What this is
- This analysis examines the effects of combining exenatide and SGLT2 inhibitors on cardiovascular and renal outcomes in type 2 diabetes.
- The study utilizes data from the EXSCEL trial, which included over 14,000 participants.
- It compares outcomes in patients using both treatments against those using either treatment alone or none.
Essence
- Combination therapy with exenatide and SGLT2 inhibitors may lower cardiovascular event risk and all-cause mortality in type 2 diabetes patients. The analysis suggests potential benefits for renal function as well.
Key takeaways
- Combination therapy with exenatide and SGLT2 inhibitors resulted in a nominally significant reduction in all-cause mortality risk compared to both exenatide alone and placebo.
- The risk for major adverse cardiovascular events () was numerically lower with the combination therapy compared to both placebo and exenatide alone.
- The estimated slope improved significantly with the combination therapy, indicating better renal function compared to both placebo and exenatide alone.
Caveats
- The analysis is observational and relies on propensity matching, which may not fully account for unmeasured confounders.
- Median follow-up time was under 2 years, limiting insights into long-term cardiovascular and renal outcomes.
- The study's moderate cohort sizes may restrict the statistical significance of the findings.
Definitions
- MACE: Major adverse cardiovascular events, including cardiovascular death, nonfatal myocardial infarction, and nonfatal stroke.
- eGFR: Estimated glomerular filtration rate, a measure of kidney function.
Simplified
Background
Members of both the glucagon-like peptide-1 receptor agonist (GLP-1 RA) and sodium-glucose cotransporter-2 inhibitor (SGLT2i) classes of anti-hyperglycemic drugs have demonstrated cardio- and reno-protective effects in cardiovascular outcomes trials (CVOTs) conducted in patients with type 2 diabetes mellitus. While the study populations, designs, and results of individual trials have varied, meta-analyses suggest that both classes reduce major adverse cardiovascular events (MACE) in participants with established atherosclerotic cardiovascular disease (ASCVD) [1–4]. These meta-analyses additionally show that SGLT2i reduce risk of hospitalization for heart failure and the risk of worsening estimated glomerular filtration rate (eGFR) or end-stage renal disease, regardless of ASCVD status [1–3].
Many patients require multiple anti-hyperglycemic agents to manage their diabetes. Given the largely distinct mechanisms, beyond glycemic control, through which GLP-1 RA and SGLT2i are hypothesized to exert their cardiorenal effects, there is considerable interest in how the combination of these two classes would effect long-term outcomes [5, 6]. The 104 week DURATION-8, 24 week AWARD-10, and 30 week SUSTAIN 9 trials demonstrated that simultaneous initiation of GLP-1 RA exenatide and SGLT2i dapagliflozin, or addition of GLP-1 RAs dulaglutide and semaglutide to open-label SGLT2i, durably improved glycemic control and cardiovascular risk factors without increasing the risk of hypoglycemia [7–10]. However, no clinical trial or real world evidence on long-term cardiovascular outcomes, mortality, and renal disease progression with combination GLP-1 RA and SGLT2i treatment have been reported to date.
The EXenatide Study of Cardiovascular Event Lowering (EXSCEL) was a randomized, placebo-controlled, global pragmatic clinical trial designed to assess the effect of subcutaneous once-weekly GLP-1 RA exenatide (EQW) 2 mg on cardiovascular outcomes in 14,752 participants with type 2 diabetes mellitus and a range of cardiovascular risk [11]. Potential participants were permitted to take up to three oral anti-hyperglycemic drugs, or insulin in combination with up to two oral anti-hyperglycemic agents, as part of usual care for their diabetes management. During the course of EXSCEL, three SGLT2i were approved and marketed.
This posthoc analysis of EXSCEL leveraged the pool of participants taking open label SGLT2i in addition to study drug to quantify the impact of this EQW+SGLT2i combination on cardiorenal outcomes, as compared with both: (1) treatment with neither EQW nor an SGLT2i, and (2) treatment with EQW but not an SGLT2i, on top of standard of care.
Methods
Population and SGLT2i usage
EXSCEL (NCT01144338) enrolled 14,752 patients in 35 countries between June 2010 and September 2015. The primary results, study design and baseline characteristics have been published [11–13]. Briefly, inclusion criteria included a hemoglobin A1c (HbA1c) of 6.5% to 10%, and any level of cardiovascular risk, targeting ~ 70% of participants with a previous cardiovascular event. Participants were excluded if they were < 18 years old, had type 1 diabetes, ≥ 2 episodes of severe hypoglycemia in the previous 12 months, an estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2, or previous pancreatitis.
All EXSCEL participants were included in this analysis except for 786 placebo arm participants that took open-label SGLT2i. The 33 EXSCEL participants who never received study drug and a further 635 participants missing required covariates were excluded from propensity matching (Additional file: Figure S1). 1
Information on SGLT2i use was collected at each 6-monthly study visit [11]. As precise dates for concomitant medication initiation and cessation were not itemized, we assumed SGLT2i initiation at the first study visit that recorded its use [14]. SGLT2i exposure time was calculated as the interval from the first visit with known usage to the last study visit with SGLT2i use recorded, regardless of gaps or switching of SGLT2i type. No lower bound on exposure was imposed. We assumed no SGLT2i use when information was missing; SGLT2i usage data was not collected before May 2013, 6 months after the first market approval of an SGLT2i. Due to the limited size of the available data, subjects were eligible for inclusion in the EQW+SGLT2i cohorts whether they discontinued study drug before SGLT2i initiation or not.
