Risk Factor Analyses for Macrovascular Complication in Nonobese NIDDM Patients: Multiclinical Study for Diabetic Macroangiopathy (MSDM)

Author:

Ito Hideki1,Harano Yutaka2,Suzuki Masaaki2,Hattori Yuichi3,Takeuchi Makoto4,Inada Hiroshi5,Inoue Junichiro1,Kawamori Ryuzo6,Murase Toshio7,Ouchi Yasuyoshi8,Umeda Fumio9,Nawata Hajime9,Orimo Hajime,

Affiliation:

1. Endocrinology Section, Tokyo Metropolitan Geriatric Hospital Tokyo

2. Atherosclerosis and Metabolism Section, the National Cardiovascular Center Osaka

3. Department of Applied Mathematics, Faculty of Science, Konan University Kobe

4. Kobe City College of Technology Kobe

5. Research Institute, the National Cardiovascular Center Osaka

6. Department of Endocrinology and Metabolism, Faculty of Medicine, Jyuntendo University Tokyo

7. Metabolism Section, Toranomon Hospital Tokyo

8. Department of Geriatric Medicine, Faculty of Medicine, Tokyo University Tokyo

9. The 3rd Department of Internal Medicine, Faculty of Medicine, Kyushu University Fukuoka, Japan

Abstract

To examine the characteristic features of risk factors for macroangiopathy (MA) in nonobese Japanese NIDDM patients, 899 NIDDM patients with and without MA were registered from 40 facilities. Of these, 386 subjects were identified as having any form of MA (total MA); these included 211 with ischemie heart disease (IHD), 163 with cerebrovascular disease (CVD), and 77 with peripheral vascular disease (PVD). Univariate analyses revealed the following common risk factors for total MA, IHD, CVD, and PVD: age, hypertension, systolic blood pressure (sBP) or diastolic blood pressure (dBP), duration of diabetes, diabetic microangiopathy (retinopathy, nephropathy, and neuropathy), low HDL cholesterol level, and higher LDL cholesterol/HDL cholesterol ratio. Additional significant risk factors for specific conditions were also identified, respectively, as male sex for total MA, IHD, and PVD, smoking for IHD and PVD, and high fasting plasma glucose level for total MA and CVD. With stepwise multivariate logistic regression analysis, older age, duration of diabetes, smoking, and low LDL cholesterol/HDL cholesterol ratio were identified as significant and independent risk factors for total MA, IHD, CVD, and PVD. Other risk factors identified were high dBP for IHD, CVD, and PVD, high sBP for total MA, and low BMI for PVD. These results clearly demonstrated that duration of diabetes, smoking, hypertension, and dyslipidemia are major risk factors for MA in NIDDM patients. Since the mean BMI was similar for both groups (∼23 kg/m2) and there were no significant differences in immunoreactive insulin levels before and after 75-g oral glucose challenge testing, obesity and hyperinsulinism at the time of the analyses were not considered to play an important role for the pathogenesis of MA in Japanese NIDDM patients. By using the χ2 test, cutoff points were determined for six of the most commonly measured risk factors. The cutoff point was the level beyond which a significantly higher prevalence of MA occurred. The cutoff points (rounded slightly upward in some cases) for fasting plasma glucose, sBP, dBP, serum total cholesterol level, serum triglyceride level, and BMI were 140 mg/dl, 140 mmHg, 80 mmHg, 180 mg/dl, 120 mg/dl, and 23 kg/m2, respectively. When these cutoff points were used as control criteria, the prevalence of MA was significantly lower in subjects whose risk factor measurements remained under the proposed control criteria for four or more of the six variables. In conclusion, in nonobese NIDDM patients, age, hypertension, and dyslipidemia were found to be risk factors for MA. Duration of diabetes was also demonstrated as an independent risk factor, indicating the close association of deranged glucose metabolism with the pathogenesis of MA in NIDDM patients. It seems to be crucial to control these risk factors for the prevention of MA in NIDDM patients.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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