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1
Association of GDF15 With Inflammation and Physical Function During Aging and Recovery After Acute Hospitalization: A Longitudinal Study of Older Patients and Age-Matched Controls.GDF15 与衰老过程中的炎症和身体功能的关系及急性住院后恢复:一项老年患者和年龄匹配对照的纵向研究。
J Gerontol A Biol Sci Med Sci. 2021 May 22;76(6):964-974. doi: 10.1093/gerona/glab011.
2
The senescence-associated secretome as an indicator of age and medical risk.衰老相关分泌表型作为年龄和医疗风险的标志物。
JCI Insight. 2020 Jun 18;5(12):133668. doi: 10.1172/jci.insight.133668.
3
Associations Between Serum GDF15 Concentrations, Muscle Mass, and Strength Show Sex-Specific Differences in Older Hospital Patients.血清 GDF15 浓度与肌肉质量和力量之间的关联在老年住院患者中存在性别特异性差异。
Rejuvenation Res. 2021 Feb;24(1):14-19. doi: 10.1089/rej.2020.2308. Epub 2020 Jun 23.
4
Patterns of Multimorbidity and Differences in Healthcare Utilization and Complexity Among Acutely Hospitalized Medical Patients (≥65 Years) - A Latent Class Approach.老年(≥65岁)急性住院内科患者的共病模式、医疗服务利用差异及复杂性——一种潜在类别分析方法
Clin Epidemiol. 2020 Feb 28;12:245-259. doi: 10.2147/CLEP.S226586. eCollection 2020.
5
Pre-frailty factors in community-dwelling 40-75 year olds: opportunities for successful ageing.社区居住的 40-75 岁老年人的虚弱前期因素:成功老龄化的机会。
BMC Geriatr. 2020 Mar 6;20(1):96. doi: 10.1186/s12877-020-1490-7.
6
A proteomic atlas of senescence-associated secretomes for aging biomarker development.衰老相关分泌表型的蛋白质组学图谱用于衰老生物标志物的开发。
PLoS Biol. 2020 Jan 16;18(1):e3000599. doi: 10.1371/journal.pbio.3000599. eCollection 2020 Jan.
7
Undulating changes in human plasma proteome profiles across the lifespan.人类血浆蛋白质组谱在整个生命周期中的波动变化。
Nat Med. 2019 Dec;25(12):1843-1850. doi: 10.1038/s41591-019-0673-2. Epub 2019 Dec 5.
8
Association between Plasma Levels of Growth Differentiation Factor-15 and Renal Function in the Elderly: Korean Frailty and Aging Cohort Study.生长分化因子 15 与老年人肾功能的关系:韩国虚弱与衰老队列研究。
Kidney Blood Press Res. 2019;44(3):405-414. doi: 10.1159/000498959. Epub 2019 Jun 4.
9
Association of growth differentiation factor 15 with other key biomarkers, functional parameters and mortality in community-dwelling older adults.生长分化因子 15 与其他关键生物标志物、功能参数及社区老年人死亡率的相关性。
Age Ageing. 2019 Jul 1;48(4):541-546. doi: 10.1093/ageing/afz022.
10
GDF15 and Growth Control.生长分化因子15与生长调控
Front Physiol. 2018 Nov 27;9:1712. doi: 10.3389/fphys.2018.01712. eCollection 2018.

一般人群中急性住院前和死亡前 GDF15 水平的纵向病程。

Longitudinal course of GDF15 levels before acute hospitalization and death in the general population.

机构信息

Department of Clinical Research, Copenhagen University Hospital Hvidovre, Kettegaard Alle 30, DK-2650, Hvidovre, Denmark.

Emergency Department, Copenhagen University Hospital Amager and Hvidovre, Kettegaard Alle 30, 2650, Hvidovre, Denmark.

出版信息

Geroscience. 2021 Aug;43(4):1835-1849. doi: 10.1007/s11357-021-00359-5. Epub 2021 Mar 24.

DOI:10.1007/s11357-021-00359-5
PMID:33763774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8492834/
Abstract

Growth differentiation 15 (GDF15) is a potential novel biomarker of biological aging. To separate the effects of chronological age and birth cohort from biological age, longitudinal studies investigating the associations of GDF15 levels with adverse health outcomes are needed. We investigated changes in GDF15 levels over 10 years in an age-stratified sample of the general population and their relation to the risk of acute hospitalization and death. Serum levels of GDF15 were measured three times in 5-year intervals in 2176 participants aged 30, 40, 50, or 60 years from the Danish population-based DAN-MONICA cohort. We assessed the association of single and repeated GDF15 measurements with the risk of non-traumatic acute hospitalizations. We tested whether changes in GDF15 levels over 10 years differed according to the frequency of hospitalizations within 2 years or survival within 20 years, after the last GDF15 measurement. The change in GDF15 levels over time was dependent on age and sex. Higher GDF15 levels and a greater increase in GDF15 levels were associated with an increased risk of acute hospitalization in adjusted Cox regression analyses. Participants with more frequent admissions within 2 years, and those who died within 20 years, after the last GDF15 measurement already had elevated GDF15 levels at baseline and experienced greater increases in GDF15 levels during the study. The change in GDF15 levels was associated with changes in C-reactive protein and biomarkers of kidney, liver, and cardiac function. Monitoring of GDF15 starting in middle-aged could be valuable for the prediction of adverse health outcomes.

摘要

生长分化因子 15(GDF15)是生物衰老的潜在新型生物标志物。为了将年龄和出生队列的影响与生物年龄分开,需要进行纵向研究,以调查 GDF15 水平与不良健康结果的关联。我们在年龄分层的一般人群样本中研究了 GDF15 水平在 10 年内的变化及其与急性住院和死亡风险的关系。在丹麦人群为基础的 DAN-MONICA 队列中,2176 名年龄在 30、40、50 或 60 岁的参与者每 5 年测量 3 次血清 GDF15 水平。我们评估了单次和重复 GDF15 测量与非创伤性急性住院风险的关联。我们测试了 10 年内 GDF15 水平的变化是否因 2 年内住院频率或最后一次 GDF15 测量后 20 年内的生存而有所不同。GDF15 水平随时间的变化取决于年龄和性别。在调整后的 Cox 回归分析中,较高的 GDF15 水平和 GDF15 水平的较大增加与急性住院风险的增加相关。在最后一次 GDF15 测量后 2 年内住院次数较多的参与者和 20 年内死亡的参与者在基线时已经具有较高的 GDF15 水平,并且在研究期间 GDF15 水平的增加更大。GDF15 水平的变化与 C 反应蛋白和肾脏、肝脏和心脏功能的生物标志物的变化相关。从中年开始监测 GDF15 可能对预测不良健康结果具有价值。