Vnitr Lek 2003, 49(7):535-540

[Microvascular reactivity in type 2 diabetes mellitus and its relation to IGF-I and its binding proteins].

M Krsek, M Prázný, J Skrha, V Justová, Z Lacinová, T Haas
III. interní klinika 1. lékarské fakulty UK a VFN, Praha.

BACKGROUND: AND AIM: System of insulin-like growth factor-I (IGF-I) and its binding proteins (IGFBP) may be involved in the pathogenesis of vascular damage in Type 2 diabetes. Aim of the study was to analyse the relationship between this system and microvascular reactivity in Type 2 diabetes as measured by laser-Doppler flowmetry.

METHODS AND RESULTS: Thirteen Type 2 diabetic patients (8 women and 5 men) with microangiopathy and fifteen healthy subjects (8 women and 7 men) were examined clinically, underwent laser-Doppler flowmetry and intima-media thickness measurements. Fasting serum levels of IGF-I, IGFBP and lipids were examined. Percentage perfusion increase in the test with postocclusive reactive hyperaemia (PORH) as well as in that with thermal hyperaemia (TH) were significantly decreased in Type 2 diabetic patients (p < 0.05). Maximal perfusion after heating (THmax) was lower in Type 2 diabetic patients. Reaction of microcirculation after heating (THmax/t) was slower in Type 2 diabetic patients (p < 0.001). The changes in microvascular reactivity didn't significantly correlate with any of measured parameters of IGF-I/IGFBP system.

CONCLUSIONS: Microvascular reactivity is impaired in Type 2 diabetic patients. The function of microcirculation is not significantly related to the particular parameters of the IGF-I/IGFBP system.

Keywords: Diabetes Mellitus, Type 2, blood, ; Diabetic Angiopathies, physiopathology, ; Female; Humans; Insulin-Like Growth Factor Binding Proteins, blood, ; Insulin-Like Growth Factor I, analysis, ; Laser-Doppler Flowmetry; Male; Microcirculation, physiology, ; Middle Aged

Published: July 1, 2003  Show citation

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Krsek M, Prázný M, Skrha J, Justová V, Lacinová Z, Haas T. [Microvascular reactivity in type 2 diabetes mellitus and its relation to IGF-I and its binding proteins]. Vnitr Lek. 2003;49(7):535-540.
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