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将生物年龄、表观遗传时钟和端粒长度整合到慢性病管理的精准营养策略中:潜在框架与当前挑战。

Integrating biological age, epigenetic clocks, and telomere length in precision nutrition strategies for chronic disease management: Potential frameworks and ongoing challenges.

作者信息

Carvalho Beatriz G, Ribeiro Amanda A, da Mota Jhulia C N L, Carvalho Lucas M, Nicoletti Carolina F

机构信息

Applied Physiology and Nutrition Research Group - School of Physical Education and Sport and Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil; Center of Lifestyle Medicine, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil.

Applied Physiology and Nutrition Research Group - School of Physical Education and Sport and Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil; Center of Lifestyle Medicine, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil; Rheumatology Division, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, Sao Paulo, Brazil.

出版信息

Nutr Res. 2025 Aug;140:135-160. doi: 10.1016/j.nutres.2025.06.010. Epub 2025 Jun 29.

Abstract

Precision nutrition is emerging as a transformative strategy for optimizing health, particularly in the context of biological aging and chronic disease prevention. This review aims to examine how biological age markers-specifically telomere length and epigenetic clocks-can be integrated into precision nutrition frameworks to personalize interventions, enhance chronic disease management, and support healthy aging. Telomere length is a widely studied biomarker of aging and chronic disease risk, while epigenetic clocks, based on DNA methylation patterns, offer complementary insights into biological age, gene expression, and disease susceptibility. Nutritional interventions rich in antioxidants, omega-3 fatty acids, polyphenols, B vitamins, and anti-inflammatory compounds have shown potential to modulate these biomarkers, supporting cellular health and delaying aging processes. In addition, lifestyle factors such as physical activity, stress management, and adequate sleep play critical roles in maintaining telomere integrity and epigenetic stability. However, challenges remain in translating these biomarkers into clinical practice. Importantly, variability is not the only barrier; most of these biomarkers still lack clinical validation, and there is no consensus on standardized protocols or reference values that would support their routine application in healthcare. Current guidelines recommend combining telomere length and epigenetic age with other molecular markers, such as multi-omics data, within integrative biological age assessment approaches. Nevertheless, translating this approach into clinical practice will require overcoming significant limitations, including the validation of biomarkers, standardization of measurement techniques, cost-effectiveness, and the development of clear clinical guidelines. Continued research is essential to confirm their predictive value and practical utility in precision nutrition strategies aimed at promoting healthy aging and preventing chronic diseases.

摘要

精准营养正在成为一种优化健康的变革性策略,尤其是在生物衰老和慢性病预防的背景下。本综述旨在探讨生物年龄标志物——特别是端粒长度和表观遗传时钟——如何能够整合到精准营养框架中,以实现个性化干预、加强慢性病管理并支持健康衰老。端粒长度是一种被广泛研究的衰老和慢性病风险生物标志物,而基于DNA甲基化模式的表观遗传时钟则为生物年龄、基因表达和疾病易感性提供了补充性见解。富含抗氧化剂、omega-3脂肪酸、多酚、B族维生素和抗炎化合物的营养干预已显示出调节这些生物标志物的潜力,有助于维持细胞健康并延缓衰老过程。此外,身体活动、压力管理和充足睡眠等生活方式因素在维持端粒完整性和表观遗传稳定性方面起着关键作用。然而,将这些生物标志物转化为临床实践仍面临挑战。重要的是,变异性并非唯一障碍;这些生物标志物大多仍缺乏临床验证,对于支持其在医疗保健中常规应用的标准化方案或参考值也没有达成共识。当前指南建议在综合生物年龄评估方法中,将端粒长度和表观遗传年龄与其他分子标志物(如多组学数据)相结合。尽管如此,将这种方法转化为临床实践将需要克服重大限制,包括生物标志物的验证、测量技术的标准化、成本效益以及明确临床指南的制定。持续的研究对于确认它们在旨在促进健康衰老和预防慢性病的精准营养策略中的预测价值和实际效用至关重要。

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