Pub Date : 2026-01-21DOI: 10.1016/j.semperi.2026.152211
Catherine Y Spong
{"title":"Advancing evidence for maternal and fetal health: Clinical trials that changed practice.","authors":"Catherine Y Spong","doi":"10.1016/j.semperi.2026.152211","DOIUrl":"https://doi.org/10.1016/j.semperi.2026.152211","url":null,"abstract":"","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152211"},"PeriodicalIF":3.2,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146030745","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.1016/j.semperi.2025.152210
Eniola R Ibirogba, Jennifer Grasch, Maged M Costantine
Hypertensive disorders of pregnancy are major contributors to adverse maternal, fetal and neonatal outcomes. This review summarizes pivotal clinical and translational studies that have shaped the clinical approach to the prevention and treatment of preeclampsia. Early preclinical trails established the pathophysiological basis and rationale for prevention strategies culminating in the standard use low dose aspirin and the emerging potential of statins. Recent randomized trials have also demonstrated that treatment of mild chronic hypertension reduces the risk preeclampsia and associated complications. Furthermore, clinical studies examining the use of magnesium sulfate for seizure prophylaxis and the optimal delivery timing have defined key aspects of evidence-based preeclampsia management. Further research to identify novel therapeutic targets and refine management strategies to mitigate the persistent burden of preeclampsia is urgently needed.
{"title":"Preeclampsia trials that changed practice.","authors":"Eniola R Ibirogba, Jennifer Grasch, Maged M Costantine","doi":"10.1016/j.semperi.2025.152210","DOIUrl":"10.1016/j.semperi.2025.152210","url":null,"abstract":"<p><p>Hypertensive disorders of pregnancy are major contributors to adverse maternal, fetal and neonatal outcomes. This review summarizes pivotal clinical and translational studies that have shaped the clinical approach to the prevention and treatment of preeclampsia. Early preclinical trails established the pathophysiological basis and rationale for prevention strategies culminating in the standard use low dose aspirin and the emerging potential of statins. Recent randomized trials have also demonstrated that treatment of mild chronic hypertension reduces the risk preeclampsia and associated complications. Furthermore, clinical studies examining the use of magnesium sulfate for seizure prophylaxis and the optimal delivery timing have defined key aspects of evidence-based preeclampsia management. Further research to identify novel therapeutic targets and refine management strategies to mitigate the persistent burden of preeclampsia is urgently needed.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152210"},"PeriodicalIF":3.2,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12818694/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145843971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-20DOI: 10.1016/j.semperi.2025.152195
Kevin S Shrestha, Alan Tn Tita
Landmark trials impact how we care for patients. These studies often have convincing data that lead to new or updated practice guidelines by professional societies and other organizations. In this review, we present four such studies of maternal interventions that defined standards of care and continue to influence what we do today. The first found that the rate of perinatal HIV transmission was reduced in women with HIV in pregnancy with treatment of zidovudine in the antepartum, intrapartum, and neonatal periods. The second found that postoperative infections and use of resources were reduced in women who received a single intravenous dose of azithromycin in addition to their standard preoperative antibiotics for cesarean delivery. The third study did not find any benefit in treating subclinical hypothyroidism or hypothyroxinemia in pregnancy preventing routine use of levothyroxine for these patients. The fourth showed that the treatment of non-severe chronic hypertension in pregnancy safely resulted in improved pregnancy outcomes.
{"title":"Trials that have changed maternal care.","authors":"Kevin S Shrestha, Alan Tn Tita","doi":"10.1016/j.semperi.2025.152195","DOIUrl":"https://doi.org/10.1016/j.semperi.2025.152195","url":null,"abstract":"<p><p>Landmark trials impact how we care for patients. These studies often have convincing data that lead to new or updated practice guidelines by professional societies and other organizations. In this review, we present four such studies of maternal interventions that defined standards of care and continue to influence what we do today. The first found that the rate of perinatal HIV transmission was reduced in women with HIV in pregnancy with treatment of zidovudine in the antepartum, intrapartum, and neonatal periods. The second found that postoperative infections and use of resources were reduced in women who received a single intravenous dose of azithromycin in addition to their standard preoperative antibiotics for cesarean delivery. The third study did not find any benefit in treating subclinical hypothyroidism or hypothyroxinemia in pregnancy preventing routine use of levothyroxine for these patients. The fourth showed that the treatment of non-severe chronic hypertension in pregnancy safely resulted in improved pregnancy outcomes.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152195"},"PeriodicalIF":3.2,"publicationDate":"2025-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145805437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1016/j.semperi.2025.152208
Mary Marchese, Victoria Adewale, Dwight J Rouse
Over the past few decades, multiple landmark studies investigating interventions for perinatal benefit have determined best practices for obstetricians worldwide. In this review, we will highlight trials that have demonstrated the effects of maternal intervention for perinatal benefit, including latency antibiotics, antenatal steroids, fetal neuroprotective measures, intrapartum group B streptococcus (GBS) prophylaxis, and delivery timing.
