The management of acne in adult females is problematic, with many having a history of treatment failure and some having a predisposition to androgen excess. Alternatives to oral antibiotics and combined oral contraceptives (COCs) are required.
Our aim was to conduct a hybrid systematic review of the evidence for benefits and potential harms of oral spironolactone in the management of acne in adult females.
The review was conducted according to a previously published protocol. Three reviewers independently selected relevant studies from the search results, extracted data, assessed the risk of bias, and rated the quality of the evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.
Ten randomized controlled trials (RCTs) and 21 case series were retrieved. All trials were assessed as being at a ‘high risk’ of bias, and the quality of evidence was rated as low or very low for all outcomes. Apart from one crossover trial that demonstrated statistical superiority of a 200 mg daily dose versus inflamed lesions compared with placebo, data from the remaining trials were unhelpful in establishing the degree of efficacy of lower doses versus active comparators or placebo. Menstrual side effects were significantly more common with the 200 mg dose; frequency could be significantly reduced by concomitant use of a COC. Pooling of results for serum potassium supported the recent recommendation that routine monitoring is not required in this patient population.
This systematic review of RCTs and case series identified evidence of limited quality to underpin the expert endorsement of spironolactone at the doses typically used (≤100 mg/day) in everyday clinical practice.
Oral spironolactone is used off-label to treat persistent and late-onset acne in adult females.
There is low-quality evidence for benefits and side effects from randomized controlled trials and case series; superiority over placebo has not been established for doses <200 mg/day.
Prescribing recommendations must continue to rely on consensus and expert opinion until high-quality evidence becomes available.
Acne is the eighth most prevalent disease globally . While this chronic inflammatory skin condition affects mostly adolescents, adult females represent a significant and increasing proportion of cases in which quality of life is severely affected [2–5].
A number of variants of acne in adult women are recognized, based on age of onset, distribution and type of lesions, recalcitrance to conventional drug-based remedies, predisposing factors (e.g. smoking, ethnicity), and endocrine disposition, most commonly polycystic ovarian syndrome (PCOS) [2, 3, 6–9]. However, many patients have no signs of peripheral hyperandrogenism other than acne. Serum profiles of androgens and gonadotrophins are often normal [10, 11].
In both teenagers and adults, acne is, de facto, a disease of sebogenesis . Beginning during adrenarche, rising levels of androgens and insulin-like growth factor (IGF)-1 mediate the onset of sebum production in both sexes . Anaerobic bacteria, particularly Propionibacterium acnes proliferate within acne-prone pilosebaceous follicles, which are blocked as a result of abnormal keratinocyte proliferation in response to signals from sebum components. This triggers leukocyte infiltration via both innate and adaptive immune mechanisms. Characteristically, a cell-mediated inflammatory response ensues, in which macrophages and T helper (Th)-1 and Th-17 cells predominate [13, 14].
Spironolactone, a synthetic 17-lactone steroid, acts as a non-selective mineralocorticoid receptor antagonist with moderate affinity for both progesterone and androgen receptors . Spironolactone is predominantly utilized in clinical practice as a potassium-sparing diuretic, however it has been used off-label for acne since the 1980s. A reduction in sebum may be achieved by blocking dihydrotestosterone binding to the androgen receptor within sebocytes and inhibiting androgen-induced sebocyte proliferation [16, 17]. The systemic effects of spironolactone on adrenal synthesis of androgen precursors may also contribute to clinical efficacy, although at therapeutic doses this may be unlikely . The diuretic effect of spironolactone may benefit women who experience a premenstrual acne flare associated with fluid retention .
Successful long-term management of acne in adult women presents a considerable therapeutic challenge. As an anti-androgen and potential inhibitor of sebogenesis, spironolactone represents a possible alternative to oral isotretinoin and combined oral contraceptives (COCs), the only licensed anti-acne medications that significantly reduce sebum secretion, but which may be associated with serious adverse effects in some patients [20, 21]. Antibiotics are often over-prescribed in acne, drive antimicrobial resistance in targeted and non-targeted bacteria, and have no effect on sebum synthesis .
A Cochrane review focusing primarily on hirsutism included only one randomized controlled trial (RCT) of oral spironolactone for acne in its analyses and concluded there was insufficient evidence for effectiveness in treating acne . In contrast, a narrative review, based largely on clinical experience, highlighted the potential therapeutic usefulness of oral spironolactone in the management of acne in adult females, and detailed recommendations about appropriate use and monitoring during therapy .
Take-home messages from these different reviews are contradictory. In view of this clinical uncertainty, we conducted a hybrid systematic review of all studies that had assessed the clinical efficacy of oral spironolactone for acne in women. The primary aim was to determine whether oral spironolactone monotherapy produces a degree of improvement in acne that is clinically important and comparable to conventional drug-based remedies. Secondary aims were to identify evidence that could better inform clinicians on the selection of patients likely to benefit, and/or reveal the most appropriate dosing regimen.
