Table 1

Baseline characteristics of participants in the trial (SPRINT or ACCORD-BP) according to the treatment assignment

VariablesIntensive treatment group (target SBP <120 mmHg; N = 5334)Standard treatment group (target SBP <140 mmHg; N = 5338)
Age, mean (SD), year65.4 (8.3)65.6 (8.5)
Female, %2191 (41.1)2161 (40.5)
Race/ethnicity, %
 Non-Hispanic White3165 (58.3)3102 (58.1)
 Non-Hispanic Black1378 (25.8)1469 (27.5)
 Hispanic489 (9.2)479 (9.0)
 Other302 (5.7)288 (5.4)
Education status, %
 Less than college3592 (67.3)3538 (66.3)
 College or above1742 (32.7)1800 (33.7)
Uninsured, %673 (12.6)666 (12.5)
Living alone, %1317 (24.7)1382 (25.9)
Smoking, %676 (12.7)719 (13.5)
SBP, mean (SD), mmHg139.2 (15.8)139.5 (15.5)
BMI, mean (SD), kg/m231.1 (5.4)31.0 (5.2)
Total cholesterol, mean (SD), mg/dL191.8 (43.0)190.9 (42.1)
HDL cholesterol, mean (SD), mg/dL49.7 (14.2)49.9 (14.6)
eGFR, mL/min/1.73 m2, %
 ≥901548 (29.0)1539 (28.9)
 60 to <902665 (50.0)2666 (49.9)
  45 to <60768 (14.4)796 (14.9)
 <45353 (6.6)337 (6.3)
Clinical CVD, %1233 (23.1)1193 (22.4)
Statin use, %2781 (52.1)2872 (53.8)
Antihypertensive use medications, %
 0534 (10.1)559 (10.9)
 11786 (33.5)1800 (33.7)
 ≥23014 (56.5)2959 (55.4)
History of diabetesa2239 (42.0)2244 (42.0)
10-year Framingham CVD risk %, median (IQR)22.7 (19.6)22.6 (19.4)
10-year ASCVD risk %, median (IQR)22.3 (12.8)22.5 (13.0)
VariablesIntensive treatment group (target SBP <120 mmHg; N = 5334)Standard treatment group (target SBP <140 mmHg; N = 5338)
Age, mean (SD), year65.4 (8.3)65.6 (8.5)
Female, %2191 (41.1)2161 (40.5)
Race/ethnicity, %
 Non-Hispanic White3165 (58.3)3102 (58.1)
 Non-Hispanic Black1378 (25.8)1469 (27.5)
 Hispanic489 (9.2)479 (9.0)
 Other302 (5.7)288 (5.4)
Education status, %
 Less than college3592 (67.3)3538 (66.3)
 College or above1742 (32.7)1800 (33.7)
Uninsured, %673 (12.6)666 (12.5)
Living alone, %1317 (24.7)1382 (25.9)
Smoking, %676 (12.7)719 (13.5)
SBP, mean (SD), mmHg139.2 (15.8)139.5 (15.5)
BMI, mean (SD), kg/m231.1 (5.4)31.0 (5.2)
Total cholesterol, mean (SD), mg/dL191.8 (43.0)190.9 (42.1)
HDL cholesterol, mean (SD), mg/dL49.7 (14.2)49.9 (14.6)
eGFR, mL/min/1.73 m2, %
 ≥901548 (29.0)1539 (28.9)
 60 to <902665 (50.0)2666 (49.9)
  45 to <60768 (14.4)796 (14.9)
 <45353 (6.6)337 (6.3)
Clinical CVD, %1233 (23.1)1193 (22.4)
Statin use, %2781 (52.1)2872 (53.8)
Antihypertensive use medications, %
 0534 (10.1)559 (10.9)
 11786 (33.5)1800 (33.7)
 ≥23014 (56.5)2959 (55.4)
History of diabetesa2239 (42.0)2244 (42.0)
10-year Framingham CVD risk %, median (IQR)22.7 (19.6)22.6 (19.4)
10-year ASCVD risk %, median (IQR)22.3 (12.8)22.5 (13.0)

SPRINT, Systolic Blood Pressure Intervention Trial; ACCORD-BP, Action to Control Cardiovascular Risk in Diabetes Blood Pressure; BMI, body mass index; SBP, systolic blood pressure; HDL, high-density lipoprotein; eGFR, estimated glomerular filtration rate; CVD, cardiovascular disease; SD, standard deviation; IQR, interquartile range; ASCVD, atherosclerotic cardiovascular disease.

a

History of diabetes was labelled as 0 for the SPRINT participants and 1 for the ACCORD-BP participants.

