Do inflammation and procoagulation biomarkers contribute to the metabolic syndrome cluster?

被引:49
作者
Kraja, Aldi T. [1 ]
Province, Michael A. [1 ]
Arnett, Donna [2 ]
Wagenknecht, Lynne [3 ]
Tang, Weihong [4 ]
Hopkins, Paul N. [5 ]
Djousse, Luc [6 ,7 ]
Borecki, Ingrid B. [1 ]
机构
[1] Washington Univ, Sch Med, Div Stat Genom, St Louis, MO 63130 USA
[2] Univ Alabama Birmingham, Dept Epidemiol, Birmingham, AL USA
[3] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27109 USA
[4] Univ Minnesota, Div Epidemiol & Community Hlth, Minneapolis, MN USA
[5] Univ Utah, Hlth Sci Ctr, Dept Internal Med, Salt Lake City, UT USA
[6] Harvard Univ, Sch Med, Boston, MA USA
[7] Brigham & Womens Hosp, Boston, MA 02115 USA
关键词
D O I
10.1186/1743-7075-4-28
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Context: The metabolic syndrome (MetS), in addition to its lipid, metabolic, and anthropomorphic characteristics, is associated with a prothrombotic and the proinflammatory state. However, the relationship of inflammatory biomarkers to MetS is not clear. Objective: To study the association between a group of thrombotic and inflammatory biomarkers and the MetS. Methods: Ten conventional MetS risk variables and ten biomarkers were analyzed. Correlations, factor analysis, hexagonal binning, and regression of each biomarker with the National Cholesterol Education Program (NCEP) MetS categories were performed in the Family Heart Study (n = 2,762). Results: Subjects in the top 75% quartile for plasminogen activator inhibitor-1 (PAII) had a 6.9 CI95 [4.2-11.2] greater odds (p < 0.0001) of being classified with the NCEP MetS. Significant associations of the corresponding top 75% quartile to MetS were identified for monocyte chemotactic protein 1 (MCPI, OR = 2.19), C-reactive protein (CRP, OR = 1.89), interleukin-6 (IL6, OR = 2.11), sICAMI (OR = 1.61), and fibrinogen (OR = 1.86). PAII correlated significantly with all obesity and dyslipidemia variables. CRP had a high correlation with serum amyloid A (0.6) and IL6 (0.51), and a significant correlation with fibrinogen (0.46). Ten conventional quantitative risk factors were utilized to perform multivariate factor analysis. Individual inclusion, in this analysis of each biomarker, showed that, PAII, CRP, IL6, and fibrinogen were the most important biomarkers that clustered with the MetS latent factors. Conclusion: PAII is an important risk factor for MetS. It correlates significantly with most of the variables studied, clusters in two latent factors related to obesity and lipids, and demonstrates the greatest relative odds of the 10 biomarkers studied with respect to the MetS. Three other biomarkers, CRP, IL6, and fibrinogen associate also importantly with the MetS cluster. These 4 biomarkers can contribute in the MetS risk assessment.
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页数:12
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共 55 条
  • [1] Factors of insulin resistance syndrome-related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic Mexican-Americans
    Arya, R
    Blangero, J
    Williams, K
    Almasy, L
    Dyer, TD
    Leach, RJ
    O'Connell, P
    Stern, MP
    Duggirala, R
    [J]. DIABETES, 2002, 51 (03) : 841 - 847
  • [2] Metabolic syndrome accompanied by hypercholesterolemia is strongly associated with proinflammatory state and impairment of fibrinolysis in patients with type 2 diabetes - Synergistic effects of plasminogen activator inhibitor-1 and thrombin-activatable fibrinolysis inhibitor
    Aso, Y
    Wakabayashi, S
    Yamamoto, R
    Matsutomo, R
    Takebayashi, K
    Inukai, T
    [J]. DIABETES CARE, 2005, 28 (09) : 2211 - 2216
  • [3] High-sensitivity C-reactive protein: Clinical importance
    Bassuk, SS
    Rifai, N
    Ridker, PM
    [J]. CURRENT PROBLEMS IN CARDIOLOGY, 2004, 29 (08) : 439 - 493
  • [4] CRP is or is not a reliable marker of ischaemic heart disease?
    Biasucci, LM
    Giubilato, G
    Graziani, F
    Piro, M
    [J]. LUPUS, 2005, 14 (09) : 752 - 755
  • [5] LEVELS OF T-LYMPHOCYTE SUBPOPULATIONS, INTERLEUKIN-1-BETA, AND SOLUBLE INTERLEUKIN-2 RECEPTOR IN ACUTE MYOCARDIAL-INFARCTION
    BLUM, A
    SCLAROVSKY, S
    REHAVIA, E
    SHOHAT, B
    [J]. AMERICAN HEART JOURNAL, 1994, 127 (05) : 1226 - 1230
  • [6] BONEU B, 1997, THROMB HAEMOSTASIS, V159
  • [7] HEXAGON MOSAIC MAPS FOR DISPLAY OF UNIVARIATE AND BIVARIATE GEOGRAPHICAL DATA
    CARR, DB
    OLSEN, AR
    WHITE, D
    [J]. CARTOGRAPHY AND GEOGRAPHIC INFORMATION SYSTEMS, 1992, 19 (04): : 228 - &
  • [8] CLAUSS A., 1957, ACTA HAEMATOL, V17, P237
  • [9] DECLERCK PJ, 1988, BLOOD, V71, P220
  • [10] Lipid and carbohydrate metabolism in mice with a targeted mutation in the IL-6 gene: absence of development of age-related obesity
    Di Gregorio, GB
    Hensley, L
    Lu, T
    Ranganathan, G
    Kern, PA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 287 (01): : E182 - E187