HDL function and subclinical atherosclerosis in juvenile idiopathic arthritis

被引:14
|
作者
Mani, Preethi [1 ]
Uno, Kiyoko [2 ]
MyNgan Duong [3 ]
Wolski, Kathy [2 ]
Spalding, Steven [4 ]
Husni, M. Elaine [4 ]
Nicholls, Stephen J. [3 ]
机构
[1] UT Southwestern Med Ctr, Dept Internal Med, Dallas, TX USA
[2] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44106 USA
[3] Univ Adelaide, South Australian Hlth & Med Res Inst, Adelaide, SA, Australia
[4] Cleveland Clin, Dept Rheumatol, Cleveland, OH 44106 USA
关键词
Arthritis; juvenile; high-density lipoproteins (HDL) cholesterol; atherosclerosis; HIGH-DENSITY-LIPOPROTEIN; INTIMA-MEDIA THICKNESS; CHOLESTEROL EFFLUX CAPACITY; CORONARY-HEART-DISEASE; SYSTEMIC-LUPUS-ERYTHEMATOSUS; FOAM CELL-TRANSFORMATION; RHEUMATOID-ARTHRITIS; CARDIOVASCULAR-DISEASE; OXIDATIVE STRESS; IFN-GAMMA;
D O I
10.3978/j.issn.2223-3652.2015.12.14
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Increasing evidence suggests that inflammation adversely impacts the protective properties of high-density lipoproteins (HDL) and progression of atherosclerosis. The impact of early chronic inflammatory conditions on HDL function and vascular risk has not been well investigated. Methods: We compared measures of HDL particle distribution and functionality, in addition to measures of carotid intima-medial thickness (cIMT) in patients with juvenile idiopathic arthritis (JIA) and age matched controls. Results: JIA patients demonstrated lower levels of HDL cholesterol [47.0 (40.0, 56.0) vs. 56.0 (53.0, 61.0) mg/dL, P=0.04], total HDL [29.5 (27.9, 32.3) vs. 32.9 (31.6, 36.3) mg/dL, P=0.05] and large HDL [5.1 (3.7, 7.3) vs. 8.0 (6.7, 9.7) mg/dL, P=0.04] particles. In association JIA patients demonstrated greater cholesterol efflux mediated via ATP binding cassette A1 (ABCA1) [17.3% (12.8, 19.7) vs. 10.0% (5.8, 16.0), P=0.05] and less efflux mediated via ATP binding cassette G-1 (ABCG1) [3.2% (2.0, 3.9) vs. 4.8% (3.5, 5.8), P=0.01] and SR-B1 [6.9% (6.0, 8.4) vs. 9.1% (8.6, 10.2), P=0.002] compared with controls. Exposure of macrophages to serum from JIA patients resulted in a smaller increase in mRNA expression of ABCA1 (2.0+/-0.95 vs. 7.1+/-5.7 fold increase, P=0.01) and greater increases in expression of ABCG1 [1.4 (0.9, 1.5) vs. 0.8 (0.7, 1.1) fold increase, P=0.04] and SR-B1 (1.3+/-0.47 vs. 0.7+/-0.3 fold increase, P=0.001) compared with controls. Arylesterase (128.9+/-27.6 vs. 152.0+/-45.2 umoles/min/mL, P=0.04) activity and endothelial cell migration (491.2+/-68.9 vs. 634.2+/-227.4 cells/field, P=0.01) were less in JIA patients. No differences in cIMT were observed between JIA patients and controls. Conclusions: The presence of JIA was associated with alterations in HDL particle distribution, cholesterol efflux and non-lipid transporting activities. The ultimate implication of these findings for cardiovascular risk requires further investigation.
引用
收藏
页码:34 / 43
页数:10
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