Impact of multiple placental pathologies on neonatal death, bronchopulmonary dysplasia, and neurodevelopmental impairment in preterm infants.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
04 2020
Historique:
received: 10 06 2019
accepted: 18 11 2019
revised: 13 11 2019
pubmed: 8 12 2019
medline: 16 6 2021
entrez: 8 12 2019
Statut: ppublish

Résumé

To determine the association of placental pathology, including multiple placental lesions, with the occurrence and severity of bronchopulmonary dysplasia (BPD), death, and neurodevelopmental impairment (NDI) in preterm infants. A retrospective cohort study of neonates <29 weeks gestational age (GA) born at Parkland Hospital from 08/2009 to 08/2012. Infants were stratified as follows: Group 1: no significant placental pathology; Group 2: single significant placental lesion; and Group 3: ≥2 placental lesions (multiple lesions). Primary outcome was death and/or BPD. Two-year neurodevelopmental follow-up was compared. In all, 42% (100/241) of infants had one placental lesion, and 34% (82/241) ≥2 lesions. As the number of the pathologic lesions increased (no lesions vs. 1 vs. ≥2), the occurrence of death or BPD increased (25%, 37%, and 52%, respectively; P = 0.004). Moreover, infants with multiple pathologic lesions were more likely to have NDI (29%, 29%, and 46%, respectively; P = 0.03). After logistic regression, infants with multiple pathologic lesions were more likely to develop moderate-to-severe BPD [P < 0.01; OR 3.9 (1.5-10.1)] but not NDI. Neonates <29 weeks GA with multiple placental pathologic lesions have an increased risk for developing BPD, suggesting an interaction between placental inflammation and vascular pathology and the pathogenesis of BPD; however, the risk of NDI is not increased.

Sections du résumé

BACKGROUND
To determine the association of placental pathology, including multiple placental lesions, with the occurrence and severity of bronchopulmonary dysplasia (BPD), death, and neurodevelopmental impairment (NDI) in preterm infants.
METHOD
A retrospective cohort study of neonates <29 weeks gestational age (GA) born at Parkland Hospital from 08/2009 to 08/2012. Infants were stratified as follows: Group 1: no significant placental pathology; Group 2: single significant placental lesion; and Group 3: ≥2 placental lesions (multiple lesions). Primary outcome was death and/or BPD. Two-year neurodevelopmental follow-up was compared.
RESULTS
In all, 42% (100/241) of infants had one placental lesion, and 34% (82/241) ≥2 lesions. As the number of the pathologic lesions increased (no lesions vs. 1 vs. ≥2), the occurrence of death or BPD increased (25%, 37%, and 52%, respectively; P = 0.004). Moreover, infants with multiple pathologic lesions were more likely to have NDI (29%, 29%, and 46%, respectively; P = 0.03). After logistic regression, infants with multiple pathologic lesions were more likely to develop moderate-to-severe BPD [P < 0.01; OR 3.9 (1.5-10.1)] but not NDI.
CONCLUSION(S)
Neonates <29 weeks GA with multiple placental pathologic lesions have an increased risk for developing BPD, suggesting an interaction between placental inflammation and vascular pathology and the pathogenesis of BPD; however, the risk of NDI is not increased.

Identifiants

pubmed: 31812153
doi: 10.1038/s41390-019-0715-y
pii: 10.1038/s41390-019-0715-y
pmc: PMC7223700
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

885-891

Subventions

Organisme : NICHD NIH HHS
ID : K23 HD083511
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

