Extracellular nucleic acids in maternal circulation as potential biomarkers for placental insufficiency
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
22364204
PubMed Central
PMC3391496
DOI
10.1089/dna.2011.1530
Knihovny.cz E-zdroje
- MeSH
- biologické markery krev MeSH
- DNA krev MeSH
- extracelulární prostor genetika MeSH
- lidé MeSH
- matky * MeSH
- placentární insuficience krev diagnóza genetika patologie MeSH
- RNA krev MeSH
- těhotenství MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- biologické markery MeSH
- DNA MeSH
- RNA MeSH
Since the placenta is being continuously remodeled during normal placental development, extracellular nucleic acids of both fetal and placental origin, packed into either trophoblast-derived apoptotic bodies or shedding syncytiotrophoblast microparticles, may be detected in maternal circulation during the course of normal gestation. Placental-insufficiency-related pregnancy complications have been shown to be associated with excessive placental trophoblast apoptosis and shedding of placenta debris. Recent advances in the field are reviewed with a focus on the diagnostic potential of particular molecular biomarkers and their eventual implementation in the currently used predictive and diagnostic algorithms for placental-insufficiency-related pregnancy complications.
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ACOG Committee on Practice Bulletins—Obstetrics. Diagnosis and management of preeclampsia and eclampsia. Obstet Gynecol. 2002;99:159–167. PubMed
Akolekar R. Minekawa R. Veduta A. Romero X.C. Nicolaides K.H. Maternal plasma inhibin A at 11–13 weeks of gestation in hypertensive disorders of pregnancy. Prenat Diagn. 2009;29:753–760. PubMed
Akolekar R. Syngelaki A. Sarquis R. Zvanca M. Nicolaides K.H. Prediction of early, intermediate and late pre-eclampsia from maternal factors, biophysical and biochemical markers at 11–13 weeks. Prenat Diagn. 2011;31:66–74. PubMed
Alberry M.S. Maddocks D.G. Hadi M.A. Metawi H. Hunt L.P. Abdel-Fattah S.A. Avent N.D. Soothill P.W. Quantification of cell free fetal DNA in maternal plasma in normal pregnancies and in pregnancies with placental dysfunction. Am J Obstet Gynecol. 2009;2009:98.e1–98.e6. PubMed
Anderson U.D. Olsson M.G. Kristensen K.H. Akerström B. Hansson S.R. Review: biochemical markers to predict preeclampsia. Placenta. 2011;33(Suppl):S42–S47. PubMed
Ason B. Darnell D.K. Wittbrodt B. Berezikov E. Kloosterman W.P. Wittbrodt J. Antin P.B. Plasterk R.H. Differences in vertebrate microRNA expression. Proc Natl Acad Sci U S A. 2006;103:14385–14389. PubMed PMC
Aspirin and pre-eclampsia. Lancet. 1986;1:328–329. PubMed
Baehrecke E.H. miRNAs: micro managers of programmed cell death. Curr Biol. 2003;13:R473–R475. PubMed
Bartel D.P. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004;116:281–297. PubMed
Beta J. Akolekar R. Ventura W. Syngelaki A. Nicolaides K.H. Prediction of spontaneous preterm delivery from maternal factors, obstetric history and placental perfusion and function at 11–13 weeks. Prenat Diagn. 2011;31:75–83. PubMed
Brennecke J. Hipfner D.R. Stark A. Russell R.B. Cohen S.M. Bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila. Cell. 2003;113:25–36. PubMed
