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Blood Pressure Variability and Outcomes Across Antihypertensive Regimens

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Abstract

Background: Blood pressure variability (BPV) is associated with cardiovascular risk beyond mean blood pressure (BP). Whether first-line antihypertensive regimens differentially affect BPV and cardiovascular outcomes remains uncertain.

Methods: We conducted a target trial emulation using pooled individual participant data from two randomised trials: ACCORD-BP and SPRINT. Propensity score matching was used for pairwise comparisons of renin–angiotensin system (RAS) inhibitors, calcium channel blockers (CCBs), and diuretics, as monotherapy or in combination. Follow-up was initiated at a predefined baseline medication assessment. The primary outcome was visit-to-visit systolic BPV, assessed using variation independent of the mean (VIM). Secondary outcomes included major adverse cardiovascular events (MACE) and its individual components.

Results: The final cohort included 5,779 participants (median of 12 BP measurements and median follow-up of 3.5 years), among whom 2,754 were included in the matched analysis. CCB-based regimens were consistently associated with significantly lower systolic BPV compared with both RAS inhibitor-based and diuretic-based regimens. This association was consistent across monotherapy (CCB vs RAS: β=-1.341, 95% CI -1.930 to -0.752, P<0.001) and combination therapies (CCB+diuretic vs RAS+diuretic: β=-1.299, 95% CI -1.852 to -0.747, P<0.001). In contrast, RAS inhibitor–based and diuretic-based regimens demonstrated comparable BPV profiles. 215 (3.7%) MACE events were observed in the overall cohort. No significant differences in MACE or individual components were observed across comparisons.

Conclusions: Among high-risk hypertensive patients receiving target-driven BP management, CCB-based regimens were associated with lower visit-to-visit systolic BPV compared with RAS inhibitor–based and diuretic-based regimens. However, these differences were not accompanied by detectable differences in cardiovascular outcomes.

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Journal Title

Hypertension

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0194-911X
1524-4563

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American Heart Association

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
British Heart Foundation (RG/F/22/110052)
British Heart Foundation (RE/24/130011)
Cambridge University Hospitals NHS Foundation Trust (CUH) (Unknown)
This research was supported by the National Natural Science Fund of China (grant number 82422024), the National Major Science and Technology Projects of Brain Science and Brain-inspired Intelligence Young Scientist Class A (grant number 2025ZD0215802), the British Heart Foundation (grant number RG/F/22/110052), and Fundamental and Interdisciplinary Disciplines Breakthrough Plan of the Ministry of Education of China (grant number JYB2025XDXM603). Infrastructural support was provided by the Cambridge British Heart Foundation Centre of Research Excellence (grant number RE/24/130011) and the Cambridge University Hospitals National Institute for Health and Care Research (NIHR) Biomedical Research Centre (grant number NIHR203312).