The protocol for this review was published in PROSPERO (http://www.crd.york.ac.uk/PROSPERO/) with the accession number 42016038496.
2.1 Search Strategies
Electronic searches were conducted between 10 and 15 May 2016 and included the Cochrane Central Register of Controlled Trials, MEDLINE, EMBASE, Science Citation Index and LILACS. The search strategy for MEDLINE and EMBASE is shown in Appendix 1 (electronic supplementary material). The following trials registers were searched using the search terms spironolactone AND acne or ‘polycystic ovarian syndrome’.
metaRegister of Controlled Trials (www.controlled-trials.com);
US National Institutes of Health Ongoing Trials Register (http://www.clinicaltrials.gov);
Australian New Zealand Clinical Trials Registry (http://www.anzctr.org.au);
World Health Organization International Clinical Trials Registry Platform (www.who.int/trialsearch);
EU Clinical Trials Register (https://www.clinicaltrialsregister.eu/).
The reference lists of all identified RCTs and key review articles were checked for citations to potentially relevant studies. No language or date restrictions were applied.
Outputs of searches were imported into Rayyan to facilitate sorting , and full-text copies of all potentially eligible studies were obtained. Two authors (AE and ZF) independently assessed the full-text papers and resolved any disagreements on the eligibility of included studies through discussion and consensus, or through a third party (EvZ).
2.2 Inclusion Criteria
We included RCTs in females of any ethnicity over 18 years of age with acne vulgaris of the face and/or trunk, or PCOS if acne status or severity was measured as an outcome. Case series were included if they provided supplementary evidence on the benefits or side effects.
2.3 Outcome Measures
The following primary outcomes were prespecified: (1) physician-assessed change in total lesion count; and (2) physician-assessed change in global acne severity using a recognized or validated scale. Prespecified secondary outcomes were (1) participant-reported improvement in global acne severity (e.g. Likert scale); (2) change in health-related quality of life (HRQOL) assessed using any validated instrument (generic, dermatology-specific, or acne-specific); (3) number and proportion of participants reporting each type of adverse event; (4) duration of remission post-treatment; and (5) time to improvement (as assessed by either primary outcome or patient-reported outcome at time points within the first 8 weeks).
2.4 Data Extraction
Data extraction using piloted forms, risk of bias assessments and analyses were carried out independently by three authors (AE, ZF and EvZ) and any disagreements were resolved by consensus. Risk of bias assessments for the RCTs were made using the Cochrane domain-based risk of bias tool and were used to support conclusions regarding the overall quality of evidence in the review . Data were analyzed using RevMan version 5.3 . Dichotomous outcomes were expressed as risk ratios (RRs) and were reported with their associated 95% confidence interval (CI), while continuous outcomes were reported as mean differences (MDs) with 95% CI. Attempts, although only partially successful, were made to obtain missing trial details by contacting the lead investigators of the studies. The protocol specified that data would be reanalyzed according to the intention-to-treat (ITT) principle; however, for the majority of trials this was not possible due to inadequate or incomplete reporting. Therefore, in general, the per-protocol (PP) population was used. Analyses of side effect rates were conducted using the ITT population with and without acne. For numbers included in each type of analysis, see Electronic Supplementary Table 1. When available, and unless otherwise stated, assessments at month 3 were used as the basis of comparison between studies. The Grading of Recommendations Assessment, Development and Evaluation (GRADE) software (GRADEpro GDT) was used to rate the quality of evidence from RCTs for the individual outcomes and to produce summary of findings tables . Following recommendations in the GRADE handbook, case series are considered to provide low quality evidence and are often further downgraded to very-low-quality evidence . Data from case series were not reanalyzed but were pooled if the studies were clinically similar.
3.1 Study Characteristics
Full details of the study selection process are reported in Fig. 1. We identified 10 RCTs [30–39], 18 case series in which acne status or severity was an outcome [40–52, 54, 55, 57, 59, 60], and three [53, 56, 58] articles reporting on the side effects of spironolactone in female patients with acne, but which contained no data on clinical outcomes. Eleven studies [61–71] were out of scope and five were unobtainable [72–76] (see Electronic Supplementary Table 2).
