Elevated serum vascular endothelial growth factor is associated with visceral fat accumulation in human obese subjects
Open accessAbstract
Aims/hypothesis Adipose tissue expresses some bioactive molecules, which may be involved in the development of obesity-associated metabolic disorders and cardiovascular diseases. Vascular endothelial growth factor (VEGF) an important angiogenic factor is implicated in normal and pathological vessel formation. The aim of this study is to investigate clinically the association between blood serum VEGF concentrations and body fat accumulation as well as distribution. The study also aims to show the effect of serum VEGF protein on gene expression of transcriptional factor E26 transformation-specific-1 (Ets-1) and matrix metalloproteinase (MMP)-3.Methods Serum VEGF concentrations were measured in 38 overweight or obese subjects. Fat distribution in the abdominal subcutaneous as well as visceral fat areas was assessed by computed tomography scans at umbilical level. Furthermore, the changes of serum VEGF concentrations following body weight reduction therapy were analyzed in eight subjects recruited from the original pool of subjects. Semi-purified circulating VEGF proteins were obtained by heparin-sepharose and its biological activities were shown to alter gene expressions in human aortic endothelial cells.Results Serum VEGF concentrations were positively correlated with BMI (r=0.433, p=0.007) and visceral fat area (r=0.488, p=0.002). Stepwise regression analysis showed the visceral fat area as the most important determinant factor for VEGF circulating levels. Following body weight reduction therapy, VEGF concentrations as well as visceral fat area were decreased. The serum semi-purified VEGF protein enhanced expressions of Ets-1 and MMP-3 in human aortic endothelial cells.Conclusion/interpretation Increased serum VEGF concentrations associated with visceral fat accumulation could influence vascular endothelial function.
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VEGF is upregulated in adipose tissue of mice fed a high-fat diet for three days, but reports in chronic obesity show both enhanced and reduced VEGF expression.
“For example, VEGF is upregulated in AT of mice fed a HFD for three days, but there are reports of both enhanced and reduced VEGF expression in chronic obesity (3,13,43,44), suggesting that sprouting angiogenesis is activated early and may or may not persist.”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [44]
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References 36 · Cited by 254
- Authors
- Miyazawa-Hoshimoto, S., Takahashi, K., Bujo, H., Hashimoto, N., & Saito, Y.
- Affiliations
- Chiba University (JP)
- Corresponding author
- Takahashi, K.
- Venue
- Diabetologia
- Published
- 2003-11-01
- Volume
- 46
- Issue
- 11
- Pages
- 1483-1488
- ISSN
- 0012-186X (ISSN-L)
- 1432-0428
- OpenAlex
- W2070821645
- Cited by
- 254
- References
- 36
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 10 · 2023: 16 · 2022: 11 · 2021: 10 · 2020: 7 · 2019: 16 · 2018: 14 · 2017: 18 · 2016: 17 · 2015: 13 · 2014: 13 · 2013: 12 · 2012: 15
- FWCI
- 4.91
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Diabetologia (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Keywords
- vascular endothelial growth factor, visceral fat, obesity, body fat distribution, ETS1, matrix metalloproteinase-3, angiogenesis, endothelial function, weight loss, human aortic endothelial cells, adipose tissue
- MeSH terms
- Adipose Tissue, Base Sequence, Female, Gene Expression Regulation, Homeostasis, Humans, Insulin Resistance, Male, Middle Aged, Obesity, Proto-Oncogene Proteins, Regression Analysis, Skin, Tomography, X-Ray Computed, Transcription Factors, Viscera, Body Mass Index, DNA Primers, Matrix Metalloproteinase 3, Reverse Transcriptase Polymerase Chain Reaction, Vascular Endothelial Growth Factor A, Proto-Oncogene Proteins c-ets, Proto-Oncogene Protein c-ets-1
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