Galectin-3 Predicts Long-Term Risk of Cerebral Disability and Mortality in Out-of-Hospital Cardiac Arrest Survivors.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Journal of Personalized Medicine Pub Date : 2024-09-19 DOI:10.3390/jpm14090994
Amr Abdelradi, Wasim Mosleh, Sharma Kattel, Zaid Al-Jebaje, Arezou Tajlil, Saraswati Pokharel, Umesh C Sharma
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Abstract

Background: Out-of-hospital cardiac arrest (OHCA) is associated with high mortality and cerebral disability in survivors. Current models of risk prediction and survival are mainly based on resuscitation duration. We examined the prognostic value of circulating biomarkers in predicting mortality and severe cerebral disability for OHCA survivors, alongside traditional clinical risk indicators.

Methods: Biomarkers including BNP, troponin I, and galectin-3 were measured at hospital admission in resuscitated OHCA patients. Prognostic significance for mortality and cerebral disability involving circulating biomarkers, resuscitation duration, demographics, and laboratory and clinical characteristics was examined via univariate and multivariate Cox proportional hazards regression models. The incremental prognostic value of the index covariates was examined through model diagnostics, focusing on the Akaike information criterion (AIC) and Harrell's concordance statistic (c-statistic).

Results: In a combinatorial analysis of 144 OHCA survivors (median follow-up 5.7 years (IQR 2.9-6.6)), BNP, galectin-3, arterial pH, and resuscitation time were significant predictors of all-cause death and severe cerebral disability, whereas troponin I levels were not. Multivariate regression, adjusting for BNP, arterial pH, and resuscitation time, identified galectin-3 as an independent predictor of long-term mortality. Multiple linear regression models also confirmed galectin-3 as the strongest predictor of cerebral disability. The incorporation of galectin-3 into models for predicting mortality and cerebral disability enhanced fit and discrimination, demonstrating the incremental value of galectin-3 beyond traditional risk predictors.

Conclusions: Galectin-3 is a significant, independent long-term risk predictor of cerebral disability and mortality in OHCA survivors. Incorporating galectin-3 into current risk stratification models may enhance early prognostication and guide targeted clinical interventions.

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Galectin-3 预测院外心脏骤停幸存者脑损伤和死亡的长期风险。
背景:院外心脏骤停(OHCA)与幸存者的高死亡率和脑残疾有关。目前的风险预测和生存模型主要基于复苏持续时间。除了传统的临床风险指标外,我们还研究了循环生物标志物在预测 OHCA 幸存者死亡率和严重脑残疾方面的预后价值:方法:在OHCA复苏患者入院时测量生物标志物,包括BNP、肌钙蛋白I和galectin-3。通过单变量和多变量 Cox 比例危险回归模型检验了循环生物标志物、复苏持续时间、人口统计学、实验室和临床特征对死亡率和脑残疾的预后意义。通过模型诊断,重点是阿凯克信息准则(AIC)和哈雷尔一致性统计量(c-统计量),检验了指标协变量的增量预后价值:在对 144 名 OHCA 幸存者(中位随访 5.7 年(IQR 2.9-6.6))进行的组合分析中,BNP、galectin-3、动脉 pH 值和复苏时间是全因死亡和严重脑残的重要预测因素,而肌钙蛋白 I 水平则不是。在对 BNP、动脉 pH 值和复苏时间进行调整后,多变量回归确定 galectin-3 是长期死亡率的独立预测因子。多元线性回归模型也证实,galectin-3 是预测脑残疾的最强指标。将galectin-3纳入预测死亡率和脑残疾的模型,提高了拟合度和辨别力,证明了galectin-3超越传统风险预测因子的增量价值:结论:在 OHCA 幸存者中,Galectin-3 是一个重要的、独立的脑残疾和死亡率长期风险预测因子。将 galectin-3 纳入当前的风险分层模型可加强早期预后并指导有针对性的临床干预。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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