TY - JOUR
T1 - Preterm birth subtypes, placental pathology findings, and risk of neurodevelopmental disabilities during childhood
AU - Raghavan, Ramkripa
AU - Helfrich, Blandine Bustamante
AU - Cerda, Sandra R.
AU - Ji, Yuelong
AU - Burd, Irina
AU - Wang, Guoying
AU - Hong, Xiumei
AU - Fu, Lingling
AU - Pearson, Colleen
AU - Daniele Fallin, M.
AU - Zuckerman, Barry
AU - Wang, Xiaobin
N1 - Funding Information:
This study is supported in part by the Health Resources and Services Administration of the U.S. Department of Health and Human Services under grant number R40MC27443 , Autism Field-initiated Innovative Research Studies Program ; and grant number UJ2MC31074 , Autism Single Investigator Innovation Program . This information or content and conclusions are those of the author and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS or the U.S. Government.
Funding Information:
The Boston Birth Cohort (the parent study) was supported in part by the March of Dimes PERI grants ( 20-FY02-56 , #21-FY07-605 ); and the National Institutes of Health grants ( R21ES011666 , R01HD041702 , R21HD066471 , U01AI090727 , R21AI079872 , R01HD086013 , 2R01HD041702 ).
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/8
Y1 - 2019/8
N2 - Introduction: Preterm birth (PTB) and in-utero inflammation are recognized risk factors of neurodevelopmental disabilities (NDDs); however, their combined role in NDDs is unknown. We examined the independent and joint association of PTB and placental histological findings with the childhood risk of NDDs (overall and by subgroups including autism spectrum disorder (ASD) and ADHD). Methods: We analyzed data from the Boston Birth Cohort, where mother-infant pairs were enrolled at birth and followed from birth onwards. Birth outcomes, placental pathology and NDDs were obtained from electronic medical records. Placental pathology was categorized using a standardized classification system proposed by the Amsterdam Placental Workshop Group. Results: PTB (all, including spontaneous, medically indicated) was an independent risk factor for NDDs. Placental histological chorioamnionitis (CA) and PTB additively increased the odds of NDDs (aOR: 2.16, 95% CI: 1.37, 3.39), as well as ADHD (aOR: 2.75, 95% CI: 1.55, 4.90), other developmental disabilities (aOR: 1.96, 95% CI: 1.18, 3.25) and possibly ASD (aOR: 2.31, 95% CI: 0.99, 5.39). The above associations were more pronounced in spontaneous than medically indicated PTB. PTB alone in the absence of CA only had a moderate association with ASD and ADHD. Placental maternal vascular malperfusion alone or in combination with PTB was not associated with the risk of NDDs. Discussion: Our study provided new insights on PTB and NDDs by further considering preterm subtypes and placental histology. We revealed that children of spontaneous PTB along with histological CA were at the highest risk for a spectrum of NDDs.
AB - Introduction: Preterm birth (PTB) and in-utero inflammation are recognized risk factors of neurodevelopmental disabilities (NDDs); however, their combined role in NDDs is unknown. We examined the independent and joint association of PTB and placental histological findings with the childhood risk of NDDs (overall and by subgroups including autism spectrum disorder (ASD) and ADHD). Methods: We analyzed data from the Boston Birth Cohort, where mother-infant pairs were enrolled at birth and followed from birth onwards. Birth outcomes, placental pathology and NDDs were obtained from electronic medical records. Placental pathology was categorized using a standardized classification system proposed by the Amsterdam Placental Workshop Group. Results: PTB (all, including spontaneous, medically indicated) was an independent risk factor for NDDs. Placental histological chorioamnionitis (CA) and PTB additively increased the odds of NDDs (aOR: 2.16, 95% CI: 1.37, 3.39), as well as ADHD (aOR: 2.75, 95% CI: 1.55, 4.90), other developmental disabilities (aOR: 1.96, 95% CI: 1.18, 3.25) and possibly ASD (aOR: 2.31, 95% CI: 0.99, 5.39). The above associations were more pronounced in spontaneous than medically indicated PTB. PTB alone in the absence of CA only had a moderate association with ASD and ADHD. Placental maternal vascular malperfusion alone or in combination with PTB was not associated with the risk of NDDs. Discussion: Our study provided new insights on PTB and NDDs by further considering preterm subtypes and placental histology. We revealed that children of spontaneous PTB along with histological CA were at the highest risk for a spectrum of NDDs.
KW - ADHD
KW - Autism
KW - Chorioamnionitis
KW - Maternal vascular malperfusion
KW - Neurodevelopmental disabilities
KW - Preterm
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U2 - 10.1016/j.placenta.2019.06.374
DO - 10.1016/j.placenta.2019.06.374
M3 - Article
C2 - 31477202
AN - SCOPUS:85067886254
SN - 0143-4004
VL - 83
SP - 17
EP - 25
JO - Placenta
JF - Placenta
ER -