Effects of exenatide and open-label SGLT2 inhibitor treatment, given in parallel or sequentially, on mortality and cardiovascular and renal outcomes in type 2 diabetes: insights from the EXSCEL trial

被引:65
作者
Clegg, Lindsay E. [1 ]
Penland, Robert C. [2 ]
Bachina, Srinivas [2 ]
Boulton, David W. [1 ]
Thuresson, Marcus [3 ]
Heerspink, Hiddo J. L. [4 ]
Gustavson, Stephanie [5 ]
Sjostrom, C. David [6 ]
Ruggles, James A. [7 ]
Hernandez, Adrian F. [8 ,9 ]
Buse, John B. [10 ]
Mentz, Robert J. [8 ,9 ]
Holman, Rury R. [11 ]
机构
[1] AstraZeneca, Clin Pharmacol & Safety Sci, R&D, 1 MedImmune Way, Gaithersburg, MD 20878 USA
[2] AstraZeneca, Clin Pharmacol & Safety Sci, R&D, Boston, MA USA
[3] Statisticon AB, Uppsala, Sweden
[4] Univ Groningen, Dept Clin Pharm & Pharmacol, Univ Med Ctr Groningen, Groningen, Netherlands
[5] AstraZeneca, BioPharmaceut R&D, Gaithersburg, MD USA
[6] AstraZeneca, BioPharmaceut R&D, Gothenburg, Sweden
[7] AstraZeneca, BioPharmaceut, Wilmington, DE USA
[8] Duke Univ, Durham, NC USA
[9] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[10] Univ N Carolina, Sch Med, Chapel Hill, NC 27515 USA
[11] Univ Oxford, Diabet Trials Unit, Oxford, England
关键词
SGLT2; inhibitor; GLP-1 receptor agonist; Exenatide; Cardiovascular outcomes; eGFR slope; Type 2 diabetes mellitus; Combination therapy; Propensity score matching; PEPTIDE-1 RECEPTOR AGONISTS; COTRANSPORTER; 2; INHIBITORS; DOUBLE-BLIND; THERAPY;
D O I
10.1186/s12933-019-0942-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Sodium-glucose cotransporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1 RA) improve cardiovascular and renal outcomes in patients with type 2 diabetes through distinct mechanisms. However, evidence on clinical outcomes in patients treated with both GLP-1 RA and SGLT2i is lacking. We aim to provide insight into the effects of open-label SGLT2i use in parallel with or shortly after once-weekly GLP-1 RA exenatide (EQW) on cardiorenal outcomes. Methods In the EXSCEL cardiovascular outcomes trial EQW arm, SGLT2i drop-in occurred in 8.7% of participants. These EQW+SGLT2i users were propensity-matched to: (1) placebo-arm participants not taking SGLT2i (n = 572 per group); and to (2) EQW-arm participants not taking SGLT2i (n = 575), based on their last measured characteristics before SGLT2i initiation, and equivalent study visit in comparator groups. Time-to-first major adverse cardiovascular event (MACE) and all-cause mortality (ACM) were compared using Cox regression analyses. eGFR slopes were quantified using mixed model repeated measurement analyses. Results In adjusted analyses, the risk for MACE with combination EQW+SGLT2i use was numerically lower compared with both placebo (adjusted hazard ratio 0.68, 95% CI 0.39-1.17) and EQW alone (0.85, 0.48-1.49). Risk of ACM was nominally significantly reduced compared with placebo (0.38, 0.16-0.90) and compared with EQW (0.41, 0.17-0.95). Combination EQW+SGLT2i use also nominally significantly improved estimated eGFR slope compared with placebo (+ 1.94, 95% CI 0.94-2.94 mL/min/1.73 m(2)/year) and EQW alone (+ 2.38, 1.40-3.35 mL/min/1.73 m(2)/year). Conclusions This post hoc analysis supports the hypothesis that combinatorial EQW and SGLT2i therapy may provide benefit on cardiovascular outcomes and mortality. Trial registration Clinicaltrials.gov, Identifying number: NCT01144338, Date of registration: June 15, 2010.
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页数:12
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