The levels of MDA-LDL in circulating immune complexes predict myocardial infarction in the VADT study

被引:38
作者
Lopes-Virella, Maria F. [1 ,2 ]
Hunt, Kelly J. [1 ,2 ]
Baker, Nathaniel L. [1 ]
Virella, Gabriel [3 ]
Moritz, Thomas [4 ]
机构
[1] Med Univ S Carolina, Dept Med, Charleston, SC 29425 USA
[2] Ralph A Johnson VA Med Ctr, Charleston, SC USA
[3] Coordinating Ctr, Hines VA Cooperat Studies Program CSP, Hines, IL USA
[4] Med Univ S Carolina, Dept Microbiol & Immunol, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
Modified LDL immune complexes; Oxidized LDL; Malondialdehyde-modified LDL; Type; 2; diabetes; Cardiovascular disease; Myocardial infarction; Biomarkers of plaque instability; Modified LDL capture assays; MALONDIALDEHYDE-MODIFIED LDL; CORONARY-ARTERY-DISEASE; LOW-DENSITY-LIPOPROTEIN; INTIMA-MEDIA THICKNESS; OXIDIZED LDL; ATHEROSCLEROTIC PLAQUES; HUMAN MACROPHAGES; MONOCYTIC CELLS; AUTOANTIBODIES; INFLAMMATION;
D O I
10.1016/j.atherosclerosis.2012.08.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Circulating immune complexes (IC) containing modified forms of LDL (mLDL) are strongly pro-inflammatory and strong predictors of cardiovascular disease (CVD) progression in type 1 diabetes. The present study was undertaken to determine whether the levels of oxidized LDL (oxLDL), malondialdehyde-LDL (MDA-LDL) and advanced glycation end products-LDL (AGE-LDL) in IC predict incident CVD events in type 2 diabetes (VADT cohort). Methods and results: Levels of mLDL in IC were measured in 907 patients of the VADT cohort, a median of two years after entry into the study. Participants were followed for an average of 3.7 years for vascular outcomes. Hazard ratios (HRs) for CV endpoints in relation to mLDL-IC quartiles were calculated by Cox proportional hazard models. The primary composite CVD endpoint included documented myocardial infarction (MI); stroke; death from CVD; congestive heart failure; cardiac, cerebrovascular, or peripheral VD surgical intervention; inoperable CVD; and amputation for ischemic gangrene. During follow-up, 4.7% and 16.8% of participants had an MI or a composite endpoint, respectively. After adjustments by conventional risk factors, individuals in the highest quartile of MDA-LDL-IC were at higher risk of MI [HR = 2.44 (95% CI: 1.03, 5.77)] and composite endpoint [HR = 1.71 (95% CI: 1.04, 2.80)], relative to individuals in the lowest quartile. Similar comparisons for oxLDL and AGE-LDL levels yielded HR values of 1.08 and 1.31 for MI and 0.91 and 1.34 for composite endpoint. Conclusions: Our study indicates that high levels of MDA-LDL in isolated IC predict future MI and acute CV events in patients with type 2 diabetes. Published by Elsevier Ireland Ltd.
引用
收藏
页码:526 / 531
页数:6
相关论文
共 30 条
[1]   Design of the cooperative study on glycemic control and complications in diabetes mellitus type 2 Veterans Affairs Diabetes Trial [J].
Abraira, C ;
Duckworth, W ;
McCarren, M ;
Emanuele, N ;
Arca, D ;
Reda, D ;
Henderson, W .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2003, 17 (06) :314-322
[2]  
ADA, 2000, DIABETES CARE, V23, pS32
[3]  
De Boer OJ, 1999, J PATHOL, V188, P174, DOI 10.1002/(SICI)1096-9896(199906)188:2<174::AID-PATH333>3.0.CO
[4]  
2-3
[5]   Oxidized LDL immune complexes and oxidized LDL differentially affect the expression of genes involved with inflammation and survival in human U937 monocytic cells [J].
Hammad, Samar M. ;
Twal, Waleed O. ;
Barth, Jeremy L. ;
Smith, Kent J. ;
Saad, Antonio F. ;
Virella, Gabriel ;
Argraves, W. Scott ;
Lopes-Virella, Maria F. .
ATHEROSCLEROSIS, 2009, 202 (02) :394-404
[6]   LOCALIZATION OF LYMPHOCYTES-T AND MACROPHAGES IN FIBROUS AND COMPLICATED HUMAN ATHEROSCLEROTIC PLAQUES [J].
HANSSON, GK ;
JONASSON, L ;
LOJSTHED, B ;
STEMME, S ;
KOCHER, O ;
GABBIANI, G .
ATHEROSCLEROSIS, 1988, 72 (2-3) :135-141
[7]   Mechanisms of disease - Inflammation, atherosclerosis, and coronary artery disease [J].
Hansson, GK .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (16) :1685-1695
[8]   Oxidized LDL and malondialdehyde-modified LDL in patients with acute coronary syndromes and stable coronary artery disease [J].
Holvoet, P ;
Vanhaecke, J ;
Janssens, S ;
Van de Werf, F ;
Collen, D .
CIRCULATION, 1998, 98 (15) :1487-1494
[9]   MALONDIALDEHYDE-MODIFIED LOW-DENSITY LIPOPROTEINS IN PATIENTS WITH ATHEROSCLEROTIC DISEASE [J].
HOLVOET, P ;
PEREZ, G ;
ZHAO, Z ;
BROUWERS, E ;
BERNAR, H ;
COLLEN, D .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2611-2619
[10]   The relationship between oxidized LDL and other cardiovascular risk factors and subclinical CVD in different ethnic groups: The Multi-Ethnic Study of Atherosclerosis (MESA) [J].
Holvoet, Paul ;
Jenny, Nancy S. ;
Schreinerc, Pamela J. ;
Tracy, Russell P. ;
Jacobs, David R. .
ATHEROSCLEROSIS, 2007, 194 (01) :245-252