4.4 Article

Probucol Trial for Secondary Prevention of Atherosclerotic Events in Patients with Coronary Heart Disease (PROSPECTIVE)

Journal

JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS
Volume 28, Issue 2, Pages 103-123

Publisher

JAPAN ATHEROSCLEROSIS SOC
DOI: 10.5551/jat.55327

Keywords

Probucol; Coronary heart disease; Prevention; Reverse cholesterol transport; Antioxidants

Funding

  1. Foundation for Biomedical Research and Innovation at Kobe
  2. AstraZeneca K.K.
  3. Dai-ichi Sankyo Co, Ltd.
  4. Astellas Pharma Inc.
  5. Novartis Pharma K.K.
  6. Chugai Pharmaceutical Co., Ltd.
  7. Otsuka Pharmaceutical Co., Ltd.
  8. Sanofi K.K.
  9. Japan Atherosclerosis Society

Ask authors/readers for more resources

The study found that despite reducing HDL-C levels, probucol may help reduce cardiovascular events in patients with coronary heart disease.
Aims: Although intensive statin therapy reduced cardiovascular risks, cardiovascular events have not been completely prevented. Probucol is a potent antioxidant and reduces tendon xanthomas in familial hypercholesterolemia patients despite reduction of high-density lipoprotein (HDL)-cholesterol (HDL-C). We investigated whether probucol can reduce cardiovascular events on top of conventional lipid-lowering therapy in patients with coronary heart disease (CHD). Methods: PROSPECTIVE is a multicenter, randomized, prospective study that recruited 876 Japanese patients with CHD and dyslipidemia with a low-density lipoprotein (LDL)-cholesterol (LDL-C) level of >= 140 mg/dL without medication or those treated with lipid-lowering drugs. Lipid-lowering agents were administered during the study period in the control group (n=438), and probucol 500 mg/day was added to lipid-lowering therapy in the probucol group (n=438). Patients were randomly assigned to two treatment groups by adjusting the LDL-C level and presence of diabetes and hypertension and followed up for more than 3 years. The primary end point was a composite of cerebrovascular and cardiovascular events (cardiovascular disease death including sudden death, nonfatal myocardial infarction, nonfatal stroke, hospitalization for unstable angina, hospitalization for heart failure, or coronary revascularization). The secondary end point was carotid intima-media thickness in a subset of patients. Results: The incidence of the primary end point showed a trend to be lower in the probucol group compared with that in the control group despite reduced HDL-C without serious adverse events. Anti-atherogenic effects of probucol may be attributed to its potent antioxidative function and enhancement of reverse cholesterol transport. Conclusion: Since there was no statistical significance between the probucol and control groups despite a marked reduction of HDL-C, further studies on the clinical outcomes of probucol on top of conventional therapy may be necessary in the future (UMIN000003307).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available