{"title":"Improving perinatal outcomes: A review of landmark trials that have changed obstetric practice.","authors":"Mary Marchese, Victoria Adewale, Dwight J Rouse","doi":"10.1016/j.semperi.2025.152208","DOIUrl":"https://doi.org/10.1016/j.semperi.2025.152208","url":null,"abstract":"<p><p>Over the past few decades, multiple landmark studies investigating interventions for perinatal benefit have determined best practices for obstetricians worldwide. In this review, we will highlight trials that have demonstrated the effects of maternal intervention for perinatal benefit, including latency antibiotics, antenatal steroids, fetal neuroprotective measures, intrapartum group B streptococcus (GBS) prophylaxis, and delivery timing.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152208"},"PeriodicalIF":3.2,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145757583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1016/j.semperi.2025.152199
Jessian L Munoz, Michael A Belfort
Fetal therapy has continued to expand in treatable conditions and surgical approaches. To maintain the evidence-based approach to optimizing patient care and outcomes, clinical trials investigating these interventions is essential. All trials must take in consideration both the potential benefit to the fetus or fetuses with the maternal and perinatal risks. In this review we discuss clinical trials in fetal therapy which have changed the field and provided the highest level of evidence possible. Large-scale trials have been performed in the management of Twin-to-Twin Transfusion Syndrome (TTTS), Spina bifida, Lower Urinary Tract Obstruction (LUTO) and Congenital Diaphragmatic Hernia (CDH). As molecular biology and advanced prenatal diagnostics continues to develop, future trials in gene and enzyme therapy remain on the horizon.
{"title":"Clinical trials in fetal surgery - changing care for complex pregnancies.","authors":"Jessian L Munoz, Michael A Belfort","doi":"10.1016/j.semperi.2025.152199","DOIUrl":"https://doi.org/10.1016/j.semperi.2025.152199","url":null,"abstract":"<p><p>Fetal therapy has continued to expand in treatable conditions and surgical approaches. To maintain the evidence-based approach to optimizing patient care and outcomes, clinical trials investigating these interventions is essential. All trials must take in consideration both the potential benefit to the fetus or fetuses with the maternal and perinatal risks. In this review we discuss clinical trials in fetal therapy which have changed the field and provided the highest level of evidence possible. Large-scale trials have been performed in the management of Twin-to-Twin Transfusion Syndrome (TTTS), Spina bifida, Lower Urinary Tract Obstruction (LUTO) and Congenital Diaphragmatic Hernia (CDH). As molecular biology and advanced prenatal diagnostics continues to develop, future trials in gene and enzyme therapy remain on the horizon.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152199"},"PeriodicalIF":3.2,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-10DOI: 10.1016/j.semperi.2025.152196
Wanlin Li, Maya Reddy, Martijn A Oudijk, Ben W Mol
Spontaneous preterm birth remains a leading global cause of neonatal morbidity and mortality, with lasting health socioeconomic consequences. Despite substantial research efforts over the past decades, preterm birth rates are not declining. Large cohort studies have shown that measurement of cervical length by transvaginal ultrasound is the best predictor for identifying women at risk of preterm birth, although sensitivity stays limited. While this has guided randomised clinical trials, preventive strategies remain suboptimal. Progestogens trials have long dominated the research landscape, and evidence synthesis though individual participant data indicates a potential reduction in preterm birth of approximately 30 % for women with a singleton pregnancy and a short cervix. Relative to progestogens, other potentially effective interventions, such as cervical cerclage and pessary have received limited attention, and were evaluated later or not at all. The optimal management of twin pregnancies, an important cause of preterm birth, remains uncertain. Our knowledge base on the prevention of preterm birth can be improved by research with greater uniformity in outcome measures, better prioritization, better evidence synthesis, more balanced resource allocation, and enhanced global collaboration.