3.2 Randomized Controlled Trials (RCTs)
All 10 RCTs were single-center studies that had been conducted in Canada (1), UK (2), India (3), Bangladesh (1), Thailand (1), Israel (1) and China (1). Baseline acne severity ranged from mild to severe and was not reported in four trials [30, 32, 34, 39]. The sites affected by acne were reported for seven trials and always included the face [31–33, 35, 36, 38, 39]. Of the four trials that included males, two reported results for females separately [33, 39] and two did not [31, 36]. Six trials did not mention any sources of funding [31, 33, 36–39], one was funded by a manufacturer of spironolactone , two were funded by non-industrial sponsors [34, 35] and one received no support from a pharmaceutical company . A spironolactone manufacturer supplied the active and placebo treatment in two trials [31, 37]. Declarations stating no conflicts of interest were provided for two trials [32, 35]. For further details, see Table 1.
3.2.1 Risk of Bias in Included RCTs
All of the trials were considered to be at ‘high risk of bias’ (plausible bias that seriously weakens confidence in the results) because one or more domains, most commonly lack of blinding, received a judgment of high risk (see Fig. 2).
3.2.2 Use of Outcome Measures Within the RCTs
Heterogeneity of outcome measures and methods of reporting meant that pooling of data from different trials versus the same comparator was not feasible. Only two studies [31, 37] reported the same outcome in the same way for a similar patient population. Of our primary outcomes, four trials included a lesion count [36–39] and five included an investigator-assessed change in global acne severity, all but one of which used recognized but different severity scales [32–35]. Of our secondary outcomes, three trials included participant-assessed global improvement [31, 32, 37], none measured changes in HRQOL and only two included a post-treatment follow-up [30, 34]. One trial included time points prior to month 3, theoretically enabling calculation of time to improvement .
All but one trial reported side effects in full; one reported side effects associated with discontinuation only . Only two trials reported the number of women experiencing any side effect [32, 38]. Seven trials monitored changes in serum potassium (risk of hyperkalemia), but none reported the number of women with raised levels as a result of treatment [31–33, 35, 36, 38, 39].
3.3 Effect of the Interventions
The ten RCTs included 16 comparisons of spironolactone versus placebo or active treatment. The quality of the evidence was assessed for all comparisons and was downgraded by several levels, principally due to limitations in study design and implementation, and imprecision due to low sample sizes, and was consequently rated low or very low for our predefined outcomes. Inadequate data reporting did not permit calculation of RRs or MDs for any of the outcomes in four trials [30, 31, 34, 36].
3.3.1 Spironolactone versus Placebo
Three trials evaluated this comparison [31, 36, 37]. One provided useful data for a 200 mg daily dose in a crossover trial that examined 29 women . For the inflamed lesion count, the MD in favor of spironolactone was 26.1 lesions fewer, despite baseline imbalance in favor of the placebo (p < 0.00001; PP population of 21, both phases combined). Data for the first phase, which would be free of any potential carryover effects, were not reported. Combined data from both phases showed that 18/21 women taking spironolactone, compared with 5/21 taking placebo, reported improvement (RR 3.6, 95% CI 1.64–7.89; p = 0.001), and 15/20 versus 4/20 had at least a 50% reduction in inflamed lesion count (RR 3.75, 95% CI 1.51–9.34; p = 0.005). In a mixed gender RCT , 24/30 participants receiving spironolactone (50 mg/day, including 27 women) improved, compared with 2/25 receiving placebo (PP population); separate data were unavailable for females. A similar problem arose in the third trial, which also included males . Data could not be extracted for three women receiving the 50 mg dose, but 6/9 women receiving doses of 100–200 mg/day improved, irrespective of which outcome measures were used (PP population). In neither mixed gender trial was the extent of improvement quantified. For details and quality of evidence, see Table 2.
3.3.2 Spironolactone versus Cimetidine
Three trials compared spironolactone with cimetidine using different daily doses of one or both drugs and different outcome measures [33, 38, 39]. One also used a shorter treatment duration (2 months) and an unspecified topical therapy in both arms . Despite these inconsistencies, none detected a difference in efficacy between the two drugs. The earliest trial  found no difference in acne severity score between spironolactone (100 mg/day) and cimetidine (1.6 g/day) [MD −4.20, 95% CI −17.48 to 9.08; p = 0.54] using the Michaëlsson scale . Similarly, the second study  found no difference between the same dose of spironolactone and cimetidine 1.4 g/day, using reduction in inflamed and non-inflamed lesions as the outcome measure. MDs were −3.3 inflamed lesions (95% CI −8.14 to 1.54; p = 0.18) and −10.70 non-inflamed lesions (95% CI −24.08 to 2.68; p = 0.12). Lesion counts were also converted to a categorical improvement in 11/15 women receiving spironolactone and 6/14 women receiving cimetidine, showing at least a 50% reduction in lesions (RR 1.71, 95% CI 0.87–3.37; p = 0.12). In the final trial , a lower dose of spironolactone (60 mg/day) was not significantly different to cimetidine for the number of participants with at least 50% reduction improvement (physician-assessed) at an initial dose of 1.2 g/day (RR 0.96, 95% CI 0.89–1.03; p = 0.25). For details and quality of evidence, see Electronic Supplementary Tables 3 and 4.
