Dietary Copper Intake and Biological Aging Among US Adults, NHANES 2003-2018.

IF 7.1 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-10-20 DOI:10.1111/acel.70272
Liujie Zheng, Guoqiang Li, Jingcheng Cao, Zihang Zhao, Liping Zhang, Zhiyong Hou
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引用次数: 0

Abstract

While the health effects of dietary copper intake have been widely studied, no research to date has specifically examined its association with biological aging. Here, we aim to explore the relationship between dietary copper intake and biological aging, while examining the mediating role of dietary inflammatory index (DII). This cross-sectional study included 18,160 adults from the 2003 to 2018 National Health and Nutrition Examination Survey (NHANES). Weighted multivariable linear regression models, subgroup analysis, trend tests, and restricted cubic spline (RCS) were used to analyze the relationship between dietary copper intake and biological aging. Biological aging was measured from different perspectives including phenotypic age (PhenoAge) and phenotypic age acceleration (PhenoAgeAccel). Additionally, mediation analysis explored the mediating role of DII in the above relationships. In this study, we found dietary copper intake was negatively associated with biological aging. Specifically, each 1-unit increase in dietary copper intake was associated with a 1.12-year decrease in PhenoAge and a 1.45-year decrease in PhenoAgeAccel. RCS models revealed a non-linear relationship between dietary copper intake and biological aging (p for nonlinear < 0.001). Specifically, the inverse association was stronger at lower intake levels, with the protective effect plateauing at higher values. Mediation analysis further indicated that DII mediated the above relationships. This study demonstrates a significant negative association between dietary copper intake and biological aging. Public health strategies that increase dietary copper intake may help reduce the burden of biological aging.

美国成年人的膳食铜摄入量和生物衰老,NHANES 2003-2018。
虽然膳食铜摄入对健康的影响已被广泛研究,但迄今为止还没有研究专门研究它与生物衰老的关系。本研究旨在探讨膳食铜摄入量与生物衰老之间的关系,同时研究膳食炎症指数(DII)的中介作用。这项横断面研究包括2003年至2018年全国健康与营养检查调查(NHANES)的18160名成年人。采用加权多变量线性回归模型、亚组分析、趋势检验和限制性三次样条(RCS)分析饲粮铜摄入量与生物衰老的关系。从表型年龄(PhenoAge)和表型年龄加速(PhenoAgeAccel)等不同角度测量生物衰老。此外,通过中介分析探讨了DII在上述关系中的中介作用。在这项研究中,我们发现饮食中铜的摄入量与生物衰老呈负相关。具体来说,每增加1个单位的膳食铜摄入量与1.12年的PhenoAge下降和1.45年的PhenoAgeAccel下降相关。RCS模型揭示了饲粮铜摄入量与生物老化之间的非线性关系(p为非线性)
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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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