Corley J, Shivappa N, Hébert J R, Starr J M, Deary I J
Dr Janie Corley, Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, 7 George Square, Edinburgh, EH8 9JZ, Scotland, UK. Phone: +44-131-650-1683. Email:
J Nutr Health Aging. 2019;23(7):628-636. doi: 10.1007/s12603-019-1221-y.
Chronic low-grade inflammation is a key underlying mechanism in several age-related chronic conditions and previous studies have shown that diet can modulate the inflammatory process. We investigated the ability of the Dietary Inflammatory Index (DII®), a summary measure of dietary inflammatory potential, to predict concentrations of plasma inflammatory markers in a sample of older people.
Cross-sectional and 3-year follow-up analysis of Lothian Birth Cohort 1936 (LBC1936) study data.
Baseline data collection occurred between 2004 and 2007 in Edinburgh, Scotland.
Men and women (n 928, age ~70 at baseline) living in Edinburgh and surrounding regions who are surviving participants of the Scottish Mental Survey of 1947.
Energy-adjusted DII (E-DII) scores at age 70 (derived from a food-frequency questionnaire), plasma concentrations of inflammatory biomarkers at age 70 (C-reactive protein (CRP), fibrinogen) and age 73 (CRP, fibrinogen, hs-CRP, Interleukin-6 (IL-6)). Analyses were performed using multivariable logistic regression adjusting for age, sex, smoking, body mass index, physical activity, and hypercholesterolaemia.
Higher E-DII scores (pro-inflammatory diet) were associated with increased odds of elevated CRP (>3mg/L) at age 70 (OR 1.12; 95% CI: 1.02, 1.24, P = 0.02), and elevated IL-6 (>1.6pg/ml) at age 73 (OR 1.11; 95% CI: 1.00, 1.23, P = 0.04), but not with fibrinogen.
These results are consistent with the ability of the DII to predict inflammatory biomarker concentrations and suggest that diet plays a role in the regulation of inflammation, even after controlling for potential confounders. This validation study provides support for using the DII in research among older populations.
慢性低度炎症是几种与年龄相关的慢性疾病的关键潜在机制,先前的研究表明饮食可调节炎症过程。我们调查了饮食炎症指数(DII®)(一种饮食炎症潜能的综合指标)预测老年人群样本中血浆炎症标志物浓度的能力。
对洛锡安出生队列1936(LBC1936)研究数据进行横断面和3年随访分析。
2004年至2007年期间在苏格兰爱丁堡进行基线数据收集。
居住在爱丁堡及其周边地区的男性和女性(n = 928,基线时年龄约70岁),他们是1947年苏格兰精神调查的幸存参与者。
70岁时的能量调整DII(E-DII)得分(源自食物频率问卷),70岁时炎症生物标志物的血浆浓度(C反应蛋白(CRP)、纤维蛋白原)以及73岁时的(CRP、纤维蛋白原、高敏CRP、白细胞介素-6(IL-6))。分析采用多变量逻辑回归,对年龄、性别、吸烟、体重指数、身体活动和高胆固醇血症进行校正。
较高的E-DII得分(促炎饮食)与70岁时CRP升高(>3mg/L)几率增加相关(OR 1.12;95%CI:1.02,1.24,P = 0.02),以及73岁时IL-6升高(>1.6pg/ml)相关(OR 1.11;95%CI:1.00,1.23,P = 0.04),但与纤维蛋白原无关。
这些结果与DII预测炎症生物标志物浓度的能力一致,并表明即使在控制潜在混杂因素后,饮食在炎症调节中也起作用。这项验证研究为在老年人群研究中使用DII提供了支持。