TY - JOUR
T1 - Age-stratified and blood-pressure-stratified effects of blood-pressure-lowering pharmacotherapy for the prevention of cardiovascular disease and death
T2 - an individual participant-level data meta-analysis
AU - The Blood Pressure Lowering Treatment Trialists’ Collaboration
AU - Rahimi, Kazem
AU - Bidel, Zeinab
AU - Nazarzadeh, Milad
AU - Copland, Emma
AU - Canoy, Dexter
AU - Wamil, Malgorzata
AU - Majert, Jeannette
AU - McManus, Richard
AU - Adler, Amanda
AU - Agodoa, Larry
AU - Algra, Ale
AU - Asselbergs, Folkert W.
AU - Beckett, Nigel S.
AU - Berge, Eivind
AU - Black, Henry
AU - Boersma, Eric
AU - Brouwers, Frank P.J.
AU - Brown, Morris
AU - Brugts, Jasper J.
AU - Bulpitt, Christopher J.
AU - Byington, Robert P.
AU - Cushman, William C.
AU - Cutler, Jeffrey
AU - Devereaux, Richard B.
AU - Dwyer, Jamie P.
AU - Estacio, Ray
AU - Fagard, Robert
AU - Fox, Kim
AU - Fukui, Tsuguya
AU - Gupta, Ajay K.
AU - Holman, Rury R.
AU - Imai, Yutaka
AU - Ishii, Masao
AU - Julius, Stevo
AU - Kanno, Yoshihiko
AU - Kjeldsen, Sverre E.
AU - Kostis, John
AU - Kuramoto, Kizuku
AU - Lanke, Jan
AU - Lewis, Edmund
AU - Lewis, Julia B.
AU - Lievre, Michel
AU - Lindholm, Lars H.
AU - Lueders, Stephan
AU - MacMahon, Stephen
AU - Mancia, Giuseppe
AU - Matsuzaki, Masunori
AU - Mehlum, Maria H.
AU - Nissen, Steven
AU - Ogawa, Hiroshi
N1 - Funding Information:
This research was funded by the British Heart Foundation (PG/18/65/33872 and FS/19/36/34346), the NIHR Oxford Biomedical Research Centre, and the Oxford Martin School. The views expressed are those of the authors and not necessarily those of the National Health Service, the NIHR, or the UK Department of Health and Social Care. This manuscript was prepared using ACCORD, ALLHAT, PEACE, and SHEP research materials obtained from the NHLBI Biologic Specimen and Data Repository Information Coordinating Centre and does not necessarily reflect the opinions or views of the ACCORD, ALLHAT, PEACE and SHEP, or the NHLBI. AASK was conducted by AASK Investigators and supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). The data from the AASK reported here were supplied by the NIDDK central repositories. This manuscript was not prepared in collaboration with Investigators of the AASK study and does not necessarily reflect the opinions or views of AASK, the NIDDK central repositories, or the NIDDK. We acknowledge original depositors of the ANBP data and the Australian Data Archive and declare that those who carried out the original analysis and collection of the data bear no responsibility for the further analysis or interpretation of the data.
Funding Information:
This research was funded by the British Heart Foundation ( PG/18/65/33872 and FS/19/36/34346 ), the NIHR Oxford Biomedical Research Centre, and the Oxford Martin School. The views expressed are those of the authors and not necessarily those of the National Health Service, the NIHR, or the UK Department of Health and Social Care. This manuscript was prepared using ACCORD, ALLHAT, PEACE, and SHEP research materials obtained from the NHLBI Biologic Specimen and Data Repository Information Coordinating Centre and does not necessarily reflect the opinions or views of the ACCORD, ALLHAT, PEACE and SHEP, or the NHLBI. AASK was conducted by AASK Investigators and supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). The data from the AASK reported here were supplied by the NIDDK central repositories. This manuscript was not prepared in collaboration with Investigators of the AASK study and does not necessarily reflect the opinions or views of AASK, the NIDDK central repositories, or the NIDDK. We acknowledge original depositors of the ANBP data and the Australian Data Archive and declare that those who carried out the original analysis and collection of the data bear no responsibility for the further analysis or interpretation of the data.
