Association of life’s essential 8 with leukocyte telomere length and mitochondrial DNA copy number: Findings from the population-based UK Biobank study

生命银行 端粒 线粒体DNA 遗传学 生物 细胞老化 DNA 基因
作者
Tian Yu,Shuang Kong,Mao Li,Guoying Wang,Jinxing He,Lei Fang,Lijin Lin,Jian Li
出处
期刊:Journal of Nutrition Health & Aging [Springer Science+Business Media]
卷期号:29 (7): 100557-100557
标识
DOI:10.1016/j.jnha.2025.100557
摘要

To explore the association of Life's Essential 8 (LE8) levels with leukocyte telomere length (LTL) and mitochondrial DNA copy number (mtDNA-CN). A cross-sectional study. 225,692 participants aged 37-73 year from the UK Biobank cohort enrolled from 2006 to 2010. The LE8 score (0-100) was divided into low (<50), moderate (50-79), and high cardiovascular health (CVH) (≥80) categories, based on health behaviors and factors defined by the American Heart Association. LTL was measured by a validated quantitative polymerase chain reaction method. mtDNA-CN was reacted by standardized SNP probe intensities. The association of CVH (as both a continuous and categorical variable) with LTL and mtDNA-CN was examined using multiple linear regression. Of 225,692 participants, 5.3% had low CVH, 81.2% had moderate CVH, and 13.4% had high CVH. Participants with higher CVH were usually younger, female, better educated, of higher socioeconomic status, and with a lower prevalence of comorbidities. After adjusting for confounders, a higher LE8 score is associated with longer LTL (Beta = 0.075, P < 0.05) and increased mtDNA-CN (Beta = 0.094, P < 0.05). We also observed that this association was evident in the health behavior score (diet, physical activity, nicotine exposure, and sleep) and the health factors score (BMI, non-HDL cholesterol, blood glucose, and blood pressure), with a stronger positive association of health factors with LTL and mtDNA-CN (Beta = 0.019, P < 0.05; Beta = 0.037, P < 0.05). Higher CVH is associated with longer LTL and increased mtDNA-CN.

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