Uremia Alters HDL Composition and Function

被引:230
作者
Holzer, Michael [1 ]
Birner-Gruenberger, Ruth [2 ]
Stojakovic, Tatjana [3 ]
El-Gamal, Dalia [1 ]
Binder, Veronika [1 ]
Wadsack, Christian [4 ]
Heinemann, Akos [1 ]
Marsche, Gunther [1 ]
机构
[1] Med Univ Graz, Inst Expt & Clin Pharmacol, A-8010 Graz, Austria
[2] Med Univ Graz, Med Res Ctr, Prote Core Facil, A-8010 Graz, Austria
[3] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, A-8010 Graz, Austria
[4] Med Univ Graz, Dept Obstet & Gynecol, A-8010 Graz, Austria
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2011年 / 22卷 / 09期
基金
奥地利科学基金会;
关键词
HIGH-DENSITY-LIPOPROTEIN; CHRONIC KIDNEY-DISEASE; STAGE RENAL-DISEASE; CARDIOVASCULAR-DISEASE; CHOLESTEROL EFFLUX; ANTIINFLAMMATORY PROPERTIES; SHOTGUN PROTEOMICS; PHOSPHOLIPASE A(2); IN-VIVO; METABOLISM;
D O I
10.1681/ASN.2010111144
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Functional impairment of HDL may contribute to the excess cardiovascular mortality experienced by patients with renal disease, but the effect of advanced renal disease on the composition and function of HDL is not well understood. Here, we used mass spectrometry and biochemical analyses to study alterations in the proteome and lipid composition of HDL isolated from patients on maintenance hemodialysis. We identified a significant increase in the amount of acute phase protein serum amyloid A1, albumin, lipoprotein-associated phospholipase A2, and apoC-III composing uremic HDL. Furthermore, uremic HDL contained reduced phospholipid and increased triglyceride and lysophospholipid. With regard to function, these changes impaired the ability of uremic HDL to promote cholesterol efflux from macrophages. In summary, the altered composition of HDL in renal disease seems to inhibit its cardioprotective properties. Assessing HDL composition and function in renal disease may help identify patients at increased risk for cardiovascular disease.
引用
收藏
页码:1631 / 1641
页数:11
相关论文
共 46 条
[1]   Role of serum amyloid A during metabolism of acute-phase HDL by macrophages [J].
Artl, A ;
Marsche, G ;
Lestavel, S ;
Sattler, W ;
Malle, E .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (03) :763-772
[2]   Antiinflammatory properties of HDL [J].
Barter, PJ ;
Nicholls, S ;
Rye, KA ;
Anantharamaiah, GM ;
Navab, M ;
Fogelman, AM .
CIRCULATION RESEARCH, 2004, 95 (08) :764-772
[3]   Apolipoprotein CIII and atherosclerosis - Beyond effects on lipid metabolism [J].
Bobik, Alex .
CIRCULATION, 2008, 118 (07) :702-704
[4]  
COETZEE GA, 1986, J BIOL CHEM, V261, P9644
[5]   Proteomic Analysis of Defined HDL Subpopulations Reveals Particle-Specific Protein Clusters Relevance to Antioxidative Function [J].
Davidson, W. Sean ;
Silva, R. A. Gangani D. ;
Chantepie, Sandrine ;
Lagor, William R. ;
Chapman, M. John ;
Kontush, Anatol .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (06) :870-U234
[6]   ATP binding cassette G1-dependent cholesterol efflux during inflammation [J].
de Beer, Maria C. ;
Ji, Ailing ;
Jahangiri, Anisa ;
Vaughan, Ashley M. ;
de Beer, Frederick C. ;
van der Westhuyzen, Deneys R. ;
Webb, Nancy R. .
JOURNAL OF LIPID RESEARCH, 2011, 52 (02) :345-353
[7]   Update on strategies to increase HDL quantity and function [J].
Duffy, Danielle ;
Rader, Daniel J. .
NATURE REVIEWS CARDIOLOGY, 2009, 6 (07) :455-463
[8]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[9]   Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization [J].
Go, AS ;
Chertow, GM ;
Fan, DJ ;
McCulloch, CE ;
Hsu, CY .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (13) :1296-1305
[10]   Investigation of an albumin-enriched fraction of human serum and its albuminome [J].
Gundry, Rebekah L. ;
Fu, Qin ;
Jelinek, Christine A. ;
Van Eyk, Jennifer E. ;
Cotter, Robert J. .
PROTEOMICS CLINICAL APPLICATIONS, 2007, 1 (01) :73-88