Endpoints
This posthoc analysis examined multiple prespecified time-to-event EXSCEL endpoints: (1) first adjudicated composite of a three-point major adverse cardiovascular event (MACE), defined as cardiovascular death, nonfatal myocardial infarction or nonfatal stroke, the primary endpoint of the trial; (2) all-cause mortality (ACM); (3) cardiovascular death; and (4) serious hypoglycemia, defined as hypoglycemia requiring third-party assistance. Change over time in MDRD eGFR was examined to quantify renal disease progression. Exploratory time-to-event analyses were performed for: (1) hospitalization for heart failure (hHF); (2) a composite of hospitalization for heart failure and cardiovascular death; (3) nonfatal myocardial infarction; (4) nonfatal stroke; (5) a composite of a persistent 40% reduction in eGFR, renal dialysis, or renal transplant (“Renal_1”), (6) a composite of Renal_1 plus new macroalbuminuria (“Renal_2”); and (7) amputation.
Propensity matching
Propensity matching was performed using the same protocol as outlined in [14], designed to balance medical history, demographics, laboratory measurements, medication use, and follow-up time. Participants taking SGLT2i in the EQW arm were matched at the first known SGLT2i use to: (1) participants in the placebo arm that did not take SGLT2i (“Placebo comparison”); and (2) participants in the EQW arm that did not take SGLT2i (“Exenatide comparison”), based on covariates at the comparable study visit. No comparison was made to placebo+SGLT2i users because a large comparator group is necessary to achieve a well-matched set of cohorts, and both the EQW+SGLT2i and placebo+SGLT2i groups in EXSCEL were moderately-sized. Matching was performed first for the baseline visit, and then subsequently for each study visit without replacement of participants already matched. Propensity scores were calculated across all available participants and visits using a generalized linear model, and matching was performed via the nearest neighbor approach, using this score and logit distance calculated at each visit. A caliper of 0.1 and a 1:1 matching ratio were used in the R package MatchIt [15]. A matched set of cohorts were accepted if the post-matching difference between treatment groups for every covariate was less than 0.1 standardized difference.
The nearest neighbor approach matches participants in a random order, resulting in changes to the cohorts if matching is repeated. To prevent selection bias, the first set of cohorts generated that met the acceptance criteria were selected for this analysis. To assess the robustness of the results to variability in matching, we repeated matching 5000 times for each comparison, and compared the distributions of estimated hazard ratios in the accepted cohorts to those in the primary analysis. We also generated cohorts matched to only subjects taking exenatide and SGLT2i simultaneously, and performed a sensitivity analysis where we censored subjects in the primary analysis at initiation of open-label GLP-1 RA (in violation of study protocol) to further probe the impact of variation in drug usage patterns within our cohorts.
Covariates used for propensity matching were: age, sex, ethnicity, smoking status (trial baseline), race, region, duration of diabetes, history of heart failure, history of prior cardiovascular disease (CVD), microalbuminuria, macroalbuminuria, BMI, eGFR, systolic blood pressure, HbA1c, total cholesterol, and use of renin-angiotensin-aldosterone system inhibitors, thiazolidinediones, metformin, dipeptidyl peptidase-4 inhibitors, and insulin. All covariates were evaluated based on the last information prior to the first known SGLT2i usage (or comparable visit in controls). For participants on SGLT2i prior to enrollment, baseline characteristics were used. Prior CVD was defined, per EXSCEL protocol, as major clinical manifestations of coronary artery disease, atherosclerotic peripheral artery disease, or ischemic cerebrovascular disease, and was updated from trial baseline status based on recorded incidence of MACE, peripheral artery or vascular disease, coronary catheterization, angioplasty or stenting, coronary artery bypass, or percutaneous coronary intervention. Similarly, history of heart failure, age, and duration of diabetes were updated from trial baseline to reflect recorded hHF and time in trial, respectively.
As EXSCEL collected only local laboratory measurements, non-physiologically-reasonable outliers were capped prior to matching using the following cut-offs: BMI > 60 kg/m2, eGFR > 250 mL/min/1.73 m2, HbA1c > 15% (140 mmol/mol), and total cholesterol > 15 mmol/L. These cutoffs were set prior to analysis based on expected physiological ranges, and we confirmed that only a small number of all trial measurements were capped: 164 BMI (0.2%), 20 eGFR (0.02%), 49 HbA1c (0.06%), and 15 cholesterol (0.02%).
