Subedi Lochan, Huang Hong, Pant Amrita, Westgate Philip M, Bada Henrietta S, Bauer John A, Giannone Peter J, Sithisarn Thitinart
Department of Pediatrics, University of Kentucky, Lexington, KY, United States.
Department of Biostatistics, College of Public Health, University of Kentucky, Lexington, KY, United States.
Front Pediatr. 2017 Nov 3;5:238. doi: 10.3389/fped.2017.00238. eCollection 2017.
Brain-derived neurotrophic factor (BDNF) is a type of growth factor that promotes growth and survival of neurons. Fetal exposure to opiates can lead to postnatal withdrawal syndrome, which is referred as neonatal abstinence syndrome (NAS). Preclinical and clinical studies have shown an association between opiates exposure and alteration in BDNF expression in the brain and serum levels in adult. However, to date, there are no data available on the effects of opiate exposure on BDNF levels in infant who are exposed to opiates and whether BDNF level may correlate with the severity of NAS.
To compare plasma BDNF levels among NAS and non-NAS infants and to determine the correlation of BDNF levels and the severity of NAS.
This is a prospective cohort study with no intervention involved. Infants ≥35 weeks of gestation were enrolled. BDNF level was measured using enzyme-linked immunosorbent assay technique from blood samples drawn within 48 h of life. The severity of NAS was determined by the length of hospital stay, number of medications required to treat NAS.
67 infants were enrolled, 34 NAS and 33 non-NAS. Mean gestational age did not differ between the two groups. Mean birth weight of NAS infants was significantly lower than the non-NAS infants (3,070 ± 523 vs. 3,340 ± 459 g, = 0.028). Mean BDNF level in NAS group was 252.2 ± 91.6 ng/ml, significantly higher than 211.3 ± 66.3 ng/ml in the non-NAS group ( = 0.04). There were no differences in BDNF levels between NAS infants that required one medication vs. more than one medication (254 ± 91 vs. 218 ± 106 ng/ml, = 0.47). There was no correlation between the BDNF levels and length of hospital stay ( = 0.68) among NAS infants. Overall, there were no significant correlations between BDNF levels and NAS scores except at around 15 h after admission (correlation 0.35, = 0.045).
Plasma BDNF level was significantly increased in NAS infants during the first 48 h when compared to non-NAS infants. The correlations between plasma BDNF levels and the severity of NAS warrant further study. These results suggest that BDNF may play a neuromodulatory role during withdrawal after opiate exposure.
脑源性神经营养因子(BDNF)是一种促进神经元生长和存活的生长因子。胎儿暴露于阿片类药物可导致产后戒断综合征,即新生儿戒断综合征(NAS)。临床前和临床研究表明,阿片类药物暴露与大脑中BDNF表达改变及成人血清水平之间存在关联。然而,迄今为止,尚无关于阿片类药物暴露对暴露于阿片类药物的婴儿BDNF水平的影响以及BDNF水平是否可能与NAS严重程度相关的数据。
比较NAS婴儿和非NAS婴儿的血浆BDNF水平,并确定BDNF水平与NAS严重程度的相关性。
这是一项无干预的前瞻性队列研究。纳入孕周≥35周的婴儿。在出生后48小时内采集血样,采用酶联免疫吸附测定技术测量BDNF水平。NAS的严重程度通过住院时间、治疗NAS所需药物数量来确定。
共纳入67例婴儿,34例NAS婴儿和33例非NAS婴儿。两组的平均孕周无差异。NAS婴儿的平均出生体重显著低于非NAS婴儿(3070±523 vs. 3340±459 g,P = 0.028)。NAS组的平均BDNF水平为252.2±91.6 ng/ml,显著高于非NAS组的211.3±66.3 ng/ml(P = 0.04)。需要一种药物治疗的NAS婴儿与需要多种药物治疗 的NAS婴儿之间的BDNF水平无差异(254±91 vs. 218±106 ng/ml,P = 0.47)。NAS婴儿中,BDNF水平与住院时间之间无相关性(P = 0.68)。总体而言,除入院后约15小时外,BDNF水平与NAS评分之间无显著相关性(相关性0.35,P = 0.045)。
与非NAS婴儿相比,NAS婴儿在出生后48小时内血浆BDNF水平显著升高。血浆BDNF水平与NAS严重程度之间的相关性值得进一步研究。这些结果表明,BDNF可能在阿片类药物暴露后的戒断过程中发挥神经调节作用。