小儿心脏骤停多中心研究中循环冷休克蛋白 FGF21 和 RBM3 的特征。

IF 0.8 4区 医学 Q4 CRITICAL CARE MEDICINE
Jeremy R Herrmann, Ericka L Fink, Anthony Fabio, Rachel P Berger, Keri Janesko-Feldman, Kiersten Gorse, Robert S B Clark, Patrick M Kochanek, Travis C Jackson
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引用次数: 0

摘要

成纤维细胞生长因子 21(FGF21)是一种由冷暴露诱导的神经保护激素,它靶向β-klotho 共受体。β-klotho在新生儿大脑中含量丰富,但随着年龄的增长会迅速减少。RNA-Binding Motif 3(RBM3)是一种在低体温条件下由 FGF21 上调的强效神经保护剂。我们通过对为评估脑损伤生物标志物而收集的样本进行二次分析,确定了一项前瞻性多中心小儿心脏骤停(CA)研究入组患者的血清 FGF21 和 RBM3 水平。研究纳入了在三个可用时间点(复苏后 0-24、24-48 或 48-72 小时)中至少两个时间点有残余血清样本的患者(n = 111)。20 名健康对照者的血清样本用于对比。FGF21 通过 Luminex 和内部验证的酶联免疫测定 (ELISA) 法进行测定。RBM3 通过内部验证的酶联免疫吸附法测定。在休克后的患者中,98 人接受了常温治疗,13 人接受了治疗性低温(TH)治疗。与对照组相比,心搏骤停后 24 小时内 FGF21 增加了 20 倍以上(681 pg/mL [200-1864] vs. 29 pg/mL [15-51],n = 99 vs. 19,p n = 40 vs. 54,p n = 7 vs. 74,p p = 0.97)。我们的结论是,在一项主要采用常温目标体温管理的多中心儿科 CA 患者研究中,与对照组相比,FGF21 在心跳骤停后明显增加,在复苏后需要 ECMO 的患者中增幅最大。RBM3 与性别有关。我们为今后研究 TH 对 FGF21 的影响或儿科 CA 后使用 FGF21 治疗提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Circulating Cold Shock Proteins FGF21 and RBM3 in a Multi-Center Study of Pediatric Cardiac Arrest.

Fibroblast Growth Factor 21 (FGF21) is a neuroprotective hormone induced by cold exposure that targets the β-klotho co-receptor. β-klotho is abundant in the newborn brain but decreases rapidly with age. RNA-Binding Motif 3 (RBM3) is a potent neuroprotectant upregulated by FGF21 in hypothermic conditions. We characterized serum FGF21 and RBM3 levels in patients enrolled in a prospective multi-center study of pediatric cardiac arrest (CA) via a secondary analysis of samples collected to evaluate brain injury biomarkers. Patients (n = 111) with remnant serum samples available from at least two of three available timepoints (0-24, 24-48 or 48-72 hours post-resuscitation) were included. Serum samples from 20 healthy controls were used for comparison. FGF21 was measured by Luminex and internally validated enzyme-linked immunoassay (ELISA). RBM3 was measured by internally validated ELISA. Of postarrest patients, 98 were managed with normothermia, while 13 were treated with therapeutic hypothermia (TH). FGF21 increased >20-fold in the first 24 hours postarrest versus controls (681 pg/mL [200-1864] vs. 29 pg/mL [15-51], n = 99 vs. 19, respectively, p < 0.0001, median [interquartile range]) with no difference in RBM3. FGF21 did not differ by sex, while RBM3 was increased in females versus males at 48-72 hours postarrest (1866 pg/mL [873-5176] vs. 1045 pg/mL [535-2728], n = 40 vs. 54, respectively, p < 0.05). Patients requiring extracorporeal membrane oxygenation (ECMO) postresuscitation had increased FGF21 versus those who did not at 48-72 hours (6550 pg/mL [1455-66,781] vs. 1213 pg/mL [480-3117], n = 7 vs 74, respectively, p < 0.05). FGF21 and RBM3 did not correlate (Spearman's rho = 0.004, p = 0.97). We conclude that in a multi-center study of pediatric CA patients where normothermic targeted temperature management was largely used, FGF21 was markedly increased postarrest versus control and highest in patients requiring ECMO postresuscitation. RBM3 was sex-dependent. We provide a framework for future studies examining the effect of TH on FGF21 or use of FGF21 therapy after pediatric CA.

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来源期刊
CiteScore
2.50
自引率
8.30%
发文量
35
期刊介绍: Therapeutic Hypothermia and Temperature Management is the first and only journal to cover all aspects of hypothermia and temperature considerations relevant to this exciting field, including its application in cardiac arrest, spinal cord and traumatic brain injury, stroke, burns, and much more. The Journal provides a strong multidisciplinary forum to ensure that research advances are well disseminated, and that therapeutic hypothermia is well understood and used effectively to enhance patient outcomes. Novel findings from translational preclinical investigations as well as clinical studies and trials are featured in original articles, state-of-the-art review articles, protocols and best practices. Therapeutic Hypothermia and Temperature Management coverage includes: Temperature mechanisms and cooling strategies Protocols, risk factors, and drug interventions Intraoperative considerations Post-resuscitation cooling ICU management.
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