Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro

被引:101
作者
Benkhalifa, M
Kasakyan, S
Clement, P
Baldi, M
Tachdjian, G
Demirol, A
Gurgan, T
Fiorentino, F
Mohammed, M
Qumsiyeh, MB
机构
[1] ATL R&D, Reprod Biol & Gent Lab, F-78960 La Verriere, France
[2] Lab Clement, Dept Genet, Le Blanc Mesnil, France
[3] Consultorio Di Genet & Genoma Labs, Rome, Italy
[4] Hop Antoine Beclere, Clamart, France
[5] Infertil & Genet Res Ctr, Ankara, Turkey
[6] Quest Diagnost Inc, San Juan Capistrano, CA USA
[7] Yale Univ, Dept Genet, Cytogenet Serv, New Haven, CT 06520 USA
[8] siParadigm, Oradell, NJ USA
关键词
first-trimester fetal loss; cell culture failure; array CGH; chromosome abnormalities; autosomal monosomy;
D O I
10.1002/pd.1230
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objectives Cytogenetic analysis of spontaneous abortion samples can be limited by culture failure. Failure to grow in vitro has traditionally been suspected to be due to in vivo death of tissue associated with spontaneous abortion (SAB) or simply technical factors of growth in culture. Method We used array comparative genomic hybridization (array CGH) to investigate chromosomal imbalances in products of conception that failed to grow in vitro. Results Our data on 26 cases of SABs that failed to grow in culture are compared and contrasted with published data on cytogenetic findings following in vitro culture. The results revealed abnormalities uncommonly seen by classic cytogenetic methods. These abnormalities include high rates of double aneuploidy and autosomal monosomy. The data taken together suggest that classic cytogenetics of spontaneous abortion may yield normal karyotypes or selected abnormal karyotypes that permit cell proliferation in vitro while Array CGH detects other abnormalities. Conclusion Array CGH is becoming an important clinical assay for unbalanced chromosome abnormalities whether cells grow in culture or not and in cases of analysis on one or few cells. Copyright Q 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:894 / 900
页数:7
相关论文
共 23 条
  • [1] Diagnosis of aneuploidy in arrival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization
    Bell, KA
    Van Deerlin, PG
    Feinberg, RF
    du Manoir, S
    Haddad, BR
    [J]. FERTILITY AND STERILITY, 2001, 75 (02) : 374 - 379
  • [2] Cytogenetic abnormalities and the failure of development after round spermatid injections
    Benkhalifa, M
    Kahraman, S
    Biricik, A
    Serteyl, S
    Domez, E
    Kumtepe, Y
    Qumsiyeh, MB
    [J]. FERTILITY AND STERILITY, 2004, 81 (05) : 1283 - 1288
  • [3] Morphological and cytogenetic analysis of intact oocytes and blocked zygotes
    Benkhalifa, M
    Kahraman, S
    Caserta, D
    Domez, E
    Qumsiyeh, MB
    [J]. PRENATAL DIAGNOSIS, 2003, 23 (05) : 397 - 404
  • [4] High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
    Bruder, CEG
    Hirvelä, C
    Tapia-Paez, I
    Fransson, I
    Segraves, R
    Hamilton, G
    Zhang, XX
    Evans, DG
    Wallace, AJ
    Baser, ME
    Zucman-Rossi, J
    Hergersberg, M
    Boltshauser, E
    Papi, L
    Rouleau, GA
    Poptodorov, G
    Jordanova, A
    Rask-Andersen, H
    Kluwe, L
    Mautner, V
    Sainio, M
    Hung, G
    Mathiesen, T
    Möller, C
    Pulst, SM
    Harder, H
    Heiberg, A
    Honda, M
    Miimura, M
    Sahlén, S
    Blennow, E
    Albertson, DG
    Pinkel, D
    Dumanski, JP
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (03) : 271 - 282
  • [5] Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization
    Daniely, M
    Aviram-Goldring, A
    Barkai, G
    Goldman, B
    [J]. HUMAN REPRODUCTION, 1998, 13 (04) : 805 - 809
  • [6] Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH) -: Re-evaluation of chromosome aberration rates in early spontaneous abortions
    Fritz, B
    Hallermann, C
    Olert, J
    Fuchs, B
    Bruns, M
    Aslan, M
    Schmidt, S
    Coerdt, W
    Müntefering, H
    Rehder, H
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (07) : 539 - 547
  • [7] Gardner RJM, 2003, OXFORD MONOGRAPHS ME
  • [8] Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease
    Handyside, AH
    Robinson, MD
    Simpson, RJ
    Omar, MB
    Shaw, MA
    Grudzinskas, JG
    Rutherford, A
    [J]. MOLECULAR HUMAN REPRODUCTION, 2004, 10 (10) : 767 - 772
  • [9] Multiple displacement amplification on single cell and possible PGD applications
    Hellani, A
    Coskun, S
    Benkhalifa, M
    Tbakhi, A
    Sakati, N
    Al-Odaib, A
    Ozand, P
    [J]. MOLECULAR HUMAN REPRODUCTION, 2004, 10 (11) : 847 - 852
  • [10] The results of aneuploidy screening in 276 couples undergoing assisted reproductive techniques
    Kahraman, S
    Benkhalifa, M
    Donmez, E
    Biricik, A
    Sertyel, S
    Findikli, N
    Berkil, H
    [J]. PRENATAL DIAGNOSIS, 2004, 24 (04) : 307 - 311