Combination blood pressure lowering in the presence or absence of background statin and aspirin therapy: a combined analysis of PROGRESS and ADVANCE Trials.
J Hypertens
; 39(8): 1689-1696, 2021 08 01.
Article
in En
| MEDLINE
| ID: mdl-33883461
ABSTRACT
OBJECTIVES:
To assess the effects of combination BP lowering on cardiovascular events and mortality in the presence of aspirin and/or statin therapy in a combined analysis of the ADVANCE and PROGRESS trials.METHODS:
We conducted an analysis of 14â682 participants allocated combination therapy with perindopril and indapamide or placebo followed up for a mean of 4.2âyears. Participants were stratified into four groups defined by background use of medications at baseline statin, aspirin, both or neither. Linear mixed effect models were used to assess differences in BP and Cox proportional hazard models were used to estimate the risks of major cardiovascular events, all-cause mortality and treatment discontinuation.RESULTS:
At baseline, 14% of patients were on both aspirin and statin, 35% on aspirin, 9% on statins and 42% on neither aspirin/statins. Compared with placebo, combination BP therapy reduced mean SBP by 5.7âmmHg in ADVANCE and 12.1âmmHg in PROGRESS, with no difference (Pâ>â0.447) between patients by baseline use of aspirin/statin. Combination BP therapy reduced the risk of major cardiovascular events (hazard ratio 0.78, 95% CI 0.71-0.86), with no significant difference (Pâ=â0.600) between aspirin/statin subgroups. Rates of treatment discontinuation were similar with combination BP therapy compared with placebo (18.4 versus 18%), with no evidence of difference across the subgroups (Pâ=â0.340).CONCLUSION:
BP lowering with perindopril and indapamide reduces the risk of major cardiovascular events independent of baseline use of aspirin and/or statins.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hydroxymethylglutaryl-CoA Reductase Inhibitors
/
Hypertension
/
Indapamide
Type of study:
Clinical_trials
Limits:
Humans
Language:
En
Journal:
J Hypertens
Year:
2021
Document type:
Article