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Blood Pressure Variability, Mortality, and Cardiovascular Outcomes in CKD Patients
Francesca Mallamaci1, Giovanni Tripepi1, Graziella D'Arrigo1
1Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension, Consiglio Nazionale Ricerche-Istituto Fisiologia Clinica, Reggio Calabria, Italy; and.
Insights
Long-term blood pressure (BP) variability, but not short-term, is linked to increased cardiovascular event risk in chronic kidney disease (CKD) patients. However, BP variability offers limited predictive value for CKD outcomes.
Area of Science:
- Nephrology
- Cardiology
- Hypertension Research
Background:
- Blood pressure (BP) variability, both short-term and long-term, is associated with cardiovascular event risk.
- This association is understudied in patients with chronic kidney disease (CKD).
- The prognostic value of BP variability in CKD is largely unknown.
Purpose of the Study:
- To investigate the association between short-term and long-term systolic BP variability and cardiovascular events in CKD patients.
- To assess the prognostic value of BP variability for risk discrimination and reclassification in this population.
Main Methods:
- A cohort of 402 CKD patients was analyzed.
- Short-term (24-hour ambulatory BP monitoring) and long-term (clinic visit to clinic visit) systolic BP variability were assessed.
- The composite endpoint was death or cardiovascular event, with follow-up durations of 4.8 and 3.2 years for short-term and long-term variability, respectively.
Main Results:
- Mean short-term systolic BP variability was 12.6±3.3 mm Hg; mean long-term was 12.7±5.1 mm Hg.
- Long-term BP variability was significantly associated with the composite endpoint (adjusted HR, 1.24 per 5-mm Hg higher SD).
- Short-term BP variability was not significantly associated with the composite endpoint (adjusted HR, 0.92 per 5-mm Hg higher SD).
Conclusions:
- In CKD patients, long-term systolic BP variability, not short-term, is associated with the risk of death and cardiovascular events.
- BP variability demonstrated limited utility in improving risk prediction models for CKD.
- Further research may be needed to clarify the role of BP variability in CKD management.
Background And Objectives:
Short-term BP variability (derived from 24-hour ambulatory BP monitoring) and long-term BP variability (from clinic visit to clinic visit) are directly related to risk for cardiovascular events, but these relationships have been scarcely investigated in patients with CKD, and their prognostic value in this population is unknown.
Design, Setting, Participants, & Measurements:
In a cohort of 402 patients with CKD, we assessed associations of short- and long-term systolic BP variability with a composite end point of death or cardiovascular event. Variability was defined as the standard deviation of observed BP measurements. We further tested the prognostic value of these parameters for risk discrimination and reclassification.
Results:
Mean ± SD short-term systolic BP variability was 12.6±3.3 mm Hg, and mean ± SD long-term systolic BP variability was 12.7±5.1 mm Hg. For short-term BP variability, 125 participants experienced the composite end point over a median follow-up of 4.8 years (interquartile range, 2.3-8.6 years). For long-term BP variability, 110 participants experienced the composite end point over a median follow-up of 3.2 years (interquartile range, 1.0-7.5 years). In adjusted analyses, long-term BP variability was significantly associated with the composite end point (hazard ratio, 1.24; 95% confidence interval, 1.01 to 1.51 per 5-mm Hg higher SD of office systolic BP), but short-term systolic BP variability was not (hazard ratio, 0.92; 95% confidence interval, 0.68 to 1.25 per 5-mm Hg higher SD of 24-hour ambulatory systolic BP). Neither estimate of BP variability improved risk discrimination or reclassification compared with a simple risk prediction model.
Conclusions:
In patients with CKD, long-term but not short-term systolic BP variability is related to the risk of death and cardiovascular events. However, BP variability has a limited role for prediction in CKD.
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