Pentraxin-3 and C-reactive protein plasma levels predict survival in older adults with or without metabolic syndrome - results of the PolSenior2 substudy.

IF 5.2 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Aleksander J Owczarek, Anna Ochman, Anna Chudek, Małgorzata Mossakowska, Monika Puzianowska-Kuźnicka, Hanna Kujawska-Danecka, Tomasz Zdrojewski, Andrzej Więcek, Jerzy Chudek, Magdalena Olszanecka-Glinianowicz
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引用次数: 0

Abstract

Objective: There are no published data on the associations between plasma concentration of pentraxin-3 (PTX-3) - a marker of vascular inflammation and mortality in older subjects with or without metabolic syndrome (MS). Therefore, we aimed to compare the prognostic significance of increased PTX-3 and CRP levels on overall survival in subjects aged 60 and older with and without MS.

Materials and methods: Study participants (N = 3534) were categorized according to the presence or absence of MS and then each of these groups was stratified into 3 subgroups based on concentrations of CRP (≤ 3 mg/dL and > 3 mg/dL) and PTX-3 (< and ≥ the sex-specific cut-off values, based on the ROC curve analysis with the Youden index): double-negative inflammatory markers (low CRP and PTX-3 plasma concentrations); single-positive inflammatory marker (increased CRP or PTX-3 plasma concentrations) and double-positive inflammatory markers subgroup (increased CRP and PTX-3 plasma concentrations). During the 4.19-year follow-up, 678 (19.2% of the entire cohort) individuals died including 401 men (22.9%) and 277 women (15.5% ).

Results: The optimal cut-off for PTX-3 plasma concentration associated with an increased risk of death was 2.07 ng/mL for men and 2.23 ng/mL for women. The death rates were increased for single-positive and were highest in double-positive subgroups both for men and women, with or without MS. Kaplan-Meier analysis showed no effect of MS on survival in men and women in subgroups within specific inflammatory marker categories. Of note, the inflammatory markers class effect on survival was already significant in the single-positive subgroups (34% and 44% higher risk for death for men and women), and even more pronounced for the double-positive subgroup (more than two and almost three times higher risk of death for men and women, respectively). In the entire study group, a weak correlation was found between plasma concentrations of PTX-3 and hs-CRP (ρ = 0.11, p < 0.001) and slightly higher in undernourished subjects with hs-CRP > 3 mg/dL (ρ = 0.28, p < 0.001).

Conclusion: Our study suggests that in the age-advanced Caucasian population, the inflammatory status with increased plasma levels of both PTX-3 and CRP is associated with a higher risk of all-cause mortality, regardless of the occurrence of MS. However, due to the retrospective study design, these results require confirmation in prospective studies with an analysis of the underlying causes of death.

pentaxin -3和c -反应蛋白血浆水平预测有或无代谢综合征的老年人的生存——PolSenior2亚研究的结果
目的:在有或没有代谢综合征(MS)的老年受试者中,血管炎症和死亡率的标志物-戊曲霉素-3 (PTX-3)的血浆浓度之间没有已发表的数据。因此,我们的目的是比较PTX-3和CRP水平升高对60岁及以上伴有和不伴有MS的受试者总体生存的预后意义。材料和方法:研究参与者(N = 3534)根据是否存在MS进行分类,然后根据CRP(≤3mg /dL和> 3mg /dL)和PTX-3浓度分为3个亚组。与死亡风险增加相关的PTX-3血浆浓度的最佳临界值男性为2.07 ng/mL,女性为2.23 ng/mL。无论有无MS,单阳性患者的死亡率均增加,双阳性亚组中男性和女性的死亡率最高,Kaplan-Meier分析显示,在特定炎症标志物类别的亚组中,MS对男性和女性的生存率没有影响。值得注意的是,炎症标志物类别对生存的影响在单阳性亚组中已经很显著(男性和女性的死亡风险分别高出34%和44%),在双阳性亚组中甚至更为明显(男性和女性的死亡风险分别高出两倍和近三倍)。在整个研究组中,发现血浆PTX-3浓度与hs-CRP之间存在弱相关性(ρ = 0.11, p 3 mg/dL) (ρ = 0.28, p)。我们的研究表明,在高龄高加索人群中,炎症状态与血浆PTX-3和CRP水平升高有关,与ms的发生无关,但由于是回顾性研究设计,这些结果需要通过分析潜在死亡原因的前瞻性研究来证实。
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来源期刊
Immunity & Ageing
Immunity & Ageing GERIATRICS & GERONTOLOGY-IMMUNOLOGY
CiteScore
10.20
自引率
3.80%
发文量
55
期刊介绍: Immunity & Ageing is a specialist open access journal that was first published in 2004. The journal focuses on the impact of ageing on immune systems, the influence of aged immune systems on organismal well-being and longevity, age-associated diseases with immune etiology, and potential immune interventions to increase health span. All articles published in Immunity & Ageing are indexed in the following databases: Biological Abstracts, BIOSIS, CAS, Citebase, DOAJ, Embase, Google Scholar, Journal Citation Reports/Science Edition, OAIster, PubMed, PubMed Central, Science Citation Index Expanded, SCImago, Scopus, SOCOLAR, and Zetoc.
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