Evening versus morning dosing regimen drug therapy for hypertension
- PMID: 38353289
- PMCID: PMC10865448
- DOI: 10.1002/14651858.CD004184.pub3
Evening versus morning dosing regimen drug therapy for hypertension
Abstract
Background: Variation in blood pressure levels display circadian rhythms. Complete 24-hour blood pressure control is the primary goal of antihypertensive treatment and reducing adverse cardiovascular outcomes is the ultimate aim. This is an update of the review first published in 2011.
Objectives: To evaluate the effectiveness of administration-time-related effects of once-daily evening versus conventional morning dosing antihypertensive drug therapy regimens on all-cause mortality, cardiovascular mortality and morbidity, total adverse events, withdrawals from treatment due to adverse effects, and reduction of systolic and diastolic blood pressure in people with primary hypertension.
Search methods: We searched the Cochrane Hypertension Specialised Register via Cochrane Register of Studies (17 June 2022), Cochrane Central Register of Controlled Trials (CENTRAL) (Issue 6, 2022); MEDLINE, MEDLINE In-Process and MEDLINE Epub Ahead of Print (1 June 2022); Embase (1 June 2022); ClinicalTrials.gov (2 June 2022); Chinese Biomedical Literature Database (CBLD) (1978 to 2009); Chinese VIP (2009 to 7 August 2022); Chinese WANFANG DATA (2009 to 4 August 2022); China Academic Journal Network Publishing Database (CAJD) (2009 to 6 August 2022); Epistemonikos (3 September 2022) and the reference lists of relevant articles. We applied no language restrictions.
Selection criteria: We included randomised controlled trials (RCTs) comparing the administration-time-related effects of evening with morning dosing monotherapy regimens in people with primary hypertension. We excluded people with known secondary hypertension, shift workers or people with white coat hypertension.
Data collection and analysis: Two to four review authors independently extracted data and assessed trial quality. We resolved disagreements by discussion or with another review author. We performed data synthesis and analyses using Review Manager Web for all-cause mortality, cardiovascular mortality and morbidity, serious adverse events, overall adverse events, withdrawals due to adverse events, change in 24-hour blood pressure and change in morning blood pressure. We assessed the certainty of the evidence using GRADE. We conducted random-effects meta-analysis, fixed-effect meta-analysis, subgroup analysis and sensitivity analysis.
Main results: We included 27 RCTs in this updated review, of which two RCTs were excluded from the meta-analyses for lack of data and number of groups not reported. The quantitative analysis included 25 RCTs with 3016 participants with primary hypertension. RCTs used angiotensin-converting enzyme inhibitors (six trials), calcium channel blockers (nine trials), angiotensin II receptor blockers (seven trials), diuretics (two trials), α-blockers (one trial), and β-blockers (one trial). Fifteen trials were parallel designed, and 10 trials were cross-over designed. Most participants were white, and only two RCTs were conducted in Asia (China) and one in Africa (South Africa). All trials excluded people with risk factors of myocardial infarction and strokes. Most trials had high risk or unclear risk of bias in at least two of several key criteria, which was most prominent in allocation concealment (selection bias) and selective reporting (reporting bias). Meta-analysis showed significant heterogeneity across trials. No RCTs reported on cardiovascular mortality and cardiovascular morbidity. There may be little to no differences in all-cause mortality (after 26 weeks of active treatment: RR 0.49, 95% CI 0.04 to 5.42; RD 0, 95% CI -0.01 to 0.01; very low-certainty evidence), serious adverse events (after 8 to 26 weeks of active treatment: RR 1.17, 95% CI 0.53 to 2.57; RD 0, 95% CI -0.02 to 0.03; very low-certainty evidence), overall adverse events (after 6 to 26 weeks of active treatment: RR 0.89, 95% CI 0.67 to 1.20; I² = 37%; RD -0.02, 95% CI -0.07 to 0.02; I² = 38%; very low-certainty evidence) and withdrawals due to adverse events (after 6 to 26 weeks active treatment: RR 0.76, 95% CI 0.47 to 1.23; I² = 0%; RD -0.01, 95% CI -0.03 to 0; I² = 0%; very low-certainty evidence), but the evidence was very uncertain.
Authors' conclusions: Due to the very limited data and the defects of the trials' designs, this systematic review did not find adequate evidence to determine which time dosing drug therapy regimen has more beneficial effects on cardiovascular outcomes or adverse events. We have very little confidence in the evidence showing that evening dosing of antihypertensive drugs is no more or less effective than morning administration to lower 24-hour blood pressure. The conclusions should not be assumed to apply to people receiving multiple antihypertensive drug regimens.
Copyright © 2024 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Conflict of interest statement
CWu: none.
