Imperial College London

ProfessorPeterSever

Faculty of MedicineNational Heart & Lung Institute

Professor of Clinical Pharmacology & Therapeutics
 
 
 
//

Contact

 

+44 (0)20 7594 1099p.sever

 
 
//

Assistant

 

Mrs Yvonne Green +44 (0)20 7594 1100

 
//

Location

 

333ICTEM buildingHammersmith Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Nazarzadeh:2022:10.1016/S2213-8587(22)00172-3,
author = {Nazarzadeh, M and Bidel, Z and Canoy, D and Copland, E and Bennett, DA and Dehghan, A and Davey, Smith G and Holman, RR and Woodward, M and Gupta, A and Adler, AI and Wamil, M and Sattar, N and Cushman, WC and McManus, RJ and Teo, K and Davis, BR and Chalmers, J and Pepine, CJ and Rahimi, K and Blood, Pressure Lowering Treatment Trialists' Collaboration},
doi = {10.1016/S2213-8587(22)00172-3},
journal = {The Lancet Diabetes and Endocrinology},
pages = {645--654},
title = {Blood pressure-lowering treatment for prevention of major cardiovascular diseases in people with and without type 2 diabetes: an individual participant-level data meta-analysis},
url = {http://dx.doi.org/10.1016/S2213-8587(22)00172-3},
volume = {10},
year = {2022}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - BACKGROUND: Controversy exists as to whether the threshold for blood pressure-lowering treatment should differ between people with and without type 2 diabetes. We aimed to investigate the effects of blood pressure-lowering treatment on the risk of major cardiovascular events by type 2 diabetes status, as well as by baseline levels of systolic blood pressure. METHODS: We conducted a one-stage individual participant-level data meta-analysis of major randomised controlled trials using the Blood Pressure Lowering Treatment Trialists' Collaboration dataset. Trials with information on type 2 diabetes status at baseline were eligible if they compared blood pressure-lowering medications versus placebo or other classes of blood pressure-lowering medications, or an intensive versus a standard blood pressure-lowering strategy, and reported at least 1000 persons-years of follow-up in each group. Trials exclusively on participants with heart failure or with short-term therapies and acute myocardial infarction or other acute settings were excluded. We expressed treatment effect per 5 mm Hg reduction in systolic blood pressure on the risk of developing a major cardiovascular event as the primary outcome, defined as the first occurrence of fatal or non-fatal stroke or cerebrovascular disease, fatal or non-fatal ischaemic heart disease, or heart failure causing death or requiring hospitalisation. Cox proportional hazard models, stratified by trial, were used to estimate hazard ratios (HRs) separately by type 2 diabetes status at baseline, with further stratification by baseline categories of systolic blood pressure (in 10 mm Hg increments from <120 mm Hg to ≥170 mm Hg). To estimate absolute risk reductions, we used a Poisson regression model over the follow-up duration. The effect of each of the five major blood pressure-lowering drug classes, including angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, β blockers, calcium channel blockers, and th
AU - Nazarzadeh,M
AU - Bidel,Z
AU - Canoy,D
AU - Copland,E
AU - Bennett,DA
AU - Dehghan,A
AU - Davey,Smith G
AU - Holman,RR
AU - Woodward,M
AU - Gupta,A
AU - Adler,AI
AU - Wamil,M
AU - Sattar,N
AU - Cushman,WC
AU - McManus,RJ
AU - Teo,K
AU - Davis,BR
AU - Chalmers,J
AU - Pepine,CJ
AU - Rahimi,K
AU - Blood,Pressure Lowering Treatment Trialists' Collaboration
DO - 10.1016/S2213-8587(22)00172-3
EP - 654
PY - 2022///
SN - 2213-8595
SP - 645
TI - Blood pressure-lowering treatment for prevention of major cardiovascular diseases in people with and without type 2 diabetes: an individual participant-level data meta-analysis
T2 - The Lancet Diabetes and Endocrinology
UR - http://dx.doi.org/10.1016/S2213-8587(22)00172-3
UR - https://www.ncbi.nlm.nih.gov/pubmed/35878651
UR - https://www.sciencedirect.com/science/article/pii/S2213858722001723?via%3Dihub
UR - http://hdl.handle.net/10044/1/99116
VL - 10
ER -