{"title":"Landmark clinical trials on preterm birth prevention that have changed clinical practice.","authors":"Wanlin Li, Maya Reddy, Martijn A Oudijk, Ben W Mol","doi":"10.1016/j.semperi.2025.152196","DOIUrl":"10.1016/j.semperi.2025.152196","url":null,"abstract":"<p><p>Spontaneous preterm birth remains a leading global cause of neonatal morbidity and mortality, with lasting health socioeconomic consequences. Despite substantial research efforts over the past decades, preterm birth rates are not declining.\u0000Large cohort studies have shown that measurement of cervical length by transvaginal ultrasound is the best predictor for identifying women at risk of preterm birth, although sensitivity stays limited. While this has guided randomised clinical trials, preventive strategies remain suboptimal. Progestogens trials have long dominated the research landscape, and evidence synthesis though individual participant data indicates a potential reduction in preterm birth of approximately 30 % for women with a singleton pregnancy and a short cervix.\u0000Relative to progestogens, other potentially effective interventions, such as cervical cerclage and pessary have received limited attention, and were evaluated later or not at all. The optimal management of twin pregnancies, an important cause of preterm birth, remains uncertain. Our knowledge base on the prevention of preterm birth can be improved by research with greater uniformity in outcome measures, better prioritization, better evidence synthesis, more balanced resource allocation, and enhanced global collaboration.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152196"},"PeriodicalIF":3.2,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145744201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-06DOI: 10.1016/j.semperi.2025.152197
Christine Henricks, David Nelson
Preterm birth is the leading cause of neonatal morbidity and mortality worldwide and contributes to substantial long-term health and economic burdens. Despite decades of research, overall rates remain largely unchanged, highlighting the urgent need for more effective predictive and preventative strategies. Traditional approaches, including risk-factor scoring, cervical length measurement, and fetal fibronectin testing, provide limited predictive value. Given the limitations of traditional approaches, emerging technologies provide new opportunities to elucidate mechanisms and improve prediction. Proteomic analyses have identified pathways, such as inflammation and angiogenesis, while metabolomics has revealed small-molecule alterations reflecting biochemical and microbial processes. Genetic investigations highlight complex contributions from both maternal and fetal genomes. Artificial intelligence and machine learning are being applied to integrate multi-omics data with clinical variables with early studies suggesting improved predictive accuracy compared with conventional models. Despite these advancements, significant challenges remain. Many prediction studies are constrained by heterogeneous definitions of preterm birth, small sample sizes, and lack of validation across diverse populations. Beyond research limitations, system-level factors such as social determinants of health, environmental exposure, and inequities in access to prenatal care contribute to disparities in both risk and outcomes. These realities underscore the need for predictive tools that are not only scientifically robust but also applicable across diverse populations and care settings. Although clinical translation of novel approaches remains limited, continued innovation, longitudinal research, and commitment to equity will be essential to achieving meaningful improvements in the prediction of preterm birth. Understanding the pathophysiology and applying proven interventions is essential to improving perinatal health outcomes.
