

People with fibromyalgia often have chronic (longer than 3 months) widespread pain, and problems with sleeping, thinking, exhaustion, and poor quality of life. There is no cure for fibromyalgia. Treatments aim to improve symptoms (pain, sleep problems, fatigue) and quality of life.

Serotonin and noradrenaline are chemicals produced by the human body and are involved in pain, sleep, and mood. Low serotonin levels have been found in people with fibromyalgia. The antidepressant, mirtazapine, increases serotonin and noradrenaline levels in the brain.

Study characteristics

In July 2018 we searched for clinical trials where mirtazapine was used to treat fibromyalgia in adults. We found three studies with 606 participants. Studies were seven to 13 weeks long. They compared mirtazapine 15 mg to 45 mg daily against a fake medication (placebo).

Key results

There was no difference between mirtazapine and placebo for any primary outcome: mirtazapine and placebo reduced pain by 50% in two of 10 people (low‐quality evidence). Only one single serious adverse event was available for evaluation of safety (very low‐quality evidence). Three of 10 participants with mirtazapine and two of 10 participants with placebo dropped out of the trial due to side effects (low‐quality evidence).

Mirtazapine reduced pain by 30% or more in five out of 10 people, compared with three out of 10 with placebo (low‐quality evidence). It was also better for average pain intensity (low‐quality evidence) and sleep problems (low‐quality evidence). Mirtazapine was not better than placebo in reducing fatigue, depression, or improving health‐related quality of life (low‐quality evidence). Mirtazapine and placebo were no different in how many participants experienced a side effect (low‐quality evidence). People dropped out at the same rate with mirtazapine and placebo or because they felt the drug did not work (low‐quality evidence). For some side effects, mirtazapine was worse than placebo. This was true for drowsiness (4 out of 10 with mirtazapine, 1 out of 10 with placebo), weight gain (2 out of 10 with mirtazapine, 0 out of 10 with placebo), and high liver enzymes (1 out of 10 with mirtazapine, 0 out of 10 with placebo) (low‐quality evidence).

Quality of the evidence

Two of the studies were of poor quality. We rated the quality of the evidence using four levels: very low, low, moderate, or high. Very low‐quality evidence means that we are very uncertain about the results. High quality evidence means that we are very confident in the results. We judged that the evidence was mostly of low‐quality, which means that while the research provides some indication of the likely effect, the true effect may be substantially different. The main issues were poor study quality, decisions about the types of people included in the studies, risk of important information not being published, and sometimes low numbers of events.

Author(s)

Patrick Welsch, Kathrin Bernardy, Sheena Derry, R Andrew Moore, Winfried Häuser

Reviewer's Conclusions

Authors' conclusions

Implications for practice For people with fibromyalgia

Only a minority of people may benefit from treatment with mirtazapine in terms of meaningful relief of pain and sleep problems, without clinically‐relevant side effects. The majority of people will not experience substantial relief of fibromyalgia symptoms, or will experience clinically‐relevant side effects (weight gain, somnolence, liver damage), or both.

For physicians

Mirtazapine is not approved for fibromyalgia in any country. Mirtazapine is approved for depressive disorders in many countries.

Because of the side effect profile of mirtazapine, an off‐label therapeutic trial might be considered in people who do not tolerate duloxetine or milnacipran due to gastrointestinal adverse events (nausea, vomiting). If mirtazapine is being considered for the treatment of fibromyalgia, a frank discussion between the physician and patient about the potential benefits and harms of the treatment options is important. The warnings (suicide risk, concomitant use of monoaminoxidase inhibitors, agranulocytosis) and precautions (hepatotoxicity, weight gain, increase of cholesterol/triglycerides) should be discussed (FDA 2017). It is important to define realistic goals of treatment (e.g. pain relief of 30% or more or improvement of daily functioning, or both; Petzke 2017).

The optimal treatment dosage of mirtazapine remains to be determined. A dose response has not yet been demonstrated. Higher doses were associated with more weight gain in one study (Yeephu 2013). Therefore a starting dose of 15 mg/d at bedtime seems reasonable. It is mandatory to continue treatment for responders only, that is to say in those who reach the predefined treatment goals with a reasonable tolerability of mirtazapine (Petzke 2017).