PZ: none.
PX: none.
CWan: none.
SS: none.
SBV: none.
SL: none.
Update of
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Evening versus morning dosing regimen drug therapy for hypertension.Cochrane Database Syst Rev. 2011 Oct 5;2011(10):CD004184. doi: 10.1002/14651858.CD004184.pub2. Cochrane Database Syst Rev. 2011. Update in: Cochrane Database Syst Rev. 2024 Feb 14;2:CD004184. doi: 10.1002/14651858.CD004184.pub3. PMID: 21975743 Free PMC article. Updated. Review.
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Mengden 1993 {published data only}
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NCT05031637 {unpublished data only}
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NCT05089448 {unpublished data only}
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Niegowska 2000 {published data only}
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Peng 2019 {published data only}
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Potter 1990 {published data only}
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Shiga 1993 {published data only}
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Sun XL 2011 {published data only}
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- Liu HQ, Yan MX, Wang SH, Sun XL. Effects of bisoprolol with different drug administration time on the renin-angiotensin-aldosterone system of non-dippers hypertension [不同时间给予比索洛尔对非杓型原发性高血压患者肾素-血管紧张素-醛固酮系统的影响]. Chinese Journal of Clinical Pharmacology and Therapeutics (中国临床药理学与治疗学) 2011;16(1):101-4.
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Tokbaeva 1996 {published data only}
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Wang JS 2011 {published data only}
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- Wang JS, Zhu YP, Fu YJ. The pharmaco-chronological effects of irbesartan on day-night rhythm of blood pressure in hypertensive patients [厄贝沙坦不同时间用药对血压昼夜节律的影响研究]. Practical Journal of Cardiac Cerebral Pneumal and Vascular Disease (实用心脑肺血管病杂志) 2011;19(11):1844-5, 1848.
Wang R 2022 {published data only}
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- Wang R, Sun J, Fan WH, Li Q. Effects of allisartan isoproxil combined with vitamin B6 at different times on ambulatory blood pressure, circadian rhythm and vascular endothelial function in elderly male patients with non-dipper H-type hypertension [不同时间服用阿利沙坦酯和维生素B6 对高龄男性非杓型H 型高血压患者动态血压、昼夜节律及血管内皮功能的影响研究]. Practical Journal of Cardiac Cerebral Pneumal and Vascular Disease (实用心脑肺血管病杂志) 2022;30(1):11-6, 21.
Wang XG 2020 {published data only}
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Wang YM 2011 {published data only}
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- Wang YM, Liu GC. Chronotherapy of telmisartan in the treatment of primary hypertension [替米沙坦治疗原发性高血压的时间治疗学]. Chinese Journal of Gerontology (中国老年学杂志) 2011;31(5):756-8.
Wen 2021 {published data only}
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- Wen XB, Ding XZ. Comparison of the value of nifedipine GITS taken at different times in the treatment of elderly patients with hypertension [硝苯地平控释片不同服用时间治疗老年高血压患者的价值对比]. Sichuan Journal of Physiological Sciences (四川生理科学杂志) 2021;43(8):1430-2.
Witte 1993 {published data only}
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- Witte K, Weisser K, Neubeck M, Mutschler E, Lehmann K, Hopf R, et al. Cardiovascular effects, pharmacokinetics, and converting enzyme inhibition of enalapril after morning versus evening administration. Clinical Pharmacology & Therapeutics 1993;54(2):177-86. - PubMed
Wright 1982 {published data only}
Wu SL 2011 {published data only}
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- Wu SL, Wang RT, Xiang YJ, Zhang ZP, Zhang ZD, Li DZ. Efficacy observation of telmisartan at different administration time in the treatment of non-dipper hypertension [替米沙坦不同时间给药治疗非杓型高血压疗效观察]. China Pharmacy (中国药房) 2011;22(14):1294-6.
Wu WY 2015 {published data only}
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- Wu WY, Zhang JH, Zhou XL. The effect of different administration times of ramipril on the circadian rhythm of blood pressure [雷米普利不同给药时间对血压昼夜节律的影响]. Chinese Journal of Gerontology (中国老年学杂志) 2015;35(4):884-6.
Xiao 2010 {published data only}
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- Xiao X, Hu WJ. Effect of irbesartan with different time on blood pressure in patients with renal hypertension [不同时间服用安博维对肾性高血压降压效果观察]. Medical Journal of West China (西部医学) 2010;22(12):2212-3.
Xu 2015 {published data only}
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- Xu Y, Hao YX, Cui AD, Liang YL, Yu CY, Hu RY. Administration time-dependent effects of nifedipine controlled release tablets on blood pressure variability in hypertensive patients [硝苯地平控释片不同时间给药对高血压患者血压变异性的影响]. Chinese Journal of Hypertension (中华高血压杂志) 2015;23(6):543-8.
