Hundscheid Tamara M, Amodeo Ilaria, Cavallaro Giacomo, Hooijmans Carlijn R, Bartoš František, Villamor Eduardo
Division of Neonatology, Department of Pediatrics, MosaKids Children's Hospital, Maastricht University Medical Center (MUMC+), Research Institute for Oncology and Reproduction (GROW), Maastricht University, 6202 AZ Maastricht, The Netherlands.
Department of Pediatrics, Clínica Universidad de Navarra, 28027 Madrid, Spain.
Biomedicines. 2025 Sep 16;13(9):2274. doi: 10.3390/biomedicines13092274.
: In congenital diaphragmatic hernia (CDH), pulmonary hypoplasia and pulmonary hypertension are major causes of morbidity and mortality. Antenatal treatment with sildenafil has shown some promising protective effects in experimental CDH, but no systematic review has yet evaluated the preclinical evidence on this topic. : PubMed and EMBASE databases were searched for studies using antenatal sildenafil in animal models of CDH. Bayesian model-averaged (BMA) meta-analysis was used to calculate Bayes factors (BFs). The BF is the ratio of the probability of the data under the alternative hypothesis (presence of effect) over the probability of the data under the null hypothesis (absence of effect). Risk of bias was assessed by the SYRCLE tool. : We included 18 studies (14 nitrofen and 4 surgical CDH). The BMA analysis showed inconclusive evidence (BF between 0.33 and 3) for the presence of an effect of sildenafil in fetal survival (7 studies, BF = 1.25) or in lung hypoplasia as assessed by the lung-to-body weight ratio (16 studies, BF = 2.04). In contrast, the BMA analysis showed conclusive evidence (BF > 3) in favor of a positive effect of sildenafil on small pulmonary arteries medial wall thickness (12 studies, BF = 1499), radial alveolar count (6 studies, BF = 167.57), interalveolar septa thickness (4 studies, BF = 56.86), distal airway complexity (3 studies, BF = 7.95), mean saccular airspace diameter (2 studies, BF = 7.61), total lung capacity (2 studies, BF = 6.91), lung compliance (2 studies, BF = 5.19), and VEGF expression (5 studies, BF = 10.62). : In preclinical models of CDH, antenatal sildenafil rescues pulmonary vascular remodeling and airway/airspace morphometric alterations.
在先天性膈疝(CDH)中,肺发育不全和肺动脉高压是发病和死亡的主要原因。产前使用西地那非治疗在实验性CDH中已显示出一些有前景的保护作用,但尚无系统评价评估该主题的临床前证据。在PubMed和EMBASE数据库中检索了在CDH动物模型中使用产前西地那非的研究。采用贝叶斯模型平均(BMA)荟萃分析来计算贝叶斯因子(BFs)。BF是备择假设(存在效应)下数据的概率与原假设(无效应)下数据的概率之比。采用SYRCLE工具评估偏倚风险。我们纳入了18项研究(14项用硝基芬诱导和4项手术诱导的CDH)。BMA分析显示,关于西地那非对胎儿存活(7项研究,BF = 1.25)或通过肺与体重比评估的肺发育不全(16项研究,BF = 2.04)是否有影响的证据尚无定论(BF在0.33至3之间)。相比之下,BMA分析显示有确凿证据(BF > 3)支持西地那非对小肺动脉中膜厚度(12项研究,BF = 1499)、肺泡计数(6项研究,BF = 167.57)、肺泡间隔厚度(4项研究,BF = 56.86)、远端气道复杂性(3项研究,BF = 7.95)、平均囊状气腔直径(2项研究,BF = 7.61)、肺总量(2项研究,BF = 6.91)、肺顺应性(2项研究,BF = 5.19)和血管内皮生长因子(VEGF)表达(5项研究,BF = 10.62)有积极作用。在CDH的临床前模型中,产前西地那非可挽救肺血管重塑以及气道/气腔形态计量学改变。