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Investigational Treatment of Depressive Disorders With Neuroactive Steroids: Potential Implications for Premenstrual Dysphoric Disorder
J Clin Psychiatry 2021;82(4):20ac13853
To cite: Szpunar MJ, Freeman MP. Investigational treatment of depressive disorders with neuroactive steroids: potential implications for premenstrual dysphoric disorder. J Clin Psychiatry. 2021;82(4):20ac13853.
To share: https://doi.org/10.4088/JCP.20ac13853
© Copyright 2021 Physicians Postgraduate Press, Inc.
aAmmon-Pinizzotto Center for Women’s Mental Health, Department of Psychiatry, Massachusetts General Hospital, Boston, Massachusetts
*Corresponding author: Mercedes J. Szpunar, MD, PhD, Ammon-Pinizzotto Center for Women’s Mental Health, Department of Psychiatry, Massachusetts General Hospital, 185 Cambridge St, Suite 2200, Boston, MA 02114 (firstname.lastname@example.org).
The pathophysiology of premenstrual dysphoric disorder (PMDD) has been the subject of investigation for years.1 PMDD is defined as an increase in 5 or more mood symptoms, such as mood lability, irritability, and anxiety, during the week before menses that resolve after the onset of menses and cause significant distress or impairment,2 and it affects up to 6% of women.3,4 Past theory postulated that PMDD was due to an abnormal response to normal hormonal changes.5 More recent schema implicates changes in the production and/or signaling of ovarian-produced steroids during the menstrual cycle as a possible contributing mechanism.6–8 In a prior ASCP Corner, Carlini and Deligiannidis9 reviewed evidence-based treatments for PMDD, which include selective serotonin reuptake inhibitors (SSRIs) and combination drospirenone–ethinyl estradiol oral contraceptives. Importantly, despite these first-line treatments, many women with PMDD have residual or treatment-resistant symptoms, and more options are needed. In fact, gonadotropin-releasing hormone agonists are sometimes used, although the data are mixed, and they have potential for adverse effects.4,5,8,9 Hence, novel therapeutics are still needed for PMDD, and neuroactive steroids are an emerging class of medications of interest for the treatment of PMDD.
Neuroactive steroids are synthesized in the brain and endocrine organs to modulate behavior—including reproductive behavior—but also other essential neuroactivity including the hypothalamic pituitary adrenal (HPA) axis, neuroprotection, and immune function.7,10 By definition, neurosteroids are produced in the brain and can have effects on both excitatory and inhibitory neurotransmission.10 They can rapidly induce anxiolytic and sedative effects via positive allosteric modulation of γ-aminobutyric acid A (GABAA) receptors,11,12 but they can have other effects depending on brain region and specific neurosteroid.10 Acute stress increases the synthesis of neurosteroids, and due to their lipophilic nature, they cannot be stored and must be produced de novo.13 They are capable of passing through the blood-brain barrier.12,13 Progesterone-derived neuroactive steroids include allopregnanolone (ALLO) and its stereoisomer pregnanolone,14 and ALLO levels in brain and plasma parallel that of progesterone.10,15 In reproductive-age women, the ovary is responsible for increased ALLO during the luteal phase of the menstrual cycle, specially via production by the corpus luteum.15,16
A number of investigators have compared changes in mood with ALLO during the menstrual cycle. Prior to the addition of PMDD to the Diagnostic and Statistical Manual of Mental Disorders in 2013,2 researchers commonly studied premenstrual syndrome (PMS) in its stead.3 PMS has been described as a disorder of mood and somatic symptoms during the luteal phase of the menstrual cycle that resolves at or soon after the onset of menstruation5 and does not require any specific symptom nor number of symptoms.4 Wang and colleagues17 measured serum progesterone and ALLO during the luteal phase in women with PMS for 2 consecutive cycles. When compared with heathy women, the women with PMS had lower progesterone but no difference in ALLO. Among only the women with PMS, the participants with higher ALLO had lesser PMS symptom ratings. Similarly, Monteleone et al18 sought to determine basal progesterone and ALLO levels in women with PMS. In comparison to healthy women, women with PMS had significantly lower progesterone and ALLO during the luteal phase, but only progesterone was lower during the follicular phase.18 Both studies indicate that lower ALLO was associated with increased symptoms for the women with PMS.
