Simvastatin reduces plasma concentration of high-sensitivity C-reactive protein in type 2 diabetic patients with hyperlipidemia

被引:14
|
作者
Lee, IT
Sheu, WHH [1 ]
Lin, SY
Lee, WJ
Song, YM
Liu, HC
机构
[1] Taichung Vet Gen Hosp, Dept Internal Med, Div Endocrinol & Metab, Taichung, Taiwan
[2] Chung Shan Med Univ, Taichung, Taiwan
[3] Natl Def Med Ctr, Taipei, Taiwan
[4] Natl Yang Ming Univ, Taipei 112, Taiwan
[5] Taichung Vet Gen Hosp, Dept Med Labs, Sect Biochem, Taichung, Taiwan
关键词
coronary artery disease; hs-CRP; LDL cholesterol; statin;
D O I
10.1016/S1056-8727(02)00184-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High-sensitivity C-reactive protein (hs-CR-P) is positively associated with the prevalence of coronary artery disease by epidemiologic data. Prospective studies indicate that 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors reduced the plasma hs-CRP concentration and the risk of recurrent coronary events after myocardial infarction. Type 2 diabetes is associated with high mortality risk of coronary heart disease and this high risk may be involved in the inflammatory factors. We have therefore conducted a prospective study to assess whether simvastatin can rapidly reduce the plasma hs-CRP concentration in type 2 diabetic patients with hyperlipidemia. Seventeen type 2 diabetic patients with hyperlipidemia were enrolled in the study after 6 weeks on a lipid-lowering diet. Fourteen patients completed the study, taking simvastatin 20 mg daily for 8 weeks. Fasting blood samples were collected from each patient before and after 8-week administration of simvastatin. In response to 8-week administration of simvastatin, hs-CRP levels significantly decreased from 0.312 +/- 0.057 to 0.193 +/- 0.045 mg/dl (P < .01). Plasma LDL cholesterol also decreased significantly from 130 +/- 9 to 74 +/- 3 mg/dl (P = .001). This study shows that plasma hs-CRP concentration can be reduced by 8-week administration of simvastatin in type 2 diabetic patients with hyperlipidemia. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:382 / 385
页数:4
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