School of Life and Environmental Sciences, Faculty of Science, The University of Sydney, Sydney, New South Wales, Australia.
Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Deakin University, Geelong, Victoria, Australia.
Adv Nutr. 2022 Oct 2;13(5):1930-1946. doi: 10.1093/advances/nmac060.
The global population is living longer; however, not everyone ages at the same rate with regard to their physical and cognitive abilities and their vulnerability to certain diseases and death. This review aimed to synthesize the contribution of biological age-predictive biomarkers to nutrition research and highlight the implications for future research and clinical practice. MEDLINE, CINAHL, and Cochrane CENTRAL were systematically searched on 30 September 2021 for randomized controlled trials and cross-sectional studies examining the association between nutrition and biological age in older adults reporting on genetic, clinical, or molecular biomarkers of biological aging. Cochrane's ROB 2 and ROBINS-I were used to assess the quality of included studies. Synthesis was undertaken narratively. Of 1245 records identified from the search, 13 studies from 8 countries and territories, involving 5043 participants, were included. Seven studies assessed associations between nutrient food intake and telomere attrition, reporting protective effects for branched-chain amino acids, calcium and vitamin D, and a diet of a lower inflammatory index; whereas they found shorter telomeres in people consuming more processed foods and arachidonic acid and other proinflammatory compounds. Five studies examined the associations between plasma nutrition biomarkers and cognitive function, and found a protective effect for HDL cholesterol, lycopene, carotenoids, ω-3 and ω-6 fatty acids, and vitamins B, C, D, and E; whereas trans fatty acids and fibrinogen correlated with a decline in cognitive function. One study used Horvath's clock and reported the epigenetic rejuvenation effect of a Mediterranean diet. In conclusion, biological aging was negatively associated with an anti-inflammatory diet. However, a few studies did not control for the confounding effect of other lifestyle factors. Future research should address this and also assess the synergistic effect of different nutrients, their combinations, and evaluate their dose-response relations. Nutrition practice can incorporate updated screening procedures for older people that include relevant biological aging nutrition markers, leading to anti-aging precision nutrition therapy. The methodology of this systematic review was registered in PROSPERO (CRD42021288122).
全球人口的寿命正在延长;然而,并非每个人的身体和认知能力以及对某些疾病和死亡的易感性都以相同的速度衰老。本综述旨在综合生物年龄预测生物标志物对营养研究的贡献,并强调其对未来研究和临床实践的意义。于 2021 年 9 月 30 日,系统地检索了 MEDLINE、CINAHL 和 Cochrane CENTRAL,以查找检查营养与报告生物老化遗传、临床或分子生物标志物的老年人生物学年龄之间关联的随机对照试验和横断面研究。使用 Cochrane 的 ROB 2 和 ROBINS-I 来评估纳入研究的质量。综合采用叙述性方法进行。从检索中确定了 1245 条记录,其中包括来自 8 个国家和地区的 13 项研究,涉及 5043 名参与者。有 7 项研究评估了营养素食物摄入与端粒损耗之间的关联,报告了支链氨基酸、钙和维生素 D 以及炎症指数较低的饮食具有保护作用;而他们发现食用更多加工食品和花生四烯酸和其他促炎化合物的人端粒较短。有 5 项研究检查了血浆营养生物标志物与认知功能之间的关联,发现高密度脂蛋白胆固醇、番茄红素、类胡萝卜素、ω-3 和 ω-6 脂肪酸以及维生素 B、C、D 和 E 具有保护作用;而反式脂肪酸和纤维蛋白原与认知功能下降相关。有一项研究使用 Horvath 的时钟报告了地中海饮食的表观遗传年轻化效应。总之,生物衰老与抗炎饮食呈负相关。然而,一些研究没有控制其他生活方式因素的混杂影响。未来的研究应该解决这个问题,还应该评估不同营养素、它们的组合的协同作用,并评估它们的剂量反应关系。营养实践可以将包含相关生物衰老营养标志物的老年人更新筛查程序纳入其中,从而实现抗衰老精准营养治疗。本系统评价的方法已在 PROSPERO(CRD42021288122)中注册。