Reproductive Biology and Endocrinology (Oct 2010)

First trimester screening for trisomy 21 in gestational week 8-10 by ADAM12-S as a maternal serum marker

  • Guitton Marie,
  • Sarkissian Gaïané,
  • Wright Dave,
  • Ball Susan,
  • Tørring Niels,
  • Darbouret Bruno

DOI
https://doi.org/10.1186/1477-7827-8-129
Journal volume & issue
Vol. 8, no. 1
p. 129

Abstract

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Abstract Background A disintegrin and metalloprotease 12 (ADAM12-S) has previously been reported to be significantly reduced in maternal serum from women with fetal aneuploidy early in the first trimester and to significantly improve the quality of risk assessment for fetal trisomy 21 in prenatal screening. The aim of this study was to determine whether ADAM12-S is a useful serum marker for fetal trisomy 21 using the mixture model. Method In this case control study ADAM12-S was measured by KRYPTOR ADAM12-S immunoassay in maternal serum from gestational weeks 8 to 11 in 46 samples of fetal trisomy 21 and in 645 controls. Comparison of sensitivity and specificity of first trimester screening for fetal trisomy 21 with or without ADAM12-S included in the risk assessment using the mixture model. Results The concentration of ADAM12-S increased from week 8 to 11 and was negatively correlated with maternal weight. Log MoM ADAM12-S was positively correlated with log MoM PAPP-A (r = 0.39, P Conclusion The data show moderately decreased levels of ADAM12-S in cases of fetal aneuploidy in gestational weeks 8-11. However, including ADAM12-S in the routine risk does not improve the performance of first trimester screening for fetal trisomy 21.