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  • Predicting the effects of blood pressure-lowering treatment on major cardiovascular events for individual patients with type 2 diabetes mellitus: results from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation.

Predicting the effects of blood pressure-lowering treatment on major cardiovascular events for individual patients with type 2 diabetes mellitus: results from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation.

Hypertension (Dallas, Tex. : 1979) (2014-10-15)
Joep van der Leeuw, Frank L J Visseren, Mark Woodward, Sophia Zoungas, Andre Pascal Kengne, Yolanda van der Graaf, Paul Glasziou, Pavel Hamet, Stephen MacMahon, Neil Poulter, Diederick E Grobbee, John Chalmers
ABSTRACT

Blood pressure-lowering treatment reduces cardiovascular risk in patients with diabetes mellitus, but the effect varies between individuals. We sought to identify which patients benefit most from such treatment in a large clinical trial in type 2 diabetes mellitus. In Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation (ADVANCE) participants (n=11 140), we estimated the individual patient 5-year absolute risk of major adverse cardiovascular events with and without treatment by perindopril-indapamide (4/1.25 mg). The difference between treated and untreated risk is the estimated individual patient's absolute risk reduction (ARR). Predictions were based on a Cox proportional hazards model inclusive of demographic and clinical characteristics together with the observed relative treatment effect. The group-level effect of selectively treating patients with an estimated ARR above a range of decision thresholds was compared with treating everyone or those with a blood pressure >140/90 mm Hg using net benefit analysis. In ADVANCE, there was wide variation in treatment effects across individual patients. According to the algorithm, 43% of patients had a large predicted 5-year ARR of ≥1% (number-needed-to-treat [NNT5] ≤100) and 40% had an intermediate predicted ARR of 0.5% to 1% (NNT5=100-`200). The proportion of patients with a small ARR of ≤0.5% (NNT5≥200) was 17%. Provided that one is prepared to treat at most 200 patients for 5 years to prevent 1 adverse outcome, prediction-based treatment yielded the highest net benefit. In conclusion, a multivariable treatment algorithm can identify those individuals who benefit most from blood pressure-lowering therapy in terms of ARR of major adverse cardiovascular events and may be used to guide treatment decisions in individual patients with diabetes. http://www.clinicaltrials.gov. Unique identifier: NCT00145925.

MATERIALS
Product Number
Brand
Product Description

Perindopril tert-butylamine, European Pharmacopoeia (EP) Reference Standard
SAFC
Cholesterol, Plant-Derived, SyntheChol®
Sigma-Aldrich
Perindopril erbumine
Supelco
Indapamide, analytical standard, for drug analysis
Sigma-Aldrich
Gliclazide, powder, ≥98%
Sigma-Aldrich
Creatinine, anhydrous, ≥98%
Perindopril for stereochemical purity, European Pharmacopoeia (EP) Reference Standard
Supelco
Cholesterol solution, certified reference material, 10 mg/mL in chloroform
Supelco
Creatinine, Pharmaceutical Secondary Standard; Certified Reference Material
Indapamide, European Pharmacopoeia (EP) Reference Standard
Supelco
Cholesterol, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Indapamide, United States Pharmacopeia (USP) Reference Standard
Gliclazide, European Pharmacopoeia (EP) Reference Standard
Perindopril for peak identification, European Pharmacopoeia (EP) Reference Standard
SAFC
Cholesterol, from sheep wool, Controlled origin, meets USP/NF testing specifications
Sigma-Aldrich
Cholesterol, powder, BioReagent, suitable for cell culture, ≥99%
Sigma-Aldrich
Cholesterol, Sigma Grade, ≥99%
Sigma-Aldrich
Cholesterol, from sheep wool, ≥92.5% (GC), powder
Sigma-Aldrich
SyntheChol® NS0 Supplement, 500 ×, synthetic cholesterol, animal component-free, aqueous solution, sterile-filtered, suitable for cell culture
Sigma-Aldrich
Cholesterol, tested according to Ph. Eur.
Supelco
Gliclazide, Pharmaceutical Secondary Standard; Certified Reference Material