Cholesterol's hidden impact: the nonlinear link between remnant cholesterol (RC) and phenotypic age acceleration (PhenoAgeAccel).

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY
QianKun Yang, Shan Zhu, YanFang Luo, HongBo Ai, Lei Feng, Li Zhang, Fei Luo
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Abstract

Cholesterol metabolism disorders have been shown to correlate with multiple physiopathologic aspects of cellular aging. However, whether indicators reflecting cholesterol metabolism [e.g., remnant cholesterol (RC)] can serve as biomarkers for biological aging remains unclear. To address this gap, this study aimed to explore the relationship between RC and phenotypic age acceleration (PhenoAgeAccel) using data from the National Health and Nutrition Examination Survey (NHANES) database. First, participants with complete information on RC, PhenoAgeAccel, and other essential covariates were included and analyzed. Subsequently, multivariable generalized linear regression models, subgroup analyses, interaction tests, and restricted cubic spline (RCS) analyses were utilized to explore the association. Results showed that a total of 4,471 participants were included for analysis. After adjusting for all potential covariates, a one-unit increase in RC was associated with a 0.724-year increase in PhenoAgeAccel (β = 0.724, 95% CI: 0.106-1.341). Notably, subgroup analyses and interaction tests further revealed a more pronounced RC-PhenoAgeAccel association in individuals with diabetes (β = 4.331, 95% CI: 1.607-7.055) and hypertension (β = 2.069, 95% CI: 0.887-3.251). In addition, RCS analysis identified a positive and nonlinear association between RC and PhenoAgeAccel (P for nonlinearity < 0.001), and threshold effect analysis determined an inflection point of 0.564 mmol/L for RC. Specifically, a positive and segmented RC-PhenoAgeAccel association was observed within the 0.564-mmol/L threshold (β = 9.653, 95% CI: 7.452-11.853), and such association remained significant beyond this point (β = 1.121, 95% CI: 0.193-2.049). In conclusion, RC was positively and nonlinearly associated with accelerated aging. Thus, controlling RC below 0.564 mmol/L might contribute to anti-aging effects and thereby help prevent aging-related diseases.

胆固醇的隐性影响:残余胆固醇(RC)与表型年龄加速(PhenoAgeAccel)之间的非线性联系。
胆固醇代谢紊乱已被证明与细胞衰老的多个生理病理方面相关。然而,反映胆固醇代谢的指标[如残余胆固醇(RC)]是否可以作为生物衰老的生物标志物尚不清楚。为了解决这一差距,本研究旨在利用国家健康和营养检查调查(NHANES)数据库的数据探索RC与表型年龄加速(PhenoAgeAccel)之间的关系。首先,纳入具有完整RC、PhenoAgeAccel和其他重要协变量信息的参与者并进行分析。随后,利用多变量广义线性回归模型、亚组分析、相互作用检验和限制三次样条(RCS)分析来探讨其相关性。结果显示,共有4471名参与者被纳入分析。在对所有可能的协变量进行调整后,RC增加1个单位与表型加速增加0.724年相关(β = 0.724, 95% CI: 0.106-1.341)。值得注意的是,亚组分析和相互作用试验进一步显示,糖尿病(β = 4.331, 95% CI: 1.607-7.055)和高血压(β = 2.069, 95% CI: 0.887-3.251)患者的RC-PhenoAgeAccel相关性更明显。此外,RCS分析还发现,RC与PhenoAgeAccel呈非线性正相关(P为非线性)
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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