Muscle capillary basement membrane width in patients with vacor-induced diabetes mellitus

• Published in: The Journal of clinical investigation Vol. 78; no. 1; pp. 102 - 107
• Main Authors: FEINGOLD, K. R, TAI HEE LEE, MIN YOUNG CHUNG, SIPERSTEIN, M. D
• Format: Journal Article
• Language: English
• Published: Ann Arbor, MI American Society for Clinical Investigation 01.07.1986
• Subjects: Adult; Basement Membrane - ultrastructure; Biological and medical sciences; Capillaries - ultrastructure; Diabetes Mellitus - chemically induced; Diabetes Mellitus, Type 1 - pathology; Diabetic Retinopathy - complications; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Female; Glycated Hemoglobin A - analysis; Humans; Male; Medical sciences; Microcirculation; Muscles - blood supply; Phenylurea Compounds - adverse effects; Proteinuria - complications; Tumors. Hypoglycemia; Endocrinopathy; Human; Secondary; Toxicity; Diabetes mellitus; Etiopathogenesis; Rodenticide; Capillary tube; Basement membrane; Hyperglycemia; Microangiopathy; Ultrastructure; Poisoning; Muscle; Morphometry
• ISSN: 0021-9738; 1558-8238
• DOI: 10.1172/JCI112537

Muscle capillary basement membrane width is a sensitive marker for the presence of diabetic microangiopathy. Studies have indicated that genetic factors and alterations in glucose metabolism influence muscle capillary basement membrane width. To define the role of these factors we have measured muscle capillary basement membrane thickness in controls, insulin dependent diabetics, and individuals with diabetes secondary to the ingestion of Vacor, a rat poison, which results in hyperglycemia. Hemoglobin A1 concentrations were increased in both diabetic groups, but hemoglobin A1 levels and the duration of diabetes were similar in the two diabetic groups. The muscle capillary basement membrane width was increased to a similar extent in the insulin-dependent diabetics (control, 1,781 +/- 46 vs. IDD, 2,287 +/- 144 A, P less than 0.001) and in the Vacor diabetic group (2,320 +/- 149 A, P less than 0.001). In the insulin-dependent diabetic group, 63% of the patients had a muscle capillary basement membrane width greater than two standard deviations above the mean of the controls, while in the Vacor diabetic group this figure was 56%. Despite the relatively short duration of diabetes (6.2 +/- 0.3 yr), 44% of the Vacor diabetic patients had retinopathy and 28% had proteinuria. The present study provides strong evidence that even in the absence of genetic diabetes mellitus, hyperglycemia or some other abnormality related to insulin lack can cause microvascular changes.