Procianoy Renato S, Hentges Cláudia R, Silveira Rita C
Department of Pediatrics, Universidade Federal do Rio Grande do Sul and Newborn Section, Hospital de Clinicas de Porto Alegre, Porto Alegre, RS, Brazil.
Am J Perinatol. 2016 Apr;33(5):480-5. doi: 10.1055/s-0035-1566294. Epub 2015 Nov 3.
Bronchopulmonary dysplasia (BPD) is associated with changes in pulmonary angiogenesis. However, the role of the vascular endothelial growth factor/placental growth factor (VEGF/PlGF) heterodimer, an antiangiogenic factor, remains unknown in this disease.
To compare VEGF/PlGF levels in preterm infants with and without BPD.
This study was approved by the Institutional Review Board. Preterm neonates with birth weight <2,000 g and gestational age ≤ 34 weeks were included. Exclusion criteria were: neonates transferred from other institutions after 72 hours of life; death before blood collection; presence of major congenital malformations, inborn errors of metabolism, and early sepsis; and mothers with multiple pregnancies, TORCH infections, HIV infection, or autoimmune diseases. BPD was defined as the need for oxygen therapy for a period equal to or greater than 28 days, accompanied by radiographic changes compatible with the disease. Blood was collected from neonates in the first 72 hours of life. VEGF/PlGF levels were measured using the enzyme-linked immunosorbent assay method. The chi-square test, t-test, Mann-Whitney test, analysis of variance, and Kruskal-Wallis test were used for statistical analysis. Variables found to be significant in the univariate analysis were included in the multivariate analysis.
Seventy-three patients were included (19 with BPD, 43 without BPD, and 11 neonates who died in the first 28 days of life), with a mean (SD) gestational age of 30.32 (2.88) weeks and birth weight of 1,288 (462) g. Median VEGF/PlGF levels were higher in the groups with BPD and death in the first 28 days of life than in the group without BPD (16.46 [IQR, 12.19-44.57] and 20.64 [IQR, 13.39-50.22], respectively, vs. 9.14 [IQR, 0.02-20.64] pg/mL], p < 0.001). Higher VEGF/P1GF levels remained associated with BPD and death in the first 28 days of life in the multivariate analysis.
Higher plasma VEGF/PlGF levels were found in preterm neonates with BPD and in those who died in the first 28 days of life, suggesting an important role of this substance in pulmonary vascular development.
支气管肺发育不良(BPD)与肺血管生成的变化有关。然而,血管内皮生长因子/胎盘生长因子(VEGF/PlGF)异二聚体作为一种抗血管生成因子,在该疾病中的作用尚不清楚。
比较患有和未患有BPD的早产儿的VEGF/PlGF水平。
本研究经机构审查委员会批准。纳入出生体重<2000g且胎龄≤34周的早产儿。排除标准为:出生后72小时后从其他机构转入的新生儿;采血前死亡;存在重大先天性畸形、先天性代谢缺陷和早期败血症;以及母亲有多胎妊娠、TORCH感染、HIV感染或自身免疫性疾病。BPD定义为需要吸氧治疗等于或大于28天,并伴有与该疾病相符的影像学改变。在新生儿出生后的头72小时内采集血液。采用酶联免疫吸附测定法测量VEGF/PlGF水平。采用卡方检验、t检验、Mann-Whitney检验、方差分析和Kruskal-Wallis检验进行统计分析。单因素分析中发现有显著意义的变量纳入多因素分析。
共纳入73例患者(19例患有BPD,43例未患有BPD,11例在出生后28天内死亡的新生儿),平均(标准差)胎龄为30.32(2.88)周,出生体重为1288(462)g。患有BPD和在出生后28天内死亡的组中的VEGF/PlGF水平中位数高于未患有BPD的组(分别为16.46[四分位间距,12.19 - 44.57]和20.64[四分位间距,13.39 - 50.22]对比9.14[四分位间距,0.02 - 20.64]pg/mL),p<0.001)。在多因素分析中,较高的VEGF/P1GF水平仍然与BPD和出生后28天内死亡相关。
患有BPD的早产儿以及在出生后28天内死亡的早产儿血浆VEGF/PlGF水平较高,提示该物质在肺血管发育中起重要作用。