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. 2022 May 31;29(3):499–508. doi: 10.5603/CJ.a2020.0140

Table 1.

Characteristics of included studies.

Study Study treatment Year Randomization period Patients Median follow-up [years] Age [years] Women (%) Diabetes duration [years] HbA1c [%] ASCVD [%] Heart failure [%] eGFR [mL/min/1.73 m2] eGFR < 60 mL/min/1.73 m2
GLP-1 agonists
ELIXA Lixisenatide (up to 20 μg sc daily) 2015 2010–2013 3034/3034 2.1 60/61 30/31 9.3 / 9.5 7.7/7.6 100/100 23/22 77/75 22/25
LEADER Liraglutide (up to 1.8 mg sc daily) 2016 2010–2012 4668/4672 3.5 64/64 35/36 13/13 8.7/8.7 82/81 18/18 24/22
SUSTAIN-6 Semaglutide (0.5 mg/1.0 mg sc weekly) 2016 2013 1648/1649 2.1 65/65 39/40 14/14 8.7/8.7 60/61 23/24 28/29
EXSCEL Extended–release exenatide (2 mg sc weekly) 2017 2010–2015 7356/7396 3.2 62/62 38/38 12/12 8.0/0.0 73/73 16/17 77/76 21/22
Harmony Outcomes Albiglutide (30–50 mg sc weekly) 2018 2015–2016 4731/4732 1.6 64/64 30/31 14/14 8.8/8.7 20/20 79/79 11/11
REWIND Dulaglutide (1.5 mg sc weekly) 2019 2011–2013 4949/4952 5.4 66/66 47/46 11/11 7.3/7.4 32/31 9/9 75/75 22/23
PIONEER 6 Semaglutide (14 mg po daily) 2019 2017 1591/1592 1.3 66/66 32/31 15/15 8.2/8.2 85/85 12/13 74/74 27/27
SGLT-2 inhibitors
EMPA-REG OUTCOME Empagliflozin (10 mg/25 mg po daily) 2015 2010–2013 4687/2333 3.1 63/63 29/28 8.1/8.1 100/100 10/11 74/74 26/26
CANVAS Program Canagliflozin (100–300 mg po daily) 2017 2009–2017 5795/4347 2.4 63/63 35/37 14/14 8.2/8.2 71/74 14/15 77/76
DECLARE-TIMI 58 Dapagliflozin (10 mg po daily) 2018 2013–2015 8582/8578 4.2 64/64 37/38 11/10 8.3/8.3 41/41 10/10 85/85 7/8
CREDENCE Canagliflozin (100 mg po daily) 2019 2014–2017 2202/2199 2.6 63/63 35/33 16/16 8.3/8.3 51/50 15/15 56/56 59/59

Data are presented as second line agents/control. HbA1c — glycated hemoglobin; ASCVD — atherosclerotic cardiovascular disease; eGFR — estimated glomerular filtration rate; GLP-1 — glucagon-like peptide 1; ELIXA — evaluation of lixisenatide in acute coronary syndrome; LEADER — liraglutide effect and action in diabetes: evaluation of cardiovascular outcome results; SUSTAIN-6 — trial to evaluate cardiovascular and other long-term outcomes with semaglutide in subjects with type 2 diabetes; EXSCEL — exenatide study of cardiovascular event lowering study group; REWIND — researching cardiovascular events with a weekly incretin in diabetes; SGLT-2 — sodium glucose cotransporter 2; CANVAS — canagliflozin cardiovascular assessment study; DECLARE-TIMI 58 — dapagliflozin effect on cardiovascular events–thrombolysis in myocardial infarction 58; CREDENCE — canagliflozin and renal events in diabetes with established nephropathy clinical evaluation