{"title":"Prediction of preterm birth: past, present, and future approaches to an ongoing challenge.","authors":"Christine Henricks, David Nelson","doi":"10.1016/j.semperi.2025.152197","DOIUrl":"https://doi.org/10.1016/j.semperi.2025.152197","url":null,"abstract":"<p><p>Preterm birth is the leading cause of neonatal morbidity and mortality worldwide and contributes to substantial long-term health and economic burdens. Despite decades of research, overall rates remain largely unchanged, highlighting the urgent need for more effective predictive and preventative strategies. Traditional approaches, including risk-factor scoring, cervical length measurement, and fetal fibronectin testing, provide limited predictive value. Given the limitations of traditional approaches, emerging technologies provide new opportunities to elucidate mechanisms and improve prediction. Proteomic analyses have identified pathways, such as inflammation and angiogenesis, while metabolomics has revealed small-molecule alterations reflecting biochemical and microbial processes. Genetic investigations highlight complex contributions from both maternal and fetal genomes. Artificial intelligence and machine learning are being applied to integrate multi-omics data with clinical variables with early studies suggesting improved predictive accuracy compared with conventional models. Despite these advancements, significant challenges remain. Many prediction studies are constrained by heterogeneous definitions of preterm birth, small sample sizes, and lack of validation across diverse populations. Beyond research limitations, system-level factors such as social determinants of health, environmental exposure, and inequities in access to prenatal care contribute to disparities in both risk and outcomes. These realities underscore the need for predictive tools that are not only scientifically robust but also applicable across diverse populations and care settings. Although clinical translation of novel approaches remains limited, continued innovation, longitudinal research, and commitment to equity will be essential to achieving meaningful improvements in the prediction of preterm birth. Understanding the pathophysiology and applying proven interventions is essential to improving perinatal health outcomes.</p>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":" ","pages":"152197"},"PeriodicalIF":3.2,"publicationDate":"2025-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145696262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01DOI: 10.1016/j.semperi.2025.152146
Adam L. Numis , Marie-Coralie Cornet , Hannah C. Glass
The objective of this review is to summarize current knowledge on epilepsies presenting in the neonatal period and to highlight their implications for diagnosis and treatment. While most seizures in newborns are due to acute brain injuries, a significant minority are caused by genetic epilepsies, which require distinct clinical management. Advances in genetic testing have clarified the major etiologic categories, including channelopathies, synaptopathies, inborn errors of metabolism, and brain malformations. Bedside clinicians must be alert to a possible genetic epilepsy in a newborn with seizures, as precise diagnosis informs prognosis and directly guides therapy. Sodium channel blockers can improve seizure control in specific channelopathies, vitamin therapies are effective in certain metabolic epilepsies, dietary therapy is transformative in glucose transporter deficiency syndrome, and targeted approaches are emerging for tuberous sclerosis complex. Rapid exome and genome sequencing now enable timely diagnosis in critically ill neonates and support precision treatment. Even with improvements in seizure control, developmental outcomes often remain poor, underscoring the urgent need for disease-modifying therapies. In conclusion, early recognition of epilepsies in the neonatal intensive care unit is essential to optimize care today and to accelerate the development of future targeted treatments.
{"title":"Genetic epilepsies as a cause of seizures in Neonates","authors":"Adam L. Numis , Marie-Coralie Cornet , Hannah C. Glass","doi":"10.1016/j.semperi.2025.152146","DOIUrl":"10.1016/j.semperi.2025.152146","url":null,"abstract":"<div><div>The objective of this review is to summarize current knowledge on epilepsies presenting in the neonatal period and to highlight their implications for diagnosis and treatment. While most seizures in newborns are due to acute brain injuries, a significant minority are caused by genetic epilepsies, which require distinct clinical management. Advances in genetic testing have clarified the major etiologic categories, including channelopathies, synaptopathies, inborn errors of metabolism, and brain malformations. Bedside clinicians must be alert to a possible genetic epilepsy in a newborn with seizures, as precise diagnosis informs prognosis and directly guides therapy. Sodium channel blockers can improve seizure control in specific channelopathies, vitamin therapies are effective in certain metabolic epilepsies, dietary therapy is transformative in glucose transporter deficiency syndrome, and targeted approaches are emerging for tuberous sclerosis complex. Rapid exome and genome sequencing now enable timely diagnosis in critically ill neonates and support precision treatment. Even with improvements in seizure control, developmental outcomes often remain poor, underscoring the urgent need for disease-modifying therapies. In conclusion, early recognition of epilepsies in the neonatal intensive care unit is essential to optimize care today and to accelerate the development of future targeted treatments.</div></div>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":"49 8","pages":"Article 152146"},"PeriodicalIF":3.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145102971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01DOI: 10.1016/j.semperi.2025.152143
Elmira Bachinsky , Lauren Guyer , Riddhi Patel , Stephen K. Amoah , Diana Ortega , Shenandoah Robinson , Hawley Helmbrecht , Lauren L. Jantzie
The placenta serves as an essential communicative organ between a mother and fetus throughout gestation. The placenta is critical in the development and maintenance of pregnancy while serving as a hub for immune signaling. In the context of an ever-changing microenvironment, the placenta responds dynamically to infection, inflammation, and other potentially harmful exposures. As in chorioamnionitis and preterm birth, a placental inflammatory response can impart harm to the developing fetal brain and facilitate the presentation of perinatal brain injury. Through various functional and structural disruptions, including changes to neural networks and complex neural immune interactions, neurodevelopmental disorders can manifest. In this review, we utilize chorioamnionitis as a platform for understanding immune signaling and inflammatory cell communication along the maternal-placental-fetal axis. We delineate how immune dysfunction changes neurodevelopment and explore cellular and molecular mechanisms associated with adverse clinical outcomes after birth. Together with discussion of unique inflammatory pathophysiology and triggers of perinatal brain injury, we explore avenues for neuroimmunomodulation, novel biomarker discovery, and precision medicine approaches for clinical practice.
