Pro-inflammatory biomarkers and long term neurological outcomes in hypothermia plus melatonin treated asphyxiated newborns. A preliminary approach.

IF 3.1 3区 医学 Q1 PEDIATRICS
Antonio Jerez Calero, Francisco Contreras Chova, Ángela Benítez Feliponi, Hatim Azaryah, Jose Antonio Hurtado Suazo, M Fernanda Moreno Galdó, Antonio Molina Carballo
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引用次数: 0

Abstract

Objective: To evaluate serum neuronal and inflammatory biomarkers in asphyxiated newborns treated with hypothermia alone or hypothermia plus melatonin, and whether biomarkers correlate with neurodevelopmental outcomes.

Design: A pilot multicentre, randomized, controlled, double blind clinical trial. 25 newborns were recruited. Neonatal neural biomarkers were measured in serum samples at hospital admission (T0), 24 h (T1), 72 hours (T2) and 7-10 days of age (T3). Neurodevelopmental scales were performed at 6 and 18 months. Treated patients received a daily dose of intravenous melatonin, for 3 days.

Results: In melatonin-treated group, lower plasma levels of GM-CSF, IL-2 and IL-13 at T1 were measured vs placebo-group. We also corroborated, at T2, lower concentrations of GM-CSF, as well as IL-7 and IL-13 at T3. Throughout the study period, we found a significant decrease in GM-CSF concentrations in the treatment group. We have also observed sustained decrease over time of GM-CSF and inflammatory cytokines IL-2, IL-7 and IL-13 correlates with better neurodevelopmental outcomes at 6 and 18 months.

Conclusions: In neonates affected by hypoxic-ischemic encephalopathy, the addition of iv melatonin to hypothermia therapy affects plasma biomarker concentration in the first week of life, with a high correlation with long-term neurological prognosis.

Impact: Several plasma cytokines act as inflammatory mediators and biomarkers of hypoxia-ischemia-acquired neonatal brain damage. In animal research, melatonin has been shown to be a safe substance with proven anti-inflammatory and neuroprotective effects. Findings from our clinical trial show that melatonin affects plasma inflammatory biomarker concentration within the first week of life. This effect may be related to long-term neurological prognosis. To date, this is the only clinical trial in human infants including asphyxiated neonates treated with hypothermia and intravenous melatonin. Our study could help design future larger, well-designed clinical trials to clarify its effects in asphyxiated neonates.

低体温加褪黑素治疗窒息新生儿的前炎症生物标志物和长期神经功能预后。初步方法。
目的评估单独使用低体温或低体温加褪黑激素治疗窒息新生儿的血清神经元和炎症生物标志物,以及生物标志物是否与神经发育结果相关:多中心、随机对照、双盲临床试验。招募了 25 名新生儿。分别在入院(T0)、24 小时(T1)、72 小时(T2)和出生后 7-10 天(T3)测量血清样本中的新生儿神经生物标志物。6个月和18个月时进行神经发育量表测量。接受治疗的患者每天静脉注射褪黑激素,连续3天:结果:与安慰剂组相比,褪黑素治疗组在T1时测得的血浆GM-CSF、IL-2和IL-13水平较低。我们还证实,在 T2,GM-CSF 浓度较低,在 T3,IL-7 和 IL-13 浓度也较低。在整个研究期间,我们发现治疗组的 GM-CSF 浓度显著下降。我们还观察到,随着时间的推移,GM-CSF和炎性细胞因子IL-2、IL-7和IL-13的持续下降与6个月和18个月时更好的神经发育结果相关:结论:对于缺氧缺血性脑病新生儿,在低体温疗法中添加褪黑素会影响出生后第一周的血浆生物标志物浓度,并与神经系统的长期预后高度相关:影响:多种血浆细胞因子是缺氧缺血新生儿脑损伤的炎症介质和生物标志物。动物研究表明,褪黑素是一种安全的物质,具有公认的抗炎和神经保护作用。我们的临床试验结果表明,褪黑激素可在新生儿出生后第一周内影响血浆中炎症生物标志物的浓度。这种影响可能与神经系统的长期预后有关。迄今为止,这是唯一一项在人类婴儿中进行的临床试验,包括对窒息新生儿进行低体温和静脉注射褪黑激素治疗。我们的研究有助于设计未来更大规模、精心设计的临床试验,以明确褪黑激素对窒息新生儿的作用。
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
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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