Association of Ambulatory Arterial Pressure Index with Circadian Blood Pressure Patterns in Patients with Primary Hypertension and Coronary Artery Disease

动态动脉血压指数与原发性高血压合并冠状动脉疾病患者昼夜血压模式的相关性

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Abstract

BACKGROUND: Disruption of circadian blood pressure (BP) rhythms-manifested as non-dipper or reverse-dipper patterns-is associated with increased cardiovascular risk, especially in patients with primary hypertension (PH) and concomitant coronary artery disease (CAD). The ambulatory arterial pressure index (AAPI), a novel parameter derived from 24-hour ambulatory BP monitoring (ABPM), reflects the cumulative hemodynamic burden and may provide insight into circadian BP abnormalities. However, its relationship with BP rhythm patterns in this high-risk population remains unclear. METHODS: This retrospective observational study included 430 hospitalized patients with PH and CAD who underwent 24-hour ABPM between January 2022 and December 2023. Patients were classified into dipper (n = 51), non-dipper (n = 266), and reverse-dipper (n = 113) groups based on the nocturnal decline in systolic BP. AAPI was calculated as the ratio of diastolic to systolic pressure load over a 24-hour period. Baseline demographic, biochemical, and hemodynamic variables were compared across groups, and correlations between AAPI and BP rhythm categories were analyzed. RESULTS: The mean age was 69.1 ± 17.8 years, and 63.5% of patients were male. There were no significant differences in age, sex, renal function, or lipid profiles across circadian BP rhythm subgroups. Patients with disrupted BP rhythms (non-dipper or reverse-dipper) had significantly higher AAPI values than those with a dipper pattern (0.396 ± 0.041 vs 0.387 ± 0.043, p = 0.022). AAPI values showed a significant positive correlation with rhythm severity (r = 0.18, p = 0.004). CONCLUSION: AAPI is significantly associated with abnormal circadian BP patterns in patients with PH and CAD. As a simple, integrative hemodynamic index, AAPI may aid in the early identification of patients with rhythm disruption and provide added value for personalized cardiovascular risk stratification.

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