TY - JOUR
T1 - Cardiovascular Outcomes in Patients With Previous Myocardial Infarction and Mild Diabetes Mellitus Following Treatment With Pioglitazone
T2 - Reports of a Randomised Trial From The Japan Working Group for the Assessment Whether Pioglitazone Protects DM Patients Against Re-Infarction (PPAR Study)
AU - PPAR investigators
AU - Asakura, Masanori
AU - Kim, Jiyoong
AU - Asanuma, Hiroshi
AU - Nakama, Yasuharu
AU - Tsukahara, Kengo
AU - Higashino, Yorihiko
AU - Ishikawa, Tetsuya
AU - Koba, Shinji
AU - Tsujimoto, Mitsuru
AU - Himeno, Hideo
AU - Maruyama, Yasuyuki
AU - Ookusa, Takanori
AU - Yoda, Shunichi
AU - Suzuki, Hiroshi
AU - Okubo, Shinji
AU - Shimizu, Makoto
AU - Hashimoto, Yuji
AU - Satake, Kazuo
AU - Fujino, Susumu
AU - Uzui, Hiroyasu
AU - Nagai, Yoshiyuki
AU - Kohno, Tohru
AU - Mizuno, Sumio
AU - Nakahama, Makoto
AU - Kanaya, Hounin
AU - Murohara, Toyoaki
AU - Fukui, Kazuki
AU - Takase, Hiroyuki
AU - Ohte, Nobuyuki
AU - Shiono, Takaaki
AU - Fukunami, Masatake
AU - Endo, Tsutomu
AU - Sawada, Reimin
AU - Fujii, Kenshi
AU - Takeuchi, Motoshi
AU - Ikeda, Shuntaro
AU - Mizuno, Koichi
AU - Uematsu, Masaaki
AU - Matsubara, Taku
AU - Yano, Shoji
AU - Takahashi, Jun
AU - Ueda, Kousei
AU - Kinoshita, Yoshihiko
AU - Tamita, Koichi
AU - Hayashi, Hideki
AU - Hamasaki, Toshimitsu
AU - Kitakaze, Masafumi
N1 - Publisher Copyright:
© 2018
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Background: Secondary prevention in patients with myocardial infarction (MI) is critically important to prevent ischaemic heart failure and reduce social burden. Pioglitazone improves vascular dysfunction and prevents coronary atherosclerosis, mainly via anti-inflammatory and antiatherogenic effects by enhancing adiponectin production in addition to antihyperglycemic effects, thus suggesting that pioglitazone attenuates cardiovascular events in patients with mild (HbA1c levels < 6·5%) diabetes mellitus (DM). Therefore, we evaluated the effects of pioglitazone on cardiovascular events in patients with both previous MI and mild DM. Methods: In this multicentre, prospective, randomised, open, blinded-endpoint trial, we randomly assigned 630 patients with mild DM with a history of MI to undergo either DM therapy with (pioglitazone group) or without (control group) pioglitazone. DM was diagnosed using the 75-g oral glucose tolerance test, and mild DM was defined if HbA1c level was < 6·5%. The primary endpoint was the composite of cardiovascular death and hospitalisation caused by acute MI, unstable angina, coronary revascularisation (including percutaneous coronary intervention and cardiac bypass surgery), and stroke. Findings: HbA1C levels were 5·9 and 5·8% (p = 0·71) at baseline and 6·0 and 5·8% (p < 0·01) at 2 years for the control and pioglitazone groups, respectively. The primary endpoint was observed in 14·2% and 14·1% patients in the control and pioglitazone groups during two years (95% confidential interval (CI):0.662–1·526, p = 0·98), respectively; the incidence of MI and cerebral infarction was 0·3% and 2·2% (95%CI: 0·786–32·415, p = 0·09) and 1·0% and 0·3% (95%CI: 0·051–3·662, p = 0·44), respectively. Post-hoc analyses of the 7-year observation period showed that these trends were comparable (21·9% and 19·2% in the control and pioglitazone groups, 95%CI: 0.618–1·237, p = 0·45). Interpretation: Pioglitazone could not reduce the occurrence of cardiovascular events in patients with mild DM and previous MI.
AB - Background: Secondary prevention in patients with myocardial infarction (MI) is critically important to prevent ischaemic heart failure and reduce social burden. Pioglitazone improves vascular dysfunction and prevents coronary atherosclerosis, mainly via anti-inflammatory and antiatherogenic effects by enhancing adiponectin production in addition to antihyperglycemic effects, thus suggesting that pioglitazone attenuates cardiovascular events in patients with mild (HbA1c levels < 6·5%) diabetes mellitus (DM). Therefore, we evaluated the effects of pioglitazone on cardiovascular events in patients with both previous MI and mild DM. Methods: In this multicentre, prospective, randomised, open, blinded-endpoint trial, we randomly assigned 630 patients with mild DM with a history of MI to undergo either DM therapy with (pioglitazone group) or without (control group) pioglitazone. DM was diagnosed using the 75-g oral glucose tolerance test, and mild DM was defined if HbA1c level was < 6·5%. The primary endpoint was the composite of cardiovascular death and hospitalisation caused by acute MI, unstable angina, coronary revascularisation (including percutaneous coronary intervention and cardiac bypass surgery), and stroke. Findings: HbA1C levels were 5·9 and 5·8% (p = 0·71) at baseline and 6·0 and 5·8% (p < 0·01) at 2 years for the control and pioglitazone groups, respectively. The primary endpoint was observed in 14·2% and 14·1% patients in the control and pioglitazone groups during two years (95% confidential interval (CI):0.662–1·526, p = 0·98), respectively; the incidence of MI and cerebral infarction was 0·3% and 2·2% (95%CI: 0·786–32·415, p = 0·09) and 1·0% and 0·3% (95%CI: 0·051–3·662, p = 0·44), respectively. Post-hoc analyses of the 7-year observation period showed that these trends were comparable (21·9% and 19·2% in the control and pioglitazone groups, 95%CI: 0.618–1·237, p = 0·45). Interpretation: Pioglitazone could not reduce the occurrence of cardiovascular events in patients with mild DM and previous MI.
KW - Blood glucose-lowering
KW - Cardiovascular events
KW - Diabetes mellitus
KW - Myocardial infarction
KW - PROBE study
KW - Pioglitazone
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U2 - 10.1016/j.eclinm.2018.09.006
DO - 10.1016/j.eclinm.2018.09.006
M3 - Article
AN - SCOPUS:85064151391
SN - 2589-5370
VL - 4-5
SP - 10
EP - 24
JO - eClinicalMedicine
JF - eClinicalMedicine
ER -