Department of Pediatrics and Neonatology, Hospital Privado Universitario de Córdoba, Córdoba, Argentina; Department of Pediatrics, Instituto Universitario de Ciencias Biomédicas de Córdoba, Córdoba, Argentina.
Department of Pediatrics and Neonatology, Hospital Privado Universitario de Córdoba, Córdoba, Argentina.
J Pediatr. 2019 Feb;205:91-97. doi: 10.1016/j.jpeds.2018.09.032. Epub 2018 Oct 16.
To determine whether a sustained neonatal systemic inflammatory response was associated with poor postnatal growth among infants born very preterm during the first year of life.
We studied prospectively 192 infants born preterm (birth weight ≤1.5 kg and gestational age ≤31 weeks). Weight, length, and head circumference were measured at birth, term, 4, and 12 months of corrected age. Serial C-reactive protein and procalcitonin were measured at 1, 3, 7, 14, and 28 days of age and averaged for each infant. A sustained neonatal systemic inflammatory response was defined as an average C-reactive protein level greater than the median for the group. Analysis was undertaken with linear mixed models.
Decreases in mean z scores for weight, length, and head circumference were associated with the presence of a sustained neonatal systemic inflammatory response from birth to 12 months of corrected age (β [95% CI] = -0.282 [-0.306 to -0.258]; -1.899 [-2.028,-1.769]; -0.806 [-0.910, to -0.701], P < .001, respectively) in main effect models. This association remained significant after including interaction terms for bronchopulmonary dysplasia, neonatal sepsis, and necrotizing enterocolitis (β [95% CI] = -0.393 [-0.520 to -0.265]; -2.128 [-2.754, -1.503]; -1.102 [-1.604, -0.600]; P < .001; respectively) in interaction models.
A sustained neonatal systemic inflammatory response was associated with poor postnatal growth, particularly poor linear growth. Serial C-reactive protein and procalcitonin may be useful markers for identifying infants at risk for postnatal growth failure.
确定新生儿持续全身性炎症反应是否与早产儿在生命的第一年生长不良有关。
我们前瞻性研究了 192 名早产儿(出生体重≤1.5kg,胎龄≤31 周)。在出生、足月、4 个月和 12 个月时测量体重、身长和头围。在 1、3、7、14 和 28 天时连续测量 C 反应蛋白和降钙素原,并计算每个婴儿的平均值。新生儿持续全身性炎症反应定义为平均 C 反应蛋白水平高于组中位数。采用线性混合模型进行分析。
从出生到 12 个月校正年龄,体重、身长和头围的平均 z 评分下降与新生儿持续全身性炎症反应的存在有关(β[95%CI]=-0.282[-0.306 至-0.258];-1.899[-2.028,-1.769];-0.806[-0.910,至-0.701],P<.001)。在主要效应模型中,包括支气管肺发育不良、新生儿败血症和坏死性小肠结肠炎的交互项后,这种相关性仍然显著(β[95%CI]=-0.393[-0.520 至-0.265];-2.128[-2.754,-1.503];-1.102[-1.604,-0.600];P<.001;分别)。
新生儿持续全身性炎症反应与不良的产后生长有关,特别是线性生长不良。连续 C 反应蛋白和降钙素原可能是识别有产后生长失败风险的婴儿的有用标志物。