Bujold E. Roberge S. Lacasse Y. Bureau M. Audibert F. Marcoux S. Forest J.C. Giguere Y. Prevention of preeclampsia and intrauterine growth restriction with aspirin started in early pregnancy: a meta-analysis. Obstet Gynecol. 2010;116:402–414. PubMed
Calin G.A. Croce M.C. MicroRNA signatures in human cancers. Nat Rev Cancer. 2006;6:857–866. PubMed
Caramelli E. Rizzo N. Concu M. Simonazzi G. Carinci P. Bondavalli C. Bovicelli L. Farina A. Cell-free fetal DNA concentration in plasma of patients with abnormal uterine artery Doppler waveform and intrauterine growth restriction—a pilot study. Prenatal Diagn. 2003;23:367–371. PubMed
Chan K.C. Ding C. Gerovassili A. Yeung S.W. Chiu R.W. Leung T.N. Lau T.K. Chim S.S. Chung G.T. Nicolaides K.H. Lo Y.M. Hypermethylated RASSF1A in maternal plasma: a universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem. 2006;52:2211–2218. PubMed
Chan K.C. Zhang J. Hui A.B. Wong N. Lau T.K. Leung T.N. Lo K.W. Huang D.W. Lo Y.M. Size distributions of maternal and fetal DNA in maternal plasma. Clin Chem. 2004;50:88–92. PubMed
Chim S.S. Shing T.K. Hung E.C. Leung T.Y. Lau T.K. Chiu R.W. Lo Y.M. Detection and characterization of placental microRNAs in maternal plasma. Clin Chem. 2008;54:482–490. PubMed
Cotter A.M. Martin C.M. O'leary J.J. Daly S.F. Increased fetal DNA in the maternal circulation in early pregnancy is associated with an increased risk of preeclampsia. Am J Obstet Gynecol. 2004;191:515–520. PubMed
Department of Biological Science and Technology, Institute of Bioinformatics National Chiao Tung University; Hsinchu, Taiwan: 2011.
De Vivo A. Baviera G. Giordano D. Todarello G. Corrado F. D'anna R. Endoglin, PlGF and sFlt-1 as markers for predicting pre-eclampsia. Acta Obstet Gynecol Scand. 2008;87:837–842. PubMed
Engel K. Płonka T. Bilar M. Czajkowska E. Orzińska E. Brojer E. Ronin-Walknowska E. The analysis of the correlation between extracellular fetal DNA concentration in maternal circulation and severity of preeclampsia. Ann Acad Med Stetin. 2007;53:20–25. PubMed
Enquobahrie D.A. Abetew D.F. Sorensen T.K. Willoughby D. Chidambaram K. Williams M.A. Placental microRNA expression in pregnancies complicated by preeclampsia. Am J Obstet Gynecol. 2011;204:178.e12–178.e21. PubMed PMC
Farina A. Chan C.W.M. Chiu R.W.K. Tsui N.B.Y. Carinci P. Concu M. Banzola I. Rizzo N. Lo Y.M.D. Circulating corticotropin-releasing hormone mRNA in maternal plasma: relationship with gestational age and severity of preeclampsia. Clin Chem. 2004a;50:1851–1854. PubMed
Farina A. Sekizawa A. Purwosunu Y. Rizzo N. Banzola I. Concu M., et al. Quantitative distribution of a panel of circulating mRNA in preeclampsia versus controls. Prenat Diagn. 2006;26:1115–1120. PubMed
Farina A. Sekizawa A. Rizzo N. Concu M. Banzola I. Carinci P. Simonazzi G. Okai T. Cell-free fetal DNA (SRY locus) concentration in maternal plasma is directly correlated to the time elapsed from the onset of preeclampsia to the collection of blood. Prenat Diagn. 2004b;24:293–297. PubMed
Farina A. Sekizawa A. Sugito Y. Iwasaki M. Jimbo M. Saito H. Okai T. Fetal DNA in maternal plasma as a screening variable for preeclampsia. Prenat Diagn. 2004c;24:83–86. PubMed
Fujito N. Samura O. Miharu N. Tanigawa M. Hyodo M. Kudo Y. Increased plasma mRNAs of placenta-specific 1 (PLAC1) and glial cells-missing 1 (GCM1) in mothers with pre-eclampsia. Hiroshima J Med Sci. 2006;55:9–15. PubMed
