Polar body biopsy

Polar body biopsy is the sampling of a polar body of an oocyte. It was first applied clinically in humans in 1987 after extensive animal studies.[1] A polar body is a small haploid cell that is formed concomitantly as an egg cell during oogenesis, but which generally does not have the ability to be fertilized.

After sampling of a polar body, subsequent analysis can be used to predict viability and pregnancy chance of the oocyte, as well as the future health of a person resulting from such a pregnancy. The latter use makes it a form of preimplantation genetic screening (PGS). Compared to a blastocyst biopsy, a polar body biopsy can potentially be of lower costs, less harmful side-effects, and more sensitive in detecting abnormalities.[2]

Techniques

The first polar body is removed from the unfertilised oocyte, and the second PB from the zygote, shortly after fertilization. The biopsy and analysis of the first and second polar bodies can be completed before fertilization, which is the moment from which the zygote is generally considered an embryo and may become protected by law.

By screening the first polar body for chromosomal anomalies, non-viable eggs can be reliably identified, though eggs with normal first polar bodies can still be affected by errors. This method was initially performed with fluorescence in situ hybridization (FISH), then by hybridizing a sample into lymphocytes to observe it in metaphase, and more recently by microarrays, which are fully automated and make it easier to distinguish between chromosome vs. chromatid abnormalities.[3]

The main advantage of the use of polar bodies in PGD is that they are not necessary for successful fertilisation or normal embryonic development, thus ensuring no deleterious effect for the embryo. One of the disadvantages of PB biopsy is that it only provides information about the maternal contribution to the embryo, which is why cases of autosomal dominant and X-linked disorders that are maternally transmitted can be diagnosed, and autosomal recessive disorders can only partially be diagnosed. Another drawback is the increased risk of diagnostic error, for instance due to the degradation of the genetic material or events of recombination that lead to heterozygous first polar bodies. It is generally agreed that it is best to analyse both polar bodies in order to minimize the risk of misdiagnosis. This can be achieved by sequential biopsy, necessary if monogenic diseases are diagnosed, to be able to differentiate the first from the second polar body, or simultaneous biopsy if FISH is to be performed.

In theory, molecular analysis of polar bodies may include epigenetic profiling in the near future.[4]

Target diseases

Aneuploidy

Several studies have suggested that polar body screening for aneuploidy may not be optimal. When the majority of errors occur in chromatids rather than entire chromosomes (a condition correlated with the age of the mother), screening only the first polar body will fail to detect a large percentage of defective eggs. As mentioned earlier, chromosomal abnormality in the first polar body can result in a healthy embryo, meaning that eggs may in fact be wasted as a result of the screening. Polar body testing will also be unable to detect post-zygotic errors in an oocyte.[3]

Because euploid polar bodies contain the same chromosomes as the oocyte, they can be used as a source of genetic material that is easily accessed without destroying the egg. This presents a research advantage by minimizing damage to the oocytes under investigation.[5]

Usage

Polar body biopsy is used mainly by two PGD groups in the USA[6][7] and by groups in countries where cleavage-stage embryo selection is banned.[8]

gollark: It's not the same as actually developing the entire standard, but it's something I guess.
gollark: > In the early 1990s, O'Sullivan led a team at the CSIRO which patented, in 1996, the use of a related technique for reducing multipath interference of radio signals transmitted for computer networking. This technology is a part of all recent WiFi implementationsAh, so they contributed somewhat to WiFi.
gollark: CSIRO, that is.
gollark: It says that they came up with some sort of Fourier-transform-based thing used in the signalling?
gollark: I'm trying to confirm what you said about WiFi there.

References
  1. Galst, Joann Paley; Verp, Marion S. (2015-08-26). Prenatal and Preimplantation Diagnosis: The Burden of Choice. ISBN 9783319189116.
  2. "Delivery of a chromosomally normal child from an oocyte with reciprocal aneuploid polar bodies". Scott Jr, Richard T., Nathan R. Treff, John Stevens, Eric J. Forman, Kathleen H. Hong, Mandy G. Katz-Jaffe, William B. Schoolcraft. Journal of Assisted Reproductive Genetics Vol. 29 pp. 533-537. 2012.
  3. "Is the polar body approach best for pre-implantation genetic screening?" Delhanty, Joy. Placenta Vol. 32, pp. 268-270. 2011.
  4. Wei, Y.; Schatten, H.; Sun, Q.-Y. (2014). "Environmental epigenetic inheritance through gametes and implications for human reproduction". Human Reproduction Update. 21 (2): 194–208. doi:10.1093/humupd/dmu061. ISSN 1355-4786. PMID 25416302.
  5. Jia ZX, et al. (2012). "Age-associated alteration of oocyte-specific gene expression in polar bodies: potential markers of oocyte competence". Fertility and Sterility. 98 (2): 480–486. doi:10.1016/j.fertnstert.2012.04.035. PMC 3409302. PMID 22633262.
  6. Verlinsky Y, Ginsberg N, Lifchez A, Valle J, Moise J, Strom CM (Oct 1990). "Analysis of the first polar body: preconception genetic diagnosis". Hum. Reprod. 5 (7): 826–9. doi:10.1093/oxfordjournals.humrep.a137192. PMID 2266156.
  7. Munné S, Dailey T, Sultan KM, Grifo J, Cohen J (Apr 1995). "The use of first polar bodies for preimplantation diagnosis of aneuploidy". Hum. Reprod. 10 (4): 1014–20. doi:10.1093/oxfordjournals.humrep.a136027. PMID 7650111.
  8. Montag M, van der Ven K, Dorn C, van der Ven H (Oct 2004). "Outcome of laser-assisted polar body biopsy and aneuploidy testing". Reprod. Biomed. Online. 9 (4): 425–9. doi:10.1016/S1472-6483(10)61278-3. PMID 15511343. Retrieved 2015-02-26.
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