Several more complex studies demonstrated alterations in women with PMDD after repeat ALLO measurement or in response to its administration. Girdler and colleagues19 measured ALLO in women with PMDD and healthy women during both follicular and luteal phases and then repeated ALLO assessment 17 minutes after a stressor. Compared with healthy women during the luteal phase, the women with PMDD had higher ALLO at baseline, but stress increased ALLO 83% in the healthy women compared with only 42% in the women with PMDD, indicating a dampened response in the women with PMDD. Upon additional analysis of the PMDD cohort, the authors determined an inverse relationship between premenstrual anxiety and irritability in comparison with ALLO during the luteal phase.19 Timby et al20 did not observe any difference in ALLO between women diagnosed with PMDD when compared with healthy women during either the follicular or luteal phases. However, women with PMDD exhibited increased sensitivity to administration of intravenous ALLO during both phases of the menstrual cycle compared with the healthy women, but this response was reduced during the luteal phase.20 All together, these studies demonstrate inconsistent patterns regarding the impact of ALLO on PMDD but suggest alterations that parallel mood and sensitivity changes during the luteal phase in a subgroup of susceptible women.
Given the paucity of data specific to ALLO and PMDD, some inferences can be drawn from the literature regarding ALLO in other psychiatric disorders. Multiple investigators have implicated alterations in GABA neurotransmission in the pathogenesis of major depressive disorder (MDD)21 and specifically in women.22 In several small studies, ALLO was reduced in individuals with MDD compared with healthy controls, but it was raised to normal levels after successful treatment of depression with SSRIs.23–25 In a cohort of pregnant women, there was no relationship between second or third trimester plasma ALLO with MDD, but pregnant women with lower ALLO during the second trimester of pregnancy were more likely to develop symptoms of postpartum depression (PPD) compared with women who did not.26 In a subsequent study, lower ALLO during the second trimester of pregnancy was significantly associated with increased anxiety at 6 weeks postpartum, and lower ALLO during the second trimester trended toward increased depressive symptoms at 6 weeks postpartum.27 Hence, it is plausible that ALLO plays a role in the mechanism of psychiatric illness in a subset of individuals with underlying biologic vulnerability.
ALLO acts to positively modulate GABAA receptors and produces potent anxiolytic effects.11 Several pharmaceutical agents that mimic or oppose the action of ALLO are currently under investigation as treatment for depressive disorders including PPD and PMDD. In a randomized, placebo-controlled study, brexanolone—an intravenous, synthetic formulation of ALLO—resulted in significant reduction of depressive symptoms for women with PPD.28 Although it is the only FDA-approved medication for PPD, the treatment is a single 60-hour intravenous infusion, and available follow-up data are limited to 30 days post-infusion. Additionally, participation in a risk and evaluation mitigation strategy program is required due to risk of excessive sedation and sudden loss of consciousness.29 In contrast to the mechanism of brexanolone, isoallopregnanolone (also known as isopregnanolone) is an endogenous, negative allosteric modulator of GABAA receptors.30 Bixo and colleagues31 administered isoallopregnanolone (UC1010) subcutaneously to women with PMDD on the second day of the luteal phase to test if ALLO inhibition would alter their symptom course. Although some of their results were confounded by women with comorbid psychiatric disorders, the participants with pure PMDD experienced a 75% reduction in symptoms with isoallopregnanolone administration.31 These significant mood improvements in women with pure PMDD indicate a need to further clarify the utility of GABAA receptor modulation for this specific illness. To our knowledge, no other synthetic neuroactive steroid has been investigated specifically for PMDD.
