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Preimplantasyon Genetik Tanı

Yıl 2014, Cilt: 3 Sayı: 2, 49 - 53, 01.10.2014

Öz

Preimplantasyon Genetik Tanı, In Vitro Fertilization ve yardımcı üreme teknikleri ile elde edilen embriyolarda gebelik oluşmadan genetik incelemeyi mümkün kılan bir yöntemdir. Bu yöntemle embriyo oluşmadan veya oluşumundan birkaç gün sonra çeşitli biyopsi yöntemleri ile tek hücre veya birkaç hücresi genetik açıdan incelenmektedir. Alınan hücre veya hücrelerde ya floresan in situ hibridizasyon yöntemi ile kromozomal anomalileri ya da tüm genom amplifikasyonu sonrası Array-Comparative Genomic Hybridization=Karşılaştırmalı Genom Hibridizasyonu yöntemi ile tüm kromozomlar veya dizileme ile hedef genler incelenmektedir. Böylelikle, yapısal kromozom bozuklukları veya tek gen hastalıkları gibi genetik nedenler gebelik oluşmadan önce analiz edilerek sağlıklı embriyo seçme imkanı sağlanabilmektedir. Ayrıca preimplantasyon genetik tanı normal yolla çocuk sahibi olamayan ve yardımcı üreme tekniklerine baş vuran çiftlerde anöploidi taraması yapılarak gebelik şansını artıran ve sayısal kromozomal anomali nedeni ile gereksiz terminasyonları ortadan kaldıran bir yöntemdir. Preimplantasyon genetik tanı sadece bir tanı yöntemi olmakla kalmayıp, ailelerin sağlıklı çocuk sahibi olmasının yanında, kök hücre ile tedavisi mümkün olan hasta kardeş için HLA uyumlu doku olanağı da sunmaktadır

