Stark Ashley, Dammann Christiane, Nielsen Heber C, Volpe MaryAnn V
Tufts University School of Medicine, Boston, MA, United States.
Division of Newborn Medicine, Department of Pediatrics, Floating Hospital for Children at Tufts Medical Center, Boston, MA, United States.
Front Pediatr. 2018 Jun 13;6:125. doi: 10.3389/fped.2018.00125. eCollection 2018.
Bronchopulmonary dysplasia (BPD) and retinopathy of prematurity (ROP) are common and significant morbidities of prematurely born infants. These diseases have in common altered and pathologic vascular formation in the face of incomplete organ development. Therefore, it is reasonable to question whether factors affecting angiogenesis could have a joint pathogenic role for both diseases. Inhibition or induced expression of a single angiogenic factor is unlikely to be 100% causative or protective of either of BPD or ROP. It is more likely that interactions of multiple factors leading to disordered angiogenesis are present, increasing the likelihood of common pathways in both diseases. This review explores this possibility by assessing the evidence showing involvement of specific angiogenic factors in the vascular development and maldevelopment in each disease. Theoretical interactions of specific factors mutually contributing to BPD and ROP are proposed and, where possible, a timeline of the proposed relationships between BPD and ROP is developed. It is hoped that future research will be inspired by the theories put forth in this review to enhance the understanding of the pathogenesis in both diseases.
支气管肺发育不良(BPD)和早产儿视网膜病变(ROP)是早产婴儿常见且严重的发病情况。面对不完全的器官发育,这些疾病都存在血管形成改变和病理性改变。因此,质疑影响血管生成的因素是否对这两种疾病具有共同的致病作用是合理的。抑制或诱导单一血管生成因子的表达不太可能对BPD或ROP中的任何一种起到100%的致病或保护作用。更有可能的是存在多种导致血管生成紊乱的因素之间的相互作用,增加了两种疾病中共同途径的可能性。本综述通过评估显示特定血管生成因子参与每种疾病血管发育和发育异常的证据来探讨这种可能性。提出了特定因子对BPD和ROP相互作用的理论,并在可能的情况下制定了BPD和ROP之间拟议关系的时间线。希望本综述中提出的理论能激发未来的研究,以增强对这两种疾病发病机制的理解。