Therapy of fibromyalgia with drugs only is discouraged since current best practices in fibromyalgia guidelines recommend using the combination of pharmacological therapy with aerobic exercise and psychological therapies (Macfarlane 2017; Petzke 2017). This is especially true for symptoms where mirtazapine is ineffective, but other therapies are effective, e.g. aerobic exercise for fatigue (Bidonde 2017), and cognitive‐behavioral therapies for depression (Bernardy 2018).

Since few participants achieve a worthwhile response with mirtazapine, it is important to establish stopping rules, so that when someone does not respond within a specified time, they can be switched to an alternative treatment. This will reduce the number of participants exposed to adverse events in the absence of benefit.

For policy‐makers

Since no single treatment is effective in a majority of individuals with fibromyalgia, the relatively small number who benefit may be considered worthwhile, particularly if a) established treatment options have failed, b) appropriate switching or stopping rules are in place, and c) prescribing is under the control of physicians experienced in treating people with fibromyalgia.

For funders

Treatment with mirtazapine for fibromyalgia may be considered worthwhile, particularly if a) established treatment options have failed, and b) switching and stopping rules are in place in case the predefined treatment goals are not reached or the drug is not well‐tolerated, or both. Treatment should be supervised by a physician experienced in the use of mirtazapine.

Implications for research General

Analysis of all studies investigating mirtazapine in fibromyalgia at the level of individual patient data could provide important information, e.g. whether or not a clinically important pain response delivers large functional and quality of life benefits. Moreover, a reanalysis of the data using baseline observation carried forward, and responder analysis where discontinuation is classified as nonresponse, would allow a determination of the true efficacy of mirtazapine in fibromyalgia. All journals should follow the rules of the BMJ that reports that randomised trials will only be considered for publication if the authors commit to making the relevant anonymous patient level data available on reasonable request (Godlee 2012).

Studies in any continent with the inclusion of people with inflammatory rheumatic diseases, osteoarthritis and mental disorders (depressive and anxiety disorders, post‐traumatic stress disorder) are necessary to provide external validity of the study findings.

A standardised psychiatric interview at study entry could stratify participants according to comorbid anxiety and depressive disorders.

Generalisability of results requires study populations that are equally recruited from every continent.

It is mandatory that details of adverse event assessments (spontaneous reports, open question structured questions, symptom questionnaires) are reported by the studies because the type and frequency of adverse events is influenced by modes of assessment (Häuser 2012). Adverse events are to be reported using the International Conference on Harmonization guidelines, and coded within organ classes using the Medical Dictionary for Regulatory Activities (MedDRA version 18.0; ICH 2015). It is desirable that regulatory agencies standardise the assessment strategies of adverse events in RCTs.

It is important to control for potential effects of cointerventions on outcomes.

Measurement (endpoints)

We recommend the use of responder criteria for the key symptoms and functional domains of fibromyalgia, namely pain, sleep problems, fatigue, depression, health‐related quality of life (HRQoL) and physical function (disability). The following responder criteria (from baseline to end of treatment) for clinical trials have been suggested: ≥ 30% pain reduction; ≥ 10% improvement in SF (Short Form Health Survey)‐36 physical function or ≥ 10% improvement in Fibromyalgia Impact Questionnaire (FIQ) physical function; ≥ 20% improvement in two of the following domains: fatigue (FIQ tiredness), sleep (FIQ rested), depression (FIQ depression), anxiety (FIQ anxiety), or cognition (Multiple Ability Self‐Report Questionnaire (MASQ)) (Arnold 2012b). For HRQoL, a ≥ 20% reduction of the FIQ total score has been suggested to be clinically‐relevant (Luciano 2014).

Comparison between active treatments

It is important to compare mirtazapine not only with placebo, but also with drugs of known efficacy, such as amitriptyline or pregabalin. In addition, more studies with defined subgroups (e.g. major depression; no adequate response to a specific drug treatment) are necessary.

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