Galbiati S. Causarano V. Pinzani P. Francesca S. Orlando C. Smid M. Pasi F. Castiglioni M.T. Cavoretto P. Rovere-Querini P. Pedroni S. Calza S. Ferrari M. Cremonesi L. Evaluation of a panel of circulating DNA, RNA and protein potential markers for pathologies of pregnancy. Clin Chem Lab Med. 2010;48:791–794. PubMed
Gilad S. Meiri E. Yogev Y. Benjamin S. Lebanony D. Yerushalmi N. Benjamin H. Kushnir M. Cholakh H. Melamed N. Bentwich Z. Hod M. Goren Y. Chajut A. Serum microRNAs are promising novel biomarkers. PLoS One. 2008;3:e3148. PubMed PMC
Goetzinger K.R. Singla A. Gerkowicz S. Dicke J.M. Gray D.L. Odibo A.O. Predicting the risk of pre-eclampsia between 11 and 13 weeks' gestation by combining maternal characteristics and serum analytes, PAPP-A and free β-hCG. Prenat Diagn. 2010;30:1138–1142. PubMed PMC
Gunawardana L. Zammit S. Lewis G. Gunnell D. Hollis C. Wolke D. Harrison G. Examining the association between maternal analgesic use during pregnancy and risk of psychotic symptoms during adolescence. Schizophr Res. 2011;126:220–225. PubMed
Hromadnikova I. Benesova M. Zejskova L. The effect of DYS-14 copy number variations on extracellular fetal DNA quantification in maternal circulation. DNA Cell Biol. 2009;28:351–358. PubMed
Hromadnikova I. Kotlabova K. Doucha J. Dlouha K. Absolute and relative quantification of placental specific microRNAs in maternal circulation with placental insufficiency related complications. presented at the 5th International qPCR Symposium; Freising, Germany. Mar 28;; 2011a. Abstract no. ID109. April 1. PubMed
Hromadnikova I. Kotlabova K. Doucha J. Dlouha K. Absolute and relative quantification of placental specific microRNAs in maternal circulation with placental insufficiency related complications. presented at the 21st World Congress on Ultrasound in Obstetrics and Gynecology (ISUOG); Los Angeles, CA. Sep 18–22;.2011b. Abstract no. OP06.10. PubMed
Hromadnikova I. Kotlabova K. Doucha J. Dlouha K. Absolute and relative quantification of placental specific microRNAs in maternal circulation with placental insufficiency related complications. presented at the 15th World Congress on Controversies in Obstetrics, Gynecology and Infertility (COGI); Sanya Hainan, China. Dec 8–11;.2011c. Abstract no. 17. PubMed
Hromadnikova I. Kotlabova K. Doucha J. Dlouha K. Krofta L. Absolute and relative quantification of placental specific microRNAs in maternal circulation with placental insufficiency related complications. J Mol Diagn. 2012;14:160–167. PubMed
Hromadnikova I. Kotlabová K. Jirásek J.E. Doucha J. Detection of placenta-specific microRNAs in maternal circulation. Ceska Gynekol. 2010a;75:252–256. PubMed
Hromadnikova I. Zejskova L. Kotlabova K. Jancuskova T. Doucha J. Dlouha K., et al. Quantification of extracellular DNA using hypermethylated RASSF1A, SRY, and GLO sequences—evaluation of diagnostic possibilities for predicting placental insufficiency. DNA Cell Biol. 2010b;29:295–301. PubMed
Hu Z.Y. Liu Y.X. Liu K. Byrne S. Ny T. Feng Q. Ockleford C.D. Expression of tissue type and urokinase type plasminogen activators as well as plasminogen activator inhibitor type-1 and type-2 in human and rhesus monkey placenta. J Anat. 1999;194:183–195. PubMed PMC
