Fetal vasculitis in preterm newborns: interrelationships, modifiers, and antecedents

被引:41
作者
Dammann, O
Allred, EN
Leviton, A
Shen-Schwarz, S
Heller, D
Genest, DR
Collins, MH
机构
[1] Childrens Hosp, Neuroepidemiol Unit, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[3] Hannover Med Sch, Perinatal Infect Dis Epidemiol Unit, D-30623 Hannover, Germany
[4] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[5] St Peters Med Ctr, Dept Pathol, New Brunswick, NJ 08903 USA
[6] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pathol, Newark, NJ 07103 USA
[7] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[8] Childrens Hosp, Ctr Med, Div Pathol, Cincinnati, OH 45229 USA
关键词
D O I
10.1016/j.placenta.2004.03.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Histologic expressions of the fetal inflammatory response predict preterm delivery and neonatal disorders. We examined 1146 placentas in the Developmental Epidemiology Network data set for histologic evidence of membrane inflammation (subchorionitis, chorionitis, and chorioamnionitis) and fetal vasculitis (acute umbilical vasculitis or chorionic vasculitis). Our main findings are that (1) in the presence of membrane inflammation, fetal vasculitis is common, (2) duration of membrane rupture and gestational age appear to modify the risk of fetal vasculitis, (3) this risk modification differs for the different components of fetal vasculitis, i.e. umbilical and chorionic vasculitis, and (4) antecedents can be identified that appear to increase or decrease the risk of fetal vasculitis among births with membrane inflammation. We conclude that fetal vasculitis, the morphologic component of the fetal inflammatory response, might not be a homogeneous entity and deserves further study. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:788 / 796
页数:9
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