Suppr超能文献

肌少性肥胖、身体活动及其对美国成年人生物衰老的综合影响。

Sarcopenic obesity, physical activity, and their combined impact on biological aging in US adults.

作者信息

Wang Che, Zheng Rujie, Song Wenjuan, Sun Xiaotong, Du Xiaoyu, Lu Chengzhi

机构信息

School of Medicine, Nankai University, Tianjin, China.

Department of Cardiology, Tianjin First Central Hospital, 24 Fukang Road, Nankai District, Tianjin, 300192, China.

出版信息

BMC Public Health. 2025 Jul 2;25(1):2226. doi: 10.1186/s12889-025-23424-6.

Abstract

OBJECTIVE

Our study aimed to examine the independent and combined associations of sarcopenia, sarcopenic obesity (SO) and physical activity (PA) status with phenotypic age acceleration (PhenoAgeAccel) in US adults.

METHOD

The analyses included 9661 participants from the National Health and Nutrition Examination Survey (NHANES) 2005-2010 & 2015-2018. PhenoAgeAccel was calculated as the residuals from regressing phenotypic age (PhenoAge) on chronological age. Sarcopenia and SO were identified using the FNIH definition. Weighted multivariable logistic regression models, along with stratified and sensitivity analyses, were employed to evaluate the associations between sarcopenia, SO, and PhenoAgeAccel. Additionally, the population attributable fraction (PAF) was calculated to estimate the percentage of PhenoAgeAccel cases that could potentially be prevented by eliminating SO or PA deficiency.

RESULTS

A total of 9661 US adults were included in analysis. The weighted mean (SD) age was 32.78 (15.81) years, and 50.21% were males. Sarcopenia was not associated with PhenoAgeAccel in US adults in any subgroup or model. The multivariate-adjusted OR (95%CI) for PhenoAgeAccel with SO were 2.68 (2.13, 3.37) (p < 0.0001) for all, and 2.65 (2.10, 3.36) (p < 0.0001) for participants whose age ≤ 65 years old. Furthermore, compared to the combination of nonsarcopenia and adequate PA, combining SO and PA deficiency exhibited the highest risk of PhenoAgeAccel (OR 3.87; 95% CI 2.75, 5.46; p < 0.0001). SO increased the risk of PhenoAgeAccel by 29.3%, and adequate PA reduced the risk of PhenoAgeAccel by 9.1%, respectively. Notably, 18.5% increase was attributable to both SO and adequate PA concurrently.

CONCLUSION

SO was significantly associated with higher risk of biological aging, especially in middle or young adults. Combining SO and PA deficiency enhanced the risk of accelerated aging. These findings underscore the importance of addressing SO through comprehensive lifestyle interventions to promote healthy aging and enhance health span.

摘要

目的

我们的研究旨在探讨肌肉减少症、肌肉减少性肥胖(SO)和身体活动(PA)状态与美国成年人表型年龄加速(PhenoAgeAccel)之间的独立关联和联合关联。

方法

分析纳入了来自2005 - 2010年及2015 - 2018年美国国家健康与营养检查调查(NHANES)的9661名参与者。PhenoAgeAccel通过将表型年龄(PhenoAge)对实际年龄进行回归分析得到的残差来计算。肌肉减少症和SO根据美国国立卫生研究院(FNIH)的定义进行识别。采用加权多变量逻辑回归模型以及分层和敏感性分析来评估肌肉减少症、SO与PhenoAgeAccel之间的关联。此外,计算人群归因分数(PAF)以估计通过消除SO或PA缺乏可能预防的PhenoAgeAccel病例的百分比。

结果

总共9661名美国成年人纳入分析。加权平均(标准差)年龄为32.78(15.81)岁,男性占50.21%。在美国成年人的任何亚组或模型中,肌肉减少症与PhenoAgeAccel均无关联。对于所有人群,伴有SO的PhenoAgeAccel的多变量调整优势比(95%置信区间)为2.68(2.13,3.37)(p < 0.0001),对于年龄≤65岁的参与者为2.65(2.10,3.36)(p < 0.0001)。此外,与非肌肉减少症和充足PA的组合相比,SO与PA缺乏的组合表现出最高的PhenoAgeAccel风险(优势比3.87;95%置信区间2.75,5.46;p < 0.0001)。SO使PhenoAgeAccel风险增加29.3%,充足的PA使PhenoAgeAccel风险降低9.1%。值得注意的是,18.5%的增加同时归因于SO和充足的PA。

结论

SO与更高的生物衰老风险显著相关,尤其是在中青年成年人中。SO与PA缺乏相结合会增加加速衰老的风险。这些发现强调了通过全面的生活方式干预来解决SO问题以促进健康衰老和延长健康寿命的重要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验