SGLT-2 Inhibitors And Cardiorenal Outcomes in Patients With Or Without Type 2 Diabetes: A Meta-analysis Of 11 CVOTs
Mar 18, 2022
Dario Giugliano1,2* , Miriam Longo1, Lorenzo Scappaticcio2, Giuseppe Bellastella1,2, Maria Ida Maiorino2,3 and
Katherine Esposito2,3
Abstract
Background: It has been suggested that sodium-glucose cotransporter 2 (SGLT-2) inhibitors reduce the cardiorenal risk in patients with type 2 diabetes (T2D). The purpose of this study is to provide an update of all large cardiovascular outcome trials (CVOTs) with SGLT-2 inhibitors to assess their cardiorenal efficacy in patients with and without T2D.
Methods: An electronic search up to 30 September 2021 was conducted in PubMed, EMBASE, the Cochrane Database of Systematic Reviews, and ClinicalTrials.gov. to determine eligible trials. We included CVOTs comparing any SGLT-2 inhibitor with placebo, reporting desired cardiovascular or renal outcomes and with a follow-up duration of at least 6 months.
Results: Eleven CVOTs, with data from five SGLT-2 inhibitors (empagliflozin, canagliflozin, dapagliflozin, ertugliflozin, and sotaglifozin) and 77,541 participants, were included. In the overall analysis, the risk of the composite CV mortality or hospitalization for heart failure (HF) was reduced by 23% (HR=0.77, 95% CI 0.73–0.82, P<0.001) compared with placebo, with no significant heterogeneity (I2=26%, P=0.20), and irrespective of the presence of T2D (P for interaction=0.81) and age (>65 vs≤65 years, P for interaction=0.78). The risk of CV mortality, total mortality, and hospitalization for HF was significantly reduced by 16%, 13%, and 32%, respectively; similarly, the risk of the composite renal outcome was reduced by 35% (HR=0.65, 95% CI 0.56–0.75), with moderate heterogeneity (I2=32%). In the analysis of 6 CVOTs reporting the data, the risk of major cardiovascular events (MACE) was reduced by 12%, with low heterogeneity (I2=21.2%, P=0.19) and irrespective of the presence of established CV disease at baseline (P for interaction=0.46).
Conclusions: Therapy with SGLT-2 inhibitors in patients with cardiometabolic and renal diseases results in a sustained to moderate reduction of the composite CV death or hospitalization for HF, robust reduction of HF and renal outcomes, moderate reduction of CV mortality, total mortality, and MACE.
Keywords: Cardiovascular outcome trials, Type 2 diabetes, SGLT-2 inhibitors, Cardiorenal outcomes
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Introduction
Inhibitors of the sodium-glucose co-transporter 2 (SGLT-2) were initially developed for the treatment of type 2 diabetes (T2D) for their effect of lowering blood glucose levels through increased excretion of glucose in the urine [1]. In FDA-mandated cardiovascular safety trials, also identified as the cardiovascular outcome (CVOTs) trials [2], patients with T2D were typically divided by the presence or absence of established cardiovascular disease. However, once their efficacy in reducing the risk of heart failure or progression of chronic kidney disease was ascertained [3–6] and thought to be largely independent of baseline and time-dependent changes in glycated hemoglobin [7], the hypothesis emerged that their cardiorenal benefits might not necessarily be due to glucose-lowering and might also be found in individuals without diabetes. Te DAPA-HF (Dapagliflozin And Prevention of Adverse Outcomes in Heart Failure) trial [8] was the first one to include patients with heart failure and reduced ejection fraction irrespective of the presence of T2D: the trial showed that dapagliflozin reduced the risk of worsening heart failure events and cardiovascular death and improved symptoms in patients with or without T2D.
Methods
Search strategy and study selection
This systematic review was based on PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines [9]. The protocol has not been registered on any platform. We searched PubMed, EMBASE, the Cochrane Database of Systematic Reviews, and Clinical-Trials.gov to identify all eligible trials comparing the efficacy of SGLT-2 inhibitors with that of placebo in adult patients with or without T2D. The terms used for the research were “sodium-glucose co-transporter 2 inhibitors”, “empagliflozin”, “canagliflozin”, “dapagliflozin”, “ertugliflozin”, “sotaglifozin”, “placebo”, “cardiorenal outcomes”, “kidney outcomes”, “MACE”, “heart failure”, and “randomized controlled trials”. The search was filtered to include only randomized controlled trials (RCTs) or meta-analyses of human data. Searches were done up until September 30, 2021. We excluded observational non-randomized studies, registries, ongoing trials without results, duplicate series, meta-analysis, abstracts, and oral communications. Data were extracted by D.G. and M.L., with conflicts over study inclusion resolved by consensus. The prespecified selection criteria included: (1) randomized controlled trials comparing any SGLT-2 inhibitor with placebo; (2) RCTs reporting desired cardiovascular or renal outcomes; (3) RCTs completed before the FDA guidance of 2008 [2] and (4) follow-up duration of at least 6 months.