Kaynakça

  • 1. Gardner RL, Edwards RG. Control of the sex ratio at full term in the rabbit by transferring sexed blastocysts. Nature 1968; 27-218(5139): 346-9.
  • 2. By-passing a block to conception. Times 1978 Jul; 27: 15.
  • 3. Verlinsky Y, Ginsberg N, Lifchez A, Valle J, Moise J, Strom CM. Analysis of the first polar body: preconception genetic diagnosis. Hum Reprod 1990; 5(7): 826-9.
  • 4. Strom CM, Verlinsky Y, Milayeva S, Evsikov S, Cieslak J, Lifchez A, et al. Preconception genetic diagnosis of cystic fibrosis. Lancet 1990; 4-336(8710): 306-7.
  • 5. Kahraman S, Bahce M, Samli H, Imirzalioglu N, Yakisn K, Cengiz G, et al. Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure. Hum Reprod 2000; 15(9): 2003-7.
  • 6. Harper JC, Wilton L, Traeger-Synodinos J, Goossens V, Moutou C, SenGupta SB, et al. The ESHRE PGD Consortium: 10 years of data collection. Hum Reprod Update 2012; 18(3): 234-47.
  • 7. Simpson JL. Preimplantation genetic diagnosis at 20 years. Prenat Diagn 2010; 30(7): 682-95.
  • 8. Munne S, Weier HU, Stein J, Grifo J, Cohen J. A fast and efficient method for simultaneous X and Y in situ hybridization of human blastomeres. J Assist Reprod Genet 1993; 10(1): 82-90.
  • 9. Munne S, Bahce M, Schimmel T, Sadowy S, Cohen J. Case report: chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations. Prenat Diagn 1998; 18(13): 1450-8.
  • 10. Tur-Kaspa I, Jeelani R, Doraiswamy PM. Preimplantation genetic diagnosis for inherited neurological disorders. Nat Rev Neurol 2014; 10(7): 417-24.
  • 11. Huttelova R, Kleibl Z, Rezatova J, Krutilkova V, Foretova L, Novotny J, et al. [Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers]. Klinicka onkologie: casopis Ceske a Slovenske onkologicke spolecnosti 2009; 22: 69-74.
  • 12. Capalbo A, Bono S, Spizzichino L, Biricik A, Baldi M, Colamaria S, et al. Sequential comprehensive chromosome analysis on polar bodies, blastomeres and trophoblast: insights into female meiotic errors and chromosomal segregation in the preimplantation window of embryo development. Hum Reprod 2013; 28(2): 509-18.
  • 13. Salvaggio CN, Forman EJ, Garnsey HM, Treff NR, Scott RT, Jr. Polar body based aneuploidy screening is poorly predictive of embryo ploidy and reproductive potential. J Assist Reprod Genet 2014; 31(9): 1221-6.
  • 14. Scott KL, Hong KH, Scott RT, Jr. Selecting the optimal time to perform biopsy for preimplantation genetic testing. Fertil Steril 2013; 100(3): 608-14.
  • 15. Capalbo A, Bono S, Spizzichino L, Biricik A, Baldi M, Colamaria S, et al. Reply: Questions about the accuracy of polar body analysis for preimplantation genetic screening. Hum Reprod 2013; 28(6): 1733-6.
  • 16. Bielanska M, Jin S, Bernier M, Tan SL, Ao A. Diploidaneuploid mosaicism in human embryos cultured to the blastocyst stage. Fertil Steril 2005; 84(2): 336-42.
  • 17. Scott RT, Jr., Upham KM, Forman EJ, Zhao T, Treff NR. Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial. Fertil Steril 2013; 100(3): 624-30.
  • 18. Yang Z, Liu J, Collins GS, Salem SA, Liu X, Lyle SS, et al. Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study. Mol Cytogenet 2012; 5(1): 24.
  • 19. Adler A, Lee HL, McCulloh DH, Ampeloquio E, Clarke-Williams M, Wertz BH, et al. Blastocyst culture selects for euploid embryos: comparison of blastomere and trophectoderm biopsies. Reprodu biomed online 2014; 28(4): 485-91.
  • 20. Li G, Jin H, Xin Z, Su Y, Brezina PR, Benner AT, et al. Increased IVF pregnancy rates after microarray preimplantation genetic diagnosis due to parental translocations. Syst Biol Reprod Med 2014; 60(2): 119- 24.
  • 21. Scriven PN, Flinter FA, Khalaf Y, Lashwood A, Mackie Ogilvie C. Benefits and drawbacks of preimplantation genetic diagnosis (PGD) for reciprocal translocations: lessons from a prospective cohort study. Eur J Hum Genet: EJHG 2013 Oct; 21(10): 1035-41.
  • 22. Berger VK, Baker VL. Preimplantation diagnosis for single gene disorders. Semin Reprod Med 2014; 32(2): 107-13.
  • 23. Morton CC, Brown JA, Kirsch IR, Evans GA, Mohanakumar T, Nance WE. Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridization. Clin Genet 1986; 29(1): 62-72.
  • 24. Basille C, Frydman R, El Aly A, Hesters L, Fanchin R, Tachdjian G, et al. Preimplantation genetic diagnosis: state of the art. Eur J Obstet Gynecol Reprod Biol 2009; 145(1): 9-13.
  • 25. Verlinsky Y, Rechitsky S, Schoolcraft W, Strom C, Kuliev A. Preimplantation diagnosis for Fanconi anemia combined with HLA matching. JAMA 2001; 27-285(24): 3130-3.
  • 26. Fiorentino F, Biricik A, Karadayi H, Berkil H, Karlikaya G, Sertyel S, et al. Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching. Mol Hum Reprod 2004; 10(6): 445-60.
  • 27. Kahraman S, Beyazyurek C, Yesilipek MA, Ozturk G, Ertem M, Anak S, et al. Successful haematopoietic stem cell transplantation in 44 children from healthy siblings conceived after preimplantation HLA matching. Reprodu biomed online 2014; 29(3): 340-51.
  • 28. Sanchez-Castro M, Jimenez-Macedo AR, Sandalinas M, Blanco J. Prognostic value of sperm fluorescence in situ hybridization analysis over PGD. Hum Reprod 2009; 24(6): 1516-21.
  • 29. Mir P, Rodrigo L, Mateu E, Peinado V, Milan M, Mercader A, et al. Improving FISH diagnosis for preimplantation genetic aneuploidy screening. Hum Reprod 2010; 25(7): 1812-7.
  • 30. Qian YL, Xu CM, Jin F, Zhu YM, Luo Q, Huang HF. [Preimplantation genetic diagnosis of translocation]. Zhonghua fu chan ke za zhi 2008; 43(8): 581-3.
  • 31. Huang CC, Chang LJ, Tsai YY, Hung CC, Fang MY, Su YN, et al. A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization. Journal of the Formosan Medical Association = Taiwan yi zhi 2013; 112(9): 537-44.
  • 32. Tobler KJ, Brezina PR, Benner AT, Du L, Xu X, Kearns WG. Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates. J Assist Reprod Genet 2014; 31(7): 843-50.
  • 33. Martin J, Cervero A, Mir P, Martinez-Conejero JA, Pellicer A, Simon C. The impact of next-generation sequencing technology on preimplantation genetic diagnosis and screening. Fertil Steril 2013; 15-99(4): 1054-61 e3.
  • 34. Lu Y, Peng H, Jin Z, Cheng J, Wang S, Ma M, et al. Preimplantation genetic diagnosis for a Chinese family with autosomal recessive Meckel-Gruber syndrome type 3 (MKS3). PLoS One 2013; 8(9): 73245.

