Uric acid in chronic heart failure: A marker of chronic inflammation

被引:236
作者
Leyva, F
Anker, SD
Godsland, IF
Teixeira, M
Hellewell, PG
Kox, WJ
Poole-Wilson, PA
Coats, AJS
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, Natl Heart & Lung Inst, Dept Cardiac Med, London SW3 6LY, England
[2] Charite Berlin, Franz Volhard Klin, Berlin, Germany
[3] Humboldt Univ, Charite Berlin, Dept Anaesthesiol, Berlin, Germany
关键词
uric acid; chronic heart failure; cytokines; xanthine oxidase activity;
D O I
10.1053/euhj.1998.1188
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Chronic heart failure is associated with hyperuricaemia and elevations in circulating markers of inflammation. Activation of xanthine oxidase, through free radical release, causes leukocyte and endothelial cell activation. Associations could therefore be expected between serum uric acid level, as a marker of increased xanthine oxidase activity, and markers of inflammation. We have explored these associations in patients with chronic heart failure, taking into account the hyperuricaemic effects of diuretic therapy and insulin resistance. Methods and Results Circulating uric acid and markers of inflammation were measured in 39 male patients with chronic heart failure and 16 healthy controls. All patients underwent a metabolic assessment, which provided a measure of insulin sensitivity (intravenous glucose tolerance tests and minimal modelling analysis). Compared to controls, patients with chronic heart failure had significantly higher levels of circulating uric acid, interleukin-6, soluble tumour necrosis factor receptor (sTNFR)-1, soluble intercellular adhesion molecule-1 (ICAM-1, all P < 0.001), E-selectin and sTNFR2 (both P < 0.05). In patients with chronic heart failure, serum uric acid concentrations correlated with circulating levels of sTNFR1 (r = 0.74), interleukin-6 (r = 0.66), sTNFR2 (r = 0.63), TNF alpha (r = 0.60) (all P < 0.001), and ICAM-1 (r = 0.41, P < 0.01). In stepwise regression analyses, serum uric acid emerged as the strongest predictor of ICAM-1, interleultin-6, TNF, sTNFR1 and sTNFR2, independent of diuretic dose, age, body mass index, alcohol intake, serum creatinine,plasma insulin and glucose, and insulin sensitivity. Conclusions Serum uric acid is strongly related to circulating markers of inflammation in patients with chronic heart failure. This is consistent with a role for increased xanthine oxidase activity in the inflammatory response in patients with chronic heart failure.
引用
收藏
页码:1814 / 1822
页数:9
相关论文
共 70 条
  • [1] SENSITIVE, PRECISE RADIOIMMUNOASSAY OF SERUM-INSULIN RELYING ON CHARCOAL SEPARATION OF BOUND AND FREE HORMONE MOIETIES
    ALBANO, JDM
    EKINS, RP
    TURNER, RC
    MARITZ, G
    [J]. ACTA ENDOCRINOLOGICA, 1972, 70 (03): : 487 - +
  • [2] Anker SD, 1997, EUR HEART J, V18, P259
  • [3] Relation between serum uric acid and lower limb blood flow in patients with chronic heart failure
    Anker, SD
    Leyva, F
    PooleWilson, PA
    Kox, WJ
    Stevenson, JC
    Coats, AJS
    [J]. HEART, 1997, 78 (01) : 39 - 43
  • [4] Tumour necrosis factor alpha as a predictor of impaired peak leg blood flow in patients with chronic heart failure
    Anker, SD
    Volterrani, M
    Egerer, KR
    Felton, CV
    Kox, WJ
    Poole-Wilson, PA
    Coats, AJS
    [J]. QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS, 1998, 91 (03): : 199 - 203
  • [5] Elevated soluble CD 14 receptors and altered cytokines in chronic heart failure
    Anker, SD
    Egerer, KR
    Volk, HD
    Kox, WJ
    PooleWilson, PA
    Coats, AJS
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1997, 79 (10) : 1426 - &
  • [6] Anker SD, 1997, CIRCULATION, V96, P526
  • [7] Uric acid as independent predictor of impaired prognosis in patients with chronic heart failure
    Anker, SD
    Leyva, F
    Poole-Wilson, PA
    Coats, AJS
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (02) : 154A - 155A
  • [8] ASHRAF M, 1993, J SUBMICR CYTOL PATH, V25, P293
  • [9] BECKER BF, 1987, TOPICS PERSPECTIVES, P209
  • [10] BECKER BF, 1997, P 2 INT M WORK GROUP, P10