Publisher Copyright:
© 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2021/9/18
Y1 - 2021/9/18
N2 - Background: The effects of pharmacological blood-pressure-lowering on cardiovascular outcomes in individuals aged 70 years and older, particularly when blood pressure is not substantially increased, is uncertain. We compared the effects of blood-pressure-lowering treatment on the risk of major cardiovascular events in groups of patients stratified by age and blood pressure at baseline. Methods: We did a meta-analysis using individual participant-level data from randomised controlled trials of pharmacological blood-pressure-lowering versus placebo or other classes of blood-pressure-lowering medications, or between more versus less intensive treatment strategies, which had at least 1000 persons-years of follow-up in each treatment group. Participants with previous history of heart failure were excluded. Data were obtained from the Blood Pressure Lowering Treatment Triallists' Collaboration. We pooled the data and categorised participants into baseline age groups (<55 years, 55–64 years, 65–74 years, 75–84 years, and ≥85 years) and blood pressure categories (in 10 mm Hg increments from <120 mm Hg to ≥170 mm Hg systolic blood pressure and from <70 mm Hg to ≥110 mm Hg diastolic). We used a fixed effects one-stage approach and applied Cox proportional hazard models, stratified by trial, to analyse the data. The primary outcome was defined as either a composite of fatal or non-fatal stroke, fatal or non-fatal myocardial infarction or ischaemic heart disease, or heart failure causing death or requiring hospital admission. Findings: We included data from 358 707 participants from 51 randomised clinical trials. The age of participants at randomisation ranged from 21 years to 105 years (median 65 years [IQR 59–75]), with 42 960 (12·0%) participants younger than 55 years, 128 437 (35·8%) aged 55–64 years, 128 506 (35·8%) 65–74 years, 54 016 (15·1%) 75–84 years, and 4788 (1·3%) 85 years and older. The hazard ratios for the risk of major cardiovascular events per 5 mm Hg reduction in systolic blood pressure for each age group were 0·82 (95% CI 0·76–0·88) in individuals younger than 55 years, 0·91 (0·88–0·95) in those aged 55–64 years, 0·91 (0·88–0·95) in those aged 65–74 years, 0·91 (0·87–0·96) in those aged 75–84 years, and 0·99 (0·87–1·12) in those aged 85 years and older (adjusted pinteraction=0·050). Similar patterns of proportional risk reductions were observed for a 3 mm Hg reduction in diastolic blood pressure. Absolute risk reductions for major cardiovascular events varied by age and were larger in older groups (adjusted pinteraction=0·024). We did not find evidence for any clinically meaningful heterogeneity of relative treatment effects across different baseline blood pressure categories in any age group. Interpretation: Pharmacological blood pressure reduction is effective into old age, with no evidence that relative risk reductions for prevention of major cardiovascular events vary by systolic or diastolic blood pressure levels at randomisation, down to less than 120/70 mm Hg. Pharmacological blood pressure reduction should, therefore, be considered an important treatment option regardless of age, with the removal of age-related blood-pressure thresholds from international guidelines. Funding: British Heart Foundation, National Institute of Health Research Oxford Biomedical Research Centre, Oxford Martin School.
AB - Background: The effects of pharmacological blood-pressure-lowering on cardiovascular outcomes in individuals aged 70 years and older, particularly when blood pressure is not substantially increased, is uncertain. We compared the effects of blood-pressure-lowering treatment on the risk of major cardiovascular events in groups of patients stratified by age and blood pressure at baseline. Methods: We did a meta-analysis using individual participant-level data from randomised controlled trials of pharmacological blood-pressure-lowering versus placebo or other classes of blood-pressure-lowering medications, or between more versus less intensive treatment strategies, which had at least 1000 persons-years of follow-up in each treatment group. Participants with previous history of heart failure were excluded. Data were obtained from the Blood Pressure Lowering Treatment Triallists' Collaboration. We pooled the data and categorised participants into baseline age groups (<55 years, 55–64 years, 65–74 years, 75–84 years, and ≥85 years) and blood pressure categories (in 10 mm Hg increments from <120 mm Hg to ≥170 mm Hg systolic blood pressure and from <70 mm Hg to ≥110 mm Hg diastolic). We used a fixed effects one-stage approach and applied Cox proportional hazard models, stratified by trial, to analyse the data. The primary outcome was defined as either a composite of fatal or non-fatal stroke, fatal or non-fatal myocardial infarction or ischaemic heart disease, or heart failure causing death or requiring hospital admission. Findings: We included data from 358 707 participants from 51 randomised clinical trials. The age of participants at randomisation ranged from 21 years to 105 years (median 65 years [IQR 59–75]), with 42 960 (12·0%) participants younger than 55 years, 128 437 (35·8%) aged 55–64 years, 128 506 (35·8%) 65–74 years, 54 016 (15·1%) 75–84 years, and 4788 (1·3%) 85 years and older. The hazard ratios for the risk of major cardiovascular events per 5 mm Hg reduction in systolic blood pressure for each age group were 0·82 (95% CI 0·76–0·88) in individuals younger than 55 years, 0·91 (0·88–0·95) in those aged 55–64 years, 0·91 (0·88–0·95) in those aged 65–74 years, 0·91 (0·87–0·96) in those aged 75–84 years, and 0·99 (0·87–1·12) in those aged 85 years and older (adjusted pinteraction=0·050). Similar patterns of proportional risk reductions were observed for a 3 mm Hg reduction in diastolic blood pressure. Absolute risk reductions for major cardiovascular events varied by age and were larger in older groups (adjusted pinteraction=0·024). We did not find evidence for any clinically meaningful heterogeneity of relative treatment effects across different baseline blood pressure categories in any age group. Interpretation: Pharmacological blood pressure reduction is effective into old age, with no evidence that relative risk reductions for prevention of major cardiovascular events vary by systolic or diastolic blood pressure levels at randomisation, down to less than 120/70 mm Hg. Pharmacological blood pressure reduction should, therefore, be considered an important treatment option regardless of age, with the removal of age-related blood-pressure thresholds from international guidelines. Funding: British Heart Foundation, National Institute of Health Research Oxford Biomedical Research Centre, Oxford Martin School.
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U2 - 10.1016/S0140-6736(21)01921-8
DO - 10.1016/S0140-6736(21)01921-8
M3 - Article
C2 - 34461040
AN - SCOPUS:85114915370
SN - 0140-6736
VL - 398
SP - 1053
EP - 1064
JO - The Lancet
JF - The Lancet
IS - 10305
ER -