BACKGROUND: Inadequate inflammation resolution may contribute to persistent low-grade inflammation that accompanies many chronic conditions. Resolution of inflammation is an active process driven by Specialized Pro-resolving Mediators (SPM) that derive from long chain n-3 and n-6 fatty acids. This study examined plasma SPM in relation to sex differences, lifestyle and a broad range cardiovascular disease (CVD) risk factors in 978, 27-year olds from the Australian Raine Study. METHODS: Plasma SPM pathway intermediates (18-HEPE, 17-HDHA and 14-HDHA), and SPM (E- and D-series resolvins, PD1, MaR1) and LTB(4) were measured by liquid chromatography-tandem mass spectrometry (LCMSMS). Pearson correlations and multiple regression analyses assessed relationships between SPM and CVD risk factors. Unpaired t-tests or ANOVA assessed the effect of sex, smoking, unhealthy alcohol consumption and obesity on SPM. RESULTS: Women had higher 17-HDHA (pâ=â0.01) and lower RvE1 (pâ<â0.0001) and RvD1 (pâ=â0.05) levels compared with men. In univariate analysis, obesity associated with lower RvE1 (pâ=â0.002), whereas smoking (pâ<â0.001) and higher alcohol consumption (pâ<â0.001) associated with increased RvE1. In multiple regression analysis, plasma RvE1 was negatively associated with a range of measures of adiposity including BMI, waist circumference, waist-to-height ratio, abdominal subcutaneous fat volume, and skinfold thicknesses in both men and women. CONCLUSION: This population study suggests that a deficiency in plasma RvE1 may occur in response to increasing adiposity. This observation could be relevant to ongoing inflammation that associates with CVD and other chronic diseases.
Adiposity associates with lower plasma resolvin E1 (Rve1): a population study.
肥胖与血浆中 resolvin E1 (Rve1) 降低相关:一项人群研究
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作者:Barden Anne, Shinde Sujata, Beilin Lawrence J, Phillips Michael, Adams Leon, Bollmann Steffen, Mori Trevor A
| 期刊: | International Journal of Obesity | 影响因子: | 3.800 |
| 时间: | 2024 | 起止号: | 2024 May;48(5):725-732 |
| doi: | 10.1038/s41366-024-01482-x | 研究方向: | 其它 |
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