Key result
Higher 24-hour systolic BP variability linked to ~17% greater mortality and MACE risk.
Why the study?
High 24-h blood pressure variability increases cardiovascular risk, but the independent contributions of inherent variability and hypertensive loads to mortality and cardiovascular risk are unclear.
Does high 24-h blood pressure variability increase mortality and cardiovascular risk?
Cohort (n=1,050)
Does high 24-h blood pressure variability increase mortality and cardiovascular risk?
High average real variability in 24-h systolic blood pressure is independently associated with increased mortality and cardiovascular risk, regardless of absolute blood pressure levels.
May inform risk stratification beyond mean BP; leaves open whether targeting variability improves outcomes.
BACKGROUND: Evidence shows that high 24-h blood pressure (BP) variability increases cardiovascular risk. We investigated whether 24-h BP variability relates to mortality and cardiovascular risk due to inherent variability and/or hypertensive loads in 24-h BP. METHODS: A total of 1,050 participants from the Maracaibo Aging Study (mean age, 66 years; women, 67.2%) underwent 24-h ambulatory BP monitoring and were followed between 2001 and 2016. To evaluate inherent BP variability, we used average real variability (ARV) as it captures variability among consecutive BP readings. 24-h systolic BP load was the proportion (%) of systolic BP readings ≥130 mm Hg during the daytime and ≥110 during the nighttime. Our primary endpoint was total mortality and major adverse cardiovascular endpoints (MACE). Statistics included Cox proportional models. RESULTS: During a median follow-up of 8.3 years, 299 participants died and 210 experienced MACE. Each +2 mm Hg (corresponding to 1-standard deviation) higher 24-h systolic ARV (mean value, 9.0 ± 2.0 mm Hg) was associated with higher hazard ratios (HRs) for mortality by 1.28-fold (95% confidence interval [CI], 1.14-1.43) and for MACE by 1.24-fold (95% CI, 1.08-1.42). Each 30% higher 24-h systolic BP load (median value, 63%) was associated with mortality and MACE with HRs of 1.29 (95% CI, 1.15-1.46) and 1.28 (95% CI, 1.10-1.48); respectively. After models were additionally adjusted by BP level, only ARV was associated with mortality (HR, 1.17; 95% CI, 1.04-1.33) and MACE (HR, 1.16; 95% CI, 1.00-1.34). CONCLUSIONS: High ARV and hypertensive loads in 24-h systolic BP were associated with mortality and cardiovascular risk, however, only ARV is associated independently of the BP level.
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Melgarejo et al. (2024) conducted a cohort in Cardiovascular risk and mortality (n=1,050). 24-h blood pressure variability (average real variability) and hypertensive loads vs. Lower variability and lower hypertensive loads was evaluated on Total mortality and major adverse cardiovascular endpoints (MACE) (HR 1.28, 95% CI 1.14-1.43). Higher 24-h systolic blood pressure average real variability was independently associated with increased mortality (HR 1.17; 95% CI 1.04-1.33) and MACE (HR 1.16; 95% CI 1.00-1.34).
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