A Trial of 2 Strategies to Reduce Nocturnal Blood Pressure in Blacks With Chronic Kidney Disease
Open accessAbstract
The objective of our study was to determine the effects of 2 antihypertensive drug dose schedules (PM dose and add-on dose) on nocturnal blood pressure (BP) in comparison with usual therapy (AM dose) in blacks with hypertensive chronic kidney disease and controlled office BP. In a 3-period, crossover trial, former participants of the African American Study of Kidney Disease were assigned to receive the following 3 regimens, each lasting 6 weeks, presented in random order: AM dose (once-daily antihypertensive medications taken in the morning), PM dose (once-daily antihypertensives taken at bedtime), and add-on dose (once-daily antihypertensives taken in the morning and an additional antihypertensive medication before bedtime [diltiazem 60–120 mg, hydralazine 25 mg, or additional ramipril 5 mg]). Ambulatory BP monitoring was performed at the end of each period. The primary outcome was nocturnal systolic BP. Mean age of the study population (n=147) was 65.4 years, 64% were men, and mean estimated glomerular filtration rate was 44.9 mL/min per 1.73 m 2 . At the end of each period, mean (SE) nocturnal systolic BP was 125.6 (1.2) mm Hg in the AM dose, 123.9 (1.2) mm Hg in the PM dose, and 123.5 (1.2) mm Hg in the add-on dose. None of the pairwise differences in nocturnal, 24-hour, and daytime systolic BP was statistically significant. Among blacks with hypertensive chronic kidney disease, neither PM (bedtime) dosing of once-daily antihypertensive nor the addition of drugs taken at bedtime significantly reduced nocturnal BP compared with morning dosing of antihypertensive medications.
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Although prior analyses of randomized clinical trials found a benefit to evening versus morning dosing of antihypertensive medications, these results have not been reproduced in subsequent trials.
“Although prior analyses of randomized clinical trials found a benefit to evening versus morning dosing of antihypertensive medications (81,82), these results have not been reproduced in subsequent trials.”
From 10. Cardiovascular Disease and Risk Management: Standards of Care in Diabetes—2025 (2025) · cites this paper as [83]
The Discussion (page unavailable) reports earlier benefits from bedtime dosing, while this trial found no statistically significant reduction in nocturnal blood pressure with PM versus morning dosing. That supports a failure to reproduce a benefit in this trial, but the paper does not establish that subsequent trials generally failed to reproduce earlier results; its findings are limited to African Americans with hypertensive chronic kidney disease. (LLM, conf=0.84)
Experimental — accuracy not yet measuredThe benefit of evening versus morning antihypertensive dosing found in prior analyses has not been reproduced in subsequent trials.
“Although prior analyses of randomized clinical trials found a bene fi t to evening versus morning dosing of antihypertensive medications (74,75), these results have not been reproduced in subsequent trials.”
From 10. Cardiovascular Disease and Risk Management: <i>Standards of Care in Diabetes—2023</i> (2023) · cites this paper as [76]
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- Authors
- Rahman, M., Greene, T., Phillips, R. A., Agodoa, L. Y., Bakris, G. L., Charleston, J., Contreras, G., Gabbai, F., Hiremath, L., Jamerson, K., Kendrick, C., Kusek, J. W., Lash, J. P., Lea, J., Miller, E. R., Rostand, S., Toto, R., Wang, X., Wright, J. T., & Appel, L. J.
- Affiliations
- National Institutes of Health (US)
- ORCID
- Venue
- Hypertension
- Published
- 2013-01
- Volume
- 61
- Issue
- 1
- Pages
- 82-88
- ISSN
- 0194-911X (ISSN-L)
- 1524-4563
- PMC
- PMC3523681
- OpenAlex
- W2062987880
- Cited by
- 93
- References
- 29
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 4 · 2023: 7 · 2022: 6 · 2021: 17 · 2020: 9 · 2019: 7 · 2018: 7 · 2017: 5 · 2016: 7 · 2015: 6 · 2014: 5 · 2013: 6
- FWCI
- 3.49
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Hypertension (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (UL1TR000439)
- National Center for Research Resources (M01RR000080)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
- Health Sciences › Nursing › Nutrition and Dietetics › Sodium Intake and Health
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Keywords
- nocturnal blood pressure, chronic kidney disease, African Americans, bedtime dosing, diltiazem, hydralazine, ramipril, ambulatory blood pressure monitoring
- MeSH terms
- Aged, Aged, 80 and over, Antihypertensive Agents, Black or African American, Blood Pressure, Diltiazem, Drug Administration Schedule, Drug Therapy, Combination, Female, Glomerular Filtration Rate, Heart Rate, Humans, Hydralazine, Hypertension, Male, Middle Aged, Treatment Outcome, Ramipril, Cross-Over Studies, Blood Pressure Monitoring, Ambulatory, Renal Insufficiency, Chronic
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