TY - JOUR
T1 - Angiotensin-converting enzyme inhibitors versus angiotensin receptor blockers in hypertensive patients with myocardial infarction or heart failure
T2 - a systematic review and meta-analysis
AU - Ohtsubo, Toshio
AU - Shibata, Rei
AU - Kai, Hisashi
AU - Okamoto, Ryuji
AU - Kumagai, Eita
AU - Kawano, Hiroaki
AU - Fujiwara, Akira
AU - Kitazono, Takanari
AU - Murohara, Toyoaki
AU - Arima, Hisatomi
N1 - Funding Information:
Conflict of interest TO received honoraria from Sanwa Kagaku Kenkyusho. RS received honoraria from Medtoronic, Boehringer Ingelheim, Eli Lilly, and Otsuka Pharmaceutical Factory. HK received honoraria from Daiichi Sankyo Co., Mitsubishi Tanabe Pharma Co., Shionogi & Co., Dainippon Sumitomo Pharma Co., and Takeda Pharmaceutical Co. TK received honoraria from Daiichi Sankyo and research funding from Daiichi Sankyo, Takeda Pharmaceutical, Astellas Pharma, Chugai Pharmaceutical, MSD, Boehringer Ingel-heim, EA Pharma, Sanofi Aventis, Pfizer, Kissei Pharmaceutical, Kyowa Hakko Kirin, Asahi Kasei Medical, Otsuka Pharmaceutical, Torii Pharmaceutical, and Bayer.
Publisher Copyright:
© 2019, The Japanese Society of Hypertension.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Angiotensin-converting enzyme inhibitors (ACEIs) are considered primary drugs for the secondary prevention of myocardial infarction (MI), and angiotensin receptor blockers (ARBs) are used when ACEIs cannot be tolerated. However, it is unclear whether ACEIs or ARBs are more appropriate first-line drugs in hypertensive patients with MI or heart failure (HF). The present study aimed to compare the effects of ACEIs and those of ARBs in these patients. Sixty randomized controlled trails (RCTs) that compared the effects of ACEIs and ARBs in patients with MI or HF were extracted by searching PubMed/MEDLINE, Cochrane Database, and the Medical Central Journal database according to the PRISMA guidelines. We finally selected six eligible RCTs and identified three systematic reviews and meta-analyses. The proportion of hypertensive patients ranged from 36 to 69%. Meta-analyses were performed for recurrence or new onset of MI (risk ratio 0.97 [95% confidence interval: 0.88, 1.06]), hospitalization for HF (0.98 [0.84, 1.14]), cardiovascular or total mortality (0.98 [0.91, 1.05]), cardiovascular events or stroke (1.02 [0.94, 1.11]), and adverse events (1.40 [1.11, 1.77]). There were no significant differences between ACEIs and ARBs for all outcomes, except adverse events. Study discontinuation owing to adverse events was significantly more common with ACEIs than with ARBs. Among hypertensive patients with MI or HF, it appears desirable to select the most appropriate drugs, ACEIs or ARBs, in each case by considering the function level, patient background, comorbidity presence, blood pressure target, drug price and other such factors comprehensively in addition to considering tolerability.
AB - Angiotensin-converting enzyme inhibitors (ACEIs) are considered primary drugs for the secondary prevention of myocardial infarction (MI), and angiotensin receptor blockers (ARBs) are used when ACEIs cannot be tolerated. However, it is unclear whether ACEIs or ARBs are more appropriate first-line drugs in hypertensive patients with MI or heart failure (HF). The present study aimed to compare the effects of ACEIs and those of ARBs in these patients. Sixty randomized controlled trails (RCTs) that compared the effects of ACEIs and ARBs in patients with MI or HF were extracted by searching PubMed/MEDLINE, Cochrane Database, and the Medical Central Journal database according to the PRISMA guidelines. We finally selected six eligible RCTs and identified three systematic reviews and meta-analyses. The proportion of hypertensive patients ranged from 36 to 69%. Meta-analyses were performed for recurrence or new onset of MI (risk ratio 0.97 [95% confidence interval: 0.88, 1.06]), hospitalization for HF (0.98 [0.84, 1.14]), cardiovascular or total mortality (0.98 [0.91, 1.05]), cardiovascular events or stroke (1.02 [0.94, 1.11]), and adverse events (1.40 [1.11, 1.77]). There were no significant differences between ACEIs and ARBs for all outcomes, except adverse events. Study discontinuation owing to adverse events was significantly more common with ACEIs than with ARBs. Among hypertensive patients with MI or HF, it appears desirable to select the most appropriate drugs, ACEIs or ARBs, in each case by considering the function level, patient background, comorbidity presence, blood pressure target, drug price and other such factors comprehensively in addition to considering tolerability.
UR - http://www.scopus.com/inward/record.url?scp=85063999487&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85063999487&partnerID=8YFLogxK
U2 - 10.1038/s41440-018-0167-5
DO - 10.1038/s41440-018-0167-5
M3 - Article
C2 - 30948834
AN - SCOPUS:85063999487
SN - 0916-9636
VL - 42
SP - 641
EP - 649
JO - Hypertension Research
JF - Hypertension Research
IS - 5
ER -