Long-Term Blood Pressure Variability and Kidney Function in Participants of the ASPREE Trial

Author:

Ernst Michael E12ORCID,Fravel Michelle A1,Webb Katherine L3,Wetmore James B45,Wolfe Rory3,Chowdhury Enayet36,Reid Christopher M36,Woods Robyn L3,Beilin Lawrence7,Margolis Karen L8,Murray Anne M9ORCID,Polkinghorne Kevan R31011

Affiliation:

1. Department of Pharmacy Practice and Science, College of Pharmacy, The University of Iowa, Iowa City, Iowa, USA

2. Department of Family Medicine, Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA

3. School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia

4. Division of Nephrology, Department of Medicine, Hennepin Healthcare Systems, Minneapolis, Minnesota, USA

5. Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA

6. School of Public Health, Curtin University, Perth, Western Australia, Australia

7. Medical School Royal Perth Hospital, University of Western Australia, Perth, Western Australia, Australia

8. HealthPartners Institute, Minneapolis, Minnesota, USA

9. Division of Geriatrics, Department of Medicine, Hennepin Healthcare, Minneapolis, Minnesota, USA

10. Department of Nephrology, Monash Medical Centre, Monash Health, Melbourne, Victoria, Australia

11. Department of Medicine, Monash University, Melbourne, Victoria, Australia

Abstract

Abstract Background Whether long-term blood pressure variability (BPV) predicts kidney function decline in generally healthy older adults is unknown. We investigated this association in ASPirin in Reducing Events in the Elderly (ASPREE) trial participants. Methods Between 2010 and 2014, Australian and US individuals aged ≥70 years (≥65 if US minority) were recruited and followed with annual study visits for a median of 4.7 years. Time-to-event analyses and linear mixed effects models were used to examine associations between incident chronic kidney disease (CKD), and trajectories of estimated glomerular filtration rate (eGFR) and log albumin–creatinine ratio (log ACR) with systolic BPV as a continuous measure, and, by tertile of SD of systolic blood pressure (BP). BPV was estimated using systolic BP measures from baseline through the second annual visit, and kidney outcomes were assessed following this period. Results Incident CKD occurred in 1,829 of 6,759 participants (27.2%), and more commonly in BPV tertiles 2 (27.4%) and 3 (28.3%) than tertile 1 (25.5%); however, the risk was not significantly increased after covariate adjustment (tertile 3 hazard ratio = 1.02; 95% confidence interval: 0.91–1.14). Analysis of eGFR (n = 16,193) and log ACR trajectories (n = 15,213) showed individuals in the highest BPV tertile having the lowest eGFR and highest log ACR, cross-sectionally. However, the trajectories of eGFR and log ACR did not differ across BPV tertiles. Conclusions CKD and markers of reduced kidney function occur more commonly in individuals with higher BPV; however, BPV does not influence trajectory of decline in kidney function over time in older adults who are in generally good health. Clinical trials registration Trial Number NCT01038583 and ISRCTN83772183.

Funder

National Institute on Aging

National Cancer Institute

National Institutes of Health

National Health and Medical Research Council of Australia

Monash University

Victorian Cancer Agency

Publisher

Oxford University Press (OUP)

Subject

Internal Medicine

Reference30 articles.

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