Time-to-event analyses
Hazard ratios (HR) for time-to-first-event analyses in both sets of propensity-matched cohorts were calculated via Cox proportional hazards regression. Analyses were performed with treatment as the sole exploratory variable (unadjusted), and adjusted for: duration of diabetes, age, sex, history of CVD, prior heart failure, prior microalbuminuria, prior macroalbuminuria, eGFR, and HbA1c, to provide a “doubly robust” estimator with lower risk of bias than would be obtained via propensity matching or adjustment alone [16]. The number of adjustment covariates was constrained because of the limited size of the matched cohorts [17].
Follow-up time began at matching (SGLT2i initiation or equivalent study visit in controls), and continued until the end of trial follow-up, regardless of study drug or SGLT2i discontinuation. Participants with an event before matching were censored at time zero for analysis of that endpoint. For composite endpoints, censoring occurred at the last information on the earliest censored component. For the renal composites, renal dialysis or transplant events occurring within 30 days of the last eGFR measurement were included.
Only participants with at least two post-matching eGFR measurements were included in renal time-to-event analyses (Additional file 1: Table S3). Persistent 40% eGFR reduction was defined as two sequential post-matching eGFR measurements ≤ 60% of the last pre-match eGFR measurement, with eGFR values over 250 mL/min/1.73 m2 excluded. eGFR was calculated centrally using the MDRD formula, based on local, site-reported serum creatinine measurements [18].
Endpoints were analyzed in both comparisons, but no direct comparisons were made between the two sets of matched cohorts. Owing to the posthoc nature of this analysis, all reported p-values are nominal and no multiple test corrections were performed. A p-value < 0.05 was considered nominally significant.
eGFR slope
eGFR slope vs. time was analyzed in both sets of propensity-matched cohorts using a mixed-model repeated measures (MMRM) analysis to estimate the overall treatment effect on eGFR slope. MDRD-based eGFR was the dependent variable, with time (scheduled visit window) and baseline eGFR as linear covariates, treatment arm and visit-by-treatment interaction as fixed effects, and patient as a random effect.
Software
Data was prepared in SAS 9.4, and all analyses were performed in R version 3.4.0 [19].
Results
Full population characteristics and drug use
During the course of EXSCEL, 645 EQW arm participants used an SGLT2i at some point, with the highest SGLT2i use in Western Europe and North America (Fig. 1a). Compared with non-SGLT2i users, these participants were more likely to be male (68% vs 61%), white (84% vs. 75%), have less history of CV disease (62% vs. 74%) and heart failure (9.1% vs. 17%) at trial baseline, and have more history of albuminuria (23% vs. 16%) (Additional file 1: Table S2) [12]. This group also had higher HbA1c (8.3% vs. 8.1% (67 mmol/mol vs. 65 mmol/mol)) and eGFR (85 vs. 76 mL/min/1.73 m2), and took more anti-hyperglycemic agents aside from GLP-1 RA and SGLT2i (1.7 vs. 1.3) than non-SGLT2i users in EXSCEL (Additional file 1: Table S2).
Of the three SGLT2i taken by EXSCEL participants, dapagliflozin was the most commonly used (Additional file 1: Table S1). Median time of first known SGLT2i use in the EQW arm was 2.7 years (interquartile range (IQR) 1.5–3.8 years) (Additional file 1: Figure S2A), and median time from first to last known SGLT2i use was 9.3 months (IQR 2.5–18.1 months) (Fig. 1b).
SGLT2i usage in EXSCEL.Percentage of exenatide arm participants taking SGLT2i at some point, by drug and by region. “Multiple” indicates use of more than one SGLT2i during the trial.Histogram of time from first to last known SGLT2i use in the EXSCEL exenatide QW (light gray) and placebo (dark gray) arms. Note that, given lack of precise start/stop dates, this estimate of length of SGLT2i exposure represents a lower bound.,Time of SGLT2i initiation or matching relative to discontinuation of EQW or placebo in the propensity-matched cohorts. Blue: combination EQW+SGLT2i cohort; green: placebo cohort; red: EQW cohort a b c d
Propensity matching
Of the 623 SGLT2i users in the EQW arm with all required covariates (Additional file 1: Figure S1), 572 were matched in the placebo comparison (92%), and 575 were matched in the EQW comparison (92%), with all covariates having an imbalance of less than 0.1 standardized difference in the accepted sets of cohorts Additional file 1: Figures S3A, B), and similar propensity score distributions between cohorts (Additional file 1: Figure S4). These cohorts (Table 1) were generally similar to the overall distribution of SGLT2i users in the EQW arm (Additional file 1: Table S2), though, importantly, different than the overall population of EXSCEL [12]. 560 of the participants in the EQW+SGLT2i cohorts were identical between the two comparisons. Characteristics in the separately matched “placebo” and “EQW” comparator cohorts were generally similar, but subjects in the “EQW” cohort were older, had a longer duration of diabetes, and were less likely to be Hispanic (Additional file 1: Figure S3C), limiting validity of direct comparisons between these groups. Median follow-up time for ACM in the placebo comparison was 13.3 months (IQR 6.5–23.1) for the combination cohort and 14.2 months (IQR 4.5–27.0) for the placebo cohort. In the EQW comparison, median follow-up was 13.3 months (IQR 6.5–23.0) in the combination cohort and 15.1 months (IQR 6.0–26.7) in the exenatide cohort.
