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血管细胞黏附分子 1、可溶性 Fas 和肝细胞生长因子可预测 90 岁以上老年人的死亡率:活力 90+研究。

Vascular cell adhesion molecule 1, soluble Fas and hepatocyte growth factor as predictors of mortality in nonagenarians: the Vitality 90+ study.

机构信息

Department of Clinical Chemistry, School of Medicine, University of Tampere, Tampere, Finland; Fimlab Laboratories, Tampere, Finland.

出版信息

Exp Gerontol. 2013 Nov;48(11):1167-72. doi: 10.1016/j.exger.2013.07.009. Epub 2013 Jul 30.

DOI:10.1016/j.exger.2013.07.009
PMID:23911532
Abstract

BACKGROUND

Ageing is characteristically accompanied by changes in vascular endothelial markers and growth factor as well as increased cellular death. We analysed the associations of the plasma levels of vascular cell adhesion molecule-1 (VCAM-1), hepatocyte growth factor (HGF) and soluble Fas (sFAS), and their combinations, with 4-year mortality to identify new biomarkers.

METHODS

A total of 238 individuals, both community-dwelling and institutionalised, aged 89 91 years and participating in the Vitality 90+ study were included. Biomarkers of endothelial function (VCAM-1), growth factor (HGF) and a marker of apoptosis (sFAS) were determined from plasma using Luminex® technology. This newly-determined data was combined with earlier data, e.g., 4-year mortality and medical history.

RESULTS

Subjects who died during the follow-up had higher baseline plasma levels of VCAM-1, sFas, and HGF. When other known risk factors were adjusted for, subjects in the highest concentration tertile for VCAM-1 (HR 1.85; 95% CI, 1.12-3.05) and HGF (HR 2.22; 95% CI, 1.33-3.71) had higher mortality compared to those in the lowest tertile. In the adjusted analyses, when compared to subjects with none of the biomarkers in the highest concentration tertile, mortality was also higher when sFas and VCAM-1 were simultaneously (HR 2.03; 95% CI, 1.13-3.64) or all three were simultaneously (HR 3.63; 95% CI, 1.65-7.97) in the highest concentration tertile.

CONCLUSIONS

Our results suggest that increased concentrations of these biomarkers, separately and in combination, associate with mortality among the aged and are prognostic markers of death.

摘要

背景

衰老的特征是血管内皮标志物和生长因子的变化以及细胞死亡增加。我们分析了血管细胞黏附分子-1(VCAM-1)、肝细胞生长因子(HGF)和可溶性 Fas(sFAS)的血浆水平及其组合与 4 年死亡率的关系,以确定新的生物标志物。

方法

共纳入 238 名年龄 89-91 岁、居住在社区和机构中的参与者,参加活力 90+研究。使用 Luminex®技术从血浆中测定内皮功能(VCAM-1)、生长因子(HGF)和凋亡标志物(sFAS)的生物标志物。这些新确定的数据与早期数据(如 4 年死亡率和病史)相结合。

结果

随访期间死亡的受试者基线时 VCAM-1、sFas 和 HGF 血浆水平较高。当调整其他已知危险因素后,VCAM-1(HR 1.85;95%CI,1.12-3.05)和 HGF(HR 2.22;95%CI,1.33-3.71)最高浓度 tertile 的受试者的死亡率高于最低 tertile。在调整分析中,与最高浓度 tertile 中没有任何生物标志物的受试者相比,当 sFas 和 VCAM-1 同时处于最高浓度 tertile 时(HR 2.03;95%CI,1.13-3.64)或同时存在时(HR 3.63;95%CI,1.65-7.97),死亡率也更高。

结论

我们的结果表明,这些标志物的浓度增加,单独或联合增加,与老年人的死亡率相关,是死亡的预后标志物。

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