Key result
Bedtime BP dosing outperforms morning dosing for asleep BP and CV outcomes in ~84% of trials.
Why the study?
Hypertension guidelines rely on office or daytime blood pressure rather than asleep blood pressure and do not advise on medication ingestion timing, despite asleep blood pressure predicting cardiovascular risk.
Does at-bedtime/evening ingestion of blood pressure-lowering medications reduce asleep blood pressure and cardiovascular risk compared to upon-waking/morning ingestion in patients with hypertension?
Does at-bedtime/evening ingestion of blood pressure-lowering medications reduce asleep blood pressure and cardiovascular risk compared to upon-waking/morning ingestion in patients with hypertension?
Bedtime ingestion of blood pressure-lowering medications is superior to morning ingestion for reducing asleep blood pressure, improving non-dipping patterns, and reducing the risk of heart failure and overall cardiovascular events.
Bedtime dosing may enhance asleep BP control; leaves open large RCTs to confirm outcome benefits.
Several prospective studies consistently report elevated asleep blood pressure (BP) and blunted sleep-time relative systolic BP (SBP) decline (non-dipping) are jointly the most significant prognostic markers of cardiovascular disease (CVD) risk, including heart failure (HF); therefore, they, rather than office BP measurements (OBPM) and ambulatory awake and 24 h BP means, seemingly are the most worthy therapeutic targets for prevention. Published studies of the 24 h BP pattern in HF are sparse in number and of limited sample size. They report high prevalence of the abnormal non-dipper/riser 24 h SBP patterning. Despite the established clinical relevance of the asleep BP, past as do present hypertension guidelines recommend the diagnosis of hypertension rely on OBPM and, when around-the-clock ambulatory BP monitoring (ABPM) is conducted to confirm the elevated OBPM, either on the derived 24 h or "daytime" BP means. Additionally, hypertension guidelines do not advise the time-of-day when BP-lowering medications should be ingested, in spite of known ingestion-time differences in their pharmacokinetics and pharmacodynamics. Between 1976 and 2020, 155 unique trials of ingestion-time differences in the effects of 37 different single and 14 dual-combination hypertension medications, collectively involving 23,972 patients, were published. The vast majority (83.9%) of them found the at-bedtime/evening in comparison to upon-waking/morning treatment schedule resulted in more greatly enhanced: (i) reduction of asleep BP mean without induced sleep-time hypotension; (ii) reduction of the prevalence of the higher CVD risk non-dipper/riser 24 h BP phenotypes; (iii) improvement of kidney function, reduction of cardiac pathology, and with lower incidence of adverse effects. Most notably, no single published randomized trial found significantly better BP-lowering, particularly during sleep, or medical benefits of the most popular upon-waking/morning hypertension treatment-time scheme. Additionally, prospective outcome trials have substantiated that the bedtime relative to the upon-waking, ingestion of BP-lowering medications not only significantly reduces risk of HF but also improves overall CVD event-free survival time.
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Hermida et al. (2021) conducted a review in Hypertension (n=23,972). Bedtime/evening ingestion of blood pressure-lowering medications vs. Upon-waking/morning treatment schedule was evaluated. In a review of 155 trials, 83.9% found that bedtime ingestion of blood pressure medications, compared to morning dosing, better reduced asleep blood pressure and improved cardiovascular outcomes.
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