Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform.

Authors: Konstantinidis, M., Alfarawati, S., Hurd, D., Paolucci, M., Shovelton, J., Fragouli, E. and Wells, D.

Journal: Fertil Steril

Volume: 102

Issue: 5

Pages: 1385-1392

eISSN: 1556-5653

DOI: 10.1016/j.fertnstert.2014.07.1233

Abstract:

OBJECTIVE: To develop a microarray platform that allows simultaneous assessment of aneuploidy and quantification of mitochondrial DNA (mtDNA) in human polar bodies and embryos. DESIGN: Optimization and validation applied to cell lines and clinical samples (polar bodies, blastomeres, and trophectoderm biopsies). SETTING: University research laboratory and a preimplantation genetic diagnosis (PGD) reference laboratory. PATIENT(S): Samples from 65 couples who underwent PGD for aneuploidy and/or a single-gene disorder. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): 1) Comparison of aneuploidy screening results obtained with the use of the new microarray with those derived from two well established cytogenetic techniques. 2) mtDNA quantification. 3) Analysis of single-nucleotide polymorphisms. RESULT(S): The fully optimized microarray was estimated to have an accuracy of ≥97% for the detection of individual aneuploidies and to detect 99% of chromosomally abnormal embryos. The microarray was shown to accurately determine relative quantities of mtDNA. Information provided from polymorphic loci was sufficient to allow confirmation that an embryo was derived from specific parents. CONCLUSION(S): It is hoped that methods such as those reported here, which provide information on several aspects of oocyte/embryo genetics, could lead to improved strategies for identifying viable embryos, thereby increasing the likelihood of successful implantation. Additionally, the provision of genotyping information has the potential to reveal DNA contaminants and confirm parental origin of embryos.

Source: PubMed

Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform

Authors: Konstantinidis, M., Alfarawati, S., Hurd, D., Paolucci, M., Shovelton, J., Fragouli, E. and Wells, D.

Journal: FERTILITY AND STERILITY

Volume: 102

Issue: 5

eISSN: 1556-5653

ISSN: 0015-0282

DOI: 10.1016/j.fertnstert.2014.07.1233

Source: Web of Science (Lite)

Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform

Authors: Konstantinidis, M., Alfarawati, S., Hurd, D., Paolucci, D., Shovelton, J., Fragkouli, E. and Wells, D.

Journal: Fertility and Sterility

Volume: 102

Issue: 5

Pages: 1385-1392

Publisher: Elsevier

ISSN: 0015-0282

Source: Manual

Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform.

Authors: Konstantinidis, M., Alfarawati, S., Hurd, D., Paolucci, M., Shovelton, J., Fragouli, E. and Wells, D.

Journal: Fertility and sterility

Volume: 102

Issue: 5

Pages: 1385-1392

eISSN: 1556-5653

ISSN: 0015-0282

DOI: 10.1016/j.fertnstert.2014.07.1233

Abstract:

Objective

To develop a microarray platform that allows simultaneous assessment of aneuploidy and quantification of mitochondrial DNA (mtDNA) in human polar bodies and embryos.

Design

Optimization and validation applied to cell lines and clinical samples (polar bodies, blastomeres, and trophectoderm biopsies).

Setting

University research laboratory and a preimplantation genetic diagnosis (PGD) reference laboratory.

Patient(s)

Samples from 65 couples who underwent PGD for aneuploidy and/or a single-gene disorder.

Intervention(s)

None.

Main outcome measure(s)

1) Comparison of aneuploidy screening results obtained with the use of the new microarray with those derived from two well established cytogenetic techniques. 2) mtDNA quantification. 3) Analysis of single-nucleotide polymorphisms.

Result(s)

The fully optimized microarray was estimated to have an accuracy of ≥97% for the detection of individual aneuploidies and to detect 99% of chromosomally abnormal embryos. The microarray was shown to accurately determine relative quantities of mtDNA. Information provided from polymorphic loci was sufficient to allow confirmation that an embryo was derived from specific parents.

Conclusion(s)

It is hoped that methods such as those reported here, which provide information on several aspects of oocyte/embryo genetics, could lead to improved strategies for identifying viable embryos, thereby increasing the likelihood of successful implantation. Additionally, the provision of genotyping information has the potential to reveal DNA contaminants and confirm parental origin of embryos.

Source: Europe PubMed Central