Placental pathology predicts infantile physical development during first 18 months in Japanese population: Hamamatsu birth cohort for mothers and children (HBC Study)
Abstract:The present study aimed to investigate the relationship between placental pathological findings and physiological development during the neonate and infantile periods. Study participants were 258 infants from singleton pregnancies enrolled in the Hamamatsu Birth Cohort for Mothers and Children (HBC Study) whose placentas were stored in our pathological division. They were followed up from birth to 18 months of age. Physiological development (body weight and the ponderal index [PI]) was assessed at 0, 1, 4, 6, … Show more
“…Extensive efforts have been made over the past few decades to establish effective biomarkers through the application of ‘omics’ technologies, which may identify individuals at high risk of developing NCDs; however, only a very small number have been translated into routine health care support 39 , 40 . The present study revealed that some placental pathological findings were associated with changes in infantile neurodevelopment, in addition to our previous findings on body weight and body composition 27 in the Japanese population, suggesting that placental pathological findings are applicable as a type of biomarker for predicting neuronal as well as physical development after birth. Follow-up investigations of the offspring of the present participants are now ongoing.…”
Section: Discussionsupporting
confidence: 81%
“…After weighing and an examination of gross morphology, whole placentas were stored in our pathological division after being vacuum-sealed in plastic packages with 10% formaldehyde (0.1 M sodium citrate buffer, pH 7.4). Seven paraffin blocks were systematically obtained from each placenta for the pathological examination by systematic random sampling, as previously described 18 , 19 , 27 . In brief, 5-mm-wide linear parallel slices of placental tissue were cut at an interval of approximately 3 cm perpendicular to the greatest dimension of the placental axis.…”
Section: Methodsmentioning
confidence: 99%
“…1 A,B) as a significant predictor of a lower body weight and ‘Deciduitis’ (F i g. 1 I) as a significant predictor of a small ponderal index, i.e. lean tendency, throughout the first 18 months of life using 258 whole placentas from singleton pregnancies, which were stored in our pathological division, among 1,258 pregnant women who were enrolled in the HBC study 27 . We planned the present study as a newly evolving investigation of the previous study and conducted a comprehensive analysis to identify the relationships between infantile neurodevelopment during 10–40 months of age, Mullen Scales of Early Learning (MSEL) 28 , and placental pathological findings using the same 258 whole placentas (Table 1 , 2 ) from singleton pregnancies in the HBC study.…”
The aim of present study was to investigate the association of placental pathological findings with infantile neurodevelopment during the early 40 months of life. 258 singleton infants were enrolled in the Hamamatsu Birth Cohort for Mothers and Children (HBC Study) whose placentas were saved in our pathological division. To assess the infantile neurodevelopment, we used Mullen Scales of Early Learning (gross motor, visual reception, fine motor, receptive language, expressive language) at 10, 14, 18, 24, 32, and 40 months. For obtaining placental blocks, we carried out random sampling and assessed eleven pathological findings using mixed modeling identified ‘Accelerated villous maturation’, ‘Maternal vascular malperfusion’, and ‘Delayed villous maturation’ as significant predictors of the relatively lower MSEL composite scores in the neurodevelopmental milestones by Mullen Scales of Early Learning. On the other hand, ‘Avascular villi’, ‘Thrombosis or Intramural fibrin deposition’, ‘Fetal vascular malperfusion’, and ‘Fetal inflammatory response’ were significant predictors of the relatively higher MSEL composite scores in the neurodevelopmental milestones by Mullen Scales of Early Learning. In conclusion, the present study is the first to report that some placental pathological findings are bidirectionally associated with the progression of infantile neurodevelopment during 10–40 months of age.