Glass, H. C. et al. Outcomes for extremely premature infants. Anesth. Analg. 120, 1337–1351 (2015).
doi: 10.1213/ANE.0000000000000705
Stoll, B. J. et al. Trends in care practices, morbidity, and mortality of extremely preterm neonates, 1993-2012. JAMA 314, 1039–1051 (2015).
doi: 10.1001/jama.2015.10244
Jensen, E. A. & Schmidt, B. Epidemiology of bronchopulmonary dysplasia. Birth Defects Res. A Clin. Mol. Teratol. 100, 145–157 (2014).
doi: 10.1002/bdra.23235
Vohr, B. R. et al. Are outcomes of extremely preterm infants improving? Impact of Bayley assessment on outcomes. J. Pediatr. 161, 222.e3–228.e3 (2012).
doi: 10.1016/j.jpeds.2012.01.057
Roescher, A. M., Timmer, A., Erwich, J. J. & Bos, A. F. Placental pathology, perinatal death, neonatal outcome, and neurological development: a systematic review. PLoS ONE 9, e89419 (2014).
doi: 10.1371/journal.pone.0089419
Roescher, A. M. et al. Placental pathology and neurological morbidity in preterm infants during the first two weeks after birth. Early Hum. Dev. 90, 21–25 (2014).
doi: 10.1016/j.earlhumdev.2013.11.004
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. 13, 102–109 (2003).
doi: 10.1080/jmf.13.2.102.109
Lee, H. J. et al. Chorioamnionitis, respiratory distress syndrome and bronchopulmonary dysplasia in extremely low birth weight infants. J. Perinatol. 31, 166–170 (2011).
doi: 10.1038/jp.2010.113
Kunjunju, A. M., Gopagondanahalli, K. R., Chan, Y. & Sehgal, A. Bronchopulmonary dysplasia-associated pulmonary hypertension: clues from placental pathology. J. Perinatol. 37, 1310–1314 (2017).
doi: 10.1038/jp.2017.130
Pappas, A. et al. Chorioamnionitis and early childhood outcomes among extremely low-gestational-age neonates. JAMA Pediatr. 168, 137–147 (2014).
doi: 10.1001/jamapediatrics.2013.4248
Chisholm, K. M. et al. Correlation of preterm infant illness severity with placental histology. Placenta 39, 61–69 (2016).
doi: 10.1016/j.placenta.2016.01.012
Mestan, K. K. et al. Placental pathologic changes of maternal vascular underperfusion in bronchopulmonary dysplasia and pulmonary hypertension. Placenta 35, 570–574 (2014).
doi: 10.1016/j.placenta.2014.05.003
Greer, L. G. et al. An immunologic basis for placental insufficiency in fetal growth restriction. Am. J. Perinatol. 29, 533–538 (2012).
pubmed: 22495894
Redline, R. W., Heller, D., Keating, S. & Kingdom, J. Placental diagnostic criteria and clinical correlation-a workshop report. Placenta 26(Suppl A), S114–S117 (2005).
doi: 10.1016/j.placenta.2005.02.009
Mir, I. N. et al. Placental pathology is associated with severity of neonatal encephalopathy and adverse developmental outcomes following hypothermia. Am. J. Obstet. Gynecol. 213, 849.e1–849.e7 (2015).
doi: 10.1016/j.ajog.2015.09.072
Pinar, H., Sung, C. J., Oyer, C. E. & Singer, D. B. Reference values for singleton and twin placental weights. Pediatr. Pathol. Lab. Med. 16, 901–907 (1996).
doi: 10.1080/15513819609168713
Higgins, R. D. et al. Evaluation and management of women and newborns with a maternal diagnosis of chorioamnionitis: summary of a workshop. Obstet. Gynecol. 127, 426–436 (2016).
doi: 10.1097/AOG.0000000000001246
Papile, L.-A., Burstein, J., Burstein, R. & Koffler, H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J. Pediatr. 92, 529–534 (1978).
doi: 10.1016/S0022-3476(78)80282-0
Bell, M. J. et al. Neonatal necrotizing enterocolitis - therapeutic decisions based upon clinical staging. Ann. Surg. 187, 1–7 (1978).
doi: 10.1097/00000658-197801000-00001
Albers, C. A. & Grieve, A. J. Test Review: Bayley, N. (2006). Bayley Scales of Infant and Toddler Development–Third Edition. San Antonio, TX: Harcourt Assessment. J. Psychoeduc. Assess. 25, 180–198 (2007).
Redline, R. W., Wilson-Costello, D. & Hack, M. Placental and other perinatal risk factors for chronic lung disease in very low birth weight infants. Pediatr. Res. 52, 713–719 (2002).
doi: 10.1203/00006450-200211000-00017
Kent, A. & Dahlstrom, J. E. Chorioamnionitis/funisitis and the development of bronchopulmonary dysplasia. J. Paediatr. Child Health 40, 356–359 (2004).
doi: 10.1111/j.1440-1754.2004.00366.x
Van Marter, L. J. et al. Chorioamnionitis, mechanical ventilation, and postnatal sepsis as modulators of chronic lung disease in preterm infants. J. Pediatr. 140, 171–176 (2002).
doi: 10.1067/mpd.2002.121381
Hartling, L., Liang, Y. & Lacaze-Masmonteil, T. Chorioamnionitis as a risk factor for bronchopulmonary dysplasia: a systematic review and meta-analysis. Arch. Dis. Child. Fetal Neonatal Ed. 97, F8–F17 (2012).
doi: 10.1136/adc.2010.210187
