1Division of Cardiology, Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea
2Division of Geriatrics, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea
Copyright © 2022 Korean Diabetes Association
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
CONFLICTS OF INTEREST
No potential conflict of interest relevant to this article was reported.
FUNDING
This study was supported by a research grant from the Korea National Institute of Health (grant number: 2021-ER0901, 2021–2023).
Guidelines identifier | Year | Target populations | BP thresholds, mm Hg | BP target, mm Hg |
---|---|---|---|---|
JNC 8 | 2014 | General | Office ≥140/90 | Office <140/90 |
JNC 8 | 2014 | Diabetes | Office ≥140/90 | Office <140/90 |
ACC/AHA | 2017 | General | Office ≥130/80 | Office <130/80 |
ACC/AHA | 2017 | Diabetes | Office ≥130/80 | Office <130/80 |
ESC/ESH | 2018 | General | Office ≥140/90 | Office <140/90a |
ESC/ESH | 2018 | Diabetes | Office ≥140/90 | 120/70≤ Office ≤130/80 |
KSH | 2018 | General | Office >140/90 | Office <140/90 |
KSH | 2018 | Diabetes | Office >140/90 | Office <140/85 |
KSH | 2018 | Diabetes with CVDb | Office >140/90 | Office <130/80 |
NICE | 2019 | General | Office BP ≥140/90 | Office <140/90 |
NICE | 2019 | Diabetes | Office BP ≥140/90 | Office <140/90 |
ESC/EASD | 2019 | Diabetes | Office ≥140/90 | 120/70≤ Office ≤130/80 |
KDA | 2021 | Diabetes | - | Office <140/85 |
KDA | 2021 | Diabetes with CVD | - | Office <130/80 |
ADA | 2022 | Diabetes | Office ≥140/90 | Office <140/90 |
ADA | 2022 | Diabetes with higher CV riskc | Office ≥140/90 | Office <130/80 |
BP, blood pressure; JNC, Joint National Committee; ACC, American College of Cardiology; AHA, American Heart Association; ESC, European Society of Cardiology; ESH, European Society of Hypertension; KSH, Korean Society of Hypertension; CVD, cardiovascular disease; NICE, National Institute for Health and Care Excellence; EASD, European Association for the Study of Diabetes; KDA, Korean Diabetes Association; ADA, American Diabetes Association.
a BP target for all patients; if the treatment is well tolerated, the treated BP target should be office ≤130/80,
b Coronary artery disease, peripheral vascular disease, aortic disease, heart failure, or left ventricular hypertrophy in patients aged ≥50 years,
c Existing atherosclerotic cardiovascular disease (ASCVD) or 10-year ASCVD risk ≥15%.
Clinical trial | Population | Follow-up | Initial BP, mm Hg | Achieved BP active, mm Hg | Achieved BP control, mm Hg | Clinical outcomes |
---|---|---|---|---|---|---|
UKPDS 38, 1998 [5] | 1,148 Hypertensive participants with T2DM aged with 25–65 yr | Median 8.4 yr | Active: 159/94 | 144/82 (target: <150/85) | 154/87 (target: <180/105) | Reduced risk for diabetes related any end points risk by 24% with active control |
Control: 160/94 | Deaths related to diabetes risk by 32%, stroke risk by 44%, and heart failure risk by 56% | |||||
Microvascular end points risk by 37% | ||||||
No benefit in all-cause mortality | ||||||
HOT, 1998 [24] | 18,790 Hypertensive participants including 1,501 with T2DM | Mean 3.8 yr | 170/105 | DBP: 81.1 in target DBP ≤80 | DBP: 85.2 in target DBP ≤90 | No benefit in CV event in overall participants |
DBP: 83.2 in target DBP ≤85 | In participants with diabetes, increased major CV event risk by 2.06-fold in target DBP ≤90 compared with ≤80; Increased CV mortality risk by 3.0-fold in target DBP ≤90 compared with ≤80 | |||||
ADVANCE, 2007 [25] | 11,140 With T2DM aged with 55 yr and older with prior CVD or CV risk factors | Mean 4.3 yr | Active: 145/81 | 136/73 | 140/73 | Reduced risk of major macrovascular or microvascular event by 9%, death from CV disease by 18%, death from any cause by 14% |
Control: 145/81 | ||||||
Subgroup analysis of INVEST, 2010 [26] | 6,400 Participants of the 22,576 participants in INVEST aged at least 50 yr with T2DM and CAD | 16,893 Patient-yr | Active: 144/85 | Active SBP: 121.5 (SBP category <130) | Uncontrolled: SBP 146.1 (SBP category ≥140) | No benefit in adverse CV outcome including all-cause death, nonfatal myocardial infarction, or nonfatal stroke in active control of SBP compared with usual control |