Median study drug exposure (from trial baseline) in the propensity-matched cohorts ranged from 29.7 to 38.4 months (Additional file 1: Figure S2C, D). Median time from first to last known SGLT2i use was 9.8 months (IQR 3.1–18.8) in both comparisons. Median time from SGLT2i initiation/matching to study drug discontinuation in the placebo comparison was 3.2 months [IQR from 12.2 months before matching to 14.8 months after matching] in the placebo cohort and 4.7 months [9.7 months before to 14.8 months after] in the combination cohort (Fig. 1c). In the exenatide comparison, median time from SGLT2i initiation/matching to study drug discontinuation was 5.6 months [IQR 7.9 months before to 19.0 months after] in the EQW cohort and 4.9 months [IQR 9.2 months before to 14.8 months after] in the combination cohort (Fig. 1d). In total, 344 out of 572 participants (60%) in the placebo comparison and 348 of 575 participants (61%) in the EQW comparison started SGLT2i before EQW discontinuation.
| Placebo comparison | Exenatide comparison | |||
|---|---|---|---|---|
| Placebo,No SGLT2i | Exenatide QW + SGLT2i | Exenatide,No SGLT2i | Exenatide QW + SGLT2i | |
| Participants, n | 572 | 572 | 575 | 575 |
| Sex, male | 380 (66%) | 391 (68%) | 399 (69%) | 395 (69%) |
| Age, years | 62 (10) | 62 (9) | 63 (10) | 62 (9) |
| Race | ||||
| White | 486 (85%) | 487 (85%) | 495 (86%) | 488 (85%) |
| Black | 14 (2.4%) | 20 (3.5%) | 24 (4.2%) | 22 (3.8%) |
| Asian | 52 (9.1%) | 50 (8.7%) | 44 (7.7%) | 50 (8.7%) |
| Other/unknown | 20 (3.5%) | 15 (2.6%) | 12 (2.1%) | 15 (2.6%) |
| Region | ||||
| North America | 213 (37%) | 212 (37%) | 210 (37%) | 215 (38%) |
| Latin America | 27 (4.7%) | 27 (4.7%) | 25 (4.3%) | 26 (4.5%) |
| Asia Pacific | 53 (9.3%) | 54 (9.4%) | 50 (8.7%) | 54 (9.4%) |
| Western Europe | 200 (35%) | 182 (32%) | 190 (33%) | 186 (32%) |
| Eastern Europe | 79 (14%) | 97 (17%) | 100 (17%) | 94 (16%) |
| Ethnicity, Hispanic | 47 (8.2%) | 33 (5.8%) | 32 (5.6%) | 33 (5.7%) |
| Duration of diabetes, years | 16 (8) | 16 (8) | 17 (9) | 16 (8) |
| History of CVD (CAD, PAD, or stroke) | 377 (66%) | 379 (66%) | 395 (69%) | 378 (66%) |
| History of heart failure | 64 (11%) | 62 (11%) | 65 (11%) | 63 (11%) |
| History of retinopathy | 99 (17%) | 108 (19%) | 108 (19%) | 109 (19%) |
| History of micro- or macro-albuminuria | 172 (30%) | 159 (28%) | 164 (29%) | 160 (28%) |
| Microalbuminuria | 147 (26%) | 139 (24%) | 134 (23%) | 140 (24%) |
| Macroalbuminuria | 31 (5.4%) | 28 (4.9%) | 34 (5.9%) | 28 (4.9%) |
| Systolic blood pressure, mmHg | 133.6 (16.2) | 133.4 (15.4) | 133.1 (15.7) | 133.4 (15.5) |
| Diastolic blood pressure, mmHg | 76.6 (10.4) | 77.5 (10.0) | 77.3 (10.1) | 77.5 (10.0) |
| BMI, kg/m2 | 33.9 (6.9) | 34.1 (6.3) | 34.1 (6.5) | 34.1 (6.3) |
| HbA, %1c | 8.3 (1.5) | 8.2 (1.2) | 8.2 (1.6) | 8.2 (1.2) |
| Cholesterol, mmol/L | 4.2 (1.2) | 4.2 (1.2) | 4.2 (1.2) | 4.2 (1.2) |
| LDL, mmol/L | 2.3 (1.0) | 2.2 (1.0) | 2.2 (0.9) | 2.2 (1.0) |
| HDL, mmol/L | 1.1 (0.3) | 1.1 (0.3) | 1.1 (0.3) | 1.1 (0.3) |
| UACR (median, IQR), g/mol | 2.2 [0.9,6.6] | 1.4 [0.5,4.4] | 1.9 [0.6,5.0] | 1.4 [0.5,4.2] |
| Hemoglobin, g/L | 137.3 (15.6) | 140.2 (16.3) | 137.0 (15.4) | 140.1 (16.4) |
| eGFR, mL/min/1.73 m2 | 79.7 (26.4) | 81.1 (22.0) | 79.6 (25.8) | 81.1 (22.2) |
| eGFR<60 mL/min/1.73 m2 | 130 (23%) | 93 (16%) | 132 (23%) | 94 (16%) |
| eGFR<45 mL/min/1.73 m2 | 46 (8.0%) | 18 (3.1%) | 42 (7.3%) | 19 (3.3%) |
| Smoking | ||||
| Never | 83 (15%) | 77 (13%) | 67 (12%) | 75 (13%) |
| Past | 234 (41%) | 231 (40%) | 258 (45%) | 235 (41%) |
| Current | 255 (45%) | 264 (46%) | 250 (43%) | 265 (46%) |
| Classes of diabetes medications (n)a | 1.6 (0.9) | 1.5 (0.9) | 1.5 (0.9) | 1.5 (0.9) |
| RAASi | 458 (80%) | 461 (81%) | 471 (82%) | 463 (81%) |
| Other antihypertensives | 325 (57%) | 353 (62%) | 336 (58%) | 353 (61%) |
| Statins | 434 (76%) | 460 (80%) | 433 (75%) | 462 (80%) |
| Diuretics | 247 (43%) | 240 (42%) | 266 (46%) | 238 (41%) |
| Insulin | 312 (55%) | 324 (57%) | 321 (56%) | 323 (56%) |
| Metformin | 472 (83%) | 482 (84%) | 480 (83%) | 481 (84%) |