3.3.3 Spironolactone Plus a Combined Oral Contraceptive (COC) versus the Same or a Different COC Alone or Combined with an Anti-Androgen
Among the remaining comparisons, four compared spironolactone in combination with a COC versus a COC alone  or combined with an anti-androgen: flutamide , finasteride  or additional cyproterone acetate . One trial compared 25 mg/day spironolactone plus desogestrel/ethinyl estradiol (EE) versus cyproterone acetate/EE . Assessed using the global acne grading system , both treatments were similarly effective in reducing the acne severity score from baseline, with an MD of −2.0 (95% CI −4.59 to 0.59; p = 0.13). For details and quality of evidence, see Electronic Supplementary Table 5.
A second trial compared spironolactone (100 mg/day) plus norgestimate/EE with (1) norgestimate/EE alone and (2) cyproterone acetate/EE plus 10 mg/day additional cyproterone acetate . Randomization was 3:3:1, with fewer women in the norgestimate/EE arm. After 12 months of treatment, no significant difference was reported in the proportion of women with at least 50% improvement, using the Burke and Cunliffe acne grading system , between the three arms. Participants’ self-assessed improvement confirmed these data. For details and quality of evidence, see Electronic Supplementary Tables 6 and 7.
The remaining two trials employed multiple assessment time points, which, in one case, included the first and second month of treatment , and included post-treatment follow-up for 6 months (Table 4). Neither conducted any intergroup tests of significance and both presented data graphically, with no measures of dispersion of mean values, therefore MDs could not be calculated. Hence, the studies provided limited usable data. Using the Indian grading system , one study  found no difference in the rate of improvement or magnitude of the reduction in severity score for spironolactone plus cyproterone acetate/EE compared with finasteride plus the same COC (p > 0.05 for all time points, investigators’ calculation). The reduced acne severity score (10% of baseline value at month 12) was maintained almost unchanged during the 6-month post-treatment follow-up period. The other trial  compared spironolactone plus levonorgestrel/EE versus flutamide plus the same COC using the Cremoncini score , which included seborrhea and alopecia as well as acne. The score fell more rapidly in the flutamide plus COC arm and the reduction in score, which was maximal by month 3 in both groups, was also greater for the comparator (50% vs. 85% reduction; statistical significance not reported by the investigators. At month 9 (end of the treatment phase), 5/10 or 7/10 in the spironolactone arm (investigators’ text unclear) versus 11/12 in the flutamide arm had a lower severity score . Relapse occurred over 6 months in both arms. For further details and quality of evidence, see Electronic Supplementary Tables 8 and 9.
3.3.4 Spironolactone versus Ketoconazole and Tetracycline
Spironolactone (60 mg/day) was compared with (1) 200 mg/day ketoconazole and (2) oral tetracycline at an initial de-escalating dose of 1 g/day . All three treatments were similarly effective using the proportion of women with at least 50% improvement in lesion count as the outcome measure (Table 4). However, as the numbers of participants in each treatment arm were not equal, the study may not have been sufficiently powered to detect a difference between spironolactone (n = 63) and tetracycline (n = 14). For details and quality of evidence, see Electronic Supplementary Tables 10 and 11.
3.4 Supplementary Efficacy Data from Case Series and Comparison with RCTs
Of the 18 case series, 13 were in English, two in Spanish, and one each in French, Czech and Turkish. As well as these, three additional articles included some data on side effects in women with acne [53, 56, 58]; they did not address clinical effectiveness. One definite case series  (in Portuguese) and two possible case series (in Czech) including acne patients treated with spironolactone [72, 75] were unobtainable and had either no abstract or an uninformative abstract. Two further unobtainable articles, one in Spanish  and one in Turkish , had abstracts containing sufficient information to identify them as duplicate publications of two included case series [44, 60].
Acne severity ranged from mild to severe and was not reported in nine of the case series [41, 43, 45, 46, 50–52, 54, 55]. The location of lesions was reported in only three case series [48, 54, 57]. Seven studies did not make a clear statement about concomitant medications, making attribution of any clinical effect to spironolactone uncertain [41, 43–45, 49, 51, 55]. Further details are reported in Table 3. Insufficient data were provided to conduct any subgroup analyses on the effect of dose or duration of spironolactone therapy on efficacy or side effects. Within the case series, between 216 and 259 of 728 women (29.7–35.6%) were receiving daily doses of ≥150 mg, compared with only 35/343 women (10.2%) in the RCTs.