Huppertz B. Placental origins of preeclampsia: challenging the current hypothesis. Hypertension. 2008;51:970–975. PubMed
Huppertz B. Kingdom J.C. Apoptosis in the trophoblast—role of apoptosis in placental morphogenesis. J Soc Gynecol Investig. 2004;11:353–362. PubMed
Illanes S. Parra M. Serra R. Pino K. Fiquerosa-Diesel H. Romero C. Arraztoa J.A. Michea L. Soothill P.W. Increased free fetal DNA levels in early pregnancy plasma of women who subsequently develop preeclampsia and intrauterine growth restriction. Prenat Diagn. 2009;29:1118–1122. PubMed
Karagiannis G. Akolekar R. Sarquis R. Wright D. Nicolaides K.H. Prediction of small-for-gestation neonates from biophysical and biochemical markers at 11–13 weeks. Fetal Diagn Ther. 2011;29:148–154. PubMed
Khan K.S. Wojdyla D. Say L. Gülmezoglu A.M. Van Look P.F. WHO analysis of causes of maternal death: a systematic review. Lancet. 2006;367:1066–1074. PubMed
Khong T.Y. De Wolf F. Robertson W.B. Brosens I. Inadequate maternal vascular response to placentation in pregnancies complicated by pre-eclampsia and by small-for-gestational age infants. Br J Obstet Gynaecol. 1986;93:1049–1059. PubMed
Khvorova A. Reynolds A. Jayasena S.D. Functional siRNAs and miRNAs exhibit strand bias. Cell. 2003;115:209–216. PubMed
Kloosterman W.P. Plasterk R.H. The diverse functions of microRNAs in animal development and disease. Dev Cell. 2006;11:441–450. PubMed
Kotlabova K. Doucha J. Hromadnikova I. Placental-specific microRNA in maternal circulation–identification of appropriate pregnancy associated microRNAs with diagnostic potential. J Rep Imunol. 2011;89:185–191. PubMed
Lai E.C. MicroRNAs are complementary to 3′UTR sequence motifs that mediate negative post-transcriptional regulation. Nat Genet. 2002;23:175–205. PubMed
Lau T.W. Leung T.N. Chan L.Y. Lau T.K. Chan K.C. Tam W.H. Lo Y.M. Fetal DNA clearance from maternal plasma is impaired in preeclampsia. Clin Chem. 2002;48:2141–2146. PubMed
Leung T.N. Zhang J. Lau T.K. Chan L.Y. Lo Y.M. Increased maternal plasma fetal DNA concentrations in women who eventually develop preeclampsia. Clin Chem. 2001;47:137–139. PubMed
Levine R.J. Qian C. Leshane E.S. Yu K.F. England L.J. Schisterman E.F. Wataganara T. Romero R. Bianchi D.W. Two-stage elevation of cell-free fetal DNA in maternal sera before onset of preeclampsia. Am J Obstet Gynecol. 2004;190:707–713. PubMed
Li Y. Zimmermann B. Rusterholz C. Kang A. Holzgreve W. Hahn S. Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms. Clin Chem. 2004;50:1002–1011. PubMed
Liang Y. Ridzon D. Wong L. Chen C. Characterization of microRNA expression profiles in normal human tissues. BMC Genomics. 2007;8:166. PubMed PMC
Lo Y.M. Corbetta N. Chamberlain P.F. Rai V. Sargent I.L. Redman C.W. Wainscoat J.S. Presence of fetal DNA in maternal plasma and serum. Lancet. 1997;350:485–487. PubMed
Lo Y.M. Leung T.N. Tein M.S. Sargent I.L. Zhang J. Lau T.K. Haines C.J. Redman C.W. Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia. Clin Chem. 1999;45:184–188. PubMed
Lo Y.M. Tein M.S. Lau T.K. Haines C.J. Leung T.N. Poon P.M. Wainscoat J.S. Johnson P.J. Chang A.M. Hjelm N.M. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet. 1998;62:768–775. PubMed PMC
Lo Y.M.D. Chiu R.W.K. Chim S.S.C. Ding C. Chan K.C. Wong H.N.I. Yuen K.C.R. New fetal methylation markers. 2007. WO2007132166.