| TZD | 22 (3.8%) | 29 (5.1%) | 31 (5.4%) | 32 (5.6%) |
| DPP-4i | 192 (34%) | 176 (31%) | 186 (32%) | 172 (30%) |
| Sulfonylureas | 215 (38%) | 190 (33%) | 182 (32%) | 189 (33%) |
Time-to-event analyses
Cox proportional hazard models were used to estimate hazard ratios for MACE, ACM, CV death, and serious hypoglycemia in each of the two sets of cohorts. In both comparisons, the hazard ratio for MACE with EQW+SGLT2i was non-significantly decreased compared with placebo (adjusted HR (95% CI) 0.68 (0.39–1.17)), and compared with EQW (0.85 (0.48–1.49), Fig. 2). This reduction was driven by a nominally significant decrease in risk of CV death (aHR 0.17 (0.04–0.77) compared with placebo and 0.21 (0.05–0.93) compared with EQW); nonfatal MI and nonfatal stroke were unchanged (Additional file 1: Tables S3 and S4). All-cause mortality was also reduced (aHR vs. placebo of 0.38 (0.16–0.90) and vs. EQW of 0.41 (0.17–0.95)), with no increase in risk of serious hypoglycemia (Fig. 2). Kaplan–Meier curves are shown in Additional file 1: Figures S5–S9.
In the exploratory analysis, the composite of hHF and CV death was nominally significantly reduced in both comparisons (Additional file: Tables S3 and S4), driven by CV death, while hHF was not reduced. Event numbers were small for both renal composites, with non-significant reductions in the estimated hazard ratios (Additional file: Tables S3 and S4). Amputations were rare (5 events total) and not significantly different in either comparison (Additional file: Tables S3 and S4). 1 1 1
In the nearest neighbor method, re-matching changes the composition of the comparator cohorts, and the resultant event rates. To account for this random effect, we repeated the propensity matching procedure 5000 times, generating approximately 2000 accepted sets of cohorts for each comparison. Comparing the distributions of hazard ratio estimates in these sets to the primary case reported here confirms that those for MACE, ACM, and CV death are near the centers of the respective distributions (Additional file: Figure S10A, B). The estimate for hHF in the placebo comparison is higher than most estimates, likely due to random chance and low event numbers (Additional file: Figure S10C), with most runs suggesting a numerically lower hHF risk with EQW+SGLT2i in both comparisons. 1 1
Next, we asked whether the observed effects were similar in only subjects taking EQW and SGLT2i simultaneously. In these smaller cohorts (n = 336–340 per cohort), no MACE benefit was observed, but trends for reduced ACM and CV death were consistent with the primary analysis (Additional file: Tables S5 and S6). Additionally, censoring of subjects initiating open-label GLP-1 RA had very little impact on estimated hazard ratios (Additional file: Tables S7 and S8). 1 1
Cardiovascular, mortality, and safety outcomes with combination exenatide QW+SGLT2i in the propensity-matched cohorts. Additional details are found in Additional file: Tables S3, S4, and Kaplan–Meier curves in Additional file: Figures S5–S9. Hazard ratio adjusted for age, duration of diabetes, prior cardiovascular disease, heart failure, sex, microalbuminuria, macroalbuminuria, eGFR, and HbA1c, all evaluated at first known SGLT2i usage or equivalent visit in comparator groups. MACE: major adverse cardiovascular events; CV: cardiovascular; pt-yrs: participant-years 1 1
eGFR slope
Figure 3 shows geometric mean eGFR over time after matching in the two sets of propensity-matched cohorts. MMRM-estimated slopes in the placebo comparison were + 1.21 mL/min/1.73 m2/year (se 0.37) in the combination cohort and − 0.71 mL/min/1.73 m2/year (se 0.33) in the placebo cohort, resulting in an estimated treatment effect of + 1.94 mL/min/1.73 m2/year (95% CI 0.94–2.94, p < 0.001). Similarly, in the EQW comparison, the estimated slope was + 1.27 mL/min/1.73 m2/year (se 0.38) in the combination cohort, and − 1.11 mL/min/1.73 m2/year (se 0.32) in the EQW cohort, giving an estimated treatment effect of + 2.38 mL/min/1.73 m2/year (95% CI 1.40–3.35, p < 0.001).
