Marseglia Lucia, Gitto Eloisa, Laschi Elisa, Giordano Maurizio, Romeo Carmelo, Cannavò Laura, Toni Anna Laura, Buonocore Giuseppe, Perrone Serafina
Department of Human Pathology of the Adult and Developmental Age, University of Messina, Messina, Italy.
Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Oxid Med Cell Longev. 2021 Nov 19;2021:6308255. doi: 10.1155/2021/6308255. eCollection 2021.
Preterm infants are at risk of free radical-mediated diseases from oxidative stress (OS) injury. Increased free radical generation has been demonstrated in preterm infants during the first seven days of life. Melatonin (MEL) is a powerful antioxidant and scavenger of free radicals. In preterm neonates, melatonin deficiency has been reported. Exogenous melatonin administration appears a promising strategy in the treatment of neonatal morbidities in which OS has a leading role.
The aim was to evaluate plasma MEL concentrations and OS biomarkers in preterm newborns after early administration of melatonin.
A prospective, randomized double-blind placebo-controlled pilot study was conducted from January 2019 to September 2020. Thirty-six preterm newborns were enrolled. Starting from the first day of life, 21 received a single dose of oral melatonin 0.5 mg/kg once a day, in the morning (MEL group); 15 newborns received an equivalent dose of placebo (placebo group). Samples of 0.2 mL of plasma were collected at 24 and 48 hours after MEL administration. Plasma concentrations of melatonin, non-protein-bound iron (NPBI), advanced oxidation protein products (AOPP), and F2-isoprostanes (F2-Isopr) were measured. Babies were clinically followed until discharge.
At 24 and 48 hours after MEL administration, the MEL concentrations were significantly higher in the MEL group than in the placebo group (52759.30 ± 63529.09 vs. 28.57 ± 46.24 pg/mL and 279397.6 ± 516344.2 vs. 38.50 ± 44.01 pg/mL, respectively). NPBI and AOPP did not show any statistically significant differences between the groups both at 24 and 48 hours. At 48 hours, the mean blood concentrations of F2-Isopr were significantly lower in the MEL group than in the placebo group (36.48 ± 33.85 pg/mL 89.97 ± 52.01 pg/mL).
Early melatonin administration in preterm newborns reduces lipid peroxidation in the first days of life showing a potential role to protect high-risk newborns. . This trial is registered with NCT04785183, Early Supplementation of Melatonin in Preterm Newborns: the Effects on Oxidative Stress.
早产儿有因氧化应激(OS)损伤导致自由基介导疾病的风险。已证实在出生后的头七天内,早产儿体内自由基生成增加。褪黑素(MEL)是一种强大的抗氧化剂和自由基清除剂。据报道,早产儿存在褪黑素缺乏的情况。在治疗以OS为主导因素的新生儿疾病中,外源性给予褪黑素似乎是一种有前景的策略。
旨在评估早期给予褪黑素后早产儿的血浆MEL浓度和OS生物标志物。
于2019年1月至2020年9月进行了一项前瞻性、随机双盲安慰剂对照的试点研究。纳入了36例早产儿。从出生第一天开始,21例每天早上口服一次单剂量的褪黑素0.5mg/kg(MEL组);15例新生儿接受等量的安慰剂(安慰剂组)。在给予MEL后24小时和48小时采集0.2mL血浆样本。测量血浆中褪黑素、非蛋白结合铁(NPBI)、晚期氧化蛋白产物(AOPP)和F2-异前列腺素(F2-Isopr)的浓度。对婴儿进行临床随访直至出院。
在给予MEL后24小时和48小时,MEL组的MEL浓度显著高于安慰剂组(分别为52759.30±63529.09 vs. 28.57±46.24pg/mL和279397.6±516344.2 vs. 38.50±44.01pg/mL)。在24小时和48小时时,两组间NPBI和AOPP均未显示出任何统计学上的显著差异。在48小时时,MEL组的F2-Isopr平均血浓度显著低于安慰剂组(36.48±33.85pg/mL对89.97±52.01pg/mL)。
早产儿早期给予褪黑素可在出生后的头几天减少脂质过氧化,显示出对高危新生儿的潜在保护作用。 本试验已在ClinicalTrials.gov注册,注册号为NCT04785183,早产儿早期补充褪黑素:对氧化应激的影响。