Table 1

Baseline characteristics of participants in the trial (SPRINT or ACCORD-BP) according to the treatment assignment

VariablesIntensive treatment group (target SBP <120 mmHg; N = 5334)Standard treatment group (target SBP <140 mmHg; N = 5338)
Age, mean (SD), year65.4 (8.3)65.6 (8.5)
Female, %2191 (41.1)2161 (40.5)
Race/ethnicity, %
 Non-Hispanic White3165 (58.3)3102 (58.1)
 Non-Hispanic Black1378 (25.8)1469 (27.5)
 Hispanic489 (9.2)479 (9.0)
 Other302 (5.7)288 (5.4)
Education status, %
 Less than college3592 (67.3)3538 (66.3)
 College or above1742 (32.7)1800 (33.7)
Uninsured, %673 (12.6)666 (12.5)
Living alone, %1317 (24.7)1382 (25.9)
Smoking, %676 (12.7)719 (13.5)
SBP, mean (SD), mmHg139.2 (15.8)139.5 (15.5)
BMI, mean (SD), kg/m231.1 (5.4)31.0 (5.2)
Total cholesterol, mean (SD), mg/dL191.8 (43.0)190.9 (42.1)
HDL cholesterol, mean (SD), mg/dL49.7 (14.2)49.9 (14.6)
eGFR, mL/min/1.73 m2, %
 ≥901548 (29.0)1539 (28.9)
 60 to <902665 (50.0)2666 (49.9)
  45 to <60768 (14.4)796 (14.9)
 <45353 (6.6)337 (6.3)
Clinical CVD, %1233 (23.1)1193 (22.4)
Statin use, %2781 (52.1)2872 (53.8)
Antihypertensive use medications, %
 0534 (10.1)559 (10.9)
 11786 (33.5)1800 (33.7)
 ≥23014 (56.5)2959 (55.4)
History of diabetesa2239 (42.0)2244 (42.0)
10-year Framingham CVD risk %, median (IQR)22.7 (19.6)22.6 (19.4)
10-year ASCVD risk %, median (IQR)22.3 (12.8)22.5 (13.0)
VariablesIntensive treatment group (target SBP <120 mmHg; N = 5334)Standard treatment group (target SBP <140 mmHg; N = 5338)
Age, mean (SD), year65.4 (8.3)65.6 (8.5)
Female, %2191 (41.1)2161 (40.5)
Race/ethnicity, %
 Non-Hispanic White3165 (58.3)3102 (58.1)
 Non-Hispanic Black1378 (25.8)1469 (27.5)
 Hispanic489 (9.2)479 (9.0)
 Other302 (5.7)288 (5.4)
Education status, %
 Less than college3592 (67.3)3538 (66.3)
 College or above1742 (32.7)1800 (33.7)
Uninsured, %673 (12.6)666 (12.5)
Living alone, %1317 (24.7)1382 (25.9)
Smoking, %676 (12.7)719 (13.5)
SBP, mean (SD), mmHg139.2 (15.8)139.5 (15.5)
BMI, mean (SD), kg/m231.1 (5.4)31.0 (5.2)
Total cholesterol, mean (SD), mg/dL191.8 (43.0)190.9 (42.1)
HDL cholesterol, mean (SD), mg/dL49.7 (14.2)49.9 (14.6)
eGFR, mL/min/1.73 m2, %
 ≥901548 (29.0)1539 (28.9)
 60 to <902665 (50.0)2666 (49.9)
  45 to <60768 (14.4)796 (14.9)
 <45353 (6.6)337 (6.3)
Clinical CVD, %1233 (23.1)1193 (22.4)
Statin use, %2781 (52.1)2872 (53.8)
Antihypertensive use medications, %
 0534 (10.1)559 (10.9)
 11786 (33.5)1800 (33.7)
 ≥23014 (56.5)2959 (55.4)
History of diabetesa2239 (42.0)2244 (42.0)
10-year Framingham CVD risk %, median (IQR)22.7 (19.6)22.6 (19.4)
10-year ASCVD risk %, median (IQR)22.3 (12.8)22.5 (13.0)

SPRINT, Systolic Blood Pressure Intervention Trial; ACCORD-BP, Action to Control Cardiovascular Risk in Diabetes Blood Pressure; BMI, body mass index; SBP, systolic blood pressure; HDL, high-density lipoprotein; eGFR, estimated glomerular filtration rate; CVD, cardiovascular disease; SD, standard deviation; IQR, interquartile range; ASCVD, atherosclerotic cardiovascular disease.

a

History of diabetes was labelled as 0 for the SPRINT participants and 1 for the ACCORD-BP participants.

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