Lo Y.M.D. Chiu R.W.K. Chim S.S.C. Ding C. Chan K.C. Wong H.N.I. Yuen K.C.R. Fetal methylation markers. 2009. US20090155776.
Martinhago C.D. de Oliveira R.M. Tomitão Canas Mdo C. Vagnini L.D. Alcantara Oliveira J.B. Petersen C.G. Franco Junior J.G. Accuracy of fetal gender determination in maternal plasma at 5 and 6 weeks of pregnancy. Prenat Diagn. 2006;26:1219–1223. PubMed
Mayor-Lynn K. Toloubeydokhti T. Cruz A.C. Chegini N. Expression profile of microRNAs and mRNAs in human placentas from pregnancies complicated by preeclampsia and preterm labor. Reprod Sci. 2011;18:46–56. PubMed PMC
Mikat B. Zeller A. Scherag A. Drommelschmidt K. Kimmig R. Schmidt M. βhCG and PAPP-A in first trimester: predictive factors for preeclampsia? Hypertens Pregnancy. 2011 2011 Dec 9; doi: 10.3109/10641955.2011.638956. [Epub ahead of print] PubMed DOI
Miura K. Miura S. Yamasaki K. Higashijima A. Kinoshita A. Yoshiura K. Masuzaki H. Identification of pregnancy-associated microRNAs in maternal plasma. Clin Chem. 2010;56:1767–1771. PubMed
Nelson D.M. Apoptotic changes occur in syncytiotrophoblast of human placental villi where fibrin type fibrinoid is deposited at discontinuities in the villous trophoblast. Placenta. 1996;17:387–391. PubMed
Ng E.K. Leung T.N. Tsui N.B. Lau T.K. Panesar N.S. Chiu R.W. Lo Y.M. The concentration of circulating corticotropin-releasing hormone mRNA in maternal plasma is increased in preeclampsia. Clin Chem. 2003a;49:727–731. PubMed
Ng E.K. Tsui N.B. Lau T.K. Leung T.N. Chiu R.W. Panesar N.S. Lit L.C. Chan K.W. Lo Y.M. mRNA of placental origin is readily detectable in maternal plasma. Proc Natl Acad Sci U S A. 2003b;100:4748–4753. PubMed PMC
Noack F. Ribbat-Idel J. Thorns C. Chiriac A. Axt-Fliedner R. Diedrich K. Feller A.C. miRNA expression profiling in formalin-fixed and paraffin-embedded placental tissue samples from pregnancies with severe preeclampsia. J Perinat Med. 2011;39:267–271. PubMed
Orozco A.F. Bischoff F.Z. Horne C. Popek E. Simpson J.L. Lewis D.E. Hypoxia-induced membrane-bound apoptotic DNA particles: potential mechanism of fetal DNA in maternal plasma. Ann N Y Acad Sci. 2006;1075:57–62. PubMed
Oudejans C.B. Tjoa M.L. Westerman B.A. Mulders M.A. Van Wijk I.J. Van Vugt J.M. Circulating trophoblast in maternal blood. Prenat Diagn. 2003;23:111–116. PubMed
Pang W.W. Tsui M.H. Sahota D. Leung T.Y. Lau T.K. Lo Y.M. Chiu R.W. A strategy for identifying circulating placental RNA markers for fetal growth assessment. Prenat Diagn. 2009;29:495–504. PubMed
Pineles B.L. Romero R. Montenegro D. Tarca A.L. Han Y.M. Kim Y.M. Draghici S. Espinoza J. Kusanovic J.P. Mittal P. Hassan S.S. Kim C.J. Distinct subset of microRNAs are expressed differentially in the human placentas of patients with preeclampsia. Am J Obstet Gynecol. 2007;196:261.e1–261.e6. PubMed
Poon L.C. Akolekar R. Lachmann R. Beta J. Nicolaides K.H. Hypertensive disorders in pregnancy: screening by biophysical and biochemical markers at 11–13 weeks. Ultrasound Obstet Gynecol. 2010a;35:662–670. PubMed
Poon L.C. Kametas N.A. Chelemen T. Leal A. Nicolaides K.H. Maternal risk factors for hypertensive disorders in pregnancy: a multivariate approach. J Hum Hypertens. 2010b;24:104–110. PubMed
