Bipolar dysfunction (BD) is a disabling situation characterised by episodes of mania or hypomania, alternating or co-occurring with despair (American Psychiatric Affiliation, 2013; GBD, 2019).
Analysis means that depressive signs are predominant in BD and will current higher burden in comparison with elevated options (Judd et al., 2002; Judd et al., 2003; Miller et al., 2014). Nonetheless, using antidepressants for bipolar despair is debatable, as their security and efficacy stay unsure (McGirr et al., 2016; Pacchiarotti et al., 2013; Sachs et al., 2007).
As highlighted in a Psychological Elf weblog publish by Prof Joseph Hayes, the Nationwide Institute for Well being and Care Excellence (NICE) 2014 pointers for BD (NICE, 2014) point out that fluoxetine could also be preferable to different antidepressants. The British Affiliation for Psychopharmacology 2016 pointers recommend that antidepressants in BD could be efficient, however solely together with temper stabilisers (Goodwin et al., 2016).
Proof means that the chance of mania could also be higher for tricyclic antidepressants (TCA), in comparison with selective serotonin reuptake inhibitors (SSRIs) (Goodwin et al., 2016; Tondo et al., 2010). Though findings from randomised managed trials (RCTs) are conflicting, there may be some proof that extended remedy with antidepressants could worsen manic or hypomanic signs in BD (Ghaemi et al., 2021; McGirr et al., 2016; Yatham et al., 2023).
A latest goal trial emulation by Rohde et al. 2024, aimed to shed some mild on the chance of antidepressant-induced mania in folks with bipolar despair.
Strategies
Rohde et al.’s (2024) examine employed a ‘goal trial emulation’ mannequin (Matthews et al., 2022), whereby they have been capable of leverage knowledge gathered by Danish nationwide registers whereas incorporating core traits of the gold customary in evidence-based drugs: the randomised managed trial (RCT).
In a goal trial emulation, pre-existing observational knowledge is compiled and manipulated such that the ideas that govern a conventional RCT are upheld: individuals are recognized, screened in response to rigorous standards after which the info is stratified as a proxy for randomisation. Authors assessed mania as psychiatric admission with a main analysis of a manic or hypomanic episode.
Outcomes
The ultimate examine cohort consisted of 979 sufferers with bipolar despair, 36.6% (n = 358) of whom acquired remedy with antidepressants. The intercourse and age traits have been comparable between the antidepressant and non-antidepressant teams.
Apparently, of these handled with antidepressants, solely 62.6% used them concurrently with temper stabilisers. Amongst sufferers within the antidepressant group, round 50.5% (n=181) acquired an SSRI, 14.3% (n=51) a TCA and 11.5% (n=41) a serotonin and norepinephrine reuptake inhibitors (SNRIs). The remaining 85 sufferers have been handled with one other sort of antidepressant.
Rohde et al (2024) declare that contemplating the impact measurement of a hazard ratio of 1.77 (primarily based on a meta-analysis by McGirr et al., 2016), their examine achieved energy of 90%.
- The totally adjusted fashions which included your entire pattern, confirmed no statistically important associations between antidepressant remedy and mania or hypomania, (hazard fee ratio=1.08, 95% CI=0.72 to 1.61) (a hazard ratio of 1 signifies the dearth of an affiliation).
- Antidepressant remedy was not considerably related to danger of mania or hypomania
- amongst these handled with temper stabilisers (hazard fee ratio=1.16, 95% CI=0.63 to 2.13)
- or people who did not obtain a temper stabiliser (hazard fee ratio=1.16, 95% CI=0.65 to 2.07).
- Secondary analyses indicated that the chance of bipolar despair recurrence was not related to antidepressant use (hazard ratio=0.91, 95% CI=0.65 to 1.27).
Conclusions
This was a goal trial emulation which used observational knowledge from Danish well being registers to evaluate the chance of mania in bipolar despair following antidepressant use over a interval of 1 12 months.
