Department of Food, Environmental and Nutritional Sciences (DeFENS), Division of Human Nutrition, Università degli Studi di Milano, Milano, Italy.
Geriatria, Accettazione Geriatrica e Centro di Ricerca per l'Invecchiamento, IRCCS INRCA, Ancona, Italy.
BMC Geriatr. 2024 Aug 24;24(1):707. doi: 10.1186/s12877-024-05272-y.
Older subjects are at risk of elevated intestinal permeability (IP) which can lead to immune system activation and low-grade systemic inflammation. Dietary changes are a potential strategy to reduce IP. The MaPLE project evaluated the hypothesis that increasing (poly)phenol intake would beneficially impact on several important markers and pathways related to IP. The objective of the present study was to assess the effects of the MaPLE (poly)phenol-rich diet (PR-diet) on additional IP-related biomarkers and any relationships between biomarker responses.
A randomised, controlled, crossover study was performed involving 51 participants (≥ 60 y) with increased IP, as determined by serum zonulin levels. Participants were randomly assigned to one of two intervention groups: a control diet (C-diet) or a PR-diet. Each intervention lasted 8 weeks and was separated by an 8-week washout period. For the present study, serum and faecal samples were used to measure zonula occludens-1 (ZO-1), occludin, adiponectin, calprotectin, faecal calprotectin, soluble cluster of differentiation 14 (sCD14), interleukin-6 receptor (IL-6R), and vascular endothelial-cadherin (VEC) levels using quantitative ELISA assays. Data were analysed using ANOVA, and Spearman and network correlation analysis were performed to identify the relationship among biomarkers at baseline.
Among the different markers analysed, a significant reduction was observed for faecal and serum calprotectin (p = 0.0378 and p = 0.0186, respectively) following the PR-diet, while a significant increase in ZO-1 was found (p = 0.001) after both the intervention periods (PR-diet and C-diet). In addition, a time effect was observed for VEC levels showing a reduction (p = 0.038) following the PR-diet. Based on network correlation analysis, two clusters of correlations were identified: one cluster with high levels of serum calprotectin, faecal calprotectin, sCD14, interleukin (IL)-6, tumor necrosis factor (TNF)-α, C-reactive protein (CRP) and bacterial DNAemia (16 S rRNA gene copies), with potential inflammatory-induced intestinal permeability. Differently, the other cluster had high levels of serum occludin, IL-6R, soluble intercellular adhesion molecule-1 (sICAM-1) and VEC, with potential inflammatory-induced endothelial dysfunction.
Overall, this study provides further support to the hypothesis that a (poly)phenol-rich diet may help to ameliorate intestinal permeability-associated conditions. In this regard, calprotectin might represent a promising biomarker since it is a protein that typically increases with age and it is considered indicative of intestinal and systemic inflammation. Further research is needed to develop targeted (poly)phenol-rich diets against age-related gut dysfunction and inflammation.
28/04/2017; ISRCTN10214981; https://doi.org/10.1186/ISRCTN10214981 .
老年人易发生肠道通透性(IP)升高,这可能导致免疫系统激活和低度全身炎症。饮食改变是降低 IP 的一种潜在策略。MaPLE 项目评估了增加(多)酚摄入量将如何有益地影响与 IP 相关的几个重要标志物和途径的假设。本研究的目的是评估 MaPLE(多)酚丰富饮食(PR-饮食)对其他 IP 相关生物标志物的影响,以及生物标志物反应之间的任何关系。
进行了一项随机、对照、交叉研究,涉及 51 名血清 zonulin 水平升高的 IP 患者(≥60 岁)。参与者被随机分配到两个干预组之一:对照组(C-饮食)或 PR-饮食。每个干预持续 8 周,间隔 8 周洗脱期。本研究使用定量 ELISA 检测血清和粪便样本中的紧密连接蛋白-1(ZO-1)、occludin、脂联素、钙卫蛋白、粪便钙卫蛋白、可溶性 CD14(sCD14)、白细胞介素-6 受体(IL-6R)和血管内皮钙黏蛋白(VEC)水平。使用方差分析进行数据分析,并进行 Spearman 和网络相关分析,以确定基线时生物标志物之间的关系。
在分析的不同标志物中,PR-饮食后粪便和血清钙卫蛋白显著降低(p=0.0378 和 p=0.0186),而 ZO-1 在两种干预期间均显著增加(p=0.001)。此外,VEC 水平观察到时间效应,PR-饮食后降低(p=0.038)。基于网络相关分析,确定了两个相关性簇:一个簇与血清钙卫蛋白、粪便钙卫蛋白、sCD14、白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α、C 反应蛋白(CRP)和细菌 DNAemia(16S rRNA 基因拷贝)水平较高相关,具有潜在的炎症诱导的肠道通透性。不同的是,另一个簇具有较高的血清封闭蛋白、IL-6R、可溶性细胞间黏附分子-1(sICAM-1)和 VEC 水平,具有潜在的炎症诱导的内皮功能障碍。
总的来说,这项研究进一步支持了富含(多)酚的饮食可能有助于改善与肠道通透性相关的情况的假设。在这方面,钙卫蛋白可能是一种很有前途的生物标志物,因为它是一种随着年龄增长而通常增加的蛋白质,被认为是肠道和全身炎症的标志物。需要进一步研究开发针对与年龄相关的肠道功能障碍和炎症的靶向富含(多)酚的饮食。
2017 年 4 月 28 日;ISRCTN8300532;https://doi.org/10.1186/ISRCTN8300532。