Poon L.C. Kametas N.A. Maiz N. Akolekar R. Nicolaides K.H. First-trimester prediction of hypertensive disorders in pregnancy. Hypertension. 2009;53:812–818. PubMed
Purwosunu Y. Sekizawa A. Farina A. Wibowo N. Koide K. Okazaki S. Nakamura M. Okai T. Evaluation of physiological alterations of the placenta through analysis of cell-free messenger ribonucleic acid concentrations of angiogenic factors. Am J Obstet Gynecol. 2008;198:124.e1–124.e7. PubMed
Purwosunu Y. Sekizawa A. Farina A. Wibowo N. Okazaki S. Nakamura M. Samura O. Fujito N. Okai T. Cell-free mRNA concentrations of CRH, PLAC1, and selectin-P are increased in the plasma of pregnant women with preeclampsia. Prenat Diagn. 2007a;27:772–777. PubMed
Purwosunu Y. Sekizawa A. Koide K. Farina A. Wibowo N. Wiknjosastro G.H. Okazaki S. Chiba H. Okai T. Cell-free mRNA concentrations of plasminogen activator inhibitor-1 and tissue-type plasminogen activator are increased in the plasma of pregnant women with preeclampsia. Clin Chem. 2007b;53:399–404. PubMed
Purwosunu Y. Sekizawa A. Okazaki S. Farina A. Wibowo N. Nakamura M. Rizzo N. Saito H. Okai T. Prediction of preeclampsia by analysis of cell-free messenger RNA in maternal plasma. Am J Obstet Gynecol. 2009;200:386.e1–386.e7. PubMed
Reddy A. Zhong X.Y. Rusterholz C. Hahn S. Holzgreve W. Redman C.W. Sargent I.L. The effect of labour and placental separation on the shedding of syncytiotrophoblast microparticles, cell-free DNA and mRNA in normal pregnancy and pre-eclampsia. Placenta. 2008;29:942–949. PubMed
Rosenfeld N. Aharonov R. Meiri E. Rosenwald S. Spector Y. Zepeniuk M. Benjamin H. Shabes N. Tabak S. Levy A. Lebanony D. Goren Y. Silberschein E. Targan N. Ben-Ari A. Gilad S. Sion-Vardy N. Tobar A. Feinmesser M. Kharenko O. Nativ O. Nass D. Perelman M. Yosepovich A. Shalmon B. Polak-Charcon S. Fridman E. Avniel A. Bentwich I. Bentwich Z. Cohen D. Chajut A. Barshack I. MicroRNAs accurately identify cancer tissue origin. Nat Biotechnol. 2008;26:462–469. PubMed
Schwarz D.S. Hutvágner G. Du T. Xu Z. Aronin N. Zamore P.D. Asymmetry in the assembly of the RNAi enzyme complex. Cell. 2003;115:199–208. PubMed
Sekizawa A. Jimbo M. Saito H. Iwasaki M. Matsuoka R. Okai T. Farina A. Cell-free fetal DNA in plasma of pregnant women with severe fetal growth restriction. Am J Obstet Gynecol. 2003;188:480–484. PubMed
Sifakis S. Zaravinos A. Maiz N. Spandidos D.A. Nicolaides K.H. First-trimester maternal plasma cell-free fetal DNA and preeclampsia. Am J Obstet Gynecol. 2009;201:472.e1–472.e7. PubMed
Smid M. Vassallo A. Lagona F. Valsecchi L. Maniscalco L. Danti L. Lojacono A. Ferrari A. Ferrari M. Cremonesi L. Quantitative analysis of fetal DNA in maternal plasma in pathological conditions associated with placental abnormalities. Ann N Y Acad Sci. 2001;945:132–137. PubMed
Spencer K. Cowans N.J. Nicolaides K.H. Low levels of maternal serum PAPP-A in the first trimester and the risk of pre-eclampsia. Prenat Diagn. 2008;28:7–10. PubMed
Stirnemann J. Salomon L. Benoist G. Essaoui M. Bernard J. Ville Y. Performance of routine screening for preeclampsia by maternal factors, uterine artery Doppler, arterial pressure and PAPP-A in a general population setting. presented at the 21st World Congress on Ultrasound in Obstetrics and Gynecology (ISUOG); Los Angeles, CA. Sep 18–22;.2011. Abstract no. OC03.01.
