Easy-to-use tool for evaluating the elevated acute kidney injury risk against reduced cardiovascular disease risk during intensive blood pressure control.

Pubmed ID: 31977572

Journal: Journal of hypertension

Publication Date: March 1, 2020

Affiliation: Turku Bioscience Centre, University of Turku and Åbo Akademi University.

MeSH Terms: Humans, Cardiovascular Diseases, Hypertension, Risk Assessment, Antihypertensive Agents, Acute Kidney Injury

Authors: Raitakari OT, Venäläinen MS, Klén R, Mahmoudian M, Elo LL

Cite As: Venäläinen MS, Klén R, Mahmoudian M, Raitakari OT, Elo LL. Easy-to-use tool for evaluating the elevated acute kidney injury risk against reduced cardiovascular disease risk during intensive blood pressure control. J Hypertens 2020 Mar;38(3):511-518.

Studies:

Abstract

OBJECTIVE: The Systolic Blood Pressure Intervention Trial (SPRINT) reported that lowering SBP to below 120 mmHg (intensive treatment) reduced cardiovascular morbidity and mortality among adults with hypertension but increased the incidence of adverse events, particularly acute kidney injury (AKI). The goal of this study was to develop an accurate risk estimation tool for comparing the risk of cardiovascular events and adverse kidney-related outcomes between standard and intensive antihypertensive treatment strategies. METHODS: By applying Lasso regression on the baseline characteristics and health outcomes of 8760 participants with complete baseline information in the SPRINT trial, we developed predictive models for primary cardiovascular disease (CVD) outcome and incidence of AKI. Both models were validated against an independent test set of the SPRINT trial (one third of data not used for model building) and externally against the cardiovascular and renal outcomes available in Action to Control Cardiovascular Risk in Diabetes Blood Pressure trial, consisting of 4733 participants with type 2 diabetes mellitus. RESULTS: Lasso regression identified a subset of variables that accurately predicted the primary CVD outcome and the incidence of AKI (areas under receiver-operating characteristic curves 0.70 and 0.77, respectively). Based on the validated risk models, an easy-to-use risk assessment tool was developed and made available as an easy-to-use online tool. CONCLUSION: By predicting the risks of CVD and AKI at baseline, the developed tool can be used to weigh the benefits of intensive versus standard blood pressure control and to identify those who are likely to benefit most from intensive treatment.