Key result
Higher monocyte CD11b expression is linked to increased adipose tissue inflammation and altered metabolism.
Cross-Sectional (n=17)
At a given degree of adiposity, metabolic and cardiovascular risk varies markedly between individuals. Animal studies suggest that differentially expressed systemic activation of monocytes contributes to the obesity-associated risk variability. We tested the hypothesis that systemic monocyte activation is associated with changes in adipose tissue and skeletal muscle metabolism. In 17 obese hypertensive patients, we assessed CD11b expression on circulating monocytes, gene expression in adipose tissue biopsies, and obtained blood samples and adipose tissue and skeletal muscle microdialysis samples in the fasted state and during a glucose load. Patients were stratified into groups with higher and lower CD11b expression on monocytes. Expression of the macrophage marker CD68 was increased markedly in adipose tissue of subjects with higher CD11b expression. Although no differences in systemic insulin sensitivity were found between both groups, patients with higher peripheral CD11b expression showed a markedly augmented increase in dialysate glucose in adipose tissue during oral glucose tolerance testing and increased adipose tissue lipolysis as well. Our data demonstrate that human monocyte activation is associated with tissue-specific changes in glucose and lipid metabolism. These findings may be explained in part by monocyte/macrophage infiltration of adipose tissue, which appears to interfere with insulin responsiveness.
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Boschmann et al. (2005) conducted a cross-sectional in Obesity and Hypertension (n=17). Higher CD11b expression on monocytes vs. Lower CD11b expression on monocytes was evaluated on Adipose tissue and skeletal muscle metabolism and CD68 expression. In 17 obese hypertensive patients, higher monocyte CD11b expression was associated with markedly increased adipose tissue CD68 expression, lipolysis, and dialysate glucose during OGTT.
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