Placental lesions associated with stillbirth by gestational age, according to feature importance: Results from the stillbirth collaborative research network.
Feature selection
Intrauterine fetal demise
Kernel principal covariates regression
Placental lesions
Stillbirth
Journal
Placenta
ISSN: 1532-3102
Titre abrégé: Placenta
Pays: Netherlands
ID NLM: 8006349
Informations de publication
Date de publication:
06 2023
06 2023
Historique:
received:
30
01
2023
revised:
04
04
2023
accepted:
06
04
2023
pmc-release:
01
06
2024
medline:
16
5
2023
pubmed:
21
4
2023
entrez:
20
04
2023
Statut:
ppublish
Résumé
Previous studies have identified lesions commonly found in placentas associated with stillbirth but have not distinguished across a range of gestational ages (GAs). The objective of this study was to identify lesions associated with stillbirths at different GAs by adapting methods from the chemical machine learning field to assign lesion importance based on correlation with GA. Placentas from the Stillbirth Collaborative Research Network were examined according to standard protocols. GAs at stillbirth were categorized as: <28 weeks (extreme preterm stillbirth [PTSB]), 28-33'6 weeks (early PTSB), 34-36'6 weeks (late PTSB), ≥37 weeks (term stillbirth). We identified and ranked the most discriminating placental features, as well as those that were similar across GA ranges, using Kernel Principal Covariates Regression (KPCovR). These analyses included 210 (47.2%) extreme PTSB, 85 (19.1%) early PTSB, 62 (13.9%) late PTSB, and 88 (19.8%) term stillbirths. When we compute the KPCovR, the first principal covariate indicates that there are four lesions (acute funisitis & nucleated fetal red blood cells found in extreme PTSB; multifocal reactive amniocytes & multifocal meconium found in term stillbirth) that distinguish GA ranges among all stillbirths. There are distinct placental lesions present across GA ranges in stillbirths; these lesions are identifiable using sophisticated feature selection. Further investigation may identify histologic changes across gestations that relate to fetal mortality.
Identifiants
pubmed: 37080046
pii: S0143-4004(23)00076-0
doi: 10.1016/j.placenta.2023.04.005
pmc: PMC10192128
mid: NIHMS1894910
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
59-64Subventions
Organisme : NICHD NIH HHS
ID : U10 HD045953
Pays : United States
Organisme : NICHD NIH HHS
ID : U01 HD045954
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045925
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045952
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045955
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045944
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors have no financial or other conflicts of interest to disclose.
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