Cao Linxia, Liu Xiangye, Sun Tingting, Zhang Yuan, Bao Tianping, Cheng Huaiping, Tian Zhaofang
Department of Neonatology, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huai'an 223300, China.
Children (Basel). 2023 Dec 25;11(1):24. doi: 10.3390/children11010024.
Bronchopulmonary dysplasia (BPD) is the most common respiratory complication in preterm infants, and there is a lag in the diagnosis of BPD. Inflammation is a vital pathogenic factor for BPD; we aim to evaluate the predictive and diagnostic values of systemic inflammatory indices in BPD.
Between 1 January 2019 and 31 May 2023, the clinical data of 122 premature infants with a gestational age of <32 weeks in the Department of Neonatology, the Affiliated Huai'an No. 1 People's Hospital of Nanjing Medical University, were retrospectively collected and classified into non-BPD ( = 72) and BPD ( = 50) groups based on the National Institute of Child Health and Human Development 2018 criteria. To compare the general characteristics of each group, we identified the independent risk variables for BPD using multivariate logistic regression analysis, compared the systemic inflammatory indices at birth, 72 h, 1 week, 2 weeks, and 36 weeks postmenstrual age (PMA), and constructed the receiver operating characteristic curves of neutrophil-to-lymphocyte ratio (NLR) diagnosis of BPD at different time points.
① The independent risk factors for BPD in preterm infants were birth weight, small for gestational age, and days of oxygen therapy (all < 0.05). ② At 72 h and 1 week after birth, the serum NLR of the BPD group was higher than for the non-BPD group ( < 0.05). Furthermore, the neutrophil count (N), NLR, monocyte-to-lymphocyte ratio (MLR), systemic immune-inflammation index, systemic inflammation response index (SIRI), and pan-immune-inflammation value of infants with BPD were higher than the non-BPD group at 3 weeks after birth ( < 0.05). Moreover, at 36 weeks of PMA, the serum N, NLR, MLR, and SIRI of BPD infants were higher than those of non-BPD infants ( < 0.05). ③ The NLR of infants with and without BPD gradually increased after birth, reaching a peak at 72 h and 1 week, respectively. At 3 weeks postnatal, the NLR had the highest predictive power for BPD, with an area under the curve (AUC) of 0.717 ( < 0.001); the sensitivity was 56% and specificity was 86.1%. In addition, the NLR at 36 weeks of PMA exhibited some diagnostic value for BPD. The AUC was 0.693 ( < 0.001), the sensitivity was 54%, and specificity was 83.3%.
At 3 weeks after birth and 36 weeks of PMA, some systemic inflammation indices (like N, NLR, SIRI) of preterm infants with BPD have specific predictive and diagnostic values; these indices may help the management of high-risk preterm infants with BPD.
支气管肺发育不良(BPD)是早产儿最常见的呼吸系统并发症,且BPD的诊断存在滞后性。炎症是BPD的一个重要致病因素;我们旨在评估全身炎症指标在BPD中的预测和诊断价值。
回顾性收集2019年1月1日至2023年5月31日在南京医科大学附属淮安第一人民医院新生儿科的122例孕周<32周的早产儿的临床资料,并根据美国国立儿童健康与人类发展研究所2018年标准将其分为非BPD组(n = 72)和BPD组(n = 50)。为比较每组的一般特征,我们采用多因素logistic回归分析确定BPD的独立风险变量,比较出生时、出生后72小时、1周、2周和月经龄(PMA)36周时的全身炎症指标,并构建不同时间点中性粒细胞与淋巴细胞比值(NLR)诊断BPD的受试者工作特征曲线。
①早产儿BPD的独立危险因素为出生体重、小于胎龄和氧疗天数(均P<0.05)。②出生后72小时和1周时,BPD组血清NLR高于非BPD组(P<0.05)。此外,BPD婴儿出生后3周时的中性粒细胞计数(N)、NLR、单核细胞与淋巴细胞比值(MLR)、全身免疫炎症指数、全身炎症反应指数(SIRI)和全免疫炎症值均高于非BPD组(P<0.05)。而且,在PMA 36周时,BPD婴儿的血清N、NLR、MLR和SIRI高于非BPD婴儿(P<0.05)。③有和无BPD婴儿的NLR出生后逐渐升高,分别在72小时和1周时达到峰值。出生后3周时,NLR对BPD具有最高预测能力,曲线下面积(AUC)为0.717(P<0.001);敏感性为56%,特异性为86.1%。此外,PMA 36周时的NLR对BPD具有一定诊断价值。AUC为0.693(P<0.001),敏感性为54%,特异性为83.3%。
出生后3周和PMA 36周时,BPD早产儿的一些全身炎症指标(如N、NLR、SIRI)具有特定的预测和诊断价值;这些指标可能有助于BPD高危早产儿的管理。