1. Effects of Xuezhikang in patients with dyslipidemia: a multicenter, randomized, placebo-controlled study
- Author
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Harold E. Bays, Ping Lan Liu, Simon Li, Zhenwen Duan, Shui-ping Zhao, Alan J. Reichman, Osvaldo A. Brusco, Junxian Zhao, Guoping Lu, David M. Capuzzi, Yan Zhang, Shuren Guo, Patrick M. Moriarty, Sam Lerman, Ping Ye, Fumin Zhang, Adam Karns, Shaowen Liu, Eli M. Roth, and Yuhua Liao
- Subjects
Adult ,Male ,medicine.medical_specialty ,China ,Gastrointestinal Diseases ,Endocrinology, Diabetes and Metabolism ,Placebo-controlled study ,Placebo ,Gastroenterology ,Placebos ,chemistry.chemical_compound ,Internal medicine ,Internal Medicine ,medicine ,Red yeast rice ,Humans ,In patient ,Lovastatin ,Apolipoproteins A ,Triglycerides ,Aged ,Apolipoproteins B ,Dyslipidemias ,Hypolipidemic Agents ,Biological Products ,Nutrition and Dietetics ,business.industry ,Cholesterol ,Cholesterol, HDL ,Cholesterol, LDL ,Middle Aged ,medicine.disease ,Coronary heart disease ,United States ,Endocrinology ,chemistry ,lipids (amino acids, peptides, and proteins) ,Female ,Cardiology and Cardiovascular Medicine ,business ,Dyslipidemia ,medicine.drug ,Drugs, Chinese Herbal - Abstract
Xuezhikang (XZK) is an extract of fermented red yeast rice that has lipid-lowering properties.To evaluate the effects of XZK on lipids in subjects with dyslipidemia but no coronary heart disease.A total of 116 adults with baseline non-high-density lipoprotein cholesterol (non-HDL-C) levels of approximately 208 mg/dL and low-density lipoprotein cholesterol (LDL-C) levels of approximately 175 mg/dL were randomized to either placebo or XZK 1200 or 2400 mg daily and treated for 12 weeks.A majority of the patients were white (53.4%) or Asian (37.1%). Daily XZK 1200 mg and 2400 mg for 4 to 12 weeks resulted in statistically significant (P .001) and clinically meaningful decreases in non-HDL-C (∼24% reduction) and LDL-C (∼27% reduction) compared with placebo. XZK treatment at either dose enabled approximately 50% of subjects to reduce their LDL-C levels by ≥ 30%. Doubling the XZK daily dose from 1200 to 2400 mg at treatment week 8 caused an additional 4.6% reduction in LDL-C. Significant benefits were also observed across secondary efficacy variables, including total cholesterol (TC), apolipoprotein B (Apo B), triglycerides, HDL-C, the TC/HDL-C ratio, and the Apo B/Apo A-I ratio, at treatment week 8 or 12. XZK was safe and well tolerated. Safety and tolerability profiles were similar across treatment groups. Most adverse events were gastrointestinal. No subject experienced myopathy or markedly elevated liver transaminases or creatine kinase.Xuezhikang significantly reduced non-HDL-C and LDL-C, and was well tolerated. Further, longer-term studies in more diverse patient populations are needed to corroborate these findings.
- Published
- 2014