Association between life's essential 8 and biological ageing among US adults

被引:21
|
作者
Zhang, Ronghuai [1 ]
Wu, Min [2 ]
Zhang, Wei [1 ]
Liu, Xuna [3 ]
Pu, Jie [1 ]
Wei, Tao [1 ,4 ]
Zhu, Zhanfang [5 ]
Tang, Zhiguo [1 ]
Wei, Na [1 ]
Liu, Bo [1 ]
Cui, Qianwei [1 ]
Wang, Junkui [1 ]
Liu, Fuqiang [1 ]
Lv, Ying [1 ]
机构
[1] Shaanxi Prov Peoples Hosp, Dept Cardiol, 256 Youyixi Rd, Xian 710068, Shaanxi, Peoples R China
[2] Shaanxi Prov Peoples Hosp, Shaanxi Prov Key Lab Infect & Immune Dis, Xian, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Gastroenterol, Affiliated Hosp 2, Xian 710004, Peoples R China
[4] Shaanxi Prov Peoples Hosp, Dept Cardiovasc Surg, Xian, Peoples R China
[5] Xian Jiaotong Univ Hosp, Xian, Peoples R China
关键词
Life's Essential 8; Biological Ageing; NHANES; Cardiovascular Health; AMERICAN HEART ASSOCIATIONS; CARDIOVASCULAR HEALTH; DISEASE; BRAIN; AGE; NUTRITION; HALLMARKS; GLUCOSE; SLEEP; BMI;
D O I
10.1186/s12967-023-04495-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Biological ageing is tightly linked to cardiovascular disease (CVD). We aimed to investigate the relationship between Life's Essential 8 (LE8), a currently updated measure of cardiovascular health (CVH), and biological ageing. Methods This cross-sectional study selected adults >= 20 years of age from the 2005-2010 National Health and Nutrition Examination Survey. LE8 scores (range 0-100) were obtained from measurements based on American Heart Association definitions, divided into health behavior and health factor scores. Biological ageing was assessed by different methods including phenotypic age, phenotypic age acceleration (PhenoAgeAccel), biological age and biological age acceleration (BioAgeAccel). Correlations were analyzed by weighted linear regression and restricted cubic spline models. Results Of the 11,729 participants included, the mean age was 47.41 +/- 0.36 years and 5983 (51.01%) were female. The mean phenotypic and biological ages were 42.96 +/- 0.41 and 46.75 +/- 0.39 years, respectively, and the mean LE8 score was 67.71 +/- 0.35. After adjusting for potential confounders, higher LE8 scores were associated with lower phenotypic age, biological age, PhenoAgeAccel, and BioAgeAccel, with nonlinear dose-response relationships. Negative associations were also found between health behavior and health factor scores and biological ageing, and were stronger for health factors. In health factor-specific analyses, the ss negativity was greater for blood glucose and blood pressure. The inverse correlations of LE8 scores with phenotypic age and biological age in the stratified analyses remained solid across strata. Conclusions LE8 and its subscale scores were strongly negatively related to biological ageing. Encouraging optimal CVH levels may be advantageous in preventing and slowing down ageing.
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页数:12
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