Endothelial-Vasoprotective Effects of High-Density Lipoprotein Are Impaired in Patients With Type 2 Diabetes Mellitus but Are Improved After Extended-Release Niacin Therapy

被引:346
作者
Sorrentino, Sajoscha A. [1 ,2 ]
Besler, Christian [1 ,4 ,6 ]
Rohrer, Lucia [5 ,6 ]
Meyer, Martin [1 ,4 ]
Heinrich, Kathrin [4 ]
Bahlmann, Ferdinand H. [2 ]
Mueller, Maja [1 ,4 ]
Horvath, Tibor [1 ]
Doerries, Carola [1 ,4 ]
Heinemann, Mariko [1 ]
Flemmer, Stella [1 ]
Markowski, Andrea [1 ,3 ]
Manes, Costantina [1 ,4 ]
Bahr, Matthias J. [3 ]
Haller, Hermann [2 ]
von Eckardstein, Arnold [5 ,6 ]
Drexler, Helmut [1 ]
Landmesser, Ulf [1 ,4 ,6 ]
机构
[1] Hannover Med Sch, Klin Kardiol & Angiol, D-30623 Hannover, Germany
[2] Hannover Med Sch, Klin Nieren & Hochdruck Erkrankungen, D-30623 Hannover, Germany
[3] Hannover Med Sch, Klin Gastroenterol Hepatol & Endokrinol, D-30623 Hannover, Germany
[4] Univ Zurich Hosp, Ctr Cardiovasc, CH-8091 Zurich, Switzerland
[5] Univ Zurich, Inst Clin Chem, Zurich, Switzerland
[6] Univ Zurich, Zurich Ctr Integrated Human Physiol, Zurich, Switzerland
基金
新加坡国家研究基金会;
关键词
diabetes mellitus; endothelium; free radicals; lipids; nitric oxide; REVERSE CHOLESTEROL TRANSPORT; PROGENITOR-CELL MOBILIZATION; VASCULAR OXIDATIVE STRESS; SCAVENGER RECEPTOR-BI; NITRIC-OXIDE SYNTHASE; DOUBLE-BLIND; METABOLIC SYNDROME; HDL CHOLESTEROL; TORCETRAPIB; SIMVASTATIN;
D O I
10.1161/CIRCULATIONAHA.108.836346
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-High-density lipoprotein (HDL)-raising therapies are currently under intense evaluation, but the effects of HDL may be highly heterogeneous. We therefore compared the endothelial effects of HDL from healthy subjects and from patients with type 2 diabetes mellitus and low HDL (meeting the criteria for metabolic syndrome), who are frequently considered for HDL-raising therapies. Moreover, in diabetic patients, we examined the impact of extended-release (ER) niacin therapy on the endothelial effects of HDL. Methods and Results-HDL was isolated from healthy subjects (n = 10) and patients with type 2 diabetes (n = 33) by sequential ultracentrifugation. Effects of HDL on endothelial nitric oxide and superoxide production were characterized by electron spin resonance spectroscopy analysis. Effects of HDL on endothelium-dependent vasodilation and early endothelial progenitor cell-mediated endothelial repair were examined. Patients with diabetes were randomized to a 3-month therapy with ER niacin (1500 mg/d) or placebo, and endothelial effects of HDL were characterized. HDL from healthy subjects stimulated endothelial nitric oxide production, reduced endothelial oxidant stress, and improved endothelium-dependent vasodilation and early endothelial progenitor cell-mediated endothelial repair. In contrast, these beneficial endothelial effects of HDL were not observed in HDL from diabetic patients, which suggests markedly impaired endothelial-protective properties of HDL. ER niacin therapy improved the capacity of HDL to stimulate endothelial nitric oxide, to reduce superoxide production, and to promote endothelial progenitor cell-mediated endothelial repair. Further measurements suggested increased lipid oxidation of HDL in diabetic patients, and a reduction after ER niacin therapy. Conclusions-HDL from patients with type 2 diabetes mellitus and metabolic syndrome has substantially impaired endothelial-protective effects compared with HDL from healthy subjects. ER niacin therapy not only increases HDL plasma levels but markedly improves endothelial-protective functions of HDL in these patients, which is potentially more important.
引用
收藏
页码:110 / 122
页数:13
相关论文
共 53 条
[51]   High-density lipoprotein binding to scavenger receptor-BI activates endothelial nitric oxide synthase [J].
Yuhanna, IS ;
Zhu, Y ;
Cox, BE ;
Hahner, LD ;
Osborne-Lawrence, S ;
Marcel, YL ;
Anderson, RGW ;
Mendelsohn, ME ;
Hobbs, HH ;
Shaul, PW .
NATURE MEDICINE, 2001, 7 (07) :853-857
[52]   Association between myeloperoxidase levels and risk of coronary artery disease [J].
Zhang, ZL ;
Brennan, ML ;
Fu, XM ;
Aviles, RJ ;
Pearce, GL ;
Penn, MS ;
Topol, EJ ;
Sprecher, DL ;
Hazen, SL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (17) :2136-2142
[53]   Apolipoprotein A-I is a selective target for myeloperoxidase-catalyzed oxidation and functional impairment in subjects with cardiovascular disease [J].
Zheng, LM ;
Nukuna, B ;
Brennan, ML ;
Sun, MJ ;
Goormastic, M ;
Settle, M ;
Schmitt, D ;
Fu, XM ;
Thomson, L ;
Fox, PL ;
Ischiropoulos, H ;
Smith, JD ;
Kinter, M ;
Hazen, SL .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (04) :529-541