The most commonly used outcome measure was physician-assessed global improvement in acne severity, which was reported in all but three case series [46, 49, 54]. Some used a 4- or 5-point Likert-like improvement scale, whereas others simply recorded improved/not improved without further categorization. Dichotomizing the pooled data shows that acne improved (to any extent) in 427/550 women (77.6%, ITT population) receiving spironolactone at any dose. Using the PP population, the proportion who improved was 427/454 (94.1%). These improvement rates are significantly higher than in the RCTs that also assessed this outcome (164/213, 76.1%; PP population, not calculable for ITT population due to incomplete reporting; RR 1.22, 95% CI 1.13–1.32; p < 0.00001).
The only other clinical outcomes reported in the case series were change in acne grade [43, 59], change in lesion count [54, 60] and post-treatment relapse rate [40, 60]. Using their own grading method , Burke and Cunliffe  observed a 35% reduction in acne severity at month 3, and an average 52% reduction at month 6, in eight women receiving a spironolactone dose of 200 mg/day (no measures of dispersion or p values were reported). Turowski and James  recorded a dramatic improvement in acne score in 39 women, from a median of two pretreatment to eight post-treatment (no measure of dispersion) on a scale of 1–10 (lower is worse). Most of the women in this study, which used spironolactone doses of 50–100 mg/day, were receiving concomitant medications and were treated for an average of 19.5 months. In the study by Yemisci et al. , the mean lesion count in 28 women (PP population) had decreased by month 3, from 32.86 (standard deviation [SD] 16.15) to 6.92 (SD 4.99), a reduction of 78.9% with spironolactone monotherapy at 100 mg/day (p < 0.001, investigators’ calculation). Furthermore, in the study by Saint-Jean et al. , the mean inflamed lesion count fell from 9.0 to 4.6, and the non-inflamed lesion count fell from 15.0 to 8.5 (no measures of dispersion and no p-values) in 14 women treated with a spironolactone dose of 75–150 mg/day for an average of 17 months. Two studies [46, 51] did not report any quantifiable outcomes data and two followed-up patients after treatment ended [40, 60]. In the study by Azizlerli et al. , 5 of 14 women (35.7%) followed for 3–18 months relapsed, while in the study by Yemisci et al. , acne returned in 5/28 women (17.9%) during the 6-month follow-up period. Interestingly, Bravo Garcia et al.  observed that residual acne post-treatment in 23/30 women was purely comedonal, whereas only 10/53 had exclusively comedonal acne prior to treatment (p < 0.00001, Chi-squared).
3.5 Side Effects Reported in RCTs and Case Series
None of the studies carried a clear statement as to how information on side effects had been elicited, e.g. spontaneous reporting versus an open-ended question at each visit. Within the RCTs, there was no difference in the proportion of participants who dropped out due to side effects: 14/303 (4.6%) receiving spironolactone at any dose versus 10/343 (2.9%) receiving the comparators (RR 1.58, 95% CI 0.71–3.52; p = 0.26). Dropout rates due to side effects could not be calculated for two trials [31, 36]. In the case series, 49/729 (6.7%) women dropped out due to the side effects of spironolactone (ITT population). This was not significantly different to the rate in the RCTs (RR 0.69, 95% CI 0.39–1.23; p = 0.20).
Due to inadequate reporting in 8/10 RCTs, the proportion of women experiencing any side effect(s) could not be calculated [30, 31, 33–37, 39]. In the case series, at least 241 women experienced side effects equivalent to 48.0% of the PP and 43.9% of the ITT population. Reported rates varied from 0 to 90.7%, with the highest rates associated with the 200 mg/day dose [46, 55]. The most common side effect in both the RCTs and case series was menstrual irregularities: 38/264 (14.4%) in the RCTs and 216/543 (39.8%) in the case series (RR 0.36, 95% CI 0.26–0.49; p < 0.00001). From the case series, it was apparent these were dose-related: 137/176 women receiving 200 mg/day experienced menstrual disturbances, compared with 66/349 on lower daily doses (RR 4.12, 95% CI 3.27–5.19; p < 0.00001).
Within the RCTs, it was possible to compare the incidence of menstrual disturbances in women receiving spironolactone with and without concomitant use of a COC. The incidence appeared significantly lower when spironolactone was combined with a COC: 32/146 without a COC versus 6/112 with a COC (RR 0.24, 95% CI 0.11–0.56; p = 0.001). This was also observed by Hughes and Cunliffe , who studied the incidence of side effects in a series of 53 women receiving a dose of 200 mg/day. The number of women with menstrual irregularities was 12/23 receiving a COC versus 21/24 receiving spironolactone monotherapy (RR 0.60, 95% CI 0.39–0.91; p = 0.02). In a minority of women with abnormal menses, spironolactone therapy was reported to normalize the menstrual cycle [41, 52, 57].
