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The association between lutein and zeaxanthin intake and multi-level biological aging

叶黄素 玉米黄质 生物途径 生物 转录组 类胡萝卜素 内科学 内分泌学 医学 生理学 食品科学 生物化学 基因表达 基因
作者
Meiyi Tao,Lin Zhang,Chun‐Lei Jiang,Xiang Jia,Shipeng Chen,Songwen Tan,Shengli Sun
出处
期刊:Frontiers in Nutrition [Frontiers Media]
卷期号:12: 1618158-1618158 被引量:1
标识
DOI:10.3389/fnut.2025.1618158
摘要

Objective This study investigates the potential association between lutein and zeaxanthin (LZ) intake, particularly lutein, and biological aging. The study aims to explore how LZ intake affects the biological aging progression, particularly in organs like the liver, kidneys, and cardiovascular system, and explore the potential mechanism of lutein as the main carotenoid mediating this effect. Methods We analyzed biological aging using biological age calculations based on data from the NHANES 2007–2015 database. Various adjusted models were used to assess the relationship between LZ intake and aging phenotypes. Transcriptome analysis was conducted to explore the potential mechanisms underlying the anti-aging effects of lutein. Results A higher intake of LZ was associated with a slower biological aging rate ( P < 0.01), observed in major organs such as the liver and kidneys, as well as the cardiovascular system. LZ intake showed a significant negative correlation with biological aging acceleration ( P < 0.05). Enrichment analysis suggested that lutein's anti-aging effects might be mediated through telomere regulation and modulation of aging-related metabolic pathways. Additionally, lutein intake appeared to reduce pro-inflammatory Th1 cell abundance, further suggesting a potential anti-aging effect by suppressing inflammation. Sustained lutein intake also led to a decrease in the expression of aging phenotype-related molecules. However, in the evaluation of linear relationships, excessive lutein intake beyond a certain threshold may not yield additional benefits. Conclusion Combined LZ intake is associated with attenuated multi-level biological aging [OR (95% CI): 0.93 (0.88, 0.93), P = 0.016] and high LZ intake significantly reduce the risk of all-cause death ( P < 0.001), with lutein driving systemic effects via telomere regulation and inflammation suppression. These findings highlight lutein's translatable potential for aging interventions and provide insights for dietary strategies in aging health management.
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