Authors concluded: “findings recommend that the chance of antidepressant-induced mania is negligible” and highlighted the necessity for additional analysis. Nevertheless, proof from different research means that extended remedy with antidepressants is linked with elevated danger of manic or hypomanic signs in BD (McGirr et al., 2016; Yatham et al., 2023; Tondo et al., 2010).
Though the examine by Rohde and colleagues (2024) improved our understanding of the so-called “temper swap” following remedy with antidepressants in BD, given its methodological limitations and the conflicting findings from the literature, additional analysis on this matter is warranted.
Strengths and limitations
Rohde et al.’s implementation of a goal trial emulation mannequin supplied them with some notable methodological advantages:
- Giant pattern measurement: their use of Danish nationwide registers supplied them with a remaining cohort of 979 – this, they observe, meant their examine was bigger than any of the earlier antidepressant trials with bipolar despair sufferers.
- Prolonged ‘follow-up’ interval: this examine adopted sufferers for a 12 months, until both readmission or demise occurred. This represents one of many longest follow-up durations for a examine of this subject.
Nevertheless, regardless of the assorted upsides to their examine design, there stay quite a few limitations and disadvantages. In any case, whereas goal trial emulations search to approximate the scientific rigour of RCTs by making use of their ideas to observational knowledge, they’re not an ideal substitute for correctly managed ‘dwell’ research.
- Restricted administration of individuals: Rohde et al. have been capable of assign individuals to circumstances, however couldn’t prohibit their course of remedy. Greater than 1 / 4 of these initially assigned to the non-antidepressant situation on this trial finally began a course of antidepressants.
- Restricted utility of findings: Rohde et al.’s knowledge didn’t facilitate distinctions between bipolar I and II issues. Which means that their examine can not inform as as to if there’s a distinction in charges of antidepressant-induced [hypo]mania between the 2 sorts.
- Decreased generalisability: the eligibility standards for this examine excluded individuals who skilled an episode with out being hospitalised, thereby limiting the examine’s relevance to sufferers who’ve been admitted at the very least as soon as.
Implications for follow
The authors clarify how their findings point out that the chance of antidepressants inflicting mania in bipolar dysfunction sufferers is negligible, and that whereas widespread in sufferers handled with antidepressants, manic episodes are doubtlessly merely a consequence of the recurrent nature of the dysfunction and never a facet impact of remedy. Furthermore, the outcomes of their emulation examine help the notion that antidepressants don’t essentially trigger mania.
As knowledge continues to build up on this space, we could finally witness a shift in clinicians’ attitudes in the direction of the prescription of antidepressants as remedy for bipolar despair, particularly within the short-term. Nevertheless, present pointers for bipolar dysfunction don’t suggest monotherapy of antidepressants (Goodwin et al 2016). At the moment, as famous by Rohde et al., clinicians are significantly cautious when contemplating prescribing antidepressants for sufferers with bipolar dysfunction, given the prevailing view that there’s an elevated danger of mania. Rohde et al. recommend that this warning could also be mirrored of their knowledge, with their findings indicating a extra extreme medical course amongst sufferers that have been not handled with an antidepressant. This cohort, on common, noticed the next variety of hospital admissions, outpatient contacts and episodes of mania than these of their antidepressant-using counterparts.
Whereas the findings of Rohde et al. do serve to bolster a rising physique of proof towards the notion that antidepressants are essentially at fault for elevated charges of manic episodes, they aren’t conclusive. That is due in no small half to the constraints of the examine described beforehand. To this finish, we consider that additional analysis is merited with a purpose to totally perceive whether or not:
- individuals who chorus from taking antidepressants for everything of a future examine (together with follow-up) fare higher or worse than these which can be prescribed with antidepressants throughout a trial;
- distinctions between bipolar I and II are additional mirrored by way of their response to antidepressant remedy; and
- the severity of manic signs is, on common, higher amongst these taking antidepressants – no matter whether or not they have been or are hospitalised resulting from a bipolar episode.