Other commonly reported side effects in the RCTs and case series are shown in Table 4. No side effect, apart from menstrual disturbances, had an incidence above 5% in the RCTs or case series. Uncommon side effects (0.1–1.0%) were postural hypotension, depression, diarrhea, muscle pain, increased appetite, drowsiness, rashes/drug eruptions, chloasma-like skin pigmentation, polydipsia, weakness, edema of the legs, change in libido, and palpitations. Some investigators mentioned that certain side effects were considered beneficial: breast enlargement, reduced symptoms of premenstrual syndrome, and less greasy skin and hair [31, 46, 57]. Due to the use of concomitant medications, especially COCs, in many of the studies, side effects could not be unambiguously attributed to spironolactone. Among the 10 case series of spironolactone monotherapy in 370 women in which concomitant therapies were not mentioned [41, 43–45, 49, 51, 55] or were not permitted [42, 52, 60], the only common side effects reported were nausea (11), abdominal pain (≥10), polyuria (4) and breast tenderness (4).
3.6 Risk of Hyperkalemia
Serum electrolytes were measured in 7/10 RCTs [31–33, 35, 36, 38, 39] involving 157 women (PP population) and 10/18 case series [41, 45, 47, 49–52, 55, 57, 60] involving 312 women (PP population) as a means of detecting possible adverse effects of spironolactone on fluid balance and kidney function. Serum electrolyte data reporting was inadequate in almost all cases and no results were presented for two RCTs that monitored this [36, 38]. No women in the remaining five RCTs were reported to have elevated levels. Fourteen women (4.5%) in two case series [51, 57], one that used doses ≥200 mg/day (4/18) and the other 50–100 mg/day (10/73), were reported to have slightly raised levels post-treatment. In an earlier study (not one of the 18 case series), serum potassium was measured in otherwise healthy women with acne treated with 50–150 mg/day of spironolactone . Mild hyperkalemia was detected in 6/60 (10%) women. It is impossible to determine whether the women in the later study were a separate group to those in the earlier study, and thus whether these were independent samples. Most recently, Plovanich et al.  conducted a retrospective analysis of serum potassium levels in 974 women aged 18–45 years taking 50–200 mg/day of spironolactone for acne, seen in two US hospitals between December 2000 and March 2014. Among 1802 measurements, 13 were slightly elevated, yielding a mild hyperkalemia rate of 0.72%, similar to the expected baseline rate of 0.76% derived from all available serum potassium measurements for females of the same age (32/4209). Repeat testing in 6/13 women yielded values within the normal range, suggesting initial measurements could have been erroneous.
Two authors of this review (JDR, AML) confirm that, based on their extensive experience of successful use of the drug to treat large numbers of women with persistent or late-onset acne, spironolactone is pivotal to their clinical practice. Such experience suggests that the important role of spironolactone in this hard-to-manage patient population has been largely underrecognized and provided the rationale for this systematic review. What the review has highlighted is a paucity of high-quality evidence for the effectiveness of oral spironolactone in the management of acne in adult females. The results should not be misinterpreted to mean that the drug is ineffective at safe dosages, but rather that there is a lack of robust evidence in support of expert opinion, which currently drives treatment recommendations either for or against more widespread use.
Every one of the 10 RCTs was at high risk of bias, with the most common reason being lack of blinding. Even in the more recent trials, sample sizes were not justified by reporting of power calculations or the assumptions on which they had been based. This lack of difference in efficacy between treatments might have been due, at least in part, to insufficient power. Moreover, as no single outcome measure had been used consistently across the trials, pooling of data from similar comparisons was not possible.
The trials fell into two categories: (1) comparisons of spironolactone monotherapy versus placebo; and (2) comparisons of mono or combination therapy versus active treatment. GRADE assessments of the quality of the evidence showed that all of the comparisons versus placebo were rated ‘very low quality’ and all of the comparisons versus active therapy were of low or very low quality. With one exception , the choices of active comparator did not include standard oral therapies such as antibiotics or isotretinoin, nor was there any direct head-to-head comparison of spironolactone monotherapy with a COC of proven anti-acne efficacy, such as cyproterone acetate plus ethinyl estradiol.
Despite the somewhat limited evidence available, some tentative conclusions can still be drawn. First, at a daily dose of 200 mg, spironolactone was found to be significantly superior to placebo versus inflamed lesions in a crossover trial in which 21 of 29 women completed 3 months of treatment. Baseline imbalance and a possible carryover effect of spironolactone into the second phase would have reduced the magnitude of the difference in efficacy between spironolactone and placebo, which was already large. This statistically significant result was not reported by the authors of a frequently cited Cochrane review, which evaluated the effects of spironolactone for hirsutism and acne . Equally, the Cochrane review may have also inadvertently misled authors of subsequent reports by stating that “there was no evidence for effectiveness [of spironolactone] for the treatment of acne vulgaris”. In contrast to the crossover trial, no conclusions can be drawn from the two parallel group comparisons versus placebo regarding the absolute efficacy of lower doses of spironolactone. Spironolactone appeared to be more effective than placebo, but by how much was not quantified and indeed the difference may not have been clinically significant. The very-low-quality evidence provided by the case series consistently shows that lower doses do have a measure of anti-acne activity, but they contributed no information on relative efficacy.
