基于生物标志物的方法:Galectin-3 和可溶性 CD146 识别严重烧伤患者的心肾损伤。

IF 2.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Cardiorenal Medicine Pub Date : 2024-01-01 Epub Date: 2024-08-12 DOI:10.1159/000540845
Louis Boutin, Sabri Soussi, Angèle Garcia Lavello, Elisabeth Masson Fron, Banjamin Deniau, Matthieu Legrand, Marcel Blot-Chabaud, Stefanny Muriel Figueroa, Christos Envangelos Chadjichristos, Feriel Azibani, Fançois Dépret
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引用次数: 0

摘要

导言:急性肾损伤(AKI)和心肌损伤(MI)是严重烧伤患者的严重并发症,二者结合则更为严重,被称为心肾综合征(CRS)。确定一种独特的心肾表型可大大提高对这些患者的治疗效果。Galectin-3 (Gal3) 和可溶性 CD146 (sCD146) 是肾脏和心脏损伤的生物标志物。本研究旨在评估这些生物标志物在识别严重烧伤患者的 CRS 方面的发生率和可靠性:本研究是一项涉及严重烧伤患者的单中心前瞻性概念验证研究。在患者入院后的最初 7 天内,每天收集血浆样本以测定 Gal3 和 sCD146。入院 24 小时后,根据 AKI 1 期或 1 期以上(KDIGO 定义)和高敏肌钙蛋白(hsTnT)(变化> 20 %基线值或绝对值> 40 ng/mL)定义的心肌梗死(MI)来定义 CRS:40名患者符合纳入标准并被纳入本研究。38名患者患有CRS。入院 7 天后 Gal3 的汇总值或 Gal3 和 sCD146 的组合值与 CRS 相关,OR 值分别为 1.145 [CI 95% (1.081-1.211)], p < 0.001 和 1.147 [CI 95% (1.085-1.212)], p < 0.001。入院时(D0)的Gal3值对CRS的预测性为0.78 [CI 95% (0.63-0.93)],当使用入院时(D0)的Gal3和sCD146值组合时,预测性有所提高,AUC为0.81 [CI 95% (0.66-0.96)]。前 7 天的 Gal3 水平与患者发生 AKI 和无心肌梗死有关,OR 为 1.129 [CI 95% (1.065-1.195)], p < 0.001,与无 AKI 的心肌梗死有关,OR 为 1.095 [CI 95% (1.037-1.167)], p < 0.001:结论:在严重烧伤患者中,心肾综合征是一种常见且严重的疾病。结论:在严重烧伤患者中,心肾综合征是一种常见的严重病症,入院后前 7 天的 Gal3 值与心肾综合征有关。使用 sCD146 和 Gal3 提高了对 CRS 鉴定的预测性能。使用此类生物标志物来鉴别心肾综合征非常重要,需要在其他研究中加以证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Galectin-3 and Soluble CD146 Identify Cardiorenal Injuries in Severe Burn Patients: A Biomarker-Based Approach.

Introduction: Acute kidney injury (AKI) and myocardial injury (MI) are severe conditions in patients with severe burn injury, and combination of both is even worst and is called the cardiorenal syndrome (CRS). Identifying a distinct cardiorenal phenotype could significantly enhance the management of these patients. Galectin-3 (Gal3) and soluble CD146 (sCD146) are biomarkers for renal and cardiac injuries. This study aims to assess the occurrence and reliability of these biomarkers in recognizing CRS in individuals who have been severely burn.

Methods: This study is a single-center prospective proof-of-concept study involving patients with severe burn injuries. Plasma samples for Gal3 and sCD146 measurements were collected daily during the initial 7 days following admission. CRS was defined after 24 h of admission by the association of AKI stage 1 or more (KDIGO definition) and MI defined on high sensitive troponin (hsTnT) (variation >20% baseline value or absolute value >40 ng/mL).

Results: Forty patients met the inclusion criteria and were included in this study. Thirty-eight patients had CRS. The pooled values of Gal3 or combination of Gal3 and sCD146 values following 7 days after admission were associated with CRS with an odds ratio (OR) of 1.145 (95% CI: 1.081-1.211), p < 0.001, and 1.147 (95% CI: 1.085-1.212), p < 0.001, respectively. Gal3 values at admission (D0) had a predictive performance for CRS with an AUC of 0.78 (95% CI: 0.63-0.93), and this performance improved when using the combination of Gal3 and sCD146 values at admission (D0), with an AUC of 0.81 (95% CI: 0.66-0.96). Gal3 levels during the first 7 days were associated with patients experiencing AKI and no MI, with an OR of 1.129 (95% CI: 1.065-1.195), p < 0.001, and MI without AKI with an OR of 1.095 (95% CI: 1.037-1.167), p < 0.001. sCD146 alone was not associated with AKI without MI or MI without AKI and was poorly associated with CRS.

Conclusion: In severely burned patients, CRS is a frequent and severe condition. Gal3 values during the first 7 days following admission were associated with CRS. The use of sCD146 with Gal3 improved prediction performance for CRS identification. The use of such biomarkers to identify CRS is important and needs to be confirmed in other studies.

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来源期刊
Cardiorenal Medicine
Cardiorenal Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-UROLOGY & NEPHROLOGY
CiteScore
5.40
自引率
2.60%
发文量
25
审稿时长
>12 weeks
期刊介绍: The journal ''Cardiorenal Medicine'' explores the mechanisms by which obesity and other metabolic abnormalities promote the pathogenesis and progression of heart and kidney disease (cardiorenal metabolic syndrome). It provides an interdisciplinary platform for the advancement of research and clinical practice, focussing on translational issues.
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