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PMID: 19706590 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Fetal growth restriction and chronic lung disease among infants born before the 28th week of gestation.

Pediatrics ·Vol. 124 ·No. 3 ·2009-09-00 ·Pages e450-8

Bose C, Van Marter LJ, Laughon M, O'Shea TM, Allred EN, Karna P, Ehrenkranz RA, Boggess K, Leviton A, Extremely Low Gestational Age Newborn Study Investigators

Abstract

Improvement in survival of extremely premature infants over the past several decades has resulted in an increase in the number of infants with chronic lung disease (CLD). Historical neonatal exposures associated with CLD now less frequently precede the disease. There is now increasing interest in exposures and events before delivery that predict CLD. The objective of this study was to identify current prenatal predictors of CLD. We collected data about prenatal, placental, and neonatal characteristics of 1241 newborns who were delivered before completion of the 28th week of gestation. Associations between prenatal factors, microbiologic and histologic characteristics of the placenta, and selected neonatal characteristics and CLD risk were first evaluated in univariate analyses. Subsequent multivariate analyses investigated the contribution of prenatal factors, particularly fetal growth restriction (FGR), to CLD risk. Among the prenatal factors, birth weight z scores, used as a marker of FGR, provided the most information about CLD risk. Indicators of placental inflammation and infection were not associated with increased risk of CLD. Within nearly all strata of prenatal, placental, and neonatal variables, growth-restricted infants were at increased CLD risk, compared with infants who were not growth-restricted. FGR was the only maternal or prenatal characteristic that was highly predictive of CLD after adjustment for other risk factors. FGR is independently associated with the risk of CLD. Thus, factors that control fetal somatic growth may have a significant impact on vulnerability to lung injury and in this way increase CLD risk.

MeSH Terms
Chronic Disease Female Fetal Growth Retardation Gestational Age Humans Infant, Newborn Infant, Premature Infant, Premature, Diseases/epidemiology,etiology Lung Diseases/epidemiology,etiology Male Risk Factors
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Bose Carl
Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA. [email protected]
Van Marter Linda J
Laughon Matthew
O'Shea T Michael
Allred Elizabeth N
Karna Padmani
Ehrenkranz Richard A
Boggess Kim
Leviton Alan
Extremely Low Gestational Age Newborn Study Investigators
Investigators
15 investigators, click to expand
Dammann Olaf
Shah Bhavesh L
Martin Camilia
Insoft Robert
Kuban Karl
Bednarek Francis
Fiascone John
Engelke Stephen C
Poortenga Mariel
Beaumont Ed
Paneth Nigel
Schreiber Michael D
Batton Daniel
Pavlov Greg
Hirtz Deborah
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Article Info
Journal
Pediatrics
Abbr.
Pediatrics
ISSN
1098-4275
Published
2009-09-00
Epub
2009-00-17
Pages
e450-8
Language
English
Region
United States
NLM ID
0376422
PMCID
PMC2891899
Subset
IM
Grants
NINDS NIH HHS · U01 NS040069 · United States
NINDS NIH HHS · U01 NS040069-04 · United States
NINDS NIH HHS · 5U01NS040069-04 · United States
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