“…Extensive efforts have been made over the past few decades to establish effective biomarkers through the application of ‘omics’ technologies, which may identify individuals at high risk of developing NCDs; however, only a very small number have been translated into routine health care support 39 , 40 . The present study revealed that some placental pathological findings were associated with changes in infantile neurodevelopment, in addition to our previous findings on body weight and body composition 27 in the Japanese population, suggesting that placental pathological findings are applicable as a type of biomarker for predicting neuronal as well as physical development after birth. Follow-up investigations of the offspring of the present participants are now ongoing.…”
Section: Discussionsupporting
confidence: 81%
“…After weighing and an examination of gross morphology, whole placentas were stored in our pathological division after being vacuum-sealed in plastic packages with 10% formaldehyde (0.1 M sodium citrate buffer, pH 7.4). Seven paraffin blocks were systematically obtained from each placenta for the pathological examination by systematic random sampling, as previously described 18 , 19 , 27 . In brief, 5-mm-wide linear parallel slices of placental tissue were cut at an interval of approximately 3 cm perpendicular to the greatest dimension of the placental axis.…”
Section: Methodsmentioning
confidence: 99%
“…1 A,B) as a significant predictor of a lower body weight and ‘Deciduitis’ (F i g. 1 I) as a significant predictor of a small ponderal index, i.e. lean tendency, throughout the first 18 months of life using 258 whole placentas from singleton pregnancies, which were stored in our pathological division, among 1,258 pregnant women who were enrolled in the HBC study 27 . We planned the present study as a newly evolving investigation of the previous study and conducted a comprehensive analysis to identify the relationships between infantile neurodevelopment during 10–40 months of age, Mullen Scales of Early Learning (MSEL) 28 , and placental pathological findings using the same 258 whole placentas (Table 1 , 2 ) from singleton pregnancies in the HBC study.…”
The aim of present study was to investigate the association of placental pathological findings with infantile neurodevelopment during the early 40 months of life. 258 singleton infants were enrolled in the Hamamatsu Birth Cohort for Mothers and Children (HBC Study) whose placentas were saved in our pathological division. To assess the infantile neurodevelopment, we used Mullen Scales of Early Learning (gross motor, visual reception, fine motor, receptive language, expressive language) at 10, 14, 18, 24, 32, and 40 months. For obtaining placental blocks, we carried out random sampling and assessed eleven pathological findings using mixed modeling identified ‘Accelerated villous maturation’, ‘Maternal vascular malperfusion’, and ‘Delayed villous maturation’ as significant predictors of the relatively lower MSEL composite scores in the neurodevelopmental milestones by Mullen Scales of Early Learning. On the other hand, ‘Avascular villi’, ‘Thrombosis or Intramural fibrin deposition’, ‘Fetal vascular malperfusion’, and ‘Fetal inflammatory response’ were significant predictors of the relatively higher MSEL composite scores in the neurodevelopmental milestones by Mullen Scales of Early Learning. In conclusion, the present study is the first to report that some placental pathological findings are bidirectionally associated with the progression of infantile neurodevelopment during 10–40 months of age.
“…Three researchers (Y.H., N.I., and M.M.) macroscopically evaluated 5,201 placentas delivered at Hamamatsu University Hospital between April 2010 and March 2017, among which 1380 placentas were pathologically examined according to the criteria of S1 Table as previously described [ 15 ]. Written informed consent was obtained from the participating parturient during pregnancy after a full explanation of the study.…”
Section: Methodsmentioning
confidence: 99%
“…After they had been weighed and their gross morphology examined, whole placentas were stored in our pathological division after being vacuum-sealed in plastic packages with 10% formaldehyde, as described previously. Seven paraffin blocks were systematically obtained from each placenta for the pathological examination by systematic random sampling as previously described [ 15 ]. Two rolls of extraplacental membranes per placenta were together embedded in a block to make a single section.…”
An opaque fetal membrane based on gross appearance is traditionally indicative of histological chorioamnionitis; however, to the best of our knowledge, there is currently no supportive evidence, and its diagnostic efficiency has not yet been scientifically demonstrated. The present study aimed to provide scientific insights into the traditional concept of an opaque fetal membrane based on gross appearance being an indicator of histological chorioamnionitis. We examined the placental pathology after screening of the placental gross appearance and perinatal complications and did not examine uncomplicated deliveries. We investigated the relationship between the presence of an opaque fetal membrane and histological chorioamnionitis (Cohort 1, 571 placentas) or the outcomes of neonates delivered at term (Cohort 2, 409 placentas) at Hamamatsu University School of Medicine between 2010 and 2017. The judgment of a positive opaque fetal membrane based on gross appearance correlated with histological chorioamnionitis (Cohort 1). Its sensitivity and specificity were 66.7 and 89.9%, respectively, while positive and negative predictive values were 86.8 and 73.0%, respectively. The judgment of a positive opaque fetal membrane based on gross appearance significantly correlated with chorioamnionitis-related complications in term newborns after adjustments for confounding factors (OR;1.82 [1.07–3.11], P<0.05) (Cohort 2). A correlation was observed even after adjustments for confounding factors. The present study is the first to demonstrate that the judgment of a positive opaque fetal membrane based on gross appearance correlated with histological chorioamnionitis as well as chorioamnionitis-related complications in newborns delivered at term. The present results provide support for the traditionally-described importance of gross inspections for an opaque fetal membrane soon after birth.
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