Preimplantation Genetic Diagnosis

Yıl 2014, Cilt: 3 Sayı: 2, 49 - 53, 01.10.2014

Öz

Preimplantation Genetic Diagnosis is a procedure which enables genetic analysis in the embryos obtained by In Vitro Fertilization or assisted reproductive techniques before pregnancy begins. By this procedure, before embryo formation or in the first few days after embryo development a single cell or a few cells are analysed genetically by various biopsy methods. The cell or cells are examined for chromosomal abnormalitites by fluorescent in situ hybridization or all chromosomes are examined by Array-Comparative Genomic Hybridization after whole genome amplification or target genes are analysed by sequencing. Thus, genetic reasons such as structural chromosomal abnormalities or single gene diseases are detected before pregnancy begins which gives the opportunity to choose the healthy embryos. Besides, in infertile couples who apply for assisted reproductive techniques preimplantation genetic diagnosis is a procedure increasing the chance of pregnancy by aneuploidy scanning and eliminating unnecessary pregnancy terminations because of numerical chromosomal abnormalities. Preimplantation genetic diagnosis is not only a technique for the diagnosis, but besides offering the chance of to provide a healthy baby to the families, it also provides the possibility of HLA compatible tissue for the sick sibling in whom cure is likely by stem cell therapy as well