Data extraction and quality assessment Results in trial reports (primary trial results and subsequent secondary publications), and their accompanying supplementary materials, were used as the primary source of information. The retrieved data included study characteristics, characteristics of patients, interventions, and outcome measures, that included the hazard ratios (HR) and confidence intervals (CI) for cardiorenal outcomes. In more recent trials examining the effects of some SGLT-2 inhibitors (dapagliflozin or empagliflozin) independent of the presence of T2D, we did subgroups analysis assessing the effect of the SGLT-2 inhibitors on the primary outcome (CV death or hospitalization for HF) in subjects with T2D vs subjects without T2D, or in subjects>65 years vs. subjects≤65 years of age. The Cochrane Collaboration Risk-of-Bias tool was used for quality assessment of the RCTs [10], including sequence generation, allocation concealment, blinding, incomplete outcome data, and selective outcome reporting. The risk of bias was graded as unclear, high, or low.
Data synthesis and analysis Data were analyzed using Stata, version 16.0 (Stata Corp., College Station, TX). All statistical tests were two-sided, and P values<0.05 were regarded as significant. The efficacy outcomes for this meta-analysis were the effect of SGLT-2 inhibitors on the incidence of the composite of CV mortality or hospitalization for HF, CV mortality, total mortality, hospitalization for HF, kidney outcomes, and MACE. Subgroup analyses were done for the incidence of the composite of CV mortality or hospitalization for HF according to the presence of T2D at baseline (YES vs NO) or in subjects of 65 years of age or younger vs patients older than 65 years of age, as well as for incidence of MACE according to the presence of CV disease at baseline (YES vs NO). Hazard ratios (HRs) and 95% CI (confidence interval) for efficacy outcomes were synthesized. Heterogeneity between studies was evaluated by using Cochran’s Q test. The proportion of variation in observed effects due to heterogeneity rather than sampling error was evaluated by using the I2 index [11] and thresholds of I2 describing the degree of heterogeneity were 25% or lower (low), 26–75% (moderate), and greater than 75% (high). A Q statistic P-value of<0.10 was considered significant Pooled summary estimates and 95% CIs for efficacy outcomes were calculated according to a random-effects model using the Paule-Mandel method [12]. Publication bias was assessed with the Egger test [13]. The trim-and-fill method [14] was used to estimate the effect of publication bias (if any).
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Results
Characteristics of the included studies
Of 160 articles screened for eligibility, 11 RCTs [8, 15–29] were eligible and included in the meta-analysis (Additional file 1: Fig. S1). Their characteristics are summarized in Table 1. The participants were all adult (>18 years old) patients. All trials were multinational and sponsored by industry. The trials have been published between 2015 and 2021, with 3 trials published in 2021. All trials were of parallel-group, double-blind design, and their mean duration ranged from 0.75 to 4.2 years. The populations studied ranged in size from 1222 (SOLOISTWHF) to 17,160 (DECLARE) and were of similar age (range 61.3–71.9 years). Data from 77,541 participants were included in the analysis.
EMPA-REG OUTCOME compared empagliflozin to placebo in 7020 patients with T2D and established CV disease [15, 25]. CANVAS compared canagliflozin to placebo in 10,142 patients with T2D and established CV disease or CV risk factors only [16]. DECLARE compared dapagliflozin to placebo in 17,160 patients with T2DM and established CV disease or CV risk factors only [17]. CREDENCE compared canagliflozin to placebo in 4401 patients with T2D and diabetic kidney disease [18, 26]. DAPA-HF compared dapagliflozin to placebo in 4744 patients with or without T2D and heart failure with reduced ejection fraction [8, 27, 28]. DAPA-CKD compared dapagliflozin to placebo in 4304 patients with or without T2D and chronic kidney disease [19, 29]. VERTIS-CV compared ertugliflozin to placebo in 8246 patients with T2D and established CV disease [20]. EMPEROR-R compared empagliflozin to placebo in 3730 patients with or without T2D and heart failure with reduced ejection fraction [21]. SCORED compared sotaglifozin to placebo in 10,584 patients with T2D and chronic kidney disease [22]. SOLOIST-WHF compared sotaglifozin to placebo in 1222 patients with T2D who were recently hospitalized for worsening heart failure [23]. EMPEROR-P compared empagliflozin to placebo in 5988 patients with or without T2D and heart failure with preserved ejection fraction [24]. The primary outcomes for the 11 trials are given in Table 1. According to the Cochrane collaboration's tool for assessing the risk of bias, there was no major risk of bias in any study (Additional file 1: Fig. S2, Table S1).
