Skip to Content
MilliporeSigma
  • 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

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