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. 2019 Dec 19;9(1):e014328. doi: 10.1161/JAHA.119.014328

Table 2.

Kaplan‐Meier Estimates for Risk of MACEs by Baseline HbA1c in Patients With DM in the ACCELERATE Trial

End Point HbA1c, % P Value
<6.0 (N=1418) 6.0–<6.5 (N=1620) 6.5–<7.0 N=1554) 7.0–<7.5 (N=1111) 7.5–<8.0 (N=792) ≥8.0 (N=1650)
MACE 168 (12.6) 212 (14.5) 201 (14.0) 163 (16.1) 117 (16.3) 278 (18.2) <0.001
Cardiovascular death/MI/stroke 101 (7.8) 130 (8.9) 111 (7.8) 83 (7.9) 58 (8.0) 172 (11.3) 0.003
Cardiovascular death 45 (3.4) 41 (3.0) 42 (2.9) 36 (3.6) 18 (2.6) 63 (4.3) 0.21
All‐cause mortality 63 (4.8) 69 (5.0) 71 (4.9) 50 (5.0) 35 (5.1) 88 (5.9) 0.21
Nonfatal MI 41 (3.1) 84 (5.6) 58 (4.1) 46 (4.3) 35 (5.0) 106 (7.0) <0.001
Stroke 27 (2.3) 22 (1.5) 27 (2.0) 14 (1.4) 13 (1.8) 35 (2.4) 0.45
Revascularization 96 (7.3) 142 (9.6) 125 (8.9) 99 (10.3) 75 (10.4) 168 (11.1) 0.001
Hospitalization for unstable angina 31 (2.3) 25 (1.8) 40 (2.8) 46 (5.0) 23 (3.1) 52 (3.4) 0.003

Data are given as number of patients (Kaplan‐Meier estimate). MACEs include cardiovascular death, nonfatal MI, cerebrovascular accident, hospitalization for unstable angina, and revascularization. ACCELERATE indicates Assessment of Clinical Effects of Cholesteryl Ester Transfer Protein Inhibition With Evacetrapib in Patients at a High Risk for Vascular Outcomes; DM, diabetes mellitus; HbA1c, hemoglobin A1c; MACE, major adverse cardiovascular event; MI, myocardial infarction.