Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
J Nutr Health Aging. 2024 Aug;28(8):100304. doi: 10.1016/j.jnha.2024.100304. Epub 2024 Jun 25.
Diet can modulate systemic inflammation, while inflammation is a critical contributory factor of frailty. However, longitudinal data on the association between dietary inflammatory index (DII) and frailty are limited, and the intermediate mechanisms remain unclear. This study aimed to examine the association between DII and incident frailty and the potential mediating roles of frailty-related biomarkers.
Prospective cohort study.
The Mr. OS and Ms. OS (Hong Kong) study.
A total of 3,035 community-dwelling men and women aged above 65 years without frailty at baseline were included.
DII scores were calculated using the locally validated food frequency questionnaire. Incident frailty at year four was defined using the Fried frailty phenotype. Logistic regression was used to examine the association between DII and frailty onset. Mediation analysis was used to explore the mediating roles of frailty-related biomarkers in the DII-frailty association.
During four years of follow-up, 208 individuals developed frailty. Compared with the lowest tertile of DII, the highest tertile was associated with an increased risk of incident frailty (OR: 1.82; 95% CI: 1.17-2.82; p = 0.008) after adjustment for relevant confounders. The DII-frailty association was significant in men but not in women. Furthermore, increasing serum homocysteine, decreasing serum folate, and reducing estimated glomerular filtration rate (eGFR) mediated 11.6%, 7.1%, and 9.6 % of the total relation between DII and frailty onset, respectively.
In this cohort study, a pro-inflammatory diet was associated with a higher risk of frailty onset, mediated by homocysteine, folate, and renal function.
饮食可以调节全身炎症,而炎症是衰弱的一个关键促成因素。然而,关于饮食炎症指数(DII)与衰弱之间的关联的纵向数据有限,其潜在的中介机制仍不清楚。本研究旨在探讨 DII 与衰弱发生的相关性以及与衰弱相关的生物标志物的潜在中介作用。
前瞻性队列研究。
香港男性和女性老龄化纵向研究(Mr. OS 和 Ms. OS 研究)。
共纳入 3035 名年龄在 65 岁以上、基线时无衰弱的社区居住的男性和女性。
使用经过本地验证的食物频率问卷计算 DII 评分。在第四年发生的衰弱定义为 Fried 衰弱表型。使用逻辑回归检验 DII 与衰弱发病的相关性。采用中介分析探讨与衰弱相关的生物标志物在 DII 与衰弱关联中的中介作用。
在四年的随访期间,208 人出现衰弱。与 DII 最低三分位相比,最高三分位与发生衰弱的风险增加相关(OR:1.82;95%CI:1.17-2.82;p=0.008),校正了相关混杂因素后。DII 与衰弱的关联在男性中显著,但在女性中不显著。此外,血清同型半胱氨酸升高、血清叶酸降低和估算肾小球滤过率(eGFR)降低分别介导了 DII 与衰弱发病之间总关系的 11.6%、7.1%和 9.6%。
在这项队列研究中,促炎饮食与衰弱发病风险增加相关,其机制与同型半胱氨酸、叶酸和肾功能有关。