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体重指数对老年人细胞衰老生物标志物的影响。

The Influence of Body Mass Index on Biomarkers of Cellular Senescence in Older Adults.

作者信息

Palmer Allyson K, St Sauver Jennifer, Fielding Roger A, Atkinson Elizabeth, White Thomas A, McGree Michaela, Weston Susan, LeBrasseur Nathan K

机构信息

Robert and Arlene Kogod Center on Aging, Mayo Clinic, College of Medicine, Rochester, Minnesota, USA.

Division of Hospital Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2025 Mar 7;80(4). doi: 10.1093/gerona/glae251.

Abstract

Obesity accelerates the onset and progression of age-related conditions. In preclinical models, obesity drives cellular senescence, a cell fate that compromises tissue health and function, in part through a robust and diverse secretome. In humans, components of the secretome have been used as senescence biomarkers that are predictive of age-related disease, disability, and mortality. Here, using biospecimens and clinical data from two large and independent cohorts of older adults, we tested the hypothesis that the circulating concentrations of senescence biomarkers are influenced by body mass index. After adjusting for age, sex, and race, we observed significant increases in activin A, Fas, MDC, PAI1, PARC, TNFR1, and VEGFA, and a significant decrease in RAGE, from normal weight, to overweight, to obesity body mass index categories by linear regression in both cohorts (all p < .05). These results highlight the influence of body mass index on circulating concentrations of senescence biomarkers.

摘要

肥胖会加速与年龄相关疾病的发病和进展。在临床前模型中,肥胖会驱动细胞衰老,这是一种损害组织健康和功能的细胞命运,部分原因是通过强大且多样的分泌组。在人类中,分泌组的成分已被用作衰老生物标志物,可预测与年龄相关的疾病、残疾和死亡率。在此,我们利用来自两个大型独立老年人群队列的生物样本和临床数据,检验了衰老生物标志物的循环浓度受体重指数影响这一假设。在对年龄、性别和种族进行调整后,通过线性回归分析,我们在两个队列中均观察到,从正常体重、超重到肥胖体重指数类别,激活素A、Fas、巨噬细胞来源趋化因子(MDC)、纤溶酶原激活物抑制剂1(PAI1)、颗粒溶素(PARC)、肿瘤坏死因子受体1(TNFR1)和血管内皮生长因子A(VEGFA)的循环浓度显著升高,而晚期糖基化终末产物受体(RAGE)则显著降低(所有p < 0.05)。这些结果突出了体重指数对衰老生物标志物循环浓度的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9727/11949428/a7abc3696d96/glae251_fig1.jpg

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