Maternal-fetal interactions, predictive markers for preeclampsia, and programming

被引:24
作者
Huppertz, Berthold [1 ]
机构
[1] Med Univ Graz, Inst Cell Biol Histol & Embryol, A-8010 Graz, Austria
关键词
Preeclampsia; Biomarker; Prediction; Pregnancy; Programming; PLACENTAL GROWTH-FACTOR; CIRCULATING ANGIOGENIC FACTORS; ONSET PREECLAMPSIA; PROTEIN; 13; 1ST-TRIMESTER; HEMOGLOBIN; PREGNANCY; RISK; TROPHOBLAST; EXPRESSION;
D O I
10.1016/j.jri.2014.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During pregnancy close interactions between the maternal system and the fetal system via the placenta exist that result in a powerful crosstalk between both individuals. Looking for predictive biomarkers in maternal blood is extremely difficult because of this crosstalk as such markers may be derived from only maternal sources, only placental sources or both. In particular, the concentrations of markers derived from both sources may vary because of the huge variety of reasons and sources. During the last decade this has misled a number of scientists and clinicians who tried to decipher the sources of markers and the impact of the placenta and/or the maternal vascular system. A few examples for predictive biomarkers are presented, the placenta-specific marker placental protein 13 (PP13) and the angiogenic marker P1GF being released from both mother and placenta. Finally, a further reason why biomarkers may not be successful in predicting all cases of preeclampsia is that different causative routes lead to the development of preeclampsia. The differences in the development of preeclampsia not only explain why markers may or may not have a predictive value, but also why some mothers and/or children may display long-term effects later in life. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:26 / 32
页数:7
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