As soon as these points are addressed, not solely will we all know with higher confidence the general affect of antidepressant remedy inside the context of bipolar dysfunction, however clinicians will likely be extra knowledgeable as as to if a given affected person may stand to profit from such a course of remedy, primarily based on their distinctive circumstances (e.g., sort of bipolar dysfunction and up to date symptom severity).
Assertion of pursuits
Paul Leeks declares no conflicts of curiosity. Michail Kalfas has acquired honoraria from Neurocentrx Pharma.
Hyperlinks
Major paper
Rohde C, Østergaard SD, Jefsen OH. (2024). A Nationwide Goal Trial Emulation Assessing the Danger of Antidepressant-Induced Mania Amongst Sufferers With Bipolar Melancholy. The American Journal of Psychiatry 181(7) 630–638. https://doi.org/10.1176/appi.ajp.20230477
Different references
American Psychiatric Affiliation. (2013) Diagnostic and statistical handbook of psychological issues (fifth ed.).
Bobo WV. (2017) The Prognosis and Administration of Bipolar I and II Problems: Medical Follow Replace. Mayo Clinic proceedings, 92(10), 1532–1551. https://doi.org/10.1016/j.mayocp.2017.06.022
GBD 2019 Psychological Problems Collaborators. (2022) International, regional, and nationwide burden of 12 psychological issues in 204 nations and territories, 1990–2019: a scientific evaluation for the International Burden of Illness Research 2019. Lancet Psychiatry 9(2) 137-150.
Ghaemi SN, Whitham EA, Vohringer PA. et al (2021) Citalopram for Acute and Preventive Efficacy in Bipolar Melancholy (CAPE-BD): A Randomized, Double-Blind, Placebo-Managed Trial. The Journal of medical psychiatry 82(1) 19m13136.
Goodwin GM, Haddad PM, Ferrier IN. et al (2016) Proof-based pointers for treating bipolar dysfunction: Revised third version suggestions from the British Affiliation for Psychopharmacology. Journal of psychopharmacology (Oxford, England) 30(6) 495–553.
Judd LL, Akiskal HS, Schettler PJ. et al (2003) A potential investigation of the pure historical past of the long-term weekly symptomatic standing of bipolar II dysfunction. Archives of basic psychiatry 60(3) 261–269.
Judd LL, Akiskal HS, Schettler PJ. et al (2002) The long-term pure historical past of the weekly symptomatic standing of bipolar I dysfunction. Archives of basic psychiatry 59(6) 530-537.
Matthews A A, Danaei G, Islam N. et al (2022) Goal trial emulation: making use of ideas of randomised trials to observational research BMJ 378:e071108 doi:10.1136/bmj-2022-071108
McGirr A, Vöhringer PA, Ghaemi SN. et al (2016) Security and efficacy of adjunctive second-generation antidepressant remedy with a temper stabiliser or an atypical antipsychotic in acute bipolar despair: a scientific assessment and meta-analysis of randomised placebo-controlled trials. Lancet Psychiatry 3(12) 1138-1146.
Miller S, Dell’Osso B, Ketter TA. (2014) The prevalence and burden of bipolar despair. Journal of affective issues 169(1) S3-11.
Nationwide Institute for Well being and Care Excellence [NICE] (2014) Bipolar Dysfunction: evaluation and steerage. NICE medical guideline CG185.
Pacchiarotti I, Bond DJ, Baldessarini RJ. et al (2013) The Worldwide Society for Bipolar Problems (ISBD) job drive report on antidepressant use in bipolar issues. The American journal of psychiatry 170(11) 1249–1262.
Sachs GS, Nierenberg AA, Calabrese JR. et al (2007) Effectiveness of adjunctive antidepressant remedy for bipolar despair. The New England journal of drugs 356(17) 1711–1722.
Tondo L, Vázquez G, Baldessarini RJ. (2010) Mania related to antidepressant remedy: complete meta-analytic assessment. Acta psychiatrica Scandinavica 121(6) 404–414.
Yatham LN, Arumugham SS, Kesavan M. et al (2023) Period of Adjunctive Antidepressant Upkeep in Bipolar I Melancholy. The New England journal of drugs 389(5) 430–440.