Abman, S. H. Bronchopulmonary dysplasia: “a vascular hypothesis”. Am. J. Respir. Crit. Care Med. 164(Pt 1), 1755–1756 (2001).
doi: 10.1164/ajrccm.164.10.2109111c
Thebaud, B. & Abman, S. H. Bronchopulmonary dysplasia: where have all the vessels gone? Roles of angiogenic growth factors in chronic lung disease. Am. J. Respir. Crit. Care Med. 175, 978–985 (2007).
doi: 10.1164/rccm.200611-1660PP
Tang, J. R., Karumanchi, S. A., Seedorf, G., Markham, N. & Abman, S. H. Excess soluble vascular endothelial growth factor receptor-1 in amniotic fluid impairs lung growth in rats: linking preeclampsia with bronchopulmonary dysplasia. Am. J. Physiol. Lung Cell. Mol. Physiol. 302, L36–L46 (2012).
doi: 10.1152/ajplung.00294.2011
Strouss, L., Goldstein, N. D., Locke, R. & Paul, D. A. Vascular placental pathology and the relationship between hypertensive disorders of pregnancy and neonatal outcomes in very low birth weight infants. J. Perinatol. 38, 324–331 (2018).
doi: 10.1038/s41372-017-0032-4
Rozance, P. J. et al. Intrauterine growth restriction decreases pulmonary alveolar and vessel growth and causes pulmonary artery endothelial cell dysfunction in vitro in fetal sheep. Am. J. Physiol. Lung Cell. Mol. Physiol. 301, L860–L871 (2011).
doi: 10.1152/ajplung.00197.2011
Ghezzi, F. et al. Elevated interleukin-8 concentrations in amniotic fluid of mothers whose neonates subsequently develop bronchopulmonary dysplasia. Eur. J. Obstet. Gynecol. Reprod. Biol. 78, 5–10 (1998).
doi: 10.1016/S0301-2115(97)00236-4
Yoon, B. H. et al. Amniotic fluid cytokines (interleukin-6, tumor necrosis factor-alpha, interleukin-1 beta, and interleukin-8) and the risk for the development of bronchopulmonary dysplasia. Am. J. Obstet. Gynecol. 177, 825–830 (1997).
doi: 10.1016/S0002-9378(97)70276-X
Been, J. V. et al. Chorioamnionitis alters the response to surfactant in preterm infants. J. Pediatr. 156, 10.e1–15.e1 (2010).
doi: 10.1016/j.jpeds.2009.07.044
Schelonka, R. L., Katz, B., Waites, K. B. & Benjamin, D. K. Jr Critical appraisal of the role of Ureaplasma in the development of bronchopulmonary dysplasia with metaanalytic techniques. Pediatr. Infect. Dis. J. 24, 1033–1039 (2005).
doi: 10.1097/01.inf.0000190632.31565.83
Wu, Y. W. & Colford, J. M. Jr Chorioamnionitis as a risk factor for cerebral palsy: a meta-analysis. JAMA 284, 1417–1424 (2000).
doi: 10.1001/jama.284.11.1417
Andrews, W. W. et al. Early preterm birth: association between in utero exposure to acute inflammation and severe neurodevelopmental disability at 6 years of age. Am. J. Obstet. Gynecol. 198, 466.e1–466.e11 (2008).
doi: 10.1016/j.ajog.2007.12.031
Vinnars, M. T., Vollmer, B., Nasiell, J., Papadogiannakis, N. & Westgren, M. Association between cerebral palsy and microscopically verified placental infarction in extremely preterm infants. Acta Obstet. Gynecol. Scand. 94, 976–982 (2015).
doi: 10.1111/aogs.12688
Rezaie, P. & Dean, A. Periventricular leukomalacia, inflammation and white matter lesions within the developing nervous system. Neuropathology 22, 106–132 (2002).
doi: 10.1046/j.1440-1789.2002.00438.x
Blair, E., de Groot, J. & Nelson, K. B. Placental infarction identified by macroscopic examination and risk of cerebral palsy in infants at 35 weeks of gestational age and over. Am. J. Obstet. Gynecol. 205, 124.e1–124.e7 (2011).
doi: 10.1016/j.ajog.2011.05.022
Leviton, A. et al. Microbiologic and histologic characteristics of the extremely preterm infant's placenta predict white matter damage and later cerebral palsy. the ELGAN study. Pediatr. Res. 67, 95–101 (2010).
doi: 10.1203/PDR.0b013e3181bf5fab

Auteurs

Imran N Mir (IN)

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, UT Southwestern Medical School, Dallas, TX, 75390, USA. imran.mir@utsouthwestern.edu.

Lina F Chalak (LF)

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, UT Southwestern Medical School, Dallas, TX, 75390, USA.

L Steven Brown (LS)

Parkland Health and Hospital Systems, UT Southwestern Medical School, Dallas, TX, 75390, USA.

Sarah Johnson-Welch (S)

Department of Pathology, UT Southwestern Medical School, Dallas, TX, 75390, USA.

Roy Heyne (R)

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, UT Southwestern Medical School, Dallas, TX, 75390, USA.

Charles R Rosenfeld (CR)

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, UT Southwestern Medical School, Dallas, TX, 75390, USA.

Vishal S Kapadia (VS)

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, UT Southwestern Medical School, Dallas, TX, 75390, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH