Severe hypertriglyceridemia with insulin resistance is associated with systemic inflammation: Reversal with bezafibrate therapy in a randomized controlled trial

被引:135
作者
Jonkers, IJ
Mohrschladt, MF
Westendorp, RG
van der Laarse, A
Smelt, AH
机构
[1] Leiden Univ, Med Ctr, Dept Gen Internal Med, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Cardiol, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1016/S0002-9343(01)01123-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PURPOSE: To determine whether hypertriglyceridemia is associated with systemic inflammation, which may contribute to the increased cardiovascular risk in patients who have hypertriglyceridernia. In addition, we investigated whether fibrates reverse this inflammatory state. PATIENTS AND METHODS: Serum lipid levels, body mass index, insulin resistance, and inflammatory parameters were compared between 18 patients who had severe hypertriglyceridemia without cardiovascular disease and 20 normolipidemic controls. We measured the ex vivo production capacity of tumor necrosis factor (TNF)-alpha and interleukin (IL)-6 after whole-blood stimulation with lipopolysaccharide, as well as circulating levels of C-reactive protein and fibrinogen. A randomized controlled trial was conducted to determine whether bezafibrate (400 mg administered daily for 6 weeks) affected these parameters in hypertriglyceridemic patients. RESULTS: When compared with normolipidemic controls, hypertriglyceridemic patients had significantly lower high-density lipoprotein (HDL) cholesterol and higher triglyceride levels, body mass index, and insulin resistance. In addition, hypertriglyceridemic patients had a significantly higher production capacity of TNF-alpha (mean difference, 11 700 pg/mL; 95% confidence interval [CI]: 7800 to 15 700 pg/mL]) and IL-6 (mean difference, 20 400 pg/mL; 95% CI: 7800 to 32 900 pg/mL), and higher levels of C-reactive protein (mean difference, 0.8 mg/L; 95% CI: 0.1 to 2.4 mg/L) and fibrinogen (mean difference, 0.8 g/dL; 95% CI: 0.3 to 1.3 g/dL). Bezafibrate therapy significantly increased HDL cholesterol levels, reduced triglyceride and insulin resistance levels, and reduced production capacity of TNF-alpha and IL-6, as well as levels of C-reactive protein and fibrinogen. CONCLUSION: Systemic inflammation is present in patients who have the clinical phenotype that is associated with severe hypertriglyceridemia, and may contribute to the increased risk of cardiovascular disease in these patients. Bezafibrate has anti-inflammatory effects in these patients. (C)2002 by Excerpta Medica, Inc.
引用
收藏
页码:275 / 280
页数:6
相关论文
共 38 条
  • [1] Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study
    Albert, MA
    Danielson, E
    Rifai, N
    Ridker, PM
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01): : 64 - 70
  • [2] [Anonymous], HUMAN CYTOKINES THEI
  • [3] Hypertriglyceridemia as a cardiovascular risk factor
    Austin, MA
    Hokanson, JE
    Edwards, KL
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1998, 81 (4A) : 7B - 12B
  • [4] FIBRINOLYSIS IN HYPERTRIGLYCERIDEMIC SUBJECTS IN RESPONSE TO VENOUS OCCLUSION
    AVELLONE, G
    DIGARBO, V
    CORDOVA, R
    RANELI, G
    DESIMONE, R
    BOMPIANI, GD
    [J]. BLOOD COAGULATION & FIBRINOLYSIS, 1993, 4 (03) : 429 - 433
  • [5] HIGH-DENSITY-LIPOPROTEINS INHIBIT CYTOKINE-INDUCED EXPRESSION OF ENDOTHELIAL-CELL ADHESION MOLECULES
    COCKERILL, GW
    RYE, KA
    GAMBLE, JR
    VADAS, MA
    BARTER, PJ
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (11) : 1987 - 1994
  • [6] Cortellaro M, 2000, THROMB HAEMOSTASIS, V83, P549
  • [7] DE GD, 1992, CYTOKINE, V4, P239
  • [8] Not acute but chronic hypertriglyceridemia is associated with impaired endothelium-dependent vasodilation - Reversal after lipid-lowering therapy by atorvastatin
    de Man, FH
    Weverling-Rijnsburger, AWE
    van der Laarse, A
    Smelt, AHM
    Jukema, JW
    Blauw, GJ
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (03) : 744 - 750
  • [9] Peroxisome proliferator-activated receptor α negatively regulates the vascular inflammatory gene response by negative cross-talk with transcription factors NF-κB and AP-1
    Delerive, P
    De Bosscher, K
    Besnard, S
    Vanden Berghe, W
    Peters, JM
    Gonzalez, FJ
    Fruchart, JC
    Tedgui, A
    Haegeman, G
    Staels, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) : 32048 - 32054
  • [10] The PPAR alpha-leukotriene B-4 pathway to inflammation control
    Devchand, PR
    Keller, H
    Peters, JM
    Vazquez, M
    Gonzalez, FJ
    Wahli, W
    [J]. NATURE, 1996, 384 (6604) : 39 - 43