Long-Term Variability of Blood Pressure, Cardiovascular Outcomes, and Mortality: The Look AHEAD Study

Author:

Kaze Arnaud D1,Santhanam Prasanna2,Erqou Sebhat3,Yuyun Matthew4,Bertoni Alain G5,Ahima Rexford S2,Echouffo-Tcheugui Justin B2ORCID

Affiliation:

1. Department of Medicine, University of Maryland Medical Center, Baltimore, Maryland, USA

2. Department of Medicine, Division of Endocrinology, Diabetes & Metabolism, Johns Hopkins School of Medicine, Baltimore, Maryland, USA

3. Department of Medicine, Providence Veterans Affairs Medical Center and Alpert Medical School of Brown University, Providence, Rhode Island, USA

4. Department of Medicine, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA

5. Department of Epidemiology and Prevention, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA

Abstract

Abstract BACKGROUND We evaluated the associations of visit-to-visit blood pressure (BP) variability with incident cardiovascular disease (CVD) and deaths in adults with type 2 diabetes. METHODS We analyzed 4,152 participants in Look AHEAD (Action for Health in Diabetes) free of CVD events and deaths during the first 36 months of follow-up. Variability of systolic BP (SBP) and diastolic BP (DBP) across 4 annual visits was assessed using the intraindividual SD, variation independent of the mean, and coefficient of variation. Cox regression was used to generate the adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) for CVD (myocardial infarction [MI], stroke, or CVD-related deaths) and mortality. RESULTS Over a median of 6.6 years, there were 220 MIs, 105 stroke cases, 62 CVD-related deaths, and 236 deaths. After adjustment for confounders including average BP, the aHRs for the highest (vs. lowest) tertile of SD of SBP were 1.98 (95% CI 1.01–3.92), 1.25 (95% CI 0.90–1.72), 1.26 (95% CI 0.96–1.64), 1.05 (95% CI 0.75–1.46), and 1.64 (95% CI 0.99–2.72) for CVD mortality, all-cause mortality, CVD, MI, and stroke, respectively. The equivalent aHRs for SD of DBP were 1.84 (95% CI 0.98–3.48), 1.43 (95% CI 1.03–1.98), 1.19 (95% CI 0.91–1.56), 1.14 (95% CI 0.82–1.58), and 0.97 (95% CI 0.58–1.60), respectively. CONCLUSIONS In a large sample of individuals with type 2 diabetes, a greater variability in SBP was associated with higher cardiovascular mortality and CVD events; a higher variability in DBP was linked to increased overall and cardiovascular mortality.

Funder

NIH

NHLBI

Publisher

Oxford University Press (OUP)

Subject

Internal Medicine

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