Comparison of risk factors of macrovascular complications - Peripheral vascular disease, cerebral vascular disease, and coronary heart disease in Japanese Type 2 diabetes mellitus patients

被引:23
作者
Asakawa, H [1 ]
Tokunaga, K [1 ]
Kawakami, F [1 ]
机构
[1] Itami City Hosp, Dept Endocrinol & Metab, Itami, Hyogo 6648540, Japan
关键词
fibrinogen; thrombin-antithrombin III complex; lipoprotein (a); macroangiopathy; a risk factor;
D O I
10.1016/S1056-8727(00)00092-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although macroangiopathies such as peripheral vascular disease (PVD), cerebral Vascular disease (CVD), and coronary heart disease (CHD) can often be observed in patients with diabetes mellitus, they are not specific for diabetes mellitus. Moreover, it is unclear whether their progressive mechanism is different. In the present study, we compared the risk factors among the diabetic macrovascular complications. Univariate analyses showed that in all patients, age at examination, duration of diabetes, thrombin-antithrombin III complex (TAT) level, fibrinogen level, lipoprotein (a) (Lp(a)) level, total cholesterol (T-Chol) level, and existence of microagiopathy were risk factors for PVD. Age, duration of diabetes, insulin level, TAT level, fibrinogen level, HDL cholesterol (HDL-Chol) level, hypertension, and nephropathy were risk factors for CVD. Only fibrinogen level was a risk factor for CHD. Moreover, Lp(a) level was a risk factor for PVD and CVD in male patients, but not in females. On the other hand, insulin level was a risk factor for CVD in female patients, but not in males. Multivariate analyses showed that TAT level, T-Chol level, and neuropathy were independent variables for PVD and that age, TAT level, and HDL-Chol level were independent variables for CVD. On the other hand, only fibrinogen level was the independent variable far CHD in males. Our results suggest that the progressive mechanism of PVD and CVD might be different from that of CHD and might differ according to gender in Japanese diabetic patients. (C) 2000 Elsevier Science Inc. All rights reserved.
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页码:307 / 313
页数:7
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