Chon Ji-Eun, Semnani-Azad Zhila, Lai Kira Zhi Hua, Connelly Phillip W, Retnakaran Ravi, Harris Stewart B, Metherel Adam H, Jenkins David J A, Bazinet Richard P, Hanley Anthony J
Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.
Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
J Clin Endocrinol Metab. 2025 Apr 22;110(5):1324-1333. doi: 10.1210/clinem/dgae445.
Although preclinical studies have shown a beneficial impact of omega-3 (n-3) polyunsaturated fatty acids (PUFAs) on adipose tissue (AT) inflammation, the current literature from human studies is limited. Therefore, we aimed to evaluate the longitudinal associations of circulating levels of n-3 PUFAs with biomarkers of AT inflammation.
Longitudinal data from participants in the PROMISE cohort (n = 474) were used. AT inflammation was measured using circulating biomarkers at baseline and up to 2 follow-up visits. n-3 PUFAs were measured at baseline in 4 serum lipid fractions. Generalized estimating equations analyses evaluated longitudinal associations between n-3 PUFAs and AT inflammation, adjusting for covariates.
Fully adjusted generalized estimating equation models indicated that higher baseline proportions of eicosapentaenoic acid, n-3 docosapentaenoic acid, and docosahexaenoic acid in total serum were significantly inversely associated with longitudinal change in soluble CD163 (all P < .05). A significant positive association of n-3 docosapentaenoic acid and docosahexaenoic acid with longitudinal change in adiponectin (P < .05) was also observed. Generally consistent associations were observed between n-3 PUFAs and soluble CD163 and adiponectin in the four lipid fractions.
These findings will add to the limited evidence on the potential role n-3 PUFAs have in the prevention and management of AT inflammation in humans and may help inform future interventions targeting chronic inflammation at the level of AT.
尽管临床前研究已表明ω-3(n-3)多不饱和脂肪酸(PUFA)对脂肪组织(AT)炎症有有益影响,但目前来自人体研究的文献有限。因此,我们旨在评估n-3 PUFA循环水平与AT炎症生物标志物之间的纵向关联。
使用了PROMISE队列(n = 474)参与者的纵向数据。在基线和最多2次随访时,使用循环生物标志物测量AT炎症。在基线时测量4种血清脂质组分中的n-3 PUFA。广义估计方程分析评估了n-3 PUFA与AT炎症之间的纵向关联,并对协变量进行了调整。
完全调整后的广义估计方程模型表明,总血清中二十碳五烯酸、n-3二十二碳五烯酸和二十二碳六烯酸的基线比例较高与可溶性CD163的纵向变化显著负相关(所有P <.05)。还观察到n-3二十二碳五烯酸和二十二碳六烯酸与脂联素的纵向变化呈显著正相关(P <.05)。在四种脂质组分中,n-3 PUFA与可溶性CD163和脂联素之间观察到总体一致的关联。
这些发现将补充关于n-3 PUFA在人类AT炎症预防和管理中潜在作用的有限证据,并可能有助于为未来针对AT水平慢性炎症的干预措施提供信息。