FRailty and Arterial stiffness - the role of oXidative stress and Inflammation (FRAXI study).

IF 3.4 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Biomarker Insights Pub Date : 2022-10-18 eCollection Date: 2022-01-01 DOI:10.1177/11772719221130719
Ekow Mensah, Khalid Ali, Winston Banya, Frances Ann Kirkham, Manuela Mengozzi, Pietro Ghezzi, Chakravarthi Rajkumar
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引用次数: 1

Abstract

Objective: There is an association between frailty and arterial stiffness. However, arterial stiffness does not uniformly correlate with the spectrum of frailty states. Both oxidative stress and inflammaging contribute to vascular ageing. There are no human studies exploring links between arterial stiffness, oxidative stress, inflammaging and frailty. Our objective is to investigate arterial stiffness and inflammaging as predictors of frailty states.

Methods: An observational longitudinal cohort study will be used to examine the association between arterial stiffness, oxidative stress and inflammation in 50 older adults (⩾70 years) with clinical frailty scores (CFS) ⩽6 over 6 months. All study measurements will be taken at baseline. Frailty assessment will include hand-grip strength, timed-up and go test, mini-mental state examination, geriatric depression scale and sarcopenia using body composition measurements with Tanita®. Arterial stiffness measurements will include carotid-femoral pulse wave velocity (cfPWV) and carotid-radial pulse wave velocity (crPWV) using Complior (Alam Medical, France). CAVI device will measure Cardio-ankle vascular index and ankle brachial index (ABI). Oxidative stress blood markers nitrotyrosine (NT) and 8-hydroxy-2'-deoxyguanosin (8-oxo-dG) and inflammation markers high-sensitive C-reactive protein (hs-CRP) and interlukin-6(IL-6) will be measured at baseline and 6 month along with lipid profile and glycated haemoglobin.

Results data analysis plan: Descriptive statistics for continuous data using means and standard deviations for normality distributed variables or medians and inter-quartile ranges for skewed variables will be used. Participants will be categorised into CFS 1-3, and CFS 4-6. Categorical data will use frequencies and comparison between groups. Change in frailty between the groups over 6 months will be compared using paired t-test. Simple linear regression will be done between frailty measures, arterial stiffness, inflammation and oxidative stress biomarkers. Significance will be at P < .05.

Conclusion: This study data will inform a larger, multi-centre study exploring further the interplay between frailty, biomarkers and arterial stiffness parameters.

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虚弱和动脉僵硬-氧化应激和炎症的作用(FRAXI研究)。
目的:虚弱与动脉僵硬之间存在关联。然而,动脉僵硬与虚弱状态的频谱并不一致相关。氧化应激和炎症都会导致血管老化。目前还没有人类研究探索动脉硬化、氧化应激、炎症和虚弱之间的联系。我们的目的是研究动脉僵硬和炎症作为虚弱状态的预测因子。方法:一项观察性纵向队列研究将用于检查50名临床虚弱评分(CFS)≥6个月的老年人(小于或等于70岁)动脉僵硬、氧化应激和炎症之间的关联。所有研究测量将在基线时进行。虚弱评估将包括手部握力、计时和go测试、迷你精神状态检查、老年抑郁量表和肌肉减少症,使用Tanita®进行身体成分测量。动脉刚度测量将包括颈动脉-股动脉脉波速度(cfPWV)和颈动脉-桡动脉脉波速度(crPWV),使用Complior(法国Alam Medical)。CAVI装置测量心踝血管指数和踝肱指数。氧化应激血液标志物硝基酪氨酸(NT)和8-羟基-2'-脱氧鸟苷(8-氧- dg)以及炎症标志物高敏c反应蛋白(hs-CRP)和白介素-6(IL-6)将在基线和6个月时与血脂和糖化血红蛋白一起测量。结果数据分析方案:对连续数据采用描述性统计,正态分布变量采用均值和标准差,偏态变量采用中位数和四分位间距。参与者将被分为CFS 1-3和CFS 4-6。分类数据将使用频率和组间比较。使用配对t检验比较6个月内各组间虚弱程度的变化。简单的线性回归将在虚弱测量,动脉僵硬,炎症和氧化应激生物标志物之间进行。P < 0.05为显著性。结论:这项研究数据将为更大的、多中心的研究提供信息,进一步探索虚弱、生物标志物和动脉硬度参数之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomarker Insights
Biomarker Insights MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.00
自引率
0.00%
发文量
26
审稿时长
8 weeks
期刊介绍: An open access, peer reviewed electronic journal that covers all aspects of biomarker research and clinical applications.
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