Impact of the 2017 American Heart Association and American College of Cardiology hypertension guideline in aged individuals.


Journal

Journal of hypertension
ISSN: 1473-5598
Titre abrégé: J Hypertens
Pays: Netherlands
ID NLM: 8306882

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 3 8 2020
medline: 24 6 2021
entrez: 3 8 2020
Statut: ppublish

Résumé

The AHA/ACC-2017 hypertension guideline recommends an age-independent target blood pressure (BP) of less than 130/80 mmHg. In an elderly cohort without established cardiovascular disease (CVD) at baseline, we determined the impact of this guideline on the prevalence of hypertension and associated CVD risk. Nineteen thousand, one hundred and fourteen participants aged at least 65 years from the ASPirin in Reducing Events in the Elderly (ASPREE) study were grouped by baseline BP: 'pre-2017 hypertensive' (BP ≥140/90 mmHg and/or on antihypertensive drugs); 'reclassified hypertensive' (normotensive by pre-2017 guidelines; hypertensive by AHA/ACC-2017 guideline), and 'normotensive' (BP <130 and <80 mmHg). For each group, we evaluated CVD risk factors, predicted 10-year CVD risk using the Atherosclerotic Cardiovascular Disease (ASCVD) risk equation, and reported observed CVD event rates during a median 4.7-year follow-up. Overall, 74.4% (14 213/19 114) were 'pre-2017 hypertensive'; an additional 12.3% (2354/19 114) were 'reclassified hypertensive' by the AHA/ACC-2017 guideline. Of those 'reclassified hypertensive', the majority (94.5%) met criteria for antihypertensive treatment although 29% had no other traditional CVD risk factors other than age. Further, a relatively lower mean 10-year predicted CVD risk (18% versus 26%, P < 0.001) and lower CVD rates (8.9 versus 12.1/1000 person-years, P = 0.01) were observed in 'reclassified hypertensive' compared with 'pre-2017 hypertensive'. Compared with 'normotensive', a hazard ratio (95% confidence interval) for CVD events of 1.60 (1.26-2.02) for 'pre-2017 hypertensive' and 1.26 (0.93-1.71) for 'reclassified hypertensive' was observed. Applying current CVD risk calculators in the elderly 'reclassified hypertensive', as a result of shifting the BP threshold lower, increases eligibility for antihypertensive treatment but documented CVD rates remain lower than hypertensive patients defined by pre2017 BP thresholds.

Identifiants

pubmed: 32740404
doi: 10.1097/HJH.0000000000002582
pii: 00004872-202012000-00027
pmc: PMC8218338
mid: NIHMS1698921
doi:

Substances chimiques

Antihypertensive Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2527-2536

Subventions

Organisme : NIA NIH HHS
ID : P30 AG024824
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG029824
Pays : United States
Organisme : NIA NIH HHS
ID : U19 AG062682
Pays : United States

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Auteurs

Enayet Karim Chowdhury (EK)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.
School of Public Health, Curtin University, Perth, Western Australia, Australia.

Michael E Ernst (ME)

Department of Pharmacy Practice and Science, College of Pharmacy and Department of Family Medicine, Carver College of Medicine, The University of Iowa, Iowa City, USA.

Mark Nelson (M)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.
Menzies Institute for Medical Research, University of Tasmania, Hobart TAS, Australia.

Karen Margolis (K)

HealthPartners Institute, Minneapolis, Minnesota, USA.

Lawrie J Beilin (LJ)

School of Medicine, Royal Perth Hospital, University of Western Australia, Perth, Western Australia.

Collin Johnston (C)

Baker Heart and Diabetes Institute, Melbourne, Australia.

Robyn Woods (R)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Anne Murray (A)

Berman Center for Outcomes and Clinical Research, Hennepin Healthcare Research Institute (HHRI), Hennepin Healthcare.
Division of Geriatrics, Department of Medicine, Hennepin Healthcare and University of Minnesota, Minneapolis, Minnesota.

Rory Wolfe (R)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Elsdon Storey (E)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Raj C Shah (RC)

Department of Family Medicine and Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois.

Jessica Lockery (J)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Andrew Tonkin (A)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Anne Newman (A)

Center for Aging and Population Health, Department of Epidemiology, University of Pittsburgh, Pittsburgh, USA.

Walter Abhayaratna (W)

College of Health and Medicine, The Australian National University, Canberra, ACT.

Nigel Stocks (N)

Discipline of General Practice, University of Adelaide, Adelaide, SA.

Sharyn Fitzgerald (S)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Suzanne Orchard (S)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Ruth Trevaks (R)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Geoffrey Donnan (G)

Florey Institute of Neuroscience and Mental Health, University of Melbourne, Victoria, Australia.

R Grimm (R)

Division of Geriatrics, Department of Medicine, Hennepin Healthcare and University of Minnesota, Minneapolis, Minnesota.

John McNeil (J)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.

Christopher M Reid (CM)

Department of Epidemiology & Preventive Medicine, Monash University, Melbourne, Victoria.
School of Public Health, Curtin University, Perth, Western Australia, Australia.

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