ADAM12-s in coelomic fluid and maternal serum in early pregnancy

被引:11
作者
Makrydimas, George
Sotiriadis, Alexandros
Spencer, Kevin
Cowans, Nicholas J.
Nicolaides, Kypros H.
机构
[1] Univ London Kings Coll Hosp, Harris Birthright Ctr Fetal Med, London SE5 9RS, England
[2] Ioannina Univ Hosp, Dept Obstet & Gynaecol, Ioannina 45500, Greece
[3] Harold Wood Hosp, Dept Clin Biochem, Romford RM3 0BE, Essex, England
关键词
coelocentesis; ADAM; 12; first trimester; trisomy; 21; pre-eclampsia;
D O I
10.1002/pd.1581
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objectives ADAM12-s is a placental protein. In early pregnancy, reduced maternal levels, of ADAM12-s have been reported in association with foetal trisomy 21 or 18 and in cases that subsequently develop pre-eclampsia and foetal growth restriction. The aim of this study is to investigate the distribution of ADAM12-s in early pregnancy by comparing its concentration in maternal serum, amniotic fluid and coelomic fluid. Methods Coelomic fluid was obtained by coelocentesis from 13 singleton pregnancies with live foetuses at 6.9-9.3 weeks of gestation. Maternal serum was also obtained in all cases and in six cases amniotic fluid was also obtained. The concentration of ADAM12-s was measured by dissociation enhanced lanthanide fluoro-immunoassay. Results The median concentration of ADAM12-s in maternal serum was 132.7 (range 33.8-254.5) ng/mL and in coelomic fluid it was 10.5 (range 1.3-15.8) ng/mL; there were no detectable levels in five of the six amniotic fluid samples. The concentration of maternal serum ADAM12-s increased significantly with gestation (r = 0.862, p < 0.0001). There was no significant association between coelomic fluid ADAM12-s and either gestation (r = 0.255, p = 0.401) or maternal serum ADAM12-s (r = 0.302, p = 0.316). Conclusion The distribution of ADAM12-s in maternal serum and the early embryonic fluid compartments is consistent with its syncytiotrophoblastic origin. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1197 / 1200
页数:4
相关论文
共 17 条
[1]   Defect of villous cytotrophoblast differentiation into syncytiotrophoblast in Down's syndrome [J].
Frendo, JL ;
Vidaud, M ;
Guibourdenche, J ;
Luton, D ;
Muller, F ;
Bellet, D ;
Giovagrandi, Y ;
Tarrade, A ;
Porquet, D ;
Blot, P ;
Evain-Brion, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (10) :3700-3707
[2]   A novel, secreted form of human ADAM 12 (meltrin α) provokes myogenesis in vivo [J].
Gilpin, BJ ;
Loechel, F ;
Mattei, MG ;
Engvall, E ;
Albrechtsen, R ;
Wewer, UM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :157-166
[3]   Apoptosis in the trophoblast - Role of apoptosis in placental morphogenesis [J].
Huppertz, B ;
Kingdom, JCP .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2004, 11 (06) :353-362
[4]  
HUPPERTZ B, 2006, MICRON
[5]   PREGNANCY-ASSOCIATED PLASMA-PROTEIN-A LEVELS IN MATERNAL SERUM, EXTRAEMBRYONIC CELOMIC AND AMNIOTIC FLUIDS IN THE FIRST TRIMESTER [J].
ILES, RK ;
WATHEN, NC ;
SHARMA, KB ;
CAMPBELL, J ;
GRUDZINSKAS, JG ;
CHARD, T .
PLACENTA, 1994, 15 (07) :693-699
[6]   ADAMs, a disintegrin and metalloproteinases, mediate shedding of oxytocinase [J].
Ito, N ;
Nomura, S ;
Iwase, A ;
Ito, T ;
Kikkawa, F ;
Tsujimoto, M ;
Ishiura, S ;
Mizutani, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 314 (04) :1008-1013
[7]   Fluid compartments of the embryonic environment [J].
Jauniaux, E ;
Gulbis, B .
HUMAN REPRODUCTION UPDATE, 2000, 6 (03) :268-278
[8]   COELOCENTESIS - A NEW TECHNIQUE FOR EARLY PRENATAL-DIAGNOSIS [J].
JURKOVIC, D ;
JAUNIAUX, E ;
CAMPBELL, S ;
PANDYA, P ;
CARDY, DL ;
NICOLAIDES, KH .
LANCET, 1993, 341 (8861) :1623-1624
[9]   Reduction of the disintegrin and metalloprotease ADAM12 in preeclampsia [J].
Laigaard, J ;
Sorensen, T ;
Placing, S ;
Holck, P ;
Fröhlich, C ;
Wojdemann, KR ;
Sundberg, K ;
Shalmi, AC ;
Tabor, A ;
Norgaard-Pedersen, B ;
Ottesen, B ;
Christiansen, M ;
Wewer, UM .
OBSTETRICS AND GYNECOLOGY, 2005, 106 (01) :144-149
[10]   The level of ADAM12-S in maternal serum is an early first-trimester marker of fetal trisomy 18 [J].
Laigaard, J ;
Christiansen, M ;
Fröhlich, C ;
Pedersen, BN ;
Ottesen, B ;
Wewer, UM .
PRENATAL DIAGNOSIS, 2005, 25 (01) :45-46