Yan 2020 {published data only}
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- Yan XB, Zhao DT, Wang YF. Effects of different medication times of telmisartan on parameters of 24-hour ambulatory blood pressure monitoring in non-dipper patients with early morning hypertension [替米沙坦不同服药时间治疗非杓型伴清晨高血压]. Journal of MuDanJiang Medical University (牡丹江医学院学报) 2020;41(3):111-3.
Yang 2022 {published data only}
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- Yang YM, Fu SL. Clinical analysis of telmisartan treatment for hypertension at different administration times [不同给药时间替米沙坦治疗高血压的临床分析]. 保健文汇 2022;23(2):70-1.
Yu 2013 {published data only}
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- Yu M, Li L, Xiong YH. Effect of different drug administration time on blood pressure circadian rhythm and morning blood pressure of non dipper type dosing in elderly hypertensive [不同给药时间对非杓型老年高血压患者血压昼夜节律及清晨血压的影响]. Continuing Medical Education (继续医学教育) 2013;27(11):14-6.
Zaslavskaia 1994 {published data only}
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Zaslavskaia 1996 {published data only}
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- Zaslavskaia RM, Lilitsa GV, Akhmetov KZ, Teiblium MM. Time-related effect of betapressin+ in patients with essential hypertension stage II. Klinicheskaia Meditsina 1996;74(9):43-5. - PubMed
Zaslavskaia 1998a {published data only}
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- Zaslavskaia RM, Zhamankulov KA, Zhumabaeva TN, Teiblium MM. Chronopharmacodynamics of Betacap (long-acting propranolol) in patients with hypertension stage II. Klinicheskaia Meditsina 1998;76(4):38-40. - PubMed
Zaslavskaia 1998b {published data only}
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Zaslavskaia 1999b {published data only}
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Zhang L 2018 {published data only}
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Zhang YL 2012 {published data only}
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- Zhang YL, Liu AJ, Dong GJ, Zhang SG, Zhu JH. Efficacy of different time of amlodipine in non-dipper hypertension patients [氨氯地平不同时间给药对非杓型高血压患者血压的影响]. Chinese Journal of Clinical Rational Drug Use (临床合理用药杂志) 2012;5(4B):11-2.
Zhao LQ 2015 {published data only}
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- Zhao LQ, Liu SJ, Gan B. Effect of different time of taking medicine on blood pressure of elderly patients with non-dipper hypertension [不同服药时间对老年非杓型高血压患者血压的影响]. Occupation and Health (职业与健康) 2015;31(13):1794-7, 1801.
Zhao Y 2011 {published data only}
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- Zhao Y, Han N, Zhao HM. Effects of telmisartan with different administration times in patients with various type hypertension [替米沙坦不同给药时间治疗各种高血压类型疗效研究]. Chinese General Practice (中国全科医学) 2011;14(4A):1101-3.
Zhao Y 2012 {published data only}
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- Zhao Y, Han N, Zhao HM, Zhang SG. Effects of telmisartan administration time on blood pressure variability and left ventricular mass index in hypertensive patients [不同时间给予替米沙坦对高血压患者左室质量指数及血压变异性的影响]. Chinese Journal of New Drugs (中国新药杂志) 2012;21(18):2178-82.
Zhou HM 2012 {published data only}
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- Zhou HM, Li BY. Different time amlodipine non-dipper hypertensive patients blood pressure [不同时间给药对非杓型高血压的影响]. China Practical Medical (中国实用医药) 2012;7(15):47-8.
Zhou YJ 2004 {published data only}
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- Zhou YJ, Hou JY, Zhang YZ. Effect of timing of administration on antihypertensive effect of losartan and hydrochlorothiazide. Clinical Focus 2004;19(5):F2.
Zhu 2015 {published data only}
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- Zhu XF, Kang K. Efficacy and safety of losartan at different time points in the treatment of morning blood pressure surge in patients with primary hypertension [不同时间服用氯沙坦治疗原发性高血压病晨峰现象的疗效及安全性研究]. Chinese General Practice (中国全科医学) 2015;18(32):3973-6.
Zhuo LQ 2019 {published data only}
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- Zhuo LQ, Ye LQ, Xiong F. Effects of different administration time of telmisartan on ambulatory blood pressure monitoring parameters and high-sensitivity C-reactive protein levels in patients with primary mild to moderate hypertension [替米沙坦不同给药时间对轻中度原发性高血压病患者动态血压监测参数及超敏C反应蛋白水平的影响]. Evaluation and Analysis of Drug-Use in Hospitals of China (中国医院用药评价与分析) 2019;19(3):312-4.
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