TY - JOUR
T1 - Rationale, design, and baseline data of the Japanese Primary Prevention Project (JPPP)-A randomized, open-label, controlled trial of aspirin versus no aspirin in patients with multiple risk factors for vascular events
AU - Teramoto, Tamio
AU - Shimada, Kazuyuki
AU - Uchiyama, Shinichiro
AU - Sugawara, Masahiro
AU - Goto, Yoshio
AU - Yamada, Nobuhiro
AU - Oikawa, Shinichi
AU - Ando, Katsuyuki
AU - Ishizuka, Naoki
AU - Yamazaki, Tsutomu
AU - Yokoyama, Kenji
AU - Murata, Mitsuru
AU - Ikeda, Yasuo
N1 - Funding Information:
The JPPP study is funded by the Japanese Ministry of Health, Labour and Welfare (Tokyo, Japan) and the Waksman Foundation of Japan Inc (Tokyo, Japan). Enteric-coated aspirin, 100 mg, tablets are provided at no charge by Bayer Yakuhin Ltd (Osaka, Japan).
PY - 2010/3
Y1 - 2010/3
N2 - Background: Prevention of atherosclerotic disease has become an important public health priority in Japan due to the aging of the population and changes in diet and lifestyle factors. Methods: The Japanese Primary Prevention Project (JPPP) is a multicenter, open-label, randomized, parallel-group trial that is evaluating primary prevention with low-dose aspirin in Japanese patients aged 60 to 85 years with hypertension, dyslipidemia, or diabetes mellitus. The study cohort will be followed for a mean of 4 years. The primary end point is a composite of death from cardiovascular causes (including fatal myocardial infarction [MI], fatal stroke, and other cardiovascular death), nonfatal stroke (ischemic or hemorrhagic), and nonfatal MI. Key secondary end points include a composite of cardiovascular death, nonfatal stroke, nonfatal MI, transient ischemic attack, angina pectoris, or arteriosclerotic disease requiring surgery or intervention; each component of the primary end point; noncerebrovascular and noncardiovascular death; and extracranial hemorrhage requiring transfusion or hospitalization. End point assessment is done by a central adjudication committee that is blinded to treatment assignments. Results: Enrollment began in March 2005 and was completed in June 2007. A total of 14,466 patients were randomly allocated to receive enteric-coated aspirin, 100 mg/d, or no aspirin. At randomization, the study cohort had a mean (SD) age of 70.6 (6.2) years; 57.8% were women, 85.0% had hypertension, 71.7% had dyslipidemia, and 33.9% had diabetes. In the study cohort, 80.4% of patients had ≥3 risk factors. Conclusion: The JPPP is the largest primary prevention trial of aspirin in a Japanese population that is investigating whether the benefit of aspirin in reducing risk of vascular events outweighs any bleeding risk in elderly patients with multiple risk factors.
AB - Background: Prevention of atherosclerotic disease has become an important public health priority in Japan due to the aging of the population and changes in diet and lifestyle factors. Methods: The Japanese Primary Prevention Project (JPPP) is a multicenter, open-label, randomized, parallel-group trial that is evaluating primary prevention with low-dose aspirin in Japanese patients aged 60 to 85 years with hypertension, dyslipidemia, or diabetes mellitus. The study cohort will be followed for a mean of 4 years. The primary end point is a composite of death from cardiovascular causes (including fatal myocardial infarction [MI], fatal stroke, and other cardiovascular death), nonfatal stroke (ischemic or hemorrhagic), and nonfatal MI. Key secondary end points include a composite of cardiovascular death, nonfatal stroke, nonfatal MI, transient ischemic attack, angina pectoris, or arteriosclerotic disease requiring surgery or intervention; each component of the primary end point; noncerebrovascular and noncardiovascular death; and extracranial hemorrhage requiring transfusion or hospitalization. End point assessment is done by a central adjudication committee that is blinded to treatment assignments. Results: Enrollment began in March 2005 and was completed in June 2007. A total of 14,466 patients were randomly allocated to receive enteric-coated aspirin, 100 mg/d, or no aspirin. At randomization, the study cohort had a mean (SD) age of 70.6 (6.2) years; 57.8% were women, 85.0% had hypertension, 71.7% had dyslipidemia, and 33.9% had diabetes. In the study cohort, 80.4% of patients had ≥3 risk factors. Conclusion: The JPPP is the largest primary prevention trial of aspirin in a Japanese population that is investigating whether the benefit of aspirin in reducing risk of vascular events outweighs any bleeding risk in elderly patients with multiple risk factors.
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U2 - 10.1016/j.ahj.2009.11.030
DO - 10.1016/j.ahj.2009.11.030
M3 - Article
C2 - 20211296
AN - SCOPUS:77749258073
SN - 0002-8703
VL - 159
SP - 361-369.e4
JO - American heart journal
JF - American heart journal
IS - 3
ER -