The metabolic syndrome: Pathophysiology, clinical relevance, and use of niacin

被引:14
作者
Ito, MK [1 ]
机构
[1] Univ Pacific, Sch Pharm & Hlth Sci, Stockton, CA 95211 USA
[2] Vet Affairs San Diego Hlth Care Syst, Dept Pharm 119, Cardiac Rehabilat Cholesterol Clin, La Jolla, CA 92161 USA
关键词
atherogenic dyslipidemia; HDL-cholesterol; LDL particle size; metabolic syndrome; niacin; triglycerides;
D O I
10.1345/aph.1D218
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the pathophysiology and clinical relevance for using niacin to treat the metabolic syndrome. DATA SOURCES: Primary articles were identified through a MEDLINE search (1966 January 2003), and recommendations for treatment were obtained from the National Cholesterol Education Program Adult Treatment Panel (NCEP-ATP) III guidelines. STUDY SELECTION AND DATA EXTRACTION: Published studies showing the effects of the metabolic syndrome, atherogenic dyslipidemia, and niacin were evaluated and reviewed. DATA SYNTHESIS: The metabolic syndrome is a highly prevalent condition that affects 24% of American adults and significantly increases the risk of coronary heart disease (CHD). Most patients with metabolic syndrome have atherogenic dyslipidemia characterized by elevated triglycerides, low high-density-lipoprotein cholesterol (HDL-C), and small, dense low-density-lipoprotein cholesterol (LDL-C) particles. The NCEP-ATP III identifies patients with the metabolic syndrome as candidates for intensified therapy. Lifestyle modifications and drug therapy are recommended. Niacin represents a good option for treating the triad of lipid abnormalities seen in the metabolic syndrome because it raises HDL-C, lowers triglycerides, and increases LDL-C particle size. CONCLUSIONS: Treatment of the metabolic syndrome is recommended by NCEP-ATP III to further reduce CHID risk after the LDL-C target has been met. Prospective clinical studies are needed to define the impact of niacin and other lipid-modifying agents on CHD morbidity and mortality in patients with the metabolic syndrome.
引用
收藏
页码:277 / 285
页数:9
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