Serum ferritin as a component of the insulin resistance syndrome

被引:253
作者
Fernández-Real, JM
Ricart-Engel, W
Arroyo, E
Balançá, R
Casamitjana-Abella, R
Cabrero, D
Fernández-Castañer, M
Soler, J
机构
[1] Hosp Girona, Dept Endocrinol, Endocrinol Sect, Girona 17007, Spain
[2] Hosp Girona, Dept Biochem, Girona 17007, Spain
[3] Hosp Clin Barcelona, Hormonal Lab, Barcelona, Spain
[4] Hosp Llobregat, Bellvitge Hosp, Serv Endocrinol, Barcelona, Spain
关键词
D O I
10.2337/diacare.21.1.62
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - In epidemiological studies, serum ferritin was the second-strongest determinant of blood glucose (after BMI) in regression models and the third-strongest determinant of serum insulin (after BMI and age). Its concentration also correlated positively with plasma triglycerides and apolipoprotein B concentrations, and negatively with HDL2 cholesterol. We hypothesized that serum ferritin could be a marker of insulin resistance. RESEARCH DESIGN AND METHODS - Oral glucose tolerance and insulin sensitivity (S-1, minimal model method) were prospectively evaluated in 36 healthy subjects. The relationship between serum ferritin and metabolic control (as measured by HbA(1c) levels) was also studied in 76 consecutive NIDDM patients. RESULTS - In healthy subjects, log-transformed serum ferritin (LOGFER) correlated with basal serum glucose (r = 0.44, P = 0.007), but not with BMI, age, systolic or diastolic blood pressure, total cholesterol, VLDL cholesterol, HDL cholesterol, total triglycerides, VLDL triglycerides, serum insulin, or HbA(1c) (all P = NS). Identical results were obtained when the two lowest quartiles of serum ferritin were evaluated separately However, in the two highest quartiles, LOGFER correlated with BMI (0.50, P = 0.02), diastolic blood pressure (r = 0.8, P < 0.0001), serum LDL cholesterol (r = 0.57, P = 0.01), VLDL cholesterol (r = 0.48, P = 0.03), total cholesterol and HDL2 and HDL3 subfractions of HDL cholesterol (r = -0.68, -0.76, -0.55, P = 0.001, <0.0001, and 0.01, respectively), total triglycerides (r = 0.60, P = 0.006), HDL2/HDL3 quotient (P = -0.71, P = 0.001), VLDL triglycerides (r = 0.65, P = 0.004), and serum uric acid (r = 0.51, P = 0.03), but not with systolic blood pressure (r = 0.38, P = 0.15). After adjusting for BMI, only the correlations between LOGFER and diastolic blood pressure (r = 0.7, P = 0.002) and HDL2/HDL3 quotient (r = -0.63, P = 0.01) remained significant. Strong correlations between LOGFER and glucose area under the curve during oral glucose tolerance test (Pearson's r = 0.73, P = 0.001) and S-1 (r = -0.68, P = 0.001), which remained significant after controlling for BMI, were observed. LOGFER (beta = -0.44, P = 0.01) and BMI (beta = -0.52, P = 0.004) constituted independent predictors of insulin sensitivity in a multivariate analysis (R-2 = 0.68). In 76 consecutive NIDDM outpatients, serum glucose (P < 0.00001) and LOGFER (P = 0.03) independently predicted the value of HbA(1c) (R-2 = 0.40) in a multiple linear regression analysis. CONCLUSIONS - The correlations among serum ferritin and diastolic blood pressure, HDL quotient, glucose area under the curve, and S-1 suggest that serum ferritin could be a marker of the insulin resistance syndrome. Serum ferritin may also be an independent determinant of poor metabolic control in the diabetic patient.
引用
收藏
页码:62 / 68
页数:7
相关论文
共 48 条
  • [1] DIETARY IRON INTAKE AND RISK OF CORONARY-DISEASE AMONG MEN
    ASCHERIO, A
    WILLETT, WC
    RIMM, EB
    GIOVANNUCCI, EL
    STAMPFER, MJ
    [J]. CIRCULATION, 1994, 89 (03) : 969 - 974
  • [2] BARENBROCK M, 1993, CLIN NEPHROL, V40, P241
  • [3] EQUIVALENCE OF THE INSULIN SENSITIVITY INDEX IN MAN DERIVED BY THE MINIMAL MODEL METHOD AND THE EUGLYCEMIC GLUCOSE CLAMP
    BERGMAN, RN
    PRAGER, R
    VOLUND, A
    OLEFSKY, JM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (03) : 790 - 800
  • [4] Clinical and biochemical abnormalities in people heterozygous for hemochromatosis
    Bulaj, ZJ
    Griffen, LM
    Jorde, LB
    Edwards, CQ
    Kushner, JP
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (24) : 1799 - 1805
  • [5] CATALANO C, 1996, DIABETES S2, V45, pA323
  • [6] INSULIN-RESISTANCE AND HYPERINSULINEMIA IN HOMOZYGOUS BETA-THALASSEMIA
    CAVALLOPERIN, P
    PACINI, G
    CERUTTI, F
    BESSONE, A
    CONDO, C
    SACCHETTI, L
    PIGA, A
    PAGANO, G
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1995, 44 (03): : 281 - 286
  • [7] INSULIN RELEASE AND PERIPHERAL SENSITIVITY AT THE ORAL GLUCOSE-TOLERANCE TEST
    CEDERHOLM, J
    WIBELL, L
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 1990, 10 (02) : 167 - 175
  • [8] COOK JD, 1976, BLOOD, V48, P449
  • [9] INSULIN RESISTANCE AND IRON OVERLOAD
    DANDONA, P
    HUSSAIN, MAM
    VARGHESE, Z
    POLITIS, D
    FLYNN, DM
    HOFFBRAND, AV
    [J]. ANNALS OF CLINICAL BIOCHEMISTRY, 1983, 20 (MAR) : 77 - 79
  • [10] IRON-RELATED DAMAGE IN ACUTE ISCHEMIC STROKE
    DAVALOS, A
    FERNANDEZREAL, JM
    RICART, W
    SOLER, S
    MOLINS, A
    PLANAS, E
    GENIS, D
    [J]. STROKE, 1994, 25 (08) : 1543 - 1546