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      Predictive analytics in bronchopulmonary dysplasia: past, present, and future

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          Abstract

          Bronchopulmonary dysplasia (BPD) remains a significant complication of prematurity, impacting approximately 18,000 infants annually in the United States. Advances in neonatal care have not reduced BPD, and its management is challenged by the rising survival of extremely premature infants and the variability in clinical practices. Leveraging statistical and machine learning techniques, predictive analytics can enhance BPD management by utilizing large clinical datasets to predict individual patient outcomes. This review explores the foundations and applications of predictive analytics in the context of BPD, examining commonly used data sources, modeling techniques, and metrics for model evaluation. We also highlight bioinformatics’ potential role in understanding BPD's molecular basis and discuss case studies demonstrating the use of machine learning models for risk prediction and prognosis in neonates. Challenges such as data bias, model complexity, and ethical considerations are outlined, along with strategies to address these issues. Future directions for advancing the integration of predictive analytics into clinical practice include improving model interpretability, expanding data sharing and interoperability, and aligning predictive models with precision medicine goals. By overcoming current challenges, predictive analytics holds promise for transforming neonatal care and providing personalized interventions for infants at risk of BPD.

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              Bronchopulmonary dysplasia

              In the absence of effective interventions to prevent preterm births, improved survival of infants who are born at the biological limits of viability has relied on advances in perinatal care over the past 50 years. Except for extremely preterm infants with suboptimal perinatal care or major antenatal events that cause severe respiratory failure at birth, most extremely preterm infants now survive, but they often develop chronic lung dysfunction termed bronchopulmonary dysplasia (BPD; also known as chronic lung disease). Despite major efforts to minimize injurious but often life-saving postnatal interventions (such as oxygen, mechanical ventilation and corticosteroids), BPD remains the most frequent complication of extreme preterm birth. BPD is now recognized as the result of an aberrant reparative response to both antenatal injury and repetitive postnatal injury to the developing lungs. Consequently, lung development is markedly impaired, which leads to persistent airway and pulmonary vascular disease that can affect adult lung function. Greater insights into the pathobiology of BPD will provide a better understanding of disease mechanisms and lung repair and regeneration, which will enable the discovery of novel therapeutic targets. In parallel, clinical and translational studies that improve the classification of disease phenotypes and enable early identification of at-risk preterm infants should improve trial design and individualized care to enhance outcomes in preterm infants.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2822364/overviewRole: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/677646/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:
                Role: Role: Role: Role: Role: Role:
                Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/967719/overviewRole: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/2701992/overviewRole: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Pediatr
                Front Pediatr
                Front. Pediatr.
                Frontiers in Pediatrics
                Frontiers Media S.A.
                2296-2360
                20 November 2024
                2024
                : 12
                : 1483940
                Affiliations
                [ 1 ]Division of Neonatology, Department of Pediatrics, University Hospital, University of Texas Health Science Center at San Antonio , San Antonio, TX, United States
                [ 2 ]Division of Neonatology, Department of Pediatrics, Texas Children’s Hospital, Baylor College of Medicine , Houston, TX, United States
                [ 3 ]Division of Pediatric Cardiology, Department of Pediatrics, Texas Children’s Hospital, Baylor College of Medicine , Houston, TX, United States
                Author notes

                Edited by: Jing Liu, Capital Medical University, China

                Reviewed by: Daniel Vijlbrief, University Medical Center Utrecht, Netherlands

                Jonathan Michael Davis, Tufts University, United States

                [* ] Correspondence: Binoy Shivanna shivanna@ 123456bcm.edu
                Article
                10.3389/fped.2024.1483940
                11615574
                39633818
                a3a58a1e-cfb2-4480-b79d-cfe348a024ab
                © 2024 McOmber, Moreira, Kirkman, Acosta, Rusin and Shivanna.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 August 2024
                : 29 October 2024
                Page count
                Figures: 1, Tables: 2, Equations: 0, References: 84, Pages: 12, Words: 0
                Funding
                Funded by: Parker B. Francis; the National Institutes of Health (NIH) Eunice Kennedy Shriver National Institute of Child Health and Human Development
                Award ID: K23HD101701
                Funded by: NIH National Heart Lung and Blood Institute
                Award ID: 5R25HL126140-06
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by Parker B. Francis; the National Institutes of Health (NIH) Eunice Kennedy Shriver National Institute of Child Health and Human Development K23HD101701; NIH National Heart Lung and Blood Institute 5R25HL126140-06 Subaward to AM.
                Categories
                Pediatrics
                Review
                Custom metadata
                Pediatric Pulmonology

                bronchopulmonary dysplasia,predictive analytics,artificial intelligence,machine learning,personalized medicine,bioinformatics

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