Noninvasive fetal RhCE genotyping from maternal blood

BJOG: An International Journal of Obstetrics and Gynaecology

Volumn 116, Issue 2, 2009, Pages 144-151

  Geifman Holtzman, O ^a,c   Grotegut, C A ^a   Gaughan, J P ^a   Holtzman, E J ^b   Floro, C ^a   Hernandez, E ^a  

^a TEMPLE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b TEL AVIV UNIVERSITY   (Israel)

^c TEMPLE UNIVERSITY HOSPITAL   (United States)

Author keywords

Fetal cells; Fetal DNA; Fetal RhCE; Prenatal diagnosis

Indexed keywords

DNA;

ALLOIMMUNIZATION; BLOOD GROUP RHESUS SYSTEM; CELL SELECTION; CHECKLIST; CONFIDENCE INTERVAL; DIAGNOSTIC ACCURACY; FEMALE; FETUS CELL; GENOTYPE; GESTATIONAL AGE; HUMAN; MATERNAL BLOOD; NON INVASIVE PROCEDURE; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; RHCE GENOTYPING;

DNA; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; RH ISOIMMUNIZATION; RH-HR BLOOD-GROUP SYSTEM; SENSITIVITY AND SPECIFICITY;

EID: 57449089748     PISSN: 14700328     EISSN: 14710528     Source Type: Journal    
DOI: 10.1111/j.1471-0528.2008.01744.x     Document Type: Review

References (30)

1. Le Van Kim C, Mouro I, Brossard Y, Chavinie J, Cartron JP, Colin Y. PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease. Br J Haematol 1994 88 : 193 5.
2. Geifman-Holtzman O, Bernstein IM, Berry SM, Bianchi DW, Holtzman EJ. Rapid molecular determination of fetal rhesus E type. Prenat Diagn 1996 16 : 489 93.
3. Lo YM, Bowell PJ, Selinger M, Mackenzie IZ, Chamberlain P, Gillmer MD, et al. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers. Lancet 1993 341 : 1147 8.
4. Geifman-Holtzman O, Bernstein IM, Berry SM, Holtzman EJ, Vadnais TJ, DeMaria MA, et al. Fetal RhD genotyping in fetal cells flow sorted from maternal blood. Am J Obstet Gynecol 1996 174 : 818 22.
5. Amicucci P, Gennarelli M, Novelli G, Dallapiccola B. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Clin Chem 2000 46 : 301 2.
6. Saito H, Sekizawa A, Morimoto T, Suzuki M, Yanaihara T. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Lancet 2000 356 : 1170.
7. Geifman-Holtzman O, Makhlouf F, Kaufman L, Gonchoroff NJ, Holtzman EJ. The clinical utility of fetal cell sorting to determine prenatally fetal E/e or e/e Rh genotype from peripheral maternal blood. Am J Obstet Gynecol 2000 183 : 462 8.
8. Levy R, Nelson DM. To be, or not to be, that is the question. Apoptosis in human trophoblast. Placenta 2000 21 : 1 13.
9. Poon LL, Lo YM. Circulating fetal DNA in maternal plasma. Clin Chim Acta 2001 313 : 151 5.
10. Geifman-Holtzman O, Wojtowycz M, Kosmas E, Artal R. Female alloimmunization with antibodies known to cause hemolytic disease. Obstet Gynecol 1997 89 : 272 5.
11. Bianchi DW, Avent ND, Costa JM, van der Schoot CE. Noninvasive prenatal diagnosis of fetal Rhesus D: ready for Prime(r) Time. Obstet Gynecol 2005 106 : 841 4.
12. Moise KJ. Fetal RhD typing with free DNA in maternal plasma. Am J Obstet Gynecol 2005 192 : 663 5.
13. Queenan JT. Noninvasive fetal Rh genotyping: the time has come. Obstet Gynecol 2005 106 : 682 3.
14. Daniels G, Finning K, Martin P, Soothill P. Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn. Vox Sang 2004 87 : 225 32.
15. Geifman-Holtzman O, Grotegut CA, Gaughan JP. Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood-a meta-analysis. Am J Obstet Gynecol 2006 195 : 1163 73.
16. Bossuyt PM, Reitsma JB, Bruns DE, Gatsonis CA, Glasziou PP, Irwig LM, et al. Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. BMJ 2003 326 : 41 4.
17. Geifman-Holtzman O, Kaufman L, Gonchoroff N, Bernstein I, Holtzman EJ. Prenatal diagnosis of the fetal Rhc genotype from peripheral maternal blood. Obstet Gynecol 1998 91 : 506 10.
18. Legler TJ, Lynen R, Maas JH, Pindur G, Kulenkampff D, Suren A, et al. Prediction of fetal Rh D and Rh CcEe phenotype from maternal plasma with real-time polymerase chain reaction. Transfus Apher Sci 2002 27 : 217 23.
19. Hromadnikova I, Vechetova L, Vesela K, Benesova B, Doucha J, Vlk R. Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RhD-negative pregnancies. J Histochem Cytochem 2005 53 : 301 5.
20. Hromadnikova I, Vesela K, Benesova B, Nekovarova K, Duskova D, Vlk R, et al. Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies. Prenat Diagn 2005 25 : 1079 83.
21. Finning K, Martin P, Summers J, Daniels G. Fetal genotyping for the K (Kell) and Rh C, c, and E blood groups on cell-free fetal DNA in maternal plasma. Transfusion 2007 47 : 2126 33.
22. Mouro I, Colin Y, Cherif-Zahar B, Cartron JP, Le Van Kim C. Molecular genetic basis of the human Rhesus blood group system. Nat Genet 1993 5 : 62 5.
23. Avent ND, Reid ME. The Rh blood group system: a review. Blood 2000 95 : 375 87.
24. Avent ND, Finning KM, Martin PG, Soothill PW. Prenatal determination of fetal blood group status. Vox Sang 2000 78 (Suppl 2 155 62.
25. Daniels G. The molecular genetics of blood group polymorphism. Transpl Immunol 2005 14 : 143 53.
26. Cherif-Zahar B, Raynal V, D'Ambrosio AM, Cartron JP, Colin Y. Molecular analysis of the structure and expression of the RH locus in individuals with D-, Dc-, and DCw-gene complexes. Blood 1994 84 : 4354 60.
27. Yankowitz J, Li S, Weiner CP. Polymerase chain reaction determination of RhC, Rhc, and RhE blood types: an evaluation of accuracy and clinical utility. Am J Obstet Gynecol 1997 176 : 1107 11.
28. Lo YM. Fetal RhD genotyping from maternal plasma. Ann Med 1999 31 : 308 12.
29. Geifman-Holtzman O, Holtzman EJ, Vadnais TJ, Phillips VE, Capeless EL, Bianchi DW. Detection of fetal HLA-DQa sequences in maternal blood: a gender-independent technique of fetal cell identification. Prenat Diagn 1995 15 : 261 8.
30. Chan KC, Ding C, Gerovassili A, Yeung SW, Chiu RW, Leung TN, et al. Hypermethylated RASSF1A in maternal plasma: a universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem 2006 52 : 2211 8.