Geometric mean (+/− standard error) eGFR in the propensity-matched cohorts.Placebo comparison.Exenatide comparison. Time zero is the time of first visit with known SGLT2i use/matching. The small differences in eGFR at matching (t=0) also reflect restrictions on SGLT2i use in moderate renal impairment. eGFR slopes prior to matching are shown in Additional file: Figure S11. Blue: combination exenatide + SGLT2i cohorts; green: placebo cohort; red: exenatide cohort. eGFR, estimated glomerular filtration rate; SGLT2i, sodium-glucose co-transporter-2 inhibitor a b 1
Discussion
This analysis provides the first clinical support for the hypothesis that combinatorial use of GLP-1 RA and SGLT2i therapies may provide additional benefit on adjudicated cardiovascular outcomes, mortality, and renal disease progression, compared with GLP-1 RA without SGLT2i, and to standard of care with neither GLP-1 RA nor SGLT2i (Table 2). The subset of EXSCEL participants using SGLT2i provide a modestly-sized but credible cohort with rigorously collected clinical outcomes. Our analysis demonstrated numerically lower MACE risk, driven by a nominally significant reduction in cardiovascular death, compared with both EQW alone and placebo. The reduction in ACM was also nominally significant in both comparisons, as was the improvement in eGFR slope, with no increase in risk of serious hypoglycemia. We did not have enough data to probe the contributions of each drug to the observed outcomes, or to compare to SGLT2i alone, and imbalances between the EQW alone and placebo cohorts warrant caution in comparing the two sets of cohorts side-by-side. Nonetheless, the trend across cardiovascular and mortality outcomes for a numerically larger risk reduction compared with placebo than compared with exenatide supports possible beneficial contributions from both drug classes. Conversely, the similar improvement in eGFR slope in both comparisons in our population suggests the observed eGFR slope improvement may be due primarily to SGLT2i contributions when used on top of GLP-1 RA, consistent with previous GLP-1 RA studies generally showing an effect more so on macroalbuminuria than on eGFR-based endpoints [4].
In the full EXSCEL trial, the hazard ratio for MACE with EQW treatment was 0.91 (95% CI 0.83–1.00) [11], while several meta-analyses of the GLP-1 RA class estimated MACE hazard ratios from 0.87 to 0.90 [2–4, 20] for the class as a whole, with moderate evidence for intra-class heterogeneity. All three components of the MACE composite—cardiovascular death, non-fatal MI, and non-fatal stroke—appear to contribute to this outcome for the GLP-1 RA class [2, 3, 20]. While the majority of evidence supports this MACE benefit in subjects with ASCVD, there is some evidence that this benefit may extend to high-risk subjects without a previous CV event [4, 21]. In EXSCEL, the secondary end-point of ACM, while not formally tested due to the hierarchical nature of the statistical analysis plan, was nominally improved by EQW treatment (HR 0.86 (0.77–0.97) [13]. Meta-analyses suggest this mortality benefit is a class effect (hazard ratios 0.88–0.89) [4, 20], while no significant benefit on hHF or occurrence of serious hypoglycemia has been observed for the GLP-1 RA class [2, 3, 20]. In general GLP-1 RA trials point to a strong effect on new persistent macroalbuminuria [22–24], but there is limited evidence of improvement on eGFR-based endpoints: sustained eGFR decline of 40–50% for dulaglutide [23], and a small reduction in eGFR decline with liraglutide and dulaglutude in participants with moderate-to-severe CKD.
Trial design and study populations also varied across the SGLT2i class, with MACE hazard ratios in CVOTs of 0.86 to 0.93 [25–27]. Again, meta-analyses suggest a class effect benefit of 11–12% [1, 2], with this benefit restricted to a 14% improvement in participants with existing ASCVD [1]. SGLT2i appeared to have the largest benefit on the CV death component of MACE (HR 0.84 (0.75–0.94)) [2], and consistently reduce the risk of hHF (HR 0.65 to 0.73) [25–27] without increasing the risk of hypoglycemia. ACM was significantly reduced in only one SGLT2i CVOT to date [27], though there was a trend for benefit in all three completed trials [25, 26]. SGLT2i also consistently improved renal outcomes, with an estimated class benefit on worsening eGFR, ESRD, or renal death (HR 0.55 (0.48–0.64) [2]), regardless of ASCVD status and potentially also kidney disease status [1, 28]. In CREDENCE, canagliflozin reduced the relative risk of end-stage kidney disease, doubling of serum creatinine, or death from renal causes by 34%, and the relative risk of end-stage kidney disease by 32% in patients with type 2 diabetes [29].
