LDL particle size in relation to insulin, proinsulin, and insulin sensitivity -: The insulin resistance atherosclerosis study

被引:48
作者
Festa, A
D'Agostino, R
Mykkänen, L
Tracy, RP
Hales, CN
Howard, BV
Haffner, SM
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA
[2] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27109 USA
[3] Univ Vermont, Sch Med, Dept Pathol, Burlington, VT 05405 USA
[4] Medlant Res Inst, Washington, DC USA
[5] Univ Cambridge, Dept Clin Biochem, Cambridge, England
关键词
D O I
10.2337/diacare.22.10.1688
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - LDI particles are heterogeneous in terms of size and density: small dense LDL particles are considered more atherogenic than larger LDL particles. The aim of this study was to investigate the interrelationships among LDL size, insulin, proinsulin (intact and split), and insulin sensitivity in a tri-ethnic population with varying degrees of glucose tolerance (n = 1,549) in the Insulin Resistance Atherosclerosis Study. RESEARCH DESIGN AND METHODS- Insulin sensitivity was assessed by a frequently sampled intravenous glucose tolerance lest with minimal model analysis. Proinsulin levels were measured using highly sensitive assays without detectable cross-reactivity with insulin, and LDL size was determined by gradient-gel electrophoresis. RESULTS - In univariate analyses. LDL size was related to various features of the insulin resistance syndrome, including fasting insulin (r = -0.18), intact proinsulin (r = -0.24), split proinsulin (r = -0.24), the proinsulin-to-insulin ratio (r = -0.14), and insulin sensitivity (r = 0.21; all P < 0.0001). In a multivariate regression model (adjusted for age, BMI, ethnicity, and clinic), triglyceride levels (P = 0.0001), HDL cholesterol (P = 0.0001), sex (P = 0.002), and proinsulin (P = 0.01) were significantly related to LDL size. In the same model stratified by sex, LDL size was significantly inversely related to proinsulin in men (P = 0.005 and P = 0.04 after further adjustment for the glucose tolerance status), but not in women (P > 0.15). CONCLUSIONS - We found an inverse relation of proinsulin to LDL particle size in a large tri-ethnic population with varying degrees of glucose tolerance. This relation was independent of age, BMI, and triglyceride and HDL cholesterol concentrations, and was more pronounced in men than in women.
引用
收藏
页码:1688 / 1693
页数:6
相关论文
共 50 条
  • [1] AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
  • [2] BACHORIK PS, 1960, METHODS ENZ, V129, P78
  • [3] INFLUENCE OF OBESITY, IMPAIRED GLUCOSE-TOLERANCE, AND NIDDM ON LDL STRUCTURE AND COMPOSITION - POSSIBLE LINK BETWEEN HYPERINSULINEMIA AND ATHEROSCLEROSIS
    BARAKAT, HA
    CARPENTER, JW
    MCLENDON, VD
    KHAZANIE, P
    LEGGETT, N
    HEATH, J
    MARKS, R
    [J]. DIABETES, 1990, 39 (12) : 1527 - 1533
  • [4] SEX DIFFERENTIAL IN ISCHEMIC-HEART-DISEASE MORTALITY IN DIABETICS - A PROSPECTIVE POPULATION-BASED STUDY
    BARRETTCONNOR, E
    WINGARD, DL
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 1983, 118 (04) : 489 - 496
  • [5] ASSESSMENT OF INSULIN SENSITIVITY INVIVO
    BERGMAN, RN
    FINEGOOD, DT
    ADER, M
    [J]. ENDOCRINE REVIEWS, 1985, 6 (01) : 45 - 86
  • [6] Insulin resistance and coronary artery disease
    Bressler, P
    Bailey, SR
    Matsuda, M
    DeFronzo, RA
    [J]. DIABETOLOGIA, 1996, 39 (11) : 1345 - 1350
  • [7] BYRNE CD, 1994, DIABETOLOGIA, V37, P889, DOI 10.1007/BF00400944
  • [8] Optimization of glycemic control by insulin therapy decreases the proportion of small dense LDL particles in diabetic patients
    Caixas, A
    OrdonezLlanos, J
    deLeiva, A
    Payes, A
    Homs, R
    Perez, A
    [J]. DIABETES, 1997, 46 (07) : 1207 - 1213
  • [9] LOW-DENSITY-LIPOPROTEIN PARTICLE-SIZE AND CORONARY-ARTERY DISEASE
    CAMPOS, H
    GENEST, JJ
    BLIJLEVENS, E
    MCNAMARA, JR
    JENNER, JL
    ORDOVAS, JM
    WILSON, PWF
    SCHAEFER, EJ
    [J]. ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (02): : 187 - 195
  • [10] Hyperinsulinemia as an independent risk factor for ischemic heart disease
    Despres, JP
    Lamarche, B
    Mauriege, P
    Cantin, B
    Dagenais, GR
    Moorjani, S
    Lupien, PJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (15) : 952 - 957