Mitochondrial DNA levels as a marker of embryo viability in IVF
Helsinki, 4 July 2016: Despite the claims and counter-claims for new embryo assessment techniques introduced over the past two decades, the search for the holy grail of assisted reproduction – the key to the embryo destined to implant – continues. Genetic screening techniques so far have relied largely on the assessment of one component of the embryo's genetic constitution, the number of chromosomes in its cells. Studies dating back 20 years have shown beyond doubt that chromosomal abnormality is common in preimplantation embryos, and becomes even more common with increasing age. Chromosomal anomalies – or aneuploidy – are universally accepted as the main reason for miscarriage and the main cause of implantation failure
Methods that allow the screening of IVF embryos for aneuploidy are increasingly used during fertility treatments, helping doctors ensure that the embryos transferred have the correct number of chromosomes. However, even when a chromosomally normal embryo is transferred about one-third fail to produce a pregnancy.
Now, a new approach to embryo assessment described at this year's Annual Meeting of ESHRE may be able to shed light on why so many apparently healthy embryos are not viable. The approach is based on the quantification of mitochondrial DNA found in the outermost layer of cells in a five-day old embryo. The combination of chromosome analysis and mitochondrial assessment may now represent the most accurate and predictive measure of embryo viability with great potential for improving IVF outcome.
Following the presentation of these important results here in Helsinki, first author Dr Epida Fragouli from Reprogenetics UK and the University of Oxford's Nuffield Department of Obstetrics and Gynaecology in Oxford, UK, said the study "demonstrates that mitochondrial DNA levels are highly predictive of an embryo's implantation potential". Even embryos which are chromosomally normal and have a good morphological appearance under the microscope, she added, have virtually no ability to produce a baby if they have unusually high levels of mitochondrial DNA.
The evidence for mitochondrial DNA as an accurate marker of embryo viability came in a prospective study of 280 blastocysts (embryos cultured for five or six days) and tested to be chromosomally normal. The study was the first ever evaluation of the predictive power of mitochondrial DNA quantification with a prospective, blinded, non-selection design. This meant that the mitochondrial DNA levels of the blastocysts were not known at the time of transfer, so study results relied solely on a comparison of IVF outcome and mitochondrial DNA level, and were not subject to any bias.
Of the 111 single blastocyst transfers whose outcome was so far known, 78 (70%) led to ongoing pregnancies, and every single one of them (100%) had levels of mitochondrial DNA known to be normal. The remaining 33 blastocysts failed to implant, and eight of these (24%) had unusually high levels of mitochondrial DNA. Stratifying IVF outcome with mitochondrial DNA levels of low, normal and high produced an ongoing pregnancy rate of 76% (78/103) for morphologically good chromosomally-normal blastocysts with normal levels of mitochondrial DNA, but of 0% (0/8) pregnancy rate for the same type of blastocysts but with unusually high mitochondrial DNA levels. This difference, said Dr Fragouli, was highly statistically significant (P
"The results confirm that embryos with elevated levels of mitochondrial DNA rarely implant," she added, "and support the use of mitochondrial quantification as a marker of embryo viability."
Dr Fragouli described the results as "very robust", noting that the methodology has been extensively validated. This was done in a retrospective analysis of samples biopsied from over 700 blastocysts generated in multiple clinics in Europe and the USA, which confirmed, first, that blastocysts with unusually high mitochondrial DNA levels have greatly reduced implantation ability, and second, that a threshold of viability dependent on mitochondrial DNA levels was valid.
Dr Fragouli explained that mitochondrial DNA levels can be simply and quickly measured by a polymerase chain reaction (PCR) strategy, but next generation sequencing (NGS) can also be used. She also emphasised that all embryos must first be screened for aneuploidy and that the mitochondrial DNA test is only applicable to chromosomally normal embryos. "Aneuploidy is still the biggest cause of embryo implantation failure," she explained, "so mitochondrial analysis does not replace that. It is the combination of the two methods – mitochondrial DNA testing and chromosome analysis – that are so powerful." Mitochondrial DNA testing would add around £200 to the cost of aneuploidy screening. However, her group is working on an approach which would assess chromosome content and mitochondrial DNA simultaneously. "Once these are ready for application," she said, "there would be no extra cost added."
The group has started offering mitochondrial DNA quantification clinically in the USA, and has applied to the HFEA for a license for use in the UK.
Abstract O-059, Monday 4 July 2016, 16.15
Clinical implications of mitochondrial DNA quantification on pregnancy outcomes: a blinded prospective non-selection study
1. Mitochondria are structures within cells which convert the energy from food and other nutrients into a form that cells can use. Although DNA is mostly packaged in chromosomes within the cell's nucleus, mitochondria also have a small amount of their own DNA outside the cell nucleus. Each of our cells can possess hundreds of mitochondria, which are essential for giving energy to cells and organs.
The embryo screening story so far
1. While preimplantation genetic diagnosis (PGD) has always been to detect chromosome and single gene defects (such as cystic fibrosis) in the embryos of high risk cases, preimplantation genetic screening (PGS) aims to improve embryo selection for better IVF results and more efficient single embryo transfer.
2. There have been two phases of PGS. The first techniques, introduced more than 20 years ago, were only able to screen for aneuploidy in a limited number of chromosomes, and results proved disappointing. Introduction of a second phase of technology allowed "comprehensive" chromosome screening, and more encouraging results; these technologies, however, were supported by only small studies with careful patient selection. Array CGH technology has now been somewhat superseded by next generation sequencing (NGS), by which millions of DNA strands – indeed an entire human genome – can be sequenced in a relatively short time.
- A podcast of Dr Fragouli talking about this study is available at https://www.eshre2016.eu/Media/Press-releases/Fragouli/Podcast.aspx
- When obtaining outside comment, journalists are requested to ensure that their contacts are aware of the embargo on this release.
For further information on the details of this press release, contact:
Christine Bauquis at ESHRE
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Email: [email protected]