HDL function and subclinical atherosclerosis in juvenile idiopathic arthritis

被引:15
|
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
相关论文
共 50 条
  • [31] MRI Findings in Hip in Juvenile Idiopathic Arthritis
    Ostrowska, Monika
    Gietka, Piotr
    Manczak, Malgorzata
    Michalski, Emil
    Sudol-Szopinska, Iwona
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (22)
  • [32] Humoral responses against HDL are linked to lipoprotein traits, atherosclerosis, inflammation and pathogenic pathways during early arthritis stages
    Rodriguez-Carrio, Javier
    Alperi-Lopez, Mercedes
    Lopez, Patricia
    Perez-alvarez, angel, I
    Robinson, George A.
    Alonso-Castro, Sara
    Amigo-Grau, Nuria
    Atzeni, Fabiola
    Suarez, Ana
    RHEUMATOLOGY, 2023, 62 (08) : 2898 - 2907
  • [33] Management of juvenile idiopathic arthritis
    Sujata Sawhney
    The Indian Journal of Pediatrics, 2002, 69 (10) : 893 - 897
  • [34] MRI in Juvenile Idiopathic Arthritis and Juvenile Dermatomyositis
    Gardner-Medwin, Janet Mary McCrae
    Irwin, Greg
    Johnson, Karl
    MRI AND ULTRASOUND IN DIAGNOSIS AND MANAGEMENT OF RHEUMATOLOGICAL DISEASES, 2009, 1154 : 52 - 83
  • [35] Hemorheological parameters are related to subclinical atherosclerosis in systemic lupus erythematosus and rheumatoid arthritis patients
    Santos, Maria Jose
    Pedro, Luis Mendes
    Canhao, Helena
    Fernandes e Fernandes, Jose
    da Silva, Jose Canas
    Fonseca, Joao Eurico
    Saldanha, Carlota
    ATHEROSCLEROSIS, 2011, 219 (02) : 821 - 826
  • [36] Biologicals in Juvenile Idiopathic Arthritis
    Saini, Isha
    Dawman, Lesa
    Gupta, Neerja
    Kabra, S. K.
    INDIAN PEDIATRICS, 2016, 53 (03) : 260 - 261
  • [37] Audiovestibular function in patients with juvenile idiopathic arthritis (JIA)
    El-Gharib, Amani Mohamed
    El-Barbary, Amal Mohamad
    Aboelhawa, Marwa Ahmed
    Elkholy, Radwa Mostafa
    ACTA OTO-LARYNGOLOGICA, 2016, 136 (10) : 1058 - 1063
  • [38] τhe Antioxidant Function of HDL in Atherosclerosis
    Xepapadaki, Eva
    Zvintzou, Evangelia
    Kalogeropoulou, Christina
    Filou, Serafoula
    Kypreos, Kyriakos E.
    ANGIOLOGY, 2020, 71 (02) : 112 - 121
  • [39] Sexual function in female juvenile idiopathic arthritis patients
    Pitta, Ana Claudia
    Viola Ferreira, Gabriela Ribeiro
    Tomioka, Renato Bussadori
    Rodrigues Lourenco, Daniela Mencaroni
    Kozu, Katia
    Aikawa, Nadia Emi
    Elias Sallum, Adriana Maluf
    Arruda Campos, Lucia Maria
    Najjar Abdo, Carmita Helena
    Rodrigues Pereira, Rosa Maria
    Baracat, Edmund Chada
    Bonfa, Eloisa
    Silva, Clovis Artur
    ADVANCES IN RHEUMATOLOGY, 2019, 59 (1) : 13
  • [40] The detection of subclinical synovitis by ultrasound in oligoarticular juvenile idiopathic arthritis: a pilot study
    Haslam, Kirsty E.
    McCann, Liza J.
    Wyatt, Susan
    Wakefield, Richard J.
    RHEUMATOLOGY, 2010, 49 (01) : 123 - 127