Aslan Mustafa Törehan, Güney Varal İpek, Tunç Gaffari, Bağcı Onur, Ören Ayşe
Department of Neonatology, Koç University Hospital, 34010 Istanbul, Turkey.
Department of Neonatology, University of Health Sciences Bursa Yüksek İhtisas Training and Research Hospital, 16310 Bursa, Turkey.
Children (Basel). 2025 May 31;12(6):727. doi: 10.3390/children12060727.
Transient tachypnea of the newborn (TTN) is traditionally viewed as a disorder of delayed lung fluid clearance, but emerging evidence suggests inflammatory involvement. This study investigated systemic inflammatory indices [(systemic immune-inflammation index (SII-i), systemic inflammation response index (SIR-i), neutrophil-to-lymphocyte ratio (NL-r), and platelet-to-lymphocyte ratio (PL-r)] and underlying mechanisms in TTN pathogenesis for the first time. This retrospective case-control study included 199 neonates (123 with TTN and 76 healthy controls) admitted between 2022 and 2025 to a tertiary care hospital. Complete blood count parameters were collected within the first two hours of life. Inflammatory indices were calculated and compared between groups. Subgroup analyses were conducted based on gestational age (late preterm vs. term) and mode of delivery (cesarean vs. vaginal). Although not statistically significant, TTN infants showed a trend toward higher inflammatory indices with median NL-r (2.54 vs. 1.75, = 0.197) and SII-i (729,307.83 vs. 373,593.50, = 0.276). Term TTN infants had higher NL-r (3.08 vs. 2.04, = 0.022) and SII-i (729,147.74 vs. 538,928.30, = 0.133) than late preterm infants. SIR-i and NL-r values were higher in the full-term group than in the early-term and late-preterm groups ( = 0.014, = 0.022, respectively). Cesarean births showed higher NL-r (3.20 vs. 2.33, = 0.049) and SII-i ( = 0.040) than vaginal deliveries. Strong correlations existed between SII-I, NL-r (r = 0.886, < 0.01), and SII-i, SIR-i (r = 0.817, < 0.01). Elevated inflammatory indices in neonates with TTN, particularly in term infants and those delivered vaginally, suggest a supportive/potential role for systemic inflammation in TTN pathophysiology. These markers may serve as potential supplementary markers for risk stratification, though further prospective validation is required to confirm their clinical relevance. These findings suggest that the early assessment of systemic inflammatory indices may assist clinicians in identifying neonates at risk for TTN, thereby guiding initial respiratory support strategies.
新生儿短暂性呼吸急促(TTN)传统上被视为一种肺液清除延迟的疾病,但新出现的证据表明存在炎症参与。本研究首次调查了TTN发病机制中的全身炎症指标[全身免疫炎症指数(SII-i)、全身炎症反应指数(SIR-i)、中性粒细胞与淋巴细胞比值(NL-r)和血小板与淋巴细胞比值(PL-r)]及其潜在机制。这项回顾性病例对照研究纳入了2022年至2025年间入住一家三级护理医院的199例新生儿(123例TTN患儿和76例健康对照)。在出生后的头两小时内收集全血细胞计数参数。计算并比较两组之间的炎症指标。根据胎龄(晚期早产儿与足月儿)和分娩方式(剖宫产与阴道分娩)进行亚组分析。尽管差异无统计学意义,但TTN患儿的炎症指标有升高趋势,NL-r中位数(2.54对1.75,P = 0.197)和SII-i(729307.83对373593.50,P = 0.276)。足月儿TTN患儿的NL-r(3.08对2.04,P = 0.022)和SII-i(729147.74对538928.30,P = 0.133)高于晚期早产儿。足月组的SIR-i和NL-r值高于早期足月组和晚期早产组(分别为P = 0.014,P = 0.022)。剖宫产出生的婴儿的NL-r(3.20对2.33,P = 0.049)和SII-i(P = 0.040)高于阴道分娩。SII-I与NL-r(r = 0.886,P < 0.01)以及SII-i与SIR-i之间存在强相关性(r = 0.817,P < 0.01)。TTN新生儿炎症指标升高,尤其是足月儿和经阴道分娩的新生儿,提示全身炎症在TTN病理生理过程中起支持/潜在作用。这些标志物可能作为风险分层的潜在补充标志物,不过需要进一步的前瞻性验证来确认其临床相关性。这些发现表明,早期评估全身炎症指标可能有助于临床医生识别有TTN风险的新生儿,从而指导初始呼吸支持策略。