Usual: 149/85 | Usual SBP 131.2 (SBP category 130–140) | Increased risk of adverse CV outcome in uncontrolled SBP group compared with usual control by 1.46-fold | ||||
Uncontrolled: 159/86 | Increased risk of all-cause mortality in active control compared with usual control by 1.15-fold when extended follow-up | |||||
ACCORD-BP, 2010 [20] | 4,733 Participants with T2DM aged 40–79 yr with prior CVD or 55–79 yr with CV risk factors | Mean 4.7 yr | Active: 139.0/75.9 | 119.3/64.4 (target SBP: <120) | 135/70.5 (target SBP: 130–140) | No benefit in primary composite outcome including nonfatal MI, nonfatal stroke, and CV death |
Control: 139.4/76.0 | Reduced risk of stroke by 41% with active control | |||||
SAEs more common in intensive group, particularly hypotension, elevated serum creatinine and electrolyte imbalance | ||||||
SPRINT-eligible ACCORD-BP, 2017 [23] | SPRINT-eligible 1,284 participants of the 4,733 participants in ACCORD-BP aged at least 75 yr with T2DM or clinical CVD or subclnical CVD or high CV risk | - | Active: 139.8 | SBP: 120.1 (target SBP: <120) | SBP: 133.5 (target SBP: <140) | Reduced risk of composite of CV death, nonfatal MI, nonfatal stroke, any revascularization, and HF by 21% |
Control: 140.8 | Reduced risk of CV death, nonfatal MI, and nonfatal stroke by 31% | |||||
More frequent treatment-related adverse events in active control |
BP, blood pressure; UKPDS, UK Prospective Diabetes Study; T2DM, type 2 diabetes mellitus; HOT, Hypertension Optimal Treatment trial; DBP, diastolic blood pressure; CV, cardiovascular; ADVANCE, Action in Diabetes and Vascular Disease: preterAx and diamicroN-MR Controlled Evaluation trial; CVD, cardiovascular disease; INVEST, International Verapamil SR-Trandolapril Study; CAD, coronary artery disease; SBP, systolic blood pressure; ACCORD-BP, Action to Control Cardiovascular Risk in Diabetes Blood Pressure Trial; MI, myocardial infarction; SAE, serious adverse event; SPRINT, Systolic Blood Pressure Intervention Trial; HF, heart failure.
Guidelines identifier | Year | Target populations | BP thresholds, mm Hg | BP target, mm Hg |
---|---|---|---|---|
JNC 8 | 2014 | General | Office ≥140/90 | Office <140/90 |
JNC 8 | 2014 | Diabetes | Office ≥140/90 | Office <140/90 |
ACC/AHA | 2017 | General | Office ≥130/80 | Office <130/80 |
ACC/AHA | 2017 | Diabetes | Office ≥130/80 | Office <130/80 |
ESC/ESH | 2018 | General | Office ≥140/90 | Office <140/90 |
ESC/ESH | 2018 | Diabetes | Office ≥140/90 | 120/70≤ Office ≤130/80 |
KSH | 2018 | General | Office >140/90 | Office <140/90 |
KSH | 2018 | Diabetes | Office >140/90 | Office <140/85 |
KSH | 2018 | Diabetes with CVD |
Office >140/90 | Office <130/80 |
NICE | 2019 | General | Office BP ≥140/90 | Office <140/90 |
NICE | 2019 | Diabetes | Office BP ≥140/90 | Office <140/90 |
ESC/EASD | 2019 | Diabetes | Office ≥140/90 | 120/70≤ Office ≤130/80 |
KDA | 2021 | Diabetes | - | Office <140/85 |
KDA | 2021 | Diabetes with CVD | - | Office <130/80 |
ADA | 2022 | Diabetes | Office ≥140/90 | Office <140/90 |
ADA | 2022 | Diabetes with higher CV risk |
Office ≥140/90 | Office <130/80 |
Clinical trial | Population | Follow-up | Initial BP, mm Hg | Achieved BP active, mm Hg | Achieved BP control, mm Hg | Clinical outcomes |
---|---|---|---|---|---|---|
UKPDS 38, 1998 [5] | 1,148 Hypertensive participants with T2DM aged with 25–65 yr | Median 8.4 yr | Active: 159/94 | 144/82 (target: <150/85) | 154/87 (target: <180/105) | Reduced risk for diabetes related any end points risk by 24% with active control |
Control: 160/94 | Deaths related to diabetes risk by 32%, stroke risk by 44%, and heart failure risk by 56% | |||||
Microvascular end points risk by 37% | ||||||
No benefit in all-cause mortality | ||||||
