Association of Placental Fetal and Maternal Vascular Malperfusion with Bronchopulmonary Dysplasia and Mortality in Preterm Infants
Objective: This study aimed to investigate the association of placental histopathological abnormalities with bronchopulmonary dysplasia and mortality in preterm infants.
Methods: This prospective study included preterm infants ≤32 weeks and ≤1500 g who were followed in the NICU of a tertiary university hospital between May 2019 and May 2020. The infants were separated into 2 groups as those with and without bronchopulmonary dysplasia. Placentas were evaluated according to the Amsterdam Placenta Study Group.
Results: In this study, 35 preterm infants were evaluated. Birthweight was determined to be statistically significantly lower in Group 1 (1045±160.63 g) than in Group 2 (1453.95±529.08 g) (P=0.002). According to the median (min-max) gestational week at birth, the age of Group 1 [27.5 (26-29)] was statistically significantly lower than that of Group 2 [30.5 (25-32)] (P=0.001). Nosocomial sepsis was determined at a statistically higher rate in Group 1 [58.3%, n=7) than in Group 2 (13%, n=3) (P=0.015). The median length of stay in hospital was significantly longer in Group 1 [51 days (38-92)] than in Group 2 [21 days (1-74)] (P=0.001). The number of days on non-invasive ventilation was statistically significantly greater in Group 1 [11(2-57)] than in Group 2 [2(0-43)] (P=0.001). Maternal-fetal vascular malperfusion was found to be higher in Group 2. Mortality was observed in Group 2 and not in Group 1.
Conclusion: No statistically significant difference was observed in placental histopathological findings between the groups, with maternal and fetal vascular malperfusion representing the most frequent lesions. Mortality was seen exclusively in the non-BPD group. These findings suggest a potential association between placental vascular pathologies and neonatal mortality; however, larger multicenter prospective studies are required to confirm this relationship.
1. Arsan S, Korkmaz A, Oğuz S. Turkish Neonatal Society guideline on prevention and management of bronchopulmonary dysplasia. Turk Pediatri Ars. 2018 Dec 25;53(Suppl 1):S138-S150. doi: 10.5152/TurkPediatriArs.2018.01814.
2. Morrow LA, Wagner BD, Ingram DA, ET AL. Antenatal Determinants of Bronchopulmonary Dysplasia and Late Respiratory Disease in Preterm Infants. Am J Respir Crit Care Med. 2017;196(3):364-374. doi: 10.1164/rccm.201612-2414OC.
3. Kim CJ, Romero R, Chaemsaithong P, Kim JS. Chronic inflammation of the placenta: definition, classification, pathogenesis, and clinical significance. Am J Obstet Gynecol. 2015;213(4 Suppl):S53-S69. doi: 10.1016/j.ajog.2015.08.041.
4. Ogunyemi D, Murillo M, Jackson U, Hunter N, Alperson B. The relationship between placental histopathology findings and perinatal outcome in preterm infants. J Matern Fetal Neonatal Med. 2003;13(2):102-109. doi: 10.1080/jmf.13.2.102.109.
5. Erbil N, Toprak N, Açıkgöz Ö, Gelen S, Arık N. The relationship between maternal, placental and newborn parameters. Middle Black Sea Journal of Health Science. 2015;1(1):11-18. doi: 10.19127/mbsjohs.83805.
6. Altuncu E, Akman İ, Kotiloğlu E, et al. The Relationship of Placental Histology to Pregnancy and Neonatal Characteristics in Preterm Infants, J Turkish-German Gynecol Assoc. 2008;9(1):1-7.
7. Mehta R, Nanjundaswamy S, Shen-Schwarz S, Petrova A. Neonatal morbidity and placental pathology. Indian J Pediatr. 2006;73(1):25-28. doi: 10.1007/BF02758255.
8. Çakir U, Yildiz D, Kahvecioğlu D, et al. Placenta, Secret Witness of Infant Morbidities: The Relationship Between Placental Histology and Outcome of the Premature Infant. Turk Patoloji Derg. 2019;35(1):28-35. doi: 10.5146/tjpath.2018.01443.
9. Redline RW. Classification of placental lesions. Am J Obstet Gynecol. 2015;213(4 Suppl):S21-S28. doi: 10.1016/j.ajog.2015.05.056.
10. Khong TY, Mooney EE, Ariel I, et al. Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement. Arch Pathol Lab Med. 2016;140(7):698-713. doi: 10.5858/arpa.2015-0225-CC.
11. Bancalari E, Claure N. Definitions and diagnostic criteria for bronchopulmonary dysplasia. Semin Perinatol. 2006;30(4):164-170. doi: 10.1053/j.semperi.2006.05.002.
12. Walsh MC, Yao Q, Gettner P, et al.; National Institute of Child Health and Human Development Neonatal Research Network. Impact of a physiologic definition on bronchopulmonary dysplasia rates. Pediatrics. 2004;114(5):1305-1311. doi: 10.1542/peds.2004-0204.
13. Franklin A, Yallapragada S, Birkett R, Grobman W, Ernst LM, Mestan K. The impact of placental pathology discordance in multiple gestation pregnancies on bronchopulmonary dysplasia-associated pulmonary hypertension. Pulm Circ. 2020;10(1):2045894020910674. doi: 10.1177/2045894020910674.
14. Ernst LM. Maternal vascular malperfusion of the placental bed. APMIS. 2018;126(7):551-560. doi: 10.1111/apm.12833.
15. Nijman TA, van Vliet EO, Benders MJ, et al. Placental histology in spontaneous and indicated preterm birth: A case control study. Placenta. 2016;48:56-62. doi: 10.1016/j.placenta.2016.10.006.
16. Heider A. Fetal Vascular Malperfusion. Arch Pathol Lab Med. 2017;141(11):1484-1489. doi: 10.5858/arpa.2017-0212-RA.
17. Morgan TK. Role of the Placenta in Preterm Birth: A Review. Am J Perinatol. 2016;33(3):258-266. doi: 10.1055/s-0035-1570379.
18. Romero R, Kim YM, Pacora P, et al. The frequency and type of placental histologic lesions in term pregnancies with normal outcome. J Perinat Med. 2018;46(6):613-630. doi: 10.1515/jpm-2018-0055.
19. Leon RL, Sharma K, Mir IN, et al. Placental vascular malperfusion lesions in fetal congenital heart disease. Am J Obstet Gynecol. 2022;227(4):620.e1-620.e8. doi: 10.1016/j.ajog.2022.05.038.

Copyright (c) 2026 The European Research Journal
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Downloads
Article Information
- Article Type Research Article
- Submitted March 12, 2026
- Accepted June 14, 2026
- Published June 22, 2026
- Issue 2026: Online First
- Section Research Article
- Categories
The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
