Key result
BAR2 Glu allele linked to ~43% higher visceral fat in women vs Gln/Gln homozygotes.
Why the study?
The BAR2 Gln27Glu polymorphism may be associated with male-type adiposity in women and increased cardiovascular risk, but its relationship with visceral fat and coronary intima thickness was unclear.
Does the BAR2 Gln27Glu polymorphism affect visceral fat accumulation and coronary intima thickness in women?
Cross-Sectional (n=112)
No
Does the BAR2 Gln27Glu polymorphism affect visceral fat accumulation and coronary intima thickness in women?
Absolute Event Rate: 689% vs 481%
p-value: p=0.023
The Glu allele of the BAR2 gene is associated with increased visceral fat accumulation in young to middle-aged women, but not with preclinical atherosclerosis.
BACKGROUND: The beta2-adrenergic receptor (BAR2) is the main lipolytic receptor in white human adipose tissue. There is a functional glutamine 27 glutamic acid (Gln27Glu, rs 1042714) polymorphism in its gene, which has been variably associated with body mass index. This gene variant may be associated with male-type adiposity in women and thus increased cardiovascular risk. We investigated whether the BAR2 Gln27Glu polymorphism is associated with visceral fat and coronary intima thickness in women. METHODS: The amount of mesenteric and omental fat was directly measured and anthropometric measurements were done from 112 forensic autopsy cases of women aged 15 to 49 years. The thickness of the coronary intima, which reflects the severity of atherosclerosis, was measured by computerized image analysis. The BAR2 Gln27Glu polymorphism was determined by polymerase chain reaction. RESULTS: We found that the amount of visceral fat was significantly higher in women with the Glu allele (689 +/- 555 g) compared to Gln/Gln homozygotes (481 +/- 392 g, P = 0.023). The waist-hip ratio also tended to be higher in women with the Glu allele compared to Gln/Gln homozygotes (p = 0.050). There were no statistically significant differences between the genotype groups in BMI or the thickness of coronary intima. CONCLUSION: The Glu allele of the BAR2 gene may be a risk factor for visceral fat accumulation in young to middle-aged women. However, this polymorphism was not associated with preclinical atherosclerosis.
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Kunnas et al. (2009) conducted a cross-sectional in Visceral fat accumulation (n=112). BAR2 Gln27Glu polymorphism (Glu allele) vs. Gln/Gln homozygotes was evaluated on Amount of mesenteric and omental fat (g) (p=0.023). Women carrying the Glu allele of the BAR2 gene had significantly higher amounts of visceral fat (689 g vs 481 g, p=0.023) compared to Gln/Gln homozygotes.
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