Literature DB >> 24591936

Performance of MLPA as a screening method for aneuploidy in uncultured amniocytes.

Hüseyin Yurdakul1, Beyhan Durak1, Muhammed Hamza Müslümanoğlu1, Muhsin Ozdemir1, Oğuz Cilingir1, Turgay Sener2, Sevilhan Artan1.   

Abstract

OBJECTIVE: To test whether the Multiplex Ligation-dependent Probe Amplification (MLPA) technique can be used as a screening test for rapid diagnosis of aneuploidies in uncultured amniocentesis.
MATERIAL AND METHODS: In this prospective blind study, MLPA with chromosomes 13,18,21,X and Y specific probe mixes was performed in 500 amniotic fluid samples. Chromosome copy numbers were determined by analyzing size and peak area for each MLPA probe. Results were compared with those of karyotyping/FISH.
RESULTS: Conclusive test results were obtained in 98% of the samples, whereas 10 were inconclusive. In all conclusive tests, the MLPA results were concordant with that of cytogenetic and/or FISH analyses. There were no false-positive results. A case with 69,XXX triploidy could not be diagnosed by MLPA. In total, 28 aneuploidies were diagnosed. There were no false-positive results. The performance of each probe was determined.
CONCLUSION: MLPA is a rapid, simple and reliable assay for aneuploidy screening in uncultured amniocytes.

Entities:  

Keywords:  MLPA; common aneuploidies; prenatal screening; uncultured amniocytes

Year:  2010        PMID: 24591936      PMCID: PMC3939151          DOI: 10.5152/jtgga.2010.37

Source DB:  PubMed          Journal:  J Turk Ger Gynecol Assoc        ISSN: 1309-0380


  17 in total

1.  Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.

Authors:  Jan P Schouten; Cathal J McElgunn; Raymond Waaijer; Danny Zwijnenburg; Filip Diepvens; Gerard Pals
Journal:  Nucleic Acids Res       Date:  2002-06-15       Impact factor: 16.971

2.  Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA).

Authors:  Tommy Gerdes; Maria Kirchhoff; Anne-Marie Lind; Gitte Vestergaard Larsen; Marianne Schwartz; Claes Lundsteen
Journal:  Eur J Hum Genet       Date:  2005-02       Impact factor: 4.246

Review 3.  Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis.

Authors:  Lisa G Shaffer; The-Hung Bui
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-02-15       Impact factor: 3.908

4.  Diagnostic genome profiling in mental retardation.

Authors:  Bert B A de Vries; Rolph Pfundt; Martijn Leisink; David A Koolen; Lisenka E L M Vissers; Irene M Janssen; Simon van Reijmersdal; Willy M Nillesen; Erik H L P G Huys; Nicole de Leeuw; Dominique Smeets; Erik A Sistermans; Ton Feuth; Conny M A van Ravenswaaij-Arts; Ad Geurts van Kessel; Eric F P M Schoenmakers; Han G Brunner; Joris A Veltman
Journal:  Am J Hum Genet       Date:  2005-08-30       Impact factor: 11.025

5.  Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study.

Authors:  D H Spathas; A Divane; G M Maniatis; M E Ferguson-Smith; M A Ferguson-Smith
Journal:  Prenat Diagn       Date:  1994-11       Impact factor: 3.050

6.  Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications.

Authors:  Vincenzo Cirigliano; Gianfranco Voglino; Antonella Marongiu; Paz Cañadas; Elena Ordoñez; Elisabet Lloveras; Alberto Plaja; Carme Fuster; Matteo Adinolfi
Journal:  Ann N Y Acad Sci       Date:  2006-09       Impact factor: 5.691

7.  High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy.

Authors:  Damien L Bruno; Trent Burgess; Hua Ren; Sara Nouri; Mark D Pertile; David I Francis; Fiona Norris; Bronwyn K Kenney; Jan Schouten; K H Andy Choo; Howard R Slater
Journal:  Am J Med Genet A       Date:  2006-12-15       Impact factor: 2.802

8.  Global variation in copy number in the human genome.

Authors:  Richard Redon; Shumpei Ishikawa; Karen R Fitch; Lars Feuk; George H Perry; T Daniel Andrews; Heike Fiegler; Michael H Shapero; Andrew R Carson; Wenwei Chen; Eun Kyung Cho; Stephanie Dallaire; Jennifer L Freeman; Juan R González; Mònica Gratacòs; Jing Huang; Dimitrios Kalaitzopoulos; Daisuke Komura; Jeffrey R MacDonald; Christian R Marshall; Rui Mei; Lyndal Montgomery; Kunihiro Nishimura; Kohji Okamura; Fan Shen; Martin J Somerville; Joelle Tchinda; Armand Valsesia; Cara Woodwark; Fengtang Yang; Junjun Zhang; Tatiana Zerjal; Jane Zhang; Lluis Armengol; Donald F Conrad; Xavier Estivill; Chris Tyler-Smith; Nigel P Carter; Hiroyuki Aburatani; Charles Lee; Keith W Jones; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2006-11-23       Impact factor: 49.962

9.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

Review 10.  Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

Authors:  Maj A Hultén; Seema Dhanjal; Barbara Pertl
Journal:  Reproduction       Date:  2003-09       Impact factor: 3.906

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