These differences in outcomes with GLP-1 RA and SGLT2i are most likely tied to their mechanisms of action, over and above improvement of glycemia. GLP-1 RA enhance insulin secretion and inhibit glucagon secretion in a glucose-dependent manner, reduce appetite and gastric motility, increase heart rate, and exert natriuretic and vasodilatory effects in the kidney, contributing to weight loss and small blood pressure reductions [30, 31]. Effects on inflammation and endothelial function have also been observed in animals [31, 32], although clinical benefit of short-term exenatide treatment, compared to insulin glargine, on left ventricular function has not been observed [33]. SGLT2i act in an insulin-independent but glucose-dependent manner to increase urinary excretion of glucose, sodium, and water via osmotic diuresis [34–36]. These hemodynamic effects are subsequently hypothesized to reduce weight, blood pressure, and extracellular fluid via mechanisms distinct from and potentially complementary to renin-angiotensin-aldosterone system inhibitors [37]. SGLT2i also indirectly increase glucagon secretion and are hypothesized to alter inflammation, cardiac energetics, and metabolism [34–36]. These potentially complementary sets of mechanisms support the hypothesis that combination GLP-1 RA and SGLT2i treatment may results in further CV and renal benefit than observed with either class alone [5, 38, 39]. Results of the AWARD-10, SUSTAIN 9, and DURATION-8 trials and a subgroup analysis from CANVAS showed improvement in weight, triglycerides, and systolic blood pressure with different combinations of GLP-1 RA and SGLT2i, further increasing interest in this key question [8–10, 40, 41]; two additional trials are ongoing (LIRA-ADD2SGLT2i NCT02964247 and PIONEER4 NCT02863419). The results presented here support a potential added benefit for the combination of EQW and SGLT2i on ACM, at a minimum, an end-point on which both classes alone have shown some effect, and which may reflect a convergence of multiple mechanisms of action by these two drug classes. However, this analysis does not examine whether similar results would be observed with another GLP-1 RA.
The results in this analysis apply to a population with characteristics similar to the subpopulation in EXSCEL adding an SGLT2i as part of their usual glycemic care, as would be the case in a real-world analysis, and different from the populations typically found in a full randomized trial. More laboratory measurements were available here than are commonly found in registry data, allowing propensity matching based on these metrics and study visit. This approach avoids the time lag bias that can occur when comparing to participants initiating an anti-hyperglycemic medication that may be used as a different line of therapy [42]. Additionally, matching at comparable study visits avoids immortal time bias; subjects must remain in the trial for the same amount of time to be included, regardless of SGLT2i use [42]. Most participants in this analysis initiated EQW prior to an SGLT2i, in contrast to the GLP-1 RA + SGLT2i clinical trials performed to date [8–10, 40]. The propensity-matched cohorts also reflect regional patterns in SGLT2i use, with less history of CV disease but more albuminuria and a longer duration of diabetes than the overall EXSCEL trial population. Event rates were generally similar in these cohorts compared to the trial as a whole: 3.7 vs. 4.0 MACE per 100 participant-years, 2.0 vs. 2.3 ACM per 100 participant years, and 1.4 vs. 1.5 CV deaths per 100 participant-years in the EQW and placebo arms of EXSCEL, respectively [13]. These similarities in event rates are reassuring, though further study is required to assess the applicability of these results beyond the analyzed cohorts.
It is critical to consider the limitations of this analysis when interpreting the results. The posthoc nature of this analysis and the moderate sizes of the propensity-matched cohorts limit the statistical significance of our results; interpretation should focus on key, hypothesis-generating trends, and how they compare to existing knowledge in the field. While we carefully designed the propensity-matching procedure to balance patient characteristics, including metrics of disease state, medical history, laboratory measurements, and concomitant medications, we cannot exclude the possibility of bias due to unmeasured confounders [42–44]. Median follow-up time after SGLT2i initiation was under 2 years, restricting insight on CV outcomes and renal disease progression to this time-scale, which is relatively short for accrual of hard renal outcomes in this population with preserved renal function. We performed multiple analyses in two different cohorts, increasing the likelihood of type 1 error. To confirm the robustness of our results to matching variability within the study population, we re-matched and re-estimating hazard ratios; while one estimate for hHF was high relative to the resulting distribution (and thus likely a type 1 error), the estimates for MACE, ACM, and CV death were consistent with the overall distributions.
In EXSCEL, exact dates of SGLT2i initiation and cessation were not known [11]. As such, we used an “intent-to-treat”-like analysis, starting follow-up at the first known SGLT2i usage, as done previously [14]. In these cohorts, some patients added SGLT2i to their treatment plan while still taking study drug (exenatide or placebo), while others discontinued study drug (but remained in the trial) prior to SGLT2i initiation. This mix of participants, some using EQW and SGLT2i in sequence and others in parallel, is reflective of individual treatment decisions in clinical practice [45, 46]. In only subjects with overlapping EQW and SGLT2i use, we saw a similar benefit on mortality as in the primary analysis, though not on MACE. However, the limited size and resolution of this dataset constrains our ability to draw conclusions about sequential vs. parallel use of these drugs.
