Wednesday, April 20, 2016

Is Time Lapse Morphokinetics the future for embryo selection in IVF?

When we look at other industries, a rapid progress and evolution has resulted in remarkable products, specifically computers and software. Incidentally, the birth of apple computer and the birth of first IVF baby Louis Brown were achieved in the same year 1978. Looking back the technology advances in IVF are also at par with that in computer industry.

IVF Techniques have also evolved over years, with embryo cryopreservation, gamete cryopreservation, embryo biopsy, Intracytoplasmic sperm injection, assisted hatching and genetic testing introduced into day to day practice.

Various types of incubators were introduced in markets, starting from Australia introduced mini-incubator, called the MINC in 1990. Embryos are routinely cultured till the blastocyst stage, before they are transferred. However, the pregnancy and live birthrate did not go parallel with the technology innovations. It could be explained in many ways, namely aging mothers with poor egg quality and ability to treat couples with complex infertility causes.

But, embryo selection does play a part and till now they were selected based on morphology at pre-defined interval alone. The introduction of TL technology allows us to continuous monitoring of embryos without compromising the culture environment. Several different time lapse incubators with automated image capture are in use by ART specialists.

But, are TL systems for efficient in selecting good embryos than simple morphology? Few randomized studies have been conducted till now. One such study by Goodman and colleagues was published in the February, 2016 issue of Fertility and Sterility

This was a randomized controlled trial with about 300 patients, in which all embryos were cultured in TL, but in control group they were only assessed once a day and in experimental group precise timing of various kinetic events (time to pronuclear fading, two-cell, three-cell, four-cell, five-cell, eight-cell stage, start of compaction, time to morula/ blastocyst, expanded blastocyst formation) as well as cleavage anomalies were used to identify the embryo to be transferred.

Embryos were scored using these markers. It was seen that pregnancy and implantation rates were higher in TL group, but the difference was not statistically significant.
Multinucleation and uneven cleavage was seen much more clearly in TL group. So, some researchers opine that TL is a good for deselecting the embryos, which otherwise would have been transferred but would not have implanted.

One other RCT by Rubio et al., 2014 reported   a clear cut advantage of TL systems over traditional incubators, with increased implantation rates and ongoing pregnancy rate. But, it did have many limitations due to methodology and protocols in embryo transfer, using separate incubators in control and study group. Thereby limiting benefit of the undisturbed culture conditions or the selection based on morphokinetic parameters.

In the present study both control and experimental embryos were cultured in TL incubators under similar conditions, and only the selection for transfer differed. However, there may be other factors like morphokinetic parameters, chromosomal compositions and implantation potential responsible for successful live births than just selecting some competent embryos.

But, TL embryo monitoring does offer several benefits like undisturbed embryo culture, recording of embryo development for quality control, and standardization of morphologic assessment and when combined with other advance technique like array CGH does results in improved pregnancy rates.

As time goes by, the high cost of these technologies significantly decreases and their efficacy will also increase with standardized guidelines, and combining it with other techniques, the world of morphokinetics of TL systems is here to stay!


References:
http://humrep.oxfordjournals.org/content/early/2014/10/24/humrep.deu278.full
http://www.fertstert.org/article/S0015-0282(15)02020-8/references



1 comment:

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