Clara cell protein 16 concentration in mid-trimester amniotic fluid:: Association with fetal gender, fetal G > A+38 CC16 gene polymorphism and pregnancy outcome

被引:14
|
作者
Perni, SC
Vardhana, S
Kalish, R
Chasen, S
Witkin, SS
机构
[1] Cornell Univ, Weill Med Coll, Dept Obstet & Gynecol, Div Immunol Dis, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Obstet & Gynecol, Div Maternal Fetal Med, New York, NY 10021 USA
关键词
Clara cell protein 16; amniotic fluid; preterm premature rupture of membranes; race; genetic polymorphism;
D O I
10.1016/j.jri.2005.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Clara cell protein 16 (CC16) is a major immunomodulatory protein produced in the fetal lung. We hypothesized that the mid-trimester amniotic fluid concentration of CC16 would vary according to a +38 CC16 polymorphism in the fetal genome and that increased levels would be an early indicator of subsequent adverse pregnancy outcome. Mid-trimester singleton amniotic fluids from 244 women were assayed for CC16 by ELISA. DNA from fetal cells in 179 amniotic fluids were tested for the A>G polymorphism at position +38 in exon 1 by PCR. Outcome data were obtained from 233 women after completion of laboratory testing. Median CC16 levels were higher in amniotic fluids containing male fetuses than in those with females (p=0.0005). Median amniotic fluid CC16 levels were higher in Hispanics than in Whites and Asians (p<0.05). CC16*G homozygosity was associated with elevated amniotic fluid CC16 concentrations compared to CC16*A homozygotes (p=0.02). Intraamniotic CC16 levels were highest in pregnancies that subsequently resulted in preterm premature rupture of membranes (PPROM) (p=0.01). We conclude that mid-trimester intraamniotic CC16 concentrations vary by gender, ethnicity and fetal CC16 gene polymorphism. Elevated CC16 levels are predictive of subsequent development of PPROM. (C) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:85 / 90
页数:6
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