| Previous knowledge in the field |
| Multiple GLP-1 RA and SGLT2i demonstrated benefit on cardiovascular outcomes, mortality, and/or renal disease progression |
| The mechanisms underlying these effects, while not fully understood, are largely distinct |
| Combination GLP-1 RA and SGLT2i treatment improves metabolic parameters and cardiovascular risk factors, but no data on cardiovascular events, mortality, or renal function decline is available |
| New insights from this study |
| Combination exenatide QW and SGLT2i numerically lowered the hazard ratio for MACE, driven by a significant reduction in cardiovascular death compared to exenatide alone or neither drug class |
| All-cause mortality risk decreased with the combination, compared to exenatide QW alone or placebo |
| SGLT2i-mediated eGFR slope improvement was consistent on top of placebo or exenatide QW treatment |
| This data supports the hypothesis that combination GLP-1 RA and SGLT2i may provide additional cardiovascular and mortality benefit to GLP-1 RA alone, without any increase in risk of hypoglycemia |
Conclusions
This analysis provides the first insight, from a credible cohort with adjudicated CV events, into long-term cardiorenal outcomes in subjects using EQW and SGLT2i either in parallel or relatively close sequence. The results, supporting the hypothesis that this combination may provide additional benefit particularly on mortality, motivate additional, more comprehensive study of combination GLP-1 RA and SGLT2i in the future.
Supplementary information
Acknowledgements
The EXSCEL trial was conducted jointly by the Duke Clinical Research Institute and the University of Oxford Diabetes Trials Unit, in collaboration with the sponsor Amylin Pharmaceuticals, a wholly owned subsidiary of AstraZeneca. Editorial and project management support were provided by Cactus Communications. LEC is a fellow of the AstraZeneca postdoctoral program. RRH is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Prior presentation
The results presented here were presented at the American Diabetes Association 79th Scientific Sessions, June 7–11, 2019, San Francisco, California, USA, and at the 55th Annual Meeting of the European Association for the Study of Diabetes, 16–20 September, Barcelona, Spain.
Abbreviations
Authors’ contributions
All authors were involved in design of the analysis and reviewed the results and manuscript. SB prepared the dataset. LEC performed the analysis and wrote the first draft of the manuscript.
Funding
This analysis was supported by AstraZeneca.
Availability of data and materials
Requests for data access and proposals for analyses of EXSCEL can be submitted to the EXSCEL executive committee using instructions found at: https://www.dtu.ox.ac.uk/exscel/↗.
Ethics approval and consent to participate
The protocol was approved by local ethics committees and institutional review boards at each participating center. All subjects provided written informed consent.
Consent for publication
Not applicable.
Competing interests
LEC, RCP, SB, DWB, SG, CDS, and JR are employees and/or shareholders of AstraZeneca. SG’s spouse is also an employee of AstraZeneca. HJLH serves on advisory panels for Boehringer Ingelheim GmbH and Merck & Co., Inc, and is a consultant for AbbVie Inc., AstraZeneca, Fresenius SE & Co. KGaA, Janssen Research & Development, and Mitsubishi Tanabe Pharma Corporation. RCP is a stockholder of Novartis Pharmaceuticals Corporation. DWB is a stockholder of Bristol-Myers Squibb Company. MT is a consultant for AstraZeneca. RJM has received research support and honoraria from AstraZeneca, GlaxoSmithKline plc., and Merck & Co., Inc. AFH is a consultant for Bayer AG & Boehringer Ingelheim Pharmaceuticals, Inc., and receives research support from AstraZeneca, GlaxoSmithKline plc., Janssen Pharmaceuticals, Inc., Merck & Co., Inc., and Novartis Pharmaceuticals Corporation. RRH has attended advisory boards at Elcelyx Therapeutics, Inc., Merck & Co., Inc., Novartis AG, Novo Nordisk A/S, Amylin, and Eli Lilly. RRH has given lectures supported by Bayer AG, Eli Lilly, Merck & Co., Inc, and Novo Nordisk A/S, and received research support and honoraria from AstraZeneca, Bayer AG, and Merck & Co., Inc. RRH is an Emeritus NIHR Senior Investigator. JBB’s contracted consulting fees are paid to the University of North Carolina by Adocia, AstraZeneca, Dance Biopharm, Eli Lilly, MannKind, NovaTarg, Novo Nordisk, Senseonics, vTv Therapeutics, and Zafgen; grant support from Novo Nordisk, Sanofi, and vTv Therapeutics. He is a consultant to Cirius Therapeutics Inc, CSL Behring, Neurimmune AG, and Whole Biome Inc. He holds stock options in Mellitus Health, PhaseBio, Stability Health, and Whole Biome Inc. He is supported by a grant from the National Institutes of Health (UL1TR002489).
Footnotes
Supplementary information
Supplementary information accompanies this paper at 10.1186/s12933-019-0942-x.
References
Associated Data
Supplementary Materials
Data Availability Statement
Requests for data access and proposals for analyses of EXSCEL can be submitted to the EXSCEL executive committee using instructions found at: https://www.dtu.ox.ac.uk/exscel/↗.