PMID- 36326841 OWN - NLM STAT- MEDLINE DCOM- 20230628 LR - 20230701 IS - 1861-0692 (Electronic) IS - 1861-0684 (Print) IS - 1861-0684 (Linking) VI - 112 IP - 7 DP - 2023 Jul TI - Network meta-analysis of sacubitril/valsartan for the treatment of essential hypertension. PG - 855-867 LID - 10.1007/s00392-022-02120-0 [doi] AB - AIM: Sacubitril/valsartan has been demonstrated to reduce blood pressure in hypertensive patients, but the best dose remains unclear. We performed this network meta-analysis to determine the comparative efficacy and safety of three available doses of sacubitril/valsartan (i.e., 100, 200, and 400 mg). METHODS AND RESULTS: We searched four databases for relevant studies published before January 2022. Mean systolic and diastolic blood pressures in the sitting position (msSBP and msDBP) and ambulatory condition (24-h maSBP and maDBP) and adverse events (AEs) were assessed. Nine randomized controlled trials (RCTs) involving 5474 patients were included. Sacubitril/valsartan 200 mg once daily was slightly better than 400 mg once daily in lowering 24-h maDBP (MD, 1.31 mmHg; 95% CI 0.61-2.01 mmHg), slightly better than 100 mg once daily in lowering 24-h maSBP (MD, - 3.70 mmHg; 95% CI - 6.22 to - 1.18 mmHg) and 24-h maDBP (MD, - 2.98; 95% CI - 5.11 to - 0.85), and slightly better than Valsartan 160 mg once daily in lowering 24-h maSBP (MD, - 3.23 mmHg; 95% CI, - 5.25 to - 1.21). 400 mg once daily of sacubitril/valsartan was better than 200 mg once daily in lowering msDBP (MD, - 9.38 mmHg; 95% CI - 17.79 to - 0.97 mmHg). Interestingly, 400 mg once daily of sacubitril/valsartan had fewer trial-specified AEs than 200 mg once daily (OR, 0.74; 95%CI 0.55-0.99). There was no statistical difference for the remaining comparisons. CONCLUSIONS: In hypertensive patients, 200 mg once daily of sacubitril/valsartan may exert a greater reduction in ambulatory blood pressure than 100 mg once daily and 200 mg once daily may not be inferior to 400 mg once daily. Moreover, it is not clear that sacubitril/valsartan lowers blood pressure more than an angiotensin receptor blocker. Further trials are required to determine the incremental value of sacubitril/valsartan as an anti-hypertensive agent. CI - (c) 2022. The Author(s). FAU - Zhang, Yaling AU - Zhang Y AD - Department of Nephrology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. FAU - Zhao, Xiaoyu AU - Zhao X AD - Department of Cardiovascular, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. FAU - Huang, Hao AU - Huang H AD - Department of Cardiovascular, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. howardsc@foxmail.com. FAU - Li, Ming AU - Li M AD - Department of Cardiovascular, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. lmjy4788@126.com. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review DEP - 20221103 PL - Germany TA - Clin Res Cardiol JT - Clinical research in cardiology : official journal of the German Cardiac Society JID - 101264123 RN - 17ERJ0MKGI (sacubitril) RN - 0 (Angiotensin II Type 1 Receptor Blockers) RN - 0 (Tetrazoles) RN - 80M03YXJ7I (Valsartan) RN - 0 (Antihypertensive Agents) RN - 0 (Drug Combinations) RN - 0 (Angiotensin Receptor Antagonists) SB - IM MH - Humans MH - Network Meta-Analysis MH - *Angiotensin II Type 1 Receptor Blockers/therapeutic use MH - Tetrazoles/adverse effects MH - Valsartan/pharmacology MH - *Hypertension/diagnosis/drug therapy MH - Essential Hypertension/chemically induced/drug therapy MH - Antihypertensive Agents/therapeutic use MH - Blood Pressure MH - Drug Combinations MH - Angiotensin Receptor Antagonists/adverse effects MH - Randomized Controlled Trials as Topic PMC - PMC10293449 OTO - NOTNLM OT - Diastolic blood pressure OT - Hypertension OT - Network meta-analysis OT - Sacubitril/valsartan OT - Systolic blood pressure COIS- The authors have no relevant financial or non-financial interests to disclose. EDAT- 2022/11/04 06:00 MHDA- 2023/06/28 06:42 PMCR- 2022/11/03 CRDT- 2022/11/03 12:12 PHST- 2022/04/27 00:00 [received] PHST- 2022/10/19 00:00 [accepted] PHST- 2023/06/28 06:42 [medline] PHST- 2022/11/04 06:00 [pubmed] PHST- 2022/11/03 12:12 [entrez] PHST- 2022/11/03 00:00 [pmc-release] AID - 10.1007/s00392-022-02120-0 [pii] AID - 2120 [pii] AID - 10.1007/s00392-022-02120-0 [doi] PST - ppublish SO - Clin Res Cardiol. 2023 Jul;112(7):855-867. doi: 10.1007/s00392-022-02120-0. Epub 2022 Nov 3.