Plasma interleukin-6 is associated with coagulation in poorly controlled patients with Type 2 diabetes

被引:25
作者
Aso, Y
Okumura, K
Yoshida, N
Tayama, K
Kanda, T
Kobayashi, I
Takemura, Y
Inukai, T
机构
[1] Dokkyo Univ, Sch Med, Koshigaya Hosp, Dept Internal Med, Koshigaya, Saitama 3438555, Japan
[2] Kanazawa Med Univ, Dept Gen Med, Kanazawa, Ishikawa, Japan
[3] Gunma Univ, Dept Lab Med, Maebashi, Gumma 371, Japan
关键词
coagulation; D dimer; inflammation; interleukin-6; Type; 2; diabetes;
D O I
10.1046/j.1464-5491.2003.01058.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims We investigated the relationship between interleukin (IL)-6 and coagulation, i.e. whether changes in the plasma IL-6 are associated with those in coagulation markers (D dimer and fibrinogen) after glycaemic control with sulphonylurea or insulin in poorly controlled patients with Type 2 diabetes. Methods We studied 42 patients with Type 2 diabetes, including 19 subsequently treated with sulphonylurea, 23 treated with insulin and 48 control subjects. All patients were in poor glycaemic control and were hospitalized for 3 weeks. At the beginning and end of treatment, we measured plasma concentrations of IL-6, fibrinogen, and D dimer. Results Plasma concentrations of IL-6 and D dimer were significantly higher in diabetic patients than in controls (P < 0.0001 for both). In all patients with diabetes, the plasma concentration of IL-6 decreased significantly (P < 0.001) after treatment. Changes in the plasma IL-6 during hospitalization were positively correlated with those in plasma D dimer and fibrinogen (r = 0.664, P < 0.0001; r = 0.472, P = 0.0042, respectively). Treatment with sulphonylurea or insulin caused a similar fall in the plasma IL-6 concentration with a concomitant decrease in the BMI and an equal improvement in glycaemia. Conclusions In poorly controlled patients with Type 2 diabetes, plasma IL-6 concentrations were reduced significantly even by short-term metabolic control. As changes in the plasma concentrations of D dimer are related to plasma IL-6, plasma IL-6 may reflect a pro-coagulant as well as an inflammatory state in patients with Type 2 diabetes.
引用
收藏
页码:930 / 934
页数:5
相关论文
共 32 条
  • [1] Relationship between soluble thrombomodulin in plasma and coagulation or fibrinolysis in type 2 diabetes
    Aso, Y
    Fujiwara, Y
    Tayama, K
    Takebayashi, K
    Inukai, T
    Takemura, Y
    [J]. CLINICA CHIMICA ACTA, 2000, 301 (1-2) : 135 - 145
  • [2] Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss
    Bastard, JP
    Jardel, C
    Bruckert, E
    Blondy, P
    Capeau, J
    Laville, M
    Vidal, H
    Hainque, B
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (09) : 3338 - 3342
  • [3] THE ACUTE-PHASE RESPONSE
    BAUMANN, H
    GAULDIE, J
    [J]. IMMUNOLOGY TODAY, 1994, 15 (02): : 74 - 80
  • [4] Circadian relationships between interleukin (IL)-6 and hypothalamic-pituitary-adrenal axis hormones: Failure of IL-6 to cause sustained hypercortisolism in patients with early untreated rheumatoid arthritis
    Crofford, LJ
    Kalogeras, KT
    Mastorakos, G
    Magiakou, MA
    Wells, J
    Kanik, KS
    Gold, PW
    Chrousos, GP
    Wilder, RL
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) : 1279 - 1283
  • [5] Danesh J, 2001, CIRCULATION, V103, P2323
  • [6] FIBRINOGEN AS A CARDIOVASCULAR RISK FACTOR - A METAANALYSIS AND REVIEW OF THE LITERATURE
    ERNST, E
    RESCH, KL
    [J]. ANNALS OF INTERNAL MEDICINE, 1993, 118 (12) : 956 - 963
  • [7] Folsom AR, 2001, THROMB HAEMOSTASIS, V86, P366
  • [8] HYPERFIBRINOGENEMIA - AN IMPORTANT RISK FACTOR FOR VASCULAR COMPLICATIONS IN DIABETES
    GANDA, OP
    ARKIN, CF
    [J]. DIABETES CARE, 1992, 15 (10) : 1245 - 1250
  • [9] Gavin JR, 1997, DIABETES CARE, V20, P1183
  • [10] Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction
    Haffner, SM
    Lehto, S
    Rönnemaa, T
    Pyörälä, K
    Laakso, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (04) : 229 - 234