Outcomes In the overall analysis, including 11 trials with 77,541 participants, the risk of composite CV mortality or hospitalization for HF was reduced by 23% (HR=0.77, 95% CI 0.73–0.82, P < 0.001) compared with placebo, with moderate and not significant heterogeneity (I2=26%, P=0.20) (Fig. 1 and Table 2), and no evidence of publication bias (Egger test, P=0.46). In the subanalysis of participants divided according to the presence or absence of T2D (Fig. 3 and Table 2), there was no difference in the risk of the composite CV death or hospitalization for HF between the two groups (P for interaction=0.81). In the four trials that included participants with or without T2D (DAPA-HF, DAPA-CKD, EMPEROR-R, and EMPEROR-P), treatment with dapagliflozin (DAPA) or empagliflozin (EMPEROR) was associated with 26% (HR=0.74, 95% CI 0.64–0.84) and 23% (HR=0.77, 95% CI 0.64–0.91) lower risk of the composite CV death or hospitalization for HF in patients with or without T2D, respectively. Similarly, in three trials (DAPA-HF, EMPEROR-R, and EMPEROR-P) treatment with dapagliflozin or empagliflozin was associated with 25% (HR=0.75, 95% CI 0.66–0.84) and 22% (HR=0.78, 95% CI 0.68–0.88) lower risk of the composite CV death or hospitalization for HF in patients older than 65 years or 65-year-old or younger, respectively, with no significant interaction (P=0.78) (Fig. 4 and Table 2).
In the overall analysis including all the 11 CVOTs, the risk of CV mortality (Fig. 5 and Table 2), was reduced by 16% (HR=0.84, 95% CI 0.73–0.95) by treatment with SGLT-2 inhibitors, with moderate and significant heterogeneity (I2=0.42%, P=0.07) and some evidence of publication bias (Egger test, P=0.047). The trim-and-full method indicated that this publication bias did not change the statistical significance of the estimate (HR 0.85, 95% CI 0.74–0.96). Similarly, the risk of total mortality (Fig. 6 and Table 2), was reduced by 13% (HR=0.87, 95% CI 0.74–0.98) by treatment with SGLT-2 inhibitors, with moderate heterogeneity (I2=0.45%) and some evidence of publication bias (Egger test, P=0.042). Te trim-and-full method heterogeneity (I2=0%) and no evidence of publication bias (Egger test, P=0.85). Similarly, the risk of the composite renal outcome (Fig. 2, Table 2) was reduced by 35% (HR=0.65, 95% CI 0.56–0.75), with moderate but not significant heterogeneity (I2=35%) but no evidence of publication bias (Egger test, P=0.15).
In the analysis of 6 CVOTs (EMPA-REG, CANVAS, DECLARE, CREDENCE, VERTIS-CV, SCORED) (Table 2), the risk of MACE was reduced by 12%, with low heterogeneity (I2=21.2%, P=0.19). There was no difference in the risk of MACE according to the presence or absence of established CV disease at baseline (P for interaction=0.46).
In all analyses shown in Figs. 1, 2, 3, 4, 5, 6, 7, the Hazard ratios for the specific outcomes of two sotaglifozin trials (SCORED and SOLOIST-HF), when included, were like to those of the other SGLT-2 inhibitors (empagliflozin, canagliflozin, dapagliflozin, ertugliflozin).
Discussion
The present meta-analysis includes the most recent published large RCTs (SCORED, SOLOIST-WHF and EMPEROR-P), thus providing the most contemporary assessment of the total available evidence for SGLT-2 inhibitor therapy and cardiorenal outcomes in patients with or without T2D. The findings of 11 CVOTs involving
77,541 patients show that treatment with SGLT-2 inhibitors reduced the risk of the composite CV death or hospitalization for HF by 23% in the overall population, with low and not significant heterogeneity, suggesting a plausible class effect for the outcome. This interpretation seems also supported by the subgroup analyses indicating the lack of significant difference in the reduced risk of the composite outcome in patients with or without T2D, or in subjects of 65 years of age or younger vs those older than 65 years of age. Although participants in the EMPEROR-P trial [24] were grouped by different age-threshold (>70 years vs≤70 years), this may not have altered the estimation of the Hazard Ratio given the absence of heterogeneity and interaction between groups.
