Department of Nutrition and Health, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Nutr Rev. 2022 Feb 10;80(3):598-612. doi: 10.1093/nutrit/nuab095.
Dietary fat seems to affect advanced glycation end products (AGEs) and their receptors. This systematic review assesses studies that evaluated the effect of dietary fat on markers of glycation.
The aim of this systematic review was to analyze the effect of dietary fat on markers of glycation and to explore the mechanisms involved.
This study was conducted according to PRISMA guidelines. PubMed, Cochrane, and Scopus databases were searched, using descriptors related to dietary fat, AGEs, and the receptors for AGEs.
Studies were selected independently by the 3 authors. Divergent decisions were resolved by consensus. All studies that evaluated the effects of the quantity and quality of dietary fat on circulating concentrations of AGEs and their receptors in adults and elderly adults with or without chronic diseases were included. Initially, 9 studies met the selection criteria.
Three authors performed data extraction independently. Six studies were included.
Consumption of a Mediterranean diet rich in monounsaturated fatty acids (MUFAs) and low in dietary AGEs reduced serum concentrations of AGEs, reduced expression of the receptor for AGE (RAGE), and increased expression of the AGE receptor 1 (AGER1) when compared with consumption of a Western diet rich in saturated fatty acids and dietary AGEs. Supplementation with omega-3 polyunsaturated fatty acids (PUFAs) resulted in decreased concentrations of fluorescent AGEs and decreased expression of RAGE as well as increased expression of AGER1.
Increased consumption of MUFAs and omega-3 PUFAs and reduced consumption of saturated fatty acids seem to be effective strategies to beneficially affect glycation markers, which in turn may prevent and control chronic diseases.
PROSPERO registration number CRD42021220489.
膳食脂肪似乎会影响晚期糖基化终产物(AGEs)及其受体。本系统评价评估了评估膳食脂肪对糖化标志物影响的研究。
本系统评价的目的是分析膳食脂肪对糖化标志物的影响,并探讨其中涉及的机制。
本研究根据 PRISMA 指南进行。使用与膳食脂肪、AGEs 及其受体相关的描述符,检索了 PubMed、Cochrane 和 Scopus 数据库。
由 3 位作者独立选择研究。存在分歧的决策通过共识解决。所有评估膳食脂肪的数量和质量对患有或不患有慢性疾病的成年人和老年人循环中 AGEs 及其受体浓度影响的研究均被纳入。最初,有 9 项研究符合选择标准。
由 3 位作者独立进行数据提取。共纳入 6 项研究。
与摄入富含饱和脂肪酸和膳食 AGEs 的西方饮食相比,富含单不饱和脂肪酸(MUFAs)和低膳食 AGEs 的地中海饮食可降低血清 AGEs 浓度、降低 AGE 受体(RAGE)的表达并增加 AGE 受体 1(AGER1)的表达。补充ω-3 多不饱和脂肪酸(PUFAs)可降低荧光 AGEs 浓度、降低 RAGE 表达并增加 AGER1 表达。
增加 MUFA 和 ω-3 PUFAs 的摄入量,减少饱和脂肪酸的摄入量,似乎是有益影响糖化标志物的有效策略,进而可能预防和控制慢性疾病。
PROSPERO 注册号 CRD42021220489。