系统性炎症的无创、多模式炎症生物标志物发现(NOVA 研究):横断面研究方案。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Jinjoo Shim, Sinziana Muraru, Rucsandra Dobrota, Elgar Fleisch, Oliver Distler, Filipe Barata
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引用次数: 0

摘要

背景:长期的全身性炎症被认为是各种慢性炎症性疾病的主要诱因。对炎症生物标志物的日常测量可大大改善对全身炎症的疾病监测,从而有助于减轻患者和医疗保健系统的负担。然而,目前还没有一种可扩展、具有成本效益且无创的生物标记物可用于远程评估全身性炎症。为此,我们提出了一种测量炎症生物标志物的新型、多模态和无创方法:本研究旨在评估全身性炎症患者血清(金标准)中的炎症生物标志物水平与尿液、汗液、唾液、呼出气体、粪便和核心体温中的无创生物标志物水平之间的关系:本研究是一项单中心横断面研究,共包括 20 名参与者(10 名全身性炎症患者和 10 名对照组患者)。符合条件的参与者提供血清、尿液、汗液、唾液、呼出气体和粪便样本进行生物标记物分析。使用传感器测量核心体温。主要终点是 C 反应蛋白(CRP)水平。次要终点是白细胞介素(IL)-1β、IL-6、IL-8、IL-10 和肿瘤坏死因子-α 的水平。三级终点为呼出一氧化氮分数、钙蛋白和核心体温。样本将分两批采集,以便对第一批样本(每组 1-5 名患者)进行初步分析。全面分析将包括两批样本。CRP 和细胞因子水平将通过酶联免疫吸附测定法和电化学发光免疫测定法进行测定。在进行统计分析时,将使用 Shapiro-Wilk 检验来评估各变量分布的正态性。我们将采用双尾 t 检验或 Wilcoxon 秩和检验来比较系统性炎症患者和对照组患者的炎症生物标志物水平。皮尔逊和斯皮尔曼相关系数将评估非侵入性方法得出的炎症生物标志物与血清生物标志物之间的关系。我们将利用全子集回归分析,确定对血清 CRP 水平具有最高预测准确性的无创方法组合。我们将通过问卷调查评估参与者对采样方法的偏好:该研究于 2022 年 10 月 28 日获得苏黎世州独立研究伦理委员会的伦理批准。共有 20 名参与者参与了研究测量。数据收集工作于 2023 年 2 月 22 日开始,2023 年 9 月 22 日结束。参与者的平均年龄为 52.8 岁(标准差为 14.4 岁;年龄范围为 24-82 岁),其中 70% (14/20)为女性。报告结果的分析结果预计将于 2025 年公布:这项研究旨在评估对全身性炎症患者的炎症生物标志物进行无创、多模式评估的可行性。有希望的结果可能会导致无创和潜在的全身性炎症数字生物标志物的产生,从而能够在远程环境中对炎症活动进行持续监测和早期诊断:DERR1-10.2196/62877。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Noninvasive, Multimodal Inflammatory Biomarker Discovery for Systemic Inflammation (NOVA Study): Protocol for a Cross-Sectional Study.

Background: Prolonged systemic inflammation is recognized as a major contributor to the development of various chronic inflammatory diseases. Daily measurements of inflammatory biomarkers can significantly improve disease monitoring of systemic inflammation, thus contributing to reducing the burden on patients and the health care system. There exists, however, no scalable, cost-efficient, and noninvasive biomarker for remote assessment of systemic inflammation. To this end, we propose a novel, multimodal, and noninvasive approach for measuring inflammatory biomarkers.

Objective: This study aimed to evaluate the relationship between the levels of inflammatory biomarkers in serum (gold standard) and those measured noninvasively in urine, sweat, saliva, exhaled breath, stool, and core body temperature in patients with systemic inflammation.

Methods: This study is a single-center, cross-sectional study and includes a total of 20 participants (10 patients with systemic inflammation and 10 control patients). Eligible participants provide serum, urine, sweat, saliva, exhaled breath, and stool samples for biomarker analyses. Core body temperature is measured using a sensor. The primary end point is the level of C-reactive protein (CRP). The secondary end points are interleukin (IL)-1β, IL-6, IL-8, IL-10, and tumor necrosis factor-α levels. The tertiary end points are fractional exhaled nitric oxide, calprotectin, and core body temperature. Samples will be collected in 2 batches, enabling preliminary analysis of the first batch (patients 1-5 from each group). The full analysis will include both batches. CRP and cytokine levels will be measured using enzyme-linked immunosorbent assay and electrochemiluminescence immunoassay. For statistical analysis, the Shapiro-Wilk test will be used to evaluate the normality of the distribution in each variable. We will perform the 2-tailed t test or Wilcoxon rank sum test to compare the levels of inflammatory biomarkers between patients with systemic inflammations and control patients. Pearson and Spearman correlation coefficients will assess the relationship between inflammatory biomarkers from noninvasive methods and serum biomarkers. Using all-subset regression analysis, we will determine the combination of noninvasive methods yielding the highest predictive accuracy for serum CRP levels. Participants' preferences for sampling methods will be assessed through a questionnaire.

Results: The study received ethics approval from the independent research ethics committee of Canton Zurich on October 28, 2022. A total of 20 participants participated in the study measurements. Data collection started on February 22, 2023, and was completed on September 22, 2023. Participants were on average 52.8 (SD 14.4; range 24-82) years of age, and 70% (14/20) of them were women. The analysis results reporting findings are expected to be published in 2025.

Conclusions: This study aims to evaluate the feasibility of noninvasive, multimodal assessment of inflammatory biomarkers in patients with systemic inflammation. Promising results could lead to the creation of noninvasive and potentially digital biomarkers for systemic inflammation, enabling continuous monitoring and early diagnosis of inflammatory activity in a remote setting.

International registered report identifier (irrid): DERR1-10.2196/62877.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
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