The trials that assessed comparative efficacy versus the anti-androgens flutamide, finasteride, cimetidine, ketoconazole and various COCs consistently found no difference between the spironolactone arm and the anti-androgen arm. With the exception of the COCs for which anti-acne efficacy has been established beyond doubt , independent verification of the efficacy of the comparators is scarce and/or contradictory [84–92]. What these anti-androgens have in common with spironolactone and COCs is the expectation that they will reduce sebum secretion at the doses used via their effects on androgen synthesis, action or sequestration (see Table 5). Demonstrating no difference in efficacy versus these agents is unhelpful in terms of quantifying the effect size for spironolactone, especially as some of the trials most likely had too few participants to detect a significant difference, if in fact such a difference existed.
Four of the RCTs evaluated spironolactone in combination with a COC. Hirsutism or PCOS was the primary diagnosis and acne was the secondary diagnosis. Since COCs are potent anti-androgens, and are effective as monotherapy for acne, superiority of the combination needs to be demonstrated over the COC alone. Despite this, only one trial included a COC monotherapy arm and found no benefit of adding spironolactone to norgestimate/EE , although, at trend, the combination was more effective. In this three-arm trial, treatment allocation was unbalanced, with three times as many women in the combination arm as those receiving COC monotherapy. Any added benefit of spironolactone might have been revealed had treatment arms been of equal size.
One potentially more useful trial put spironolactone head-to-head against oral tetracycline and found no difference in efficacy over 8 weeks of treatment ; however, caution is necessary in interpreting the results as this trial was also unbalanced, with 63 women receiving spironolactone but only 14 receiving tetracycline. Interestingly, the duration of therapy was consistently short (2–3 months) for those RCTs in which acne was the primary diagnosis, and much longer (9–12 months) for the trials in which hirsutism was the primary diagnosis. After only 3 months of treatment, the response of acne to spironolactone may not be optimal. The case series show that clinicians often use longer courses to manage acne in the real world. Using the PP population, improvement rates were significantly higher in the case series compared with those RCTs that had also used an outcome measure that could be dichotomized. This difference in efficacy rates may be an indication that longer treatment is likely to be more successful.
Only two RCTs conducted time courses with post-treatment follow-up [30, 34]. One found  that improvement was maximal at month 3 (approximately 50% reduction vs. baseline), whereas the other showed that improvement continued until month 12, when the reduction was 89% . Both used 100 mg/day of spironolactone in combination with a COC—the former in combination with triphasic levonorgestrel/EE and the latter in combination with cyproterone acetate/EE. In the follow-up phase, acne returned to baseline levels over 6 months in those treated with spironolactone plus levonorgestrel/EE, but there was no relapse in those treated with cyproterone acetate/EE. The data for the spironolactone plus levonorgestrel/EE combination may be somewhat misleading as a non-validated scoring method which combined acne with seborrhea and alopecia was used . Neither study included a COC-only or spironolactone-only treatment arm, making it impossible to determine the contribution of spironolactone to the efficacy of the combination.
Two studies made apparently contradictory observations in respect of the efficacy of spironolactone against comedonal (non-inflamed) lesions. One case series found that residual acne was more likely to be comedonal , whereas an RCT showed what appeared to be a large reduction in comedonal acne compared with baseline and the comparator ; however, the lack of reporting of baseline data for the number of lesions in the RCT did not permit fair comparisons to be made. As only these two studies evaluated comedones, it is not possible to know whether spironolactone monotherapy is effective versus non-inflamed lesions. Expert reviews [24, 56], commentaries , and acne treatment guidelines that include spironolactone, such as the recent US guidelines , are silent on this important point. ‘Hormonal acne’ is widely perceived as predominantly inflammatory with a paucity of comedones; however, such cases represent a minority of women with acne and, in most instances, comedones will be present .
Dropout rates due to side effects in spironolactone-treated participants were low in the RCTs and case series, suggesting that most women who begin the drug will continue to take it. However, side effect rates were significantly higher for the 200 mg/day dose than for lower doses. This was especially true for menstrual irregularities, the most common side effect reported in the RCTs and case series. Pooling of data has shown that the rate of menstrual irregularities can be significantly reduced by concomitant use of a COC, a practice that is widely recommended by experts [24, 56, 111]. However, experts also recommend dose escalation [24, 56, 111, 114, 115], which, paradoxically, was rarely used in the included trials or case series as a potential, but as yet untested, means of improving tolerance and adherence.
