School of Health Sciences, College of Health Medicine and Wellbeing, The University of Newcastle, Callaghan, NSW 2308, Australia.
Hunter Medical Research Institute (HMRI) Food and Nutrition Research Program, HMRI, New Lambton Heights, NSW 2305, Australia.
Nutrients. 2023 May 21;15(10):2405. doi: 10.3390/nu15102405.
Evidence suggests that diet can play a role in modulating systemic inflammation. This study aims to examine the relationship between fatty acids (FAs) (self-reported dietary intake and red blood cell (RBC) membrane fatty acid concentrations), three diet quality scores, and the plasma concentrations of inflammatory markers (interleukin-6, IL-6; tumour necrosis factor alpha, TNF-α; and C-reactive protein, CRP) in a group of Australian adults ( = 92). Data were collected on their demographic characteristics, health status, supplement intake, dietary intake, RBC-FAs and plasma inflammatory markers over a nine-month period. Mixed-effects models were used to determine the relationship between RBC-FAs, dietary intake of FAs, diet quality scores and inflammatory markers to determine which variable most strongly predicted systemic inflammation. A significant association was identified between dietary saturated fat intake and TNF-α (β = 0.01, < 0.05). An association was also identified between RBC membrane saturated fatty acids (SFA) and CRP (β = 0.55, < 0.05). Inverse associations were identified between RBC membrane monounsaturated fatty acids (MUFAs) (β = -0.88, < 0.01), dietary polyunsaturated fatty acids (PUFAs) (β = -0.21, < 0.05) and CRP, and the Australian Eating Survey Modified Mediterranean Diet (AES-MED) score and IL-6 (β = -0.21, < 0.05). In summary, using both objective and subjective measures of fat intake and diet quality, our study has confirmed a positive association between saturated fat and inflammation, while inverse associations were observed between MUFAs, PUFAs, the Mediterranean diet, and inflammation. Our results provide further evidence that manipulating diet quality, in particular fatty acid intake, may be useful for reducing chronic systemic inflammation.
有证据表明,饮食可以在调节全身炎症中发挥作用。本研究旨在探讨澳大利亚成年人(n=92)体内脂肪酸(FA)(自我报告的饮食摄入和红细胞(RBC)膜脂肪酸浓度)、三种饮食质量评分与炎症标志物(白细胞介素-6,IL-6;肿瘤坏死因子α,TNF-α;C 反应蛋白,CRP)之间的关系。在九个月的时间里,收集了他们的人口统计学特征、健康状况、补充剂摄入、饮食摄入、RBC-FA 和血浆炎症标志物的数据。混合效应模型用于确定 RBC-FA、FA 饮食摄入、饮食质量评分和炎症标志物之间的关系,以确定哪个变量最能预测全身炎症。饮食中饱和脂肪摄入与 TNF-α之间存在显著相关性(β=0.01,<0.05)。RBC 膜饱和脂肪酸(SFA)与 CRP 之间也存在相关性(β=0.55,<0.05)。RBC 膜单不饱和脂肪酸(MUFA)(β=-0.88,<0.01)、饮食多不饱和脂肪酸(PUFA)(β=-0.21,<0.05)与 CRP 呈负相关,澳大利亚饮食调查改良地中海饮食(AES-MED)评分与 IL-6 呈负相关(β=-0.21,<0.05)。总之,本研究使用脂肪摄入和饮食质量的客观和主观测量方法,证实了饱和脂肪与炎症之间存在正相关,而 MUFA、PUFA、地中海饮食与炎症之间存在负相关。我们的研究结果提供了进一步的证据,表明通过调整饮食质量,特别是脂肪酸摄入,可能有助于减少慢性全身炎症。