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

A novel microarray platform was developed offering the possibility of combined aneuploidy screening, genetic fingerprinting, and mitochondrial DNA (mtDNA) assessment of embryos. Associations between mtDNA and maternal age are reported.

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Authors

Michalis Konstantinidis, Ph.D., Samer Alfarawati, Ph.D., Douglas Hurd, Ph.D., Marta Paolucci, Ph.D., John Shovelton, B.Sc., Elpida Fragouli, Ph.D., Dagan Wells, Ph.D.

Volume 102, Issue 5, Pages 1385–1392

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.

Read the full text at: http://www.fertstert.org/article/S0015-0282(14)01860-3/fulltext


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Editorial Office, American Society for Reproductive Medicine

Fertility and Sterility® is an international journal for obstetricians, gynecologists, reproductive endocrinologists, urologists, basic scientists and others who treat and investigate problems of infertility and human reproductive disorders. The journal publishes juried original scientific articles in clinical and laboratory research relevant to reproductive endocrinology, urology, andrology, physiology, immunology, genetics, contraception, and menopause. Fertility and Sterility® encourages and supports meaningful basic and clinical research, and facilitates and promotes excellence in professional education, in the field of reproductive medicine.

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