Abstract
Subjects characterized by a predominance of small LDL particles (pattern B) have changes in plasma triglyceride (TG) and HDL-cholesterol concentrations consistent with the presence of resistance to insulin-mediated glucose uptake. To pursue this issue, plasma glucose and insulin responses to oral glucose, insulin-mediated glucose disposal, and lipoprotein concentrations were measured in subjects categorized on the basis of LDL peak diameter measured by gradient gel electrophoresis. Subjects with pattern B had higher (P < 0.05-0.001) total integrated plasma glucose (20.7±1.0 mmol/liter · h) and insulin (1,743±293 pmol/liter · h) responses to oral glucose compared with glucose (16.3±0.4 and 19.2±0.8 mmol/liter · h) and insulin (856±60 and 1,222±168 pmol/liter · h) responses in those with either pattern A or an intermediate pattern. Pattern B individuals were shown to be more insulin resistant on the basis of higher steady state plasma glucose concentrations (SSPG, 10.4±1.0, P < 0.002, vs. 7.5±0.7 and 6.0±0.4 mmol/ liter) after a constant infusion of somatostatin, glucose, and insulin than those with either the intermediate or pattern A subclass. Pattern B subjects also had higher concentrations of (P < 0.001) TG (1.98±0.15 vs. 1.33±0.17 and 0.77±0.05 mmol/liter) and lower (P < 0.01-0.001) HDL cholesterol (1.12±0.06 vs. 1.34±0.05 vs. 1.45±0.05 mmol/liter) than those with either the intermediate or pattern A. Finally, significant (P < 0.001) correlation coefficients existed between LDL diameter and SSPG (r = -0.44); glucose (r = -0.41) and insulin (r = -0.38) responses; TG (r = -0.65) and HDL-cholesterol (r = 0.42) concentrations; and systolic (r = -0.34) and diastolic (r = -0.34) blood pressure. Thus, pattern B subjects are insulin resistant, have higher glucose, insulin, and TG, lower HDL-cholesterol levels, and higher blood pressure than those with pattern A or intermediate.
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Reaven, G. M., Chen, Y. D. I., Jeppesen, J., Maheux, P., & Krauss, R. M. (1993). Insulin resistance and hyperinsulinemia in individuals with small, dense, low density lipoprotein particles. Journal of Clinical Investigation, 92(1), 141–146. https://doi.org/10.1172/jci116541
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