Thorp J.A. Walsh S.W. Brath P.C. Low-dose aspirin inhibits thromboxane, but not prostacyclin, production by human placental arteries. Am J Obstet Gynecol. 1988;159:1381–1384. PubMed
Tsui D.W. Chan K.C. Chim S.S. Chan L.W. Leung T.Y. Lau T.K. Lo Y.M. Chiu R.W. Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia. Prenat Diagn. 2007;27:1212–1218. PubMed
Valensise H. Vasapollo B. Gagliardi G. Novelli G.P. Early and late preeclampsia two different maternal hemodynamic states in the latent phase of the disease. Hypertension. 2008;52:873–880. PubMed
Verlohren S. Galindo A. Schlembach D. Zeisler H. Herraiz I. Moertl M.G. Pape J. Dudenhausen J.W. Denk B. Stepan H. An automated method for the determination of the sFlt-1/PIGF ratio in the assessment of preeclampsia. Am J Obstet Gynecol. 2010;202:161.e1–161.e11. PubMed
Von Dadelszen P. Magee L.A. Roberts J.M. Subclassification of preeclampsia. Hypertens Pregnancy. 2003;22:143–148. PubMed
Whitley G.S. Dash P.R. Ayling L.J. Prefumo F. Thilaganathan B. Cartwright J.E. Increased apoptosis in first trimester extravillous trophoblasts from pregnancies at higher risk of developing preeclampsia. Am J Pathol. 2007;170:1903–1909. PubMed PMC
WHO. World Health Organization International Collaborative Study of Hypertensive Disorders in Pregnancy. Geographic variation in the incidence of hypertension in pregnancy. Am J Obstet Gynecol. 1988;158:80–83. PubMed
Zhang Y. Fei M. Xue G. Zhou Q. Jia Y. Li L. Xin H. Sun S. Elevated levels of hypoxia-inducible microRNA-210 in preeclampsia: new insights into molecular mechanisms for the disease. J Cell Mol Med. 2011;16:249–259. PubMed PMC
Zhao F. Wang J. Liu R. Yang J. Cui K. Wu Y. Guo J. Mu Y. Wang X. Quantification and application of the placental epigenetic signature of the RASSF1A gene in maternal plasma. Prenat Diagn. 2010;30:778–782. PubMed
Zhong X.Y. Laivuori H. Livingston J.C. Ylikorkala O. Sibai B.M. Holzgreve W. Hahn S. Elevation of both maternal and fetal extracellular circulating deoxyribonucleic acid concentrations in the plasma of pregnant women with preeclampsia. Am J Obstet Gynecol. 2001;184:414–419. PubMed
Zhong X.Y. Volgmann T. Hahn S. Holzgreve W. Large scale analysis of circulatory fetal DNA concentrations in pregnancies which subsequently develop preeclampsia using two Y chromosome specific real-time PCR assays. JTTGA. 2007;8:135–139.
Zhu X.M. Han T. Sargent I.L. Yin G.W. Yao Y.Q. Differential expression profile of microRNAs in human placentas from preeclamptic pregnancies vs normal pregnancies. AJOG. 2009;200:661.e1–661.e7. PubMed
Expression profile of C19MC microRNAs in placental tissue in pregnancy-related complications
Circulating C19MC microRNAs in preeclampsia, gestational hypertension, and fetal growth restriction