77,541 patients show that treatment with SGLT-2 inhibitors reduced the risk of the composite CV death or hospitalization for HF by 23% in the overall population, with low and not significant heterogeneity, suggesting a plausible class effect for the outcome. This interpretation seems also supported by the subgroup analyses indicating the lack of significant difference in the reduced risk of the composite outcome in patients with or without T2D, or in subjects of 65 years of age or younger vs those older than 65 years of age. Although participants in the EMPEROR-P trial [24] were grouped by different age-threshold (>70 years vs≤70 years), this may not have altered the estimation of the Hazard Ratio given the absence of heterogeneity and interaction between groups.
end-stage kidney disease, and death from CV or renal causes, adding evidence to their nephroprotective effect. While confirming nephroprotection by SGLT-2 inhibitors with a pooled reduced risk of the renal outcome by 35%, the present meta-analysis including ten CVOTs reporting the renal outcome seems to question the class effect of SGLT-2 inhibitors for the following reasons: (1) the reduced risk of renal outcome is not significant in every CVOTs; (2) apart from canagliflozin, all other inhibitors (dapagliflozin, ertugliflozin, sotaglifozin, and empagliflozin) fail to produce a significant nephroprotection in at least one CVOT; (3) there is moderate and borderline significant heterogeneity (I2=35%, P=0.10) in the present meta-analysis, probably as a consequence of the different criteria used to define the kidney outcome; and (4) the worst results, in terms of the wideness of confidence intervals, are observed in patients with HF, independent of the presence of T2D. In particular, the beneficial effect of empagliflozin on the renal outcome was significantly greater in the EMPEROR-R than in the EMPEROR-P trial [33], suggesting a major protective effect of the drug in patients with HF and a reduced ejection fraction. It is possible that the definition of the renal outcome may have played some role in the striking discordance between the effect of empagliflozin on heart failure and renal outcomes in the EMPEROR-P trial. This discordance is extraordinarily puzzling as the effects of SGLT-2 inhibitors on hospitalization for HF and the renal outcome had consistently been tracked together in previous CVOTs. As empagliflozin reduced the risk of HF hospitalization in these two populations of patients with HF (reduced or preserved ejection fraction) irrespective of their baseline diabetic status, it is conceivable that nephroprotection is not the principal mechanism by which empagliflozin may prevent HF hospitalization [34]. It has already been shown that SGLT-2 inhibitors led to greater benefits in patients with NYHA class II than in patients with NYHA class III or IV and that the reduced HF composite outcome is independent of LVEF level (<40%, 40% to<50%, or≥50%) [35, 36].
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Several hypotheses have been formulated in the attempt to explain the cardiorenal protective effects of SGLT-2 inhibitors, including, although not limited to a diuretic effect [37], altered substrate utilization and cellular signaling through increased lipolysis in adipose tissue with subsequent generation of ketone bodies [38], Fig. 5 Forest plots examining the outcome cardiovascular mortality in participants of 11 CVOTs. There is moderate heterogeneity in the analyses (I2=42% of borderline significance)Page 9 of 11 Giugliano et al. Cardiovascular Diabetology (2021) 20:236 increased erythropoietin, hemoglobin, and hematocrit levels which can improve tissue oxygenation [39] and improve the lipid profile and decrease uric acid level [40]. Moreover, the increase in the delivery of sodium to the macula densa results in vasoconstriction of the afferent arteriolar with a subsequent reduction in the intraglomerular pressure [41]. Irrespective of the exact mechanism, the improvement in cardiorenal outcomes by SGLT-2 inhibitors in patients with and without T2D suggests inherent protective properties. To date, it is not yet possible to clearly identify subpopulations of patients without T2D that would benefit the most from treatment with SGLT-2 inhibitors.
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This study has potential limitations that include the
use of aggregate trial-data levels and some difference in
the exact inclusion/exclusion criteria and definition of
outcomes among trials. Moreover, not all CVOTs have
published the subgroup data for all outcomes and therefore some trials are not included in the analysis for individual endpoints. Strengths of the present meta-analysis
are the inclusion of all CVOTs published by September
30, 2021, the very large number of participants, the high
quality of the trials which minimizes the risk of bias, and
the absence of significant heterogeneity in most analyses,
which ranged from absent to low or moderate.
The clinical relevance of these results seems also highlighted by the evidence that for some outcomes the clinical benefit is consistent irrespective of the presence of T2D, advanced age, and cardiorenal disease. On the basis of the results of CVOTs, the FDA has approved dapagliflozin (May 5, 2020) and empagliflozin (August 18, 2021) to reduce the risk for CV death and HF hospitalization in adults with HF with reduced ejection fraction regardless of whether they have diabetes [42, 43].
Conclusions
Therapy with SGLT-2 inhibitors results in a sustained to moderate reduction of the composite CV death or hospitalization for HF, robust reduction of HF and renal outcome, and moderate reduction of CV, total mortality, and MACE. The shift from a common antihyperglycemic drug to an agent with the likely indication of cardiorenal protection is underway and close to the goal. However, it is unlikely that future studies will significantly change the present scenario based on 11 CVOTs with more than 75,000 patients.
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