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Chromosomal copy number analysis of products of conception by conventional karyotyping and next-generation sequencing.
Tamura, Yuki; Santo, Mitsuo; Araki, Yasuhisa; Matsubayashi, Hidehiko; Takaya, Yukiko; Kitaya, Kotaro; Doshida, Masakazu; Yamaguchi, Kohei; Mizuta, Shimpei; Takahashi, Chie; Kim, Namhyo; Okuno, Koichiro; Takeuchi, Takumi; Ishikawa, Tomomoto.
Afiliación
  • Tamura Y; Nippon Reprogenetics Inc. Maebashi Japan.
  • Santo M; Nippon Reprogenetics Inc. Maebashi Japan.
  • Araki Y; Nippon Reprogenetics Inc. Maebashi Japan.
  • Matsubayashi H; Graduate School of Health Science Gunma Paz University Takasaki Japan.
  • Takaya Y; Reproduction Clinic Osaka Osaka Japan.
  • Kitaya K; Reproduction Clinic Tokyo Tokyo Japan.
  • Doshida M; Reproduction Clinic Osaka Osaka Japan.
  • Yamaguchi K; Reproduction Clinic Osaka Osaka Japan.
  • Mizuta S; Reproduction Clinic Tokyo Tokyo Japan.
  • Takahashi C; Reproduction Clinic Tokyo Tokyo Japan.
  • Kim N; Reproduction Clinic Osaka Osaka Japan.
  • Okuno K; Reproduction Clinic Tokyo Tokyo Japan.
  • Takeuchi T; Reproduction Clinic Tokyo Tokyo Japan.
  • Ishikawa T; Reproduction Clinic Osaka Osaka Japan.
Reprod Med Biol ; 20(1): 71-75, 2021 Jan.
Article en En | MEDLINE | ID: mdl-33488285
ABSTRACT

PURPOSE:

Chromosomal abnormalities are a major cause of spontaneous abortion, and conventional G-banded karyotyping (G-banding) is mainly utilized for chromosomal analysis. Recently, next-generation sequencing (NGS) has been introduced for chromosomal analysis. Here, we aimed to investigate the applicability and utility of NGS-based chromosomal analysis of products of conception (POC) on chorionic villus samples from spontaneous abortion.

METHODS:

The results of chromosomal analysis of 7 chorionic villus samples from spontaneous abortion were compared between conventional G-banding and NGS-based chromosomal copy number analysis. Age dependency and frequency of each chromosomal aneuploidy were evaluated for 279 cases analyzed by NGS.

RESULTS:

Excluding two cases (culture failure and maternal cell contamination), the results were consistent between G-banding and NGS. For cases analyzed by NGS, the rate of chromosomal abnormality increased in a maternal age-dependent manner. The frequency of each chromosomal aneuploidy detected by NGS was almost the same as that previously reported. Finally, NGS analysis was possible for difficult cases by G-banding analysis, such as culture failure, maternal cell contamination, long-term storage cases, and low cell number.

CONCLUSIONS:

Chromosome analysis using NGS not only obtains comparable results to conventional G-banding, but also can analyze POC more accurately and efficiently.
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