Several oral medications are under investigation as treatment for PMDD, MDD, and postmenopausal depression, but limited bioavailability of the oral neuroactive steroids has been suggested as a limitation to their efficacy.32 Recently, Comasco et al33 treated women with PMDD in a double-blind, randomized, placebo-controlled trial with a selective progesterone receptor modulator, ulipristal acetate (UPA), which acts as a progesterone antagonist. The women who received UPA 5 mg daily for 3 months had a significant reduction of symptoms as measured by the Daily Record of Severity of Problems. In fact, 85% of the women treated with UPA had partial or complete remission of symptoms.33 Dichtel and colleagues34 published results of an open-label pilot study of an oral analog of ALLO, ganaxolone (225 or 450 mg twice daily), as adjunctive treatment for postmenopausal depression. All participants were treated with an antidepressant for at least 6 weeks prior to enrollment, and duration of ganaxolone administration lasted between 7 and 10 weeks. Prior to treatment, the authors determined a positive association with baseline ALLO level and greater depression severity, although the majority of participants (6 of 10) had undetectable levels. As anticipated, ganaxolone reduced depressive symptoms, and while the participants had significant improvements in overall sleep, they also experienced daytime sleepiness.34 In a randomized, placebo-controlled trial, another synthetic neuroactive steroid, SAGE-217, was orally administered to both men and women with moderate-to-severe depression for 14 days at a dose of 30 mg once daily. At day 15, the treatment arm had a statistically significant reduction of depressive symptom severity, but the authors did not collect data beyond that time point. Similar to the trials with ganaxolone, participants experienced sedation from SAGE-217.35 In a subsequent study with over 300 male and female participants, SAGE-217 30 mg administered daily for 2 weeks did not demonstrate a difference in depression symptoms at day 15, but the investigators noted a high placebo response and lack of measurable drug concentration for 9% of participants.36 Further investigation is required to determine duration of treatment response, appropriate dosing given lower than expected drug concentrations for both oral agents, and ideal target population(s) with careful consideration of sex and disorder. Additionally, it may prove important to perform data collection with consideration of menstrual cycling.
Thus, targeting GABAA receptor signaling via neuroactive steroids may have therapeutic implications for multiple depressive disorders including PMDD, but more investigation is required to elucidate their utility. Practically speaking, oral compounds are generally preferred for patient self-administration, and some women prefer not to take exogenous hormones. Additionally, bioavailability of oral neuroactive steroids is an important concern.32 The adverse effect of sedation caused by these compounds could be utilized for benefit given likelihood of sleep disturbance in this population. Notably, the promising findings for MDD in men and women suggest a broader treatment effect beyond application to times of gonadal steroid changes in women. Larger, placebo-controlled trials are warranted to determine appropriate dose, timing of administration, and duration of these potential therapies by indication.
Published online: June 8, 2021.
Potential conflicts of interest: Dr Freeman has the following disclosures: investigator-initiated trials/research: JayMac, Sage; advisory boards: Otsuka, Alkermes, Sunovion, Eliem; independent data safety and monitoring committee: Janssen (Johnson & Johnson), Novartis; steering committee for educational activities: Medscape; educational activities: WebMD; employee of Massachusetts General Hospital (MGH) and works with the MGH National Pregnancy Registry (current registry sponsors: Teva [2018– present], Alkermes, Inc. [2016–present]; Otsuka America Pharmaceutical, Inc. [2008–present]; Forest/Actavis [2016–present], Sunovion Pharmaceuticals, Inc. [2011–present]); and as an employee of MGH, works with the MGH Clinical Trials Network and Institute, which has had research funding from multiple pharmaceutical companies and National Institute of Mental Health. Dr Szpunar reports no potential conflict of interest.
Funding/support: Dr Szpunar was supported by the Department of Veterans Affairs Advanced Fellowship in Women’s Health.
The ASCP Corner, edited by Leslie L. Citrome, MD, MPH, is a collection of brief peer-reviewed, evidence-based articles, authored by American Society of Clinical Psychopharmacology members, that examine the practice of psychopharmacology through the lens of clinical experience. The information contained herein only represents the opinion of the author(s).