A recent multicenter study in 974 women  concluded that routine monitoring of serum potassium in healthy women taking spironolactone for acne is not necessary. The findings from this systematic review support that conclusion. Occasional testing may be justified on a case-by-case basis when risk factors are present. Although 14 women with raised potassium levels were identified among 469 women in the RCTs and case series, hyperkalemia was invariably mild and clinically insignificant. Some of the side effects of spironolactone, notably nausea, fatigue, and especially muscle weakness, can be indicative of hyperkalemia and, if persistent, could be used to indicate patients in whom testing may be justified. Crucially, the non-requirement for routine testing would reduce the overall direct costs of spironolactone treatment.
While endorsing key aspects of expert opinion with hard data and providing some new insights, this systematic review has highlighted existing important gaps in the evidence about how best to utilize oral spironolactone in managing acne in women, including clarifying the optimum dose and dosing regimen to maximize benefits and minimize the risk of side effects, the lowest effective dose, the possible requirement for concomitant therapies and what these should be, which types of acne are likely to be responsive, and how effective spironolactone is compared with standard therapies. It is interesting to note that several current acne guidelines and treatment recommendations include spironolactone on the basis of consensus and/or expert opinion [112, 116, 117]. Others either do not mention spironolactone [118–121], or specifically say it is regarded as ineffective, not recommended [122, 123] or there is insufficient evidence to support its use . All, including those that purport to be evidence-based, have failed to identify the majority of studies that were included in this systematic review. Although there were five relevant studies that, to date, have proved unobtainable (two of which were almost certainly duplicate publications of included case series), we are confident that all the RCTs evaluating spironolactone for acne in women have been retrieved and no clinical trial evidence has been overlooked. Until such time as higher quality evidence becomes available, guideline developers will have to continue to rely on recommendations largely based on expert experience or reached via consensus of expert panels. While this review has identified some very-low-quality evidence which showed that the 200 mg daily dose was statistically significantly more effective than placebo versus inflamed lesions, it has also confirmed that this dose is associated with a significantly greater risk of adverse side effects than lower doses. Hence, there would appear to be no merit in using these higher doses for managing acne, except in exceptional circumstances (e.g. in obese women with PCOS). Data from the multiple case series suggest that any future RCT examining lower doses is likely to generate results that confirm the effectiveness and better safety profile of doses ≤100 mg/day.
The findings of this systematic review have several key implications for future research. First, there is an urgent need for a well-designed, adequately powered RCT versus placebo, preferably of monotherapy, so that it is possible to establish whether spironolactone is effective against inflamed and non-inflamed lesions without concomitant use of a topical agent that would inhibit comedogenesis (see Table 6). Women who are stably maintained on an oral contraceptive can be considered for inclusion in such a trial as long as they remain on the oral contraceptive throughout and have been taking it sufficiently long enough for any anti-acne effect to be maximalized. If such a study confirms the utility of spironolactone, then head-to-head comparisons versus widely used oral therapies (antibiotics, COCs, isotretinoin) could follow. The need for, and utility of, combinations could also be explored. Within these trials, validated outcome measures should be carefully selected and any dose-related effect on sebum secretion should be explored early on. Monitoring serum androgens within such RCTs is unnecessary unless the trial is intended to identify subgroups of women less/more likely to benefit based, at least in part, on a combination of hormone profiles and clinical presentation.
This systematic review has revealed a lack of high-quality evidence on the benefits and potential harms of oral spironolactone for managing acne in women. However, it has shown that (1) there is low-quality, but statistically highly significant, evidence that 200 mg/day effectively reduces inflamed lesion counts; (2) side effects, in particular menstrual irregularities, are dose-related; and (3) concomitant use of a COC significantly reduces the incidence of menstrual disturbances. It has also confirmed the recommendation of Plovanich et al.  that routine potassium monitoring is largely unnecessary unless risk factors are present.
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The authors wish to thank Helen Weir, Library Manager at Harrogate District Hospital, for her help with literature searches and the retrieval of articles; Kwan Bevan for translation of the article by Wang et al.  from Mandarin to English; and Mohammed Delowar for making it possible to obtain the publication by Mansurul and Islam .
No funding was received for the preparation of this review.
Conflict of interest
None of the authors of this article have received funding or payments of any kind from the manufacturers of any of the products included in this review.
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Layton, A.M., Eady, E.A., Whitehouse, H. et al. Oral Spironolactone for Acne Vulgaris in Adult Females: A Hybrid Systematic Review. Am J Clin Dermatol 18, 169–191 (2017). https://doi.org/10.1007/s40257-016-0245-x