Department of Epidemiology and Biostatistics, School of Public Health, Tianjin Medical University, Tianjin, China; Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China; Center for International Collaborative Research on Environment, Nutrition and Public Health, Tianjin, China.
Public Health Science and Engineering College, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Clin Nutr. 2024 Apr;43(4):943-950. doi: 10.1016/j.clnu.2024.02.022. Epub 2024 Feb 22.
BACKGROUND & AIMS: Evidence on the association between dietary inflammation and longevity is limited. We aimed to examine the association of a low-inflammatory diet with mortality and longevity, and to explore whether cardiometabolic diseases (CMDs) and lifestyle factors may play a role in this association.
Within the UK Biobank, 188,443 participants aged 39-72 years (mean 56.07) were followed for up to 16 years to detect survival status from the death registry. At baseline, dietary intake was assessed with a 24-h dietary record. An inflammatory diet index (IDI) was calculated as weighted sum of 31 food groups (including 14 anti-inflammatory and 17 pro-inflammatory) based on plasma high-sensitivity C-reactive protein levels, and tertiled as low, moderate, and high IDI scores. Baseline lifestyle beyond diet was assessed by summing the number of healthy lifestyle factors (i.e., never smoking, regular physical activity, and normal BMI) and categorized as unfavorable (≤1) and favorable (≥2). Presence of CMDs was defined as having any one of type 2 diabetes, ischemic heart disease, atrial fibrillation, heart failure, and stroke. Data were analyzed using Cox regression, Laplace regression, and generalized structural equation modelling.
During the follow-up (median 9.79 years, interquartile range: 9.68-10.57 years), 9178 (4.9%) participants died. In multi-adjusted Cox regression models, a low-inflammatory diet (i.e. low IDI score) was associated with lower risk of all-cause mortality [hazard ratio (HR) = 0.82, 95% confidence interval (CI): 0.78 to 0.86]. Laplace regression analysis showed that the multi-adjusted 10th percentile difference (10th PD, 95% CI) of death time was delayed by 0.80 (0.55, 1.06; P < 0.001) years for participants with a low IDI score compared to those with a high IDI score. In mediation analysis, 21.48% of the association between IDI and mortality was mediated by CMDs. In joint effect analysis, participants with a low IDI score and favorable lifestyle had a 42% lower risk of death (HR = 0.58, 95% CI: 0.54, 0.62) compared to those with a high IDI score and unfavorable lifestyle. There was a significant additive interaction between low IDI score and favorable lifestyle on decreased mortality.
A low-inflammatory diet is associated with a lower risk of death and could prolong survival time. CMDs may partially mediate the IDI-mortality association. A favorable lifestyle beyond diet may augment the positive effect of a low-inflammatory diet on longevity.
关于饮食炎症与长寿之间关联的证据有限。我们旨在研究低炎症饮食与死亡率和长寿之间的关联,并探讨心脏代谢疾病(CMD)和生活方式因素是否在此关联中起作用。
在英国生物银行中,188443 名年龄在 39-72 岁(平均 56.07 岁)的参与者接受了长达 16 年的随访,以从死亡登记处检测生存状态。在基线时,通过 24 小时饮食记录评估饮食摄入。根据血浆高敏 C 反应蛋白水平,炎症饮食指数(IDI)被计算为 31 种食物组(包括 14 种抗炎和 17 种促炎)的加权总和,并分为低、中、高 IDI 评分 tertile。通过将健康生活方式因素(即从不吸烟、定期进行体育锻炼和正常 BMI)的数量相加来评估基线时的生活方式,并分为不利(≤1)和有利(≥2)两类。CMD 的存在定义为患有任何一种 2 型糖尿病、缺血性心脏病、心房颤动、心力衰竭和中风。使用 Cox 回归、Laplace 回归和广义结构方程模型进行数据分析。
在随访期间(中位数 9.79 年,四分位间距:9.68-10.57 年),9178 名(4.9%)参与者死亡。在多因素调整的 Cox 回归模型中,低炎症饮食(即低 IDI 评分)与全因死亡率降低相关[风险比(HR)=0.82,95%置信区间(CI):0.78-0.86]。Laplace 回归分析表明,与高 IDI 评分相比,低 IDI 评分参与者的死亡时间的多因素调整第 10 个百分位数差异(10th PD,95%CI)延迟了 0.80 年(0.55-1.06;P<0.001)。在中介分析中,IDI 与死亡率之间的关联有 21.48%通过 CMD 进行介导。在联合效应分析中,与高 IDI 评分和不利生活方式相比,低 IDI 评分和有利生活方式的参与者死亡风险降低了 42%(HR=0.58,95%CI:0.54-0.62)。低 IDI 评分和有利生活方式之间存在显著的相加交互作用,可降低死亡率。
低炎症饮食与死亡率降低相关,并可能延长生存时间。CMD 可能部分介导了 IDI 与死亡率之间的关联。饮食以外的有利生活方式可能会增强低炎症饮食对长寿的积极影响。