Identification of Preeclamptic Placenta in Whole Slide Images Using Artificial Intelligence Placenta Analysis.


Journal

Journal of Korean medical science
ISSN: 1598-6357
Titre abrégé: J Korean Med Sci
Pays: Korea (South)
ID NLM: 8703518

Informations de publication

Date de publication:
14 Oct 2024
Historique:
received: 15 03 2024
accepted: 22 07 2024
medline: 15 10 2024
pubmed: 15 10 2024
entrez: 15 10 2024
Statut: epublish

Résumé

Preeclampsia (PE) is a hypertensive pregnancy disorder linked to placental dysfunction, often involving pathological lesions like acute atherosis, decidual vasculopathy, accelerated villous maturation, and fibrinoid deposition. However, there is no gold standard for the pathological diagnosis of PE and this limits the ability of clinicians to distinguish between PE and non-PE pregnancies. Recent advances in computational pathology have provided the opportunity to automate pathological analysis for diagnosis, classification, prediction, and prediction of disease progression. In this study, we assessed whether computational pathology could be used to identify PE placentas. A total of 168 placental whole-slide images (WSIs) of patients from Seoul National University Hospital (comprising 84 PE cases and 84 normal controls) were used for model development and internal validation. For external validation of the model, 76 placental slides (including 38 PE cases and 38 normal controls) were obtained from the Boramae Medical Center (BMC). To establish standard criteria for diagnosing PE and distinguishing it from controls using placental WSIs, patch characteristics and quantification of terminal and intermediate villi were employed. In unsupervised learning, Using ensemble modeling, we developed a model to identify PE placentas. The model showed good performance (area under the precision-recall curve [AUPRC], 0.771; 95% confidence interval [CI], 0.752-0.790), with 77.3% of sensitivity and 71.1% of specificity, whereas the clinical feature model showed an AUPRC 0.713 (95% CI, 0.694-0.732) with 55.6% sensitivity and 86.8% specificity. External validation of the predictive model employing the BMC-derived set of placental slides also showed good discrimination (AUPRC, 0.725; 95% CI, 0.720-0.730). The proposed computational pathology model demonstrated a strong ability to identify preeclamptic placentas. Computational pathology has the potential to improve the identification of PE placentas.

Sections du résumé

BACKGROUND BACKGROUND
Preeclampsia (PE) is a hypertensive pregnancy disorder linked to placental dysfunction, often involving pathological lesions like acute atherosis, decidual vasculopathy, accelerated villous maturation, and fibrinoid deposition. However, there is no gold standard for the pathological diagnosis of PE and this limits the ability of clinicians to distinguish between PE and non-PE pregnancies. Recent advances in computational pathology have provided the opportunity to automate pathological analysis for diagnosis, classification, prediction, and prediction of disease progression. In this study, we assessed whether computational pathology could be used to identify PE placentas.
METHODS METHODS
A total of 168 placental whole-slide images (WSIs) of patients from Seoul National University Hospital (comprising 84 PE cases and 84 normal controls) were used for model development and internal validation. For external validation of the model, 76 placental slides (including 38 PE cases and 38 normal controls) were obtained from the Boramae Medical Center (BMC). To establish standard criteria for diagnosing PE and distinguishing it from controls using placental WSIs, patch characteristics and quantification of terminal and intermediate villi were employed. In unsupervised learning,
RESULTS RESULTS
Using ensemble modeling, we developed a model to identify PE placentas. The model showed good performance (area under the precision-recall curve [AUPRC], 0.771; 95% confidence interval [CI], 0.752-0.790), with 77.3% of sensitivity and 71.1% of specificity, whereas the clinical feature model showed an AUPRC 0.713 (95% CI, 0.694-0.732) with 55.6% sensitivity and 86.8% specificity. External validation of the predictive model employing the BMC-derived set of placental slides also showed good discrimination (AUPRC, 0.725; 95% CI, 0.720-0.730).
CONCLUSION CONCLUSIONS
The proposed computational pathology model demonstrated a strong ability to identify preeclamptic placentas. Computational pathology has the potential to improve the identification of PE placentas.

Identifiants

pubmed: 39403751
pii: 39.e271
doi: 10.3346/jkms.2024.39.e271
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e271

Subventions

Organisme : Seoul National University Hospital
ID : 0320230180
Pays : Korea
Organisme : Electronics and Telecommunications Research Institute
ID : 23ZR1100
Pays : Korea
Organisme : National Research Foundation of Korea
ID : NRF-2021R1F1A1046707
Pays : Korea

Informations de copyright

© 2024 The Korean Academy of Medical Sciences.

Déclaration de conflit d'intérêts

The authors have no potential conflicts of interest to disclose.

Auteurs

Young Mi Jung (YM)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

Seyeon Park (S)

Department of Medical Device Development, Seoul National University College of Medicine, Seoul, Korea.
Department of Transdisciplinary Medicine, Seoul National University Hospital, Seoul, Korea.

Youngbin Ahn (Y)

Department of Transdisciplinary Medicine, Seoul National University Hospital, Seoul, Korea.
Interdisciplinary Program of Medical Informatics, Seoul National University College of Medicine, Seoul, Korea.

Haeryoung Kim (H)

Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.

Eun Na Kim (EN)

Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.

Hye Eun Park (HE)

Department of Pathology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.

Sun Min Kim (SM)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.
Department of Obstetrics and Gynecology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.

Byoung Jae Kim (BJ)

Department of Obstetrics and Gynecology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.

Jeesun Lee (J)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

Chan-Wook Park (CW)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

Joong Shin Park (JS)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

Jong Kwan Jun (JK)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

Young-Gon Kim (YG)

Department of Transdisciplinary Medicine, Seoul National University Hospital, Seoul, Korea.
Department of Medicine, Seoul National University College of Medicine, Seoul, Korea.
Innovative Medical Technology Research Institute, Seoul National University Hospital, Seoul, Korea. younggon2.kim@gmail.com.

Seung Mi Lee (SM)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.
Innovative Medical Technology Research Institute, Seoul National University Hospital, Seoul, Korea.
Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul, Korea.
Medical Big Data Research Center & Institute of Reproductive Medicine and Population, Medical Research Center, Seoul National University, Seoul, Korea. smleemd@hanmail.net.

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