Key result
Morbid obesity with low insulin resistance is associated with a 3-fold up-regulation of VEGF-A and MMP9 in adipose tissue compared to lean controls, whereas VEGF-B, VEGF-C, VEGF-D, and MMP15 are down-regulated and correlate with insulin resistance.
Cross-Sectional (n=43)
No
Effect estimate: 3-fold up-regulation
p-value: p=<0.05
Alterations in the expression of VEGF isoforms and metalloproteinases in adipose tissue are associated with the development of insulin resistance in morbidly obese patients.
Hypothesis-generating for VEGF-A/MMP9 in obesity-related insulin resistance; leaves causal role and clinical relevance open.
BACKGROUND: The expansion of adipose tissue is linked to the development of its vasculature, which appears to have the potential to regulate the onset of obesity. However, at present, there are no studies highlighting the relationship between human adipose tissue angiogenesis and obesity-associated insulin resistance (IR). RESULTS: Our aim was to analyze and compare angiogenic factor expression levels in both subcutaneous (SC) and omentum (OM) adipose tissues from morbidly obese patients (n = 26) with low (OB/L-IR) (healthy obese) and high (OB/H-IR) degrees of IR, and lean controls (n = 17). Another objective was to examine angiogenic factor correlations with obesity and IR.Here we found that VEGF-A was the isoform with higher expression in both OM and SC adipose tissues, and was up-regulated 3-fold, together with MMP9 in OB/L-IR as compared to leans. This up-regulation decreased by 23% in OB/-H-IR compared to OB/L-IR. On the contrary, VEGF-B, VEGF-C and VEGF-D, together with MMP15 was down-regulated in both OB/H-IR and OB/L-IR compared to lean patients. Moreover, MMP9 correlated positively and VEGF-C, VEGF-D and MMP15 correlated negatively with HOMA-IR, in both SC and OM. CONCLUSION: We hereby propose that the alteration in MMP15, VEGF-B, VEGF-C and VEGF-D gene expression may be caused by one of the relevant adipose tissue processes related to the development of IR, and the up-regulation of VEGF-A in adipose tissue could have a relationship with the prevention of this pathology.
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Tinahones et al. (2012) conducted a cross-sectional in Morbid obesity and insulin resistance (n=43). Morbid obesity with or without insulin resistance vs. Lean controls was evaluated on VEGF-A gene expression in omentum adipose tissue (3-fold up-regulation, p=<0.05). Morbid obesity with low insulin resistance is associated with a 3-fold up-regulation of VEGF-A and MMP9 in adipose tissue compared to lean controls, whereas VEGF-B, VEGF-C, VEGF-D, and MMP15 are down-regulated and correlate with insulin resistance.
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