Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement

被引:8
作者
Cheng, Dehua [1 ]
Hu, Liang [1 ,2 ,3 ,4 ,5 ]
Gong, Fei [1 ,2 ,3 ,4 ,5 ]
Yuan, Shimin [1 ]
Luo, Keli [1 ,2 ]
Wu, Xianhong [3 ]
Xie, Pingyuan [3 ]
Lu, Changfu [1 ,2 ,3 ,4 ]
Lu, Guangxiu [1 ,2 ,3 ,4 ,5 ]
Tan, Yue-Qiu [1 ,2 ,4 ,5 ]
Lin, Ge [1 ,2 ,3 ,4 ,5 ]
机构
[1] CITIC Xiangya, Reprod & Genet Hosp, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Inst Reprod & Stem Cell Engn, Sch Basic Med Sci, Changsha, Hunan, Peoples R China
[3] Natl Engn & Res Ctr Human Stem Cells, Changsha, Hunan, Peoples R China
[4] Cent South Univ, NHC Key Lab Human Stem Cell & Reprod Engn, Changsha, Hunan, Peoples R China
[5] Clin Res Ctr Reprod & Genet Hunan Prov, Changsha, Hunan, Peoples R China
基金
国家重点研发计划;
关键词
Preimplantation genetic testing; Chromosome-balanced rearrangement; Chromosome microdissection; Next-generation sequencing; MicroSeq; TRANSLOCATION CARRIER; DIAGNOSIS;
D O I
10.1007/s10815-020-02052-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose The purpose of this study is to summarize the clinical outcomes of apparently balanced chromosome rearrangement (ABCR) carriers in preimplantation genetic testing (PGT) cycles by next-generation sequencing following microdissecting junction region (MicroSeq) to distinguish non-carrier embryos from balanced carriers. Methods A retrospective study of 762 ABCR carrier couples who requested PGT for structural rearrangements combined with MicroSeq at the Reproductive and Genetic Hospital of CITIC-Xiangya was conducted between October 2014 and October 2019. Results Trophectoderm biopsy was performed in 4122 blastocysts derived from 917 PGT-SR cycles and 3781 blastocysts were detected. Among the 3781 blastocysts diagnosed, 1433 (37.9%, 1433/3781) were balanced, of which 739 blastocysts were carriers (51.57%, 739/1433) and 694 blastocysts were normal (48.43%, 694/1433). Approximately 26.39% of cycles had both carrier and normal embryo transfer, and the average number of biopsied blastocysts was 6.7. In the cumulative 223 biopsied cycles with normal embryo transfer, all couples chose to transfer the normal embryos. In the 225 cycles with only carrier embryos, the couples chose to transfer the carrier embryos in 169/225 (75.11%) cycles. A total of 732 frozen embryo transfer cycles were performed, resulting in 502 clinical pregnancies. Cumulatively, 326 babies were born; all of these babies were healthy and free of any developmental issues. Conclusion Our study provides the first evaluation of the clinical outcomes of a large sample with ABCR carrier couples undergoing the MicroSeq-PGT technique and reveals its powerful ability to distinguish between carrier and non-carrier balanced embryos.
引用
收藏
页码:735 / 742
页数:8
相关论文
共 18 条
[1]   Distinguishing between carrier and noncarrier embryos with the use of long-read sequencing in preimplantation genetic testing for reciprocal translocations [J].
Chow, Judy F. C. ;
Cheng, Heidi H. Y. ;
Lau, Estella Y. L. ;
Yeung, William S. B. ;
Ng, Ernest H. Y. .
GENOMICS, 2020, 112 (01) :494-500
[2]   A simple and efficient method for microdissection and microFISH [J].
Engelen, JJM ;
Albrechts, JCM ;
Hamers, GJH ;
Geraedts, JPM .
JOURNAL OF MEDICAL GENETICS, 1998, 35 (04) :265-268
[3]   ALLELIC DROP-OUT AND PREFERENTIAL AMPLIFICATION IN SINGLE CELLS AND HUMAN BLASTOMERES - IMPLICATIONS FOR PREIMPLANTATION DIAGNOSIS OF SEX AND CYSTIC-FIBROSIS [J].
FINDLAY, I ;
RAY, P ;
QUIRKE, P ;
RUTHERFORD, A ;
LILFORD, R .
HUMAN REPRODUCTION, 1995, 10 (06) :1609-1618
[4]   Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control study [J].
Franssen, MTM ;
Korevaar, JC ;
van der Veen, F ;
Leschot, NJ ;
Bossuyt, PNM ;
Goddijn, M .
BMJ-BRITISH MEDICAL JOURNAL, 2006, 332 (7544) :759-+
[5]   Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos [J].
Hu, Liang ;
Cheng, Dehua ;
Gong, Fei ;
Lu, Changfu ;
Tan, Yueqiu ;
Luo, Keli ;
Wu, Xianhong ;
He, Wenbing ;
Xie, Pingyuan ;
Feng, Tao ;
Yang, Kai ;
Lu, Guangxiu ;
Lin, Ge .
EBIOMEDICINE, 2016, 14 :139-147
[6]   Current methods for preimplantation genetic diagnosis [J].
Liss, Joanna ;
Chromik, Iwona ;
Szczyglinska, Joanna ;
Jagiello, Monika ;
Lukaszuk, Aron ;
Lukaszuk, Krzysztof .
GINEKOLOGIA POLSKA, 2016, 87 (07) :522-526
[7]   Preimplantation genetic diagnosis and human implantation -: A review [J].
Munné, S .
PLACENTA, 2003, 24 :S70-S76
[8]  
Munne Santiago, 2002, Reprod Biomed Online, V4, P183
[9]   Benefits and drawbacks of preimplantation genetic diagnosis (PGD) for reciprocal translocations: lessons from a prospective cohort study [J].
Scriven, Paul N. ;
Flinter, Frances A. ;
Khalaf, Yakoub ;
Lashwood, Alison ;
Ogilvie, Caroline Mackie .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2013, 21 (10) :1035-1041
[10]   Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier families [J].
Shamash, Jana ;
Rienstein, Shlomit ;
Wolf-Reznik, Haike ;
Pras, Elon ;
Dekel, Michal ;
Litmanovitch, Talia ;
Brengauz, Masha ;
Goldman, Boleslav ;
Yonath, Hagith ;
Dor, Jehoshua ;
Levron, Jacob ;
Aviram-Goldring, Ayala .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2011, 28 (01) :77-83