{"title":"The placenta as a window into neonatal brain injury","authors":"Elmira Bachinsky , Lauren Guyer , Riddhi Patel , Stephen K. Amoah , Diana Ortega , Shenandoah Robinson , Hawley Helmbrecht , Lauren L. Jantzie","doi":"10.1016/j.semperi.2025.152143","DOIUrl":"10.1016/j.semperi.2025.152143","url":null,"abstract":"<div><div>The placenta serves as an essential communicative organ between a mother and fetus throughout gestation. The placenta is critical in the development and maintenance of pregnancy while serving as a hub for immune signaling. In the context of an ever-changing microenvironment, the placenta responds dynamically to infection, inflammation, and other potentially harmful exposures. As in chorioamnionitis and preterm birth, a placental inflammatory response can impart harm to the developing fetal brain and facilitate the presentation of perinatal brain injury. Through various functional and structural disruptions, including changes to neural networks and complex neural immune interactions, neurodevelopmental disorders can manifest. In this review, we utilize chorioamnionitis as a platform for understanding immune signaling and inflammatory cell communication along the maternal-placental-fetal axis. We delineate how immune dysfunction changes neurodevelopment and explore cellular and molecular mechanisms associated with adverse clinical outcomes after birth. Together with discussion of unique inflammatory pathophysiology and triggers of perinatal brain injury, we explore avenues for neuroimmunomodulation, novel biomarker discovery, and precision medicine approaches for clinical practice.</div></div>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":"49 8","pages":"Article 152143"},"PeriodicalIF":3.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145065567","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01DOI: 10.1016/j.semperi.2025.152140
Katie M. Strobel , Krystle M. Perez , Hannah Benjamin , Rebecca Hoban
Human milk (HM) is the gold standard for infant feeding due to its associations with significant reductions in short and long-term serious morbidities. It is also associated with improved brain growth and development and neurodevelopmental outcomes, particularly in the preterm population. The myriad of bioactives found in HM, such as growth factors, stem cells, human milk oligosaccharides, and the human milk microbiome, presumably play a large role in these outcomes. Given the significant improvements in infant outcomes, components of HM are now being studied as targeted neurological therapy for brain injury. This narrative review will summarize the unique components of HM that are thought to be responsible for brain health and how they may affect brain structure and development in the term and preterm neonate. Neurodevelopmental improvements seen with HM feeding will also be reviewed. Finally, pre-clinical and clinical studies utilizing whole HM or HM components to treat brain injury will be summarized so that providers can better share the science of this remarkable biologic with multi-disciplinary teams and families.
{"title":"Human milk as therapy: neurodevelopment and neonatal brain injury","authors":"Katie M. Strobel , Krystle M. Perez , Hannah Benjamin , Rebecca Hoban","doi":"10.1016/j.semperi.2025.152140","DOIUrl":"10.1016/j.semperi.2025.152140","url":null,"abstract":"<div><div>Human milk (HM) is the gold standard for infant feeding due to its associations with significant reductions in short and long-term serious morbidities. It is also associated with improved brain growth and development and neurodevelopmental outcomes, particularly in the preterm population. The myriad of bioactives found in HM, such as growth factors, stem cells, human milk oligosaccharides, and the human milk microbiome, presumably play a large role in these outcomes. Given the significant improvements in infant outcomes, components of HM are now being studied as targeted neurological therapy for brain injury. This narrative review will summarize the unique components of HM that are thought to be responsible for brain health and how they may affect brain structure and development in the term and preterm neonate. Neurodevelopmental improvements seen with HM feeding will also be reviewed. Finally, pre-clinical and clinical studies utilizing whole HM or HM components to treat brain injury will be summarized so that providers can better share the science of this remarkable biologic with multi-disciplinary teams and families.</div></div>","PeriodicalId":21761,"journal":{"name":"Seminars in perinatology","volume":"49 8","pages":"Article 152140"},"PeriodicalIF":3.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}