HOT, 1998 [24] | 18,790 Hypertensive participants including 1,501 with T2DM | Mean 3.8 yr | 170/105 | DBP: 81.1 in target DBP ≤80 | DBP: 85.2 in target DBP ≤90 | No benefit in CV event in overall participants |
DBP: 83.2 in target DBP ≤85 | In participants with diabetes, increased major CV event risk by 2.06-fold in target DBP ≤90 compared with ≤80; Increased CV mortality risk by 3.0-fold in target DBP ≤90 compared with ≤80 | |||||
ADVANCE, 2007 [25] | 11,140 With T2DM aged with 55 yr and older with prior CVD or CV risk factors | Mean 4.3 yr | Active: 145/81 | 136/73 | 140/73 | Reduced risk of major macrovascular or microvascular event by 9%, death from CV disease by 18%, death from any cause by 14% |
Control: 145/81 | ||||||
Subgroup analysis of INVEST, 2010 [26] | 6,400 Participants of the 22,576 participants in INVEST aged at least 50 yr with T2DM and CAD | 16,893 Patient-yr | Active: 144/85 | Active SBP: 121.5 (SBP category <130) | Uncontrolled: SBP 146.1 (SBP category ≥140) | No benefit in adverse CV outcome including all-cause death, nonfatal myocardial infarction, or nonfatal stroke in active control of SBP compared with usual control |
Usual: 149/85 | Usual SBP 131.2 (SBP category 130–140) | Increased risk of adverse CV outcome in uncontrolled SBP group compared with usual control by 1.46-fold | ||||
Uncontrolled: 159/86 | Increased risk of all-cause mortality in active control compared with usual control by 1.15-fold when extended follow-up | |||||
ACCORD-BP, 2010 [20] | 4,733 Participants with T2DM aged 40–79 yr with prior CVD or 55–79 yr with CV risk factors | Mean 4.7 yr | Active: 139.0/75.9 | 119.3/64.4 (target SBP: <120) | 135/70.5 (target SBP: 130–140) | No benefit in primary composite outcome including nonfatal MI, nonfatal stroke, and CV death |
Control: 139.4/76.0 | Reduced risk of stroke by 41% with active control | |||||
SAEs more common in intensive group, particularly hypotension, elevated serum creatinine and electrolyte imbalance | ||||||
SPRINT-eligible ACCORD-BP, 2017 [23] | SPRINT-eligible 1,284 participants of the 4,733 participants in ACCORD-BP aged at least 75 yr with T2DM or clinical CVD or subclnical CVD or high CV risk | - | Active: 139.8 | SBP: 120.1 (target SBP: <120) | SBP: 133.5 (target SBP: <140) | Reduced risk of composite of CV death, nonfatal MI, nonfatal stroke, any revascularization, and HF by 21% |
Control: 140.8 | Reduced risk of CV death, nonfatal MI, and nonfatal stroke by 31% | |||||
More frequent treatment-related adverse events in active control |
BP, blood pressure; JNC, Joint National Committee; ACC, American College of Cardiology; AHA, American Heart Association; ESC, European Society of Cardiology; ESH, European Society of Hypertension; KSH, Korean Society of Hypertension; CVD, cardiovascular disease; NICE, National Institute for Health and Care Excellence; EASD, European Association for the Study of Diabetes; KDA, Korean Diabetes Association; ADA, American Diabetes Association. BP target for all patients; if the treatment is well tolerated, the treated BP target should be office ≤130/80, Coronary artery disease, peripheral vascular disease, aortic disease, heart failure, or left ventricular hypertrophy in patients aged ≥50 years, Existing atherosclerotic cardiovascular disease (ASCVD) or 10-year ASCVD risk ≥15%.
BP, blood pressure; UKPDS, UK Prospective Diabetes Study; T2DM, type 2 diabetes mellitus; HOT, Hypertension Optimal Treatment trial; DBP, diastolic blood pressure; CV, cardiovascular; ADVANCE, Action in Diabetes and Vascular Disease: preterAx and diamicroN-MR Controlled Evaluation trial; CVD, cardiovascular disease; INVEST, International Verapamil SR-Trandolapril Study; CAD, coronary artery disease; SBP, systolic blood pressure; ACCORD-BP, Action to Control Cardiovascular Risk in Diabetes Blood Pressure Trial; MI, myocardial infarction; SAE, serious adverse event; SPRINT, Systolic Blood Pressure Intervention Trial; HF, heart failure.