Kaynakça

  • 1. Gardner RL, Edwards RG. Control of the sex ratio at full term in the rabbit by transferring sexed blastocysts. Nature 1968; 27-218(5139): 346-9.
  • 2. By-passing a block to conception. Times 1978 Jul; 27: 15.
  • 3. Verlinsky Y, Ginsberg N, Lifchez A, Valle J, Moise J, Strom CM. Analysis of the first polar body: preconception genetic diagnosis. Hum Reprod 1990; 5(7): 826-9.
  • 4. Strom CM, Verlinsky Y, Milayeva S, Evsikov S, Cieslak J, Lifchez A, et al. Preconception genetic diagnosis of cystic fibrosis. Lancet 1990; 4-336(8710): 306-7.
  • 5. Kahraman S, Bahce M, Samli H, Imirzalioglu N, Yakisn K, Cengiz G, et al. Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure. Hum Reprod 2000; 15(9): 2003-7.
  • 6. Harper JC, Wilton L, Traeger-Synodinos J, Goossens V, Moutou C, SenGupta SB, et al. The ESHRE PGD Consortium: 10 years of data collection. Hum Reprod Update 2012; 18(3): 234-47.
  • 7. Simpson JL. Preimplantation genetic diagnosis at 20 years. Prenat Diagn 2010; 30(7): 682-95.
  • 8. Munne S, Weier HU, Stein J, Grifo J, Cohen J. A fast and efficient method for simultaneous X and Y in situ hybridization of human blastomeres. J Assist Reprod Genet 1993; 10(1): 82-90.
  • 9. Munne S, Bahce M, Schimmel T, Sadowy S, Cohen J. Case report: chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations. Prenat Diagn 1998; 18(13): 1450-8.
  • 10. Tur-Kaspa I, Jeelani R, Doraiswamy PM. Preimplantation genetic diagnosis for inherited neurological disorders. Nat Rev Neurol 2014; 10(7): 417-24.
  • 11. Huttelova R, Kleibl Z, Rezatova J, Krutilkova V, Foretova L, Novotny J, et al. [Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers]. Klinicka onkologie: casopis Ceske a Slovenske onkologicke spolecnosti 2009; 22: 69-74.
  • 12. Capalbo A, Bono S, Spizzichino L, Biricik A, Baldi M, Colamaria S, et al. Sequential comprehensive chromosome analysis on polar bodies, blastomeres and trophoblast: insights into female meiotic errors and chromosomal segregation in the preimplantation window of embryo development. Hum Reprod 2013; 28(2): 509-18.
  • 13. Salvaggio CN, Forman EJ, Garnsey HM, Treff NR, Scott RT, Jr. Polar body based aneuploidy screening is poorly predictive of embryo ploidy and reproductive potential. J Assist Reprod Genet 2014; 31(9): 1221-6.
  • 14. Scott KL, Hong KH, Scott RT, Jr. Selecting the optimal time to perform biopsy for preimplantation genetic testing. Fertil Steril 2013; 100(3): 608-14.
  • 15. Capalbo A, Bono S, Spizzichino L, Biricik A, Baldi M, Colamaria S, et al. Reply: Questions about the accuracy of polar body analysis for preimplantation genetic screening. Hum Reprod 2013; 28(6): 1733-6.
  • 16. Bielanska M, Jin S, Bernier M, Tan SL, Ao A. Diploidaneuploid mosaicism in human embryos cultured to the blastocyst stage. Fertil Steril 2005; 84(2): 336-42.
  • 17. Scott RT, Jr., Upham KM, Forman EJ, Zhao T, Treff NR. Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial. Fertil Steril 2013; 100(3): 624-30.
  • 18. Yang Z, Liu J, Collins GS, Salem SA, Liu X, Lyle SS, et al. Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study. Mol Cytogenet 2012; 5(1): 24.
  • 19. Adler A, Lee HL, McCulloh DH, Ampeloquio E, Clarke-Williams M, Wertz BH, et al. Blastocyst culture selects for euploid embryos: comparison of blastomere and trophectoderm biopsies. Reprodu biomed online 2014; 28(4): 485-91.
  • 20. Li G, Jin H, Xin Z, Su Y, Brezina PR, Benner AT, et al. Increased IVF pregnancy rates after microarray preimplantation genetic diagnosis due to parental translocations. Syst Biol Reprod Med 2014; 60(2): 119- 24.
  • 21. Scriven PN, Flinter FA, Khalaf Y, Lashwood A, Mackie Ogilvie C. Benefits and drawbacks of preimplantation genetic diagnosis (PGD) for reciprocal translocations: lessons from a prospective cohort study. Eur J Hum Genet: EJHG 2013 Oct; 21(10): 1035-41.
  • 22. Berger VK, Baker VL. Preimplantation diagnosis for single gene disorders. Semin Reprod Med 2014; 32(2): 107-13.
  • 23. Morton CC, Brown JA, Kirsch IR, Evans GA, Mohanakumar T, Nance WE. Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridization. Clin Genet 1986; 29(1): 62-72.
  • 24. Basille C, Frydman R, El Aly A, Hesters L, Fanchin R, Tachdjian G, et al. Preimplantation genetic diagnosis: state of the art. Eur J Obstet Gynecol Reprod Biol 2009; 145(1): 9-13.
  • 25. Verlinsky Y, Rechitsky S, Schoolcraft W, Strom C, Kuliev A. Preimplantation diagnosis for Fanconi anemia combined with HLA matching. JAMA 2001; 27-285(24): 3130-3.
  • 26. Fiorentino F, Biricik A, Karadayi H, Berkil H, Karlikaya G, Sertyel S, et al. Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching. Mol Hum Reprod 2004; 10(6): 445-60.
  • 27. Kahraman S, Beyazyurek C, Yesilipek MA, Ozturk G, Ertem M, Anak S, et al. Successful haematopoietic stem cell transplantation in 44 children from healthy siblings conceived after preimplantation HLA matching. Reprodu biomed online 2014; 29(3): 340-51.
  • 28. Sanchez-Castro M, Jimenez-Macedo AR, Sandalinas M, Blanco J. Prognostic value of sperm fluorescence in situ hybridization analysis over PGD. Hum Reprod 2009; 24(6): 1516-21.
  • 29. Mir P, Rodrigo L, Mateu E, Peinado V, Milan M, Mercader A, et al. Improving FISH diagnosis for preimplantation genetic aneuploidy screening. Hum Reprod 2010; 25(7): 1812-7.
  • 30. Qian YL, Xu CM, Jin F, Zhu YM, Luo Q, Huang HF. [Preimplantation genetic diagnosis of translocation]. Zhonghua fu chan ke za zhi 2008; 43(8): 581-3.
  • 31. Huang CC, Chang LJ, Tsai YY, Hung CC, Fang MY, Su YN, et al. A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization. Journal of the Formosan Medical Association = Taiwan yi zhi 2013; 112(9): 537-44.
  • 32. Tobler KJ, Brezina PR, Benner AT, Du L, Xu X, Kearns WG. Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates. J Assist Reprod Genet 2014; 31(7): 843-50.
  • 33. Martin J, Cervero A, Mir P, Martinez-Conejero JA, Pellicer A, Simon C. The impact of next-generation sequencing technology on preimplantation genetic diagnosis and screening. Fertil Steril 2013; 15-99(4): 1054-61 e3.
  • 34. Lu Y, Peng H, Jin Z, Cheng J, Wang S, Ma M, et al. Preimplantation genetic diagnosis for a Chinese family with autosomal recessive Meckel-Gruber syndrome type 3 (MKS3). PLoS One 2013; 8(9): 73245.
Toplam 34 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Derleme
Yazarlar

Cemal Ekici Bu kişi benim

Yayımlanma Tarihi 1 Ekim 2014
Yayımlandığı Sayı Yıl 2014 Cilt: 3 Sayı: 2

Kaynak Göster

APA Ekici, C. (2014). Preimplantasyon Genetik Tanı. Annals of Health Sciences Research, 3(2), 49-53.
AMA Ekici C. Preimplantasyon Genetik Tanı. Ann Health Sci Res. Ekim 2014;3(2):49-53.
Chicago Ekici, Cemal. “Preimplantasyon Genetik Tanı”. Annals of Health Sciences Research 3, sy. 2 (Ekim 2014): 49-53.
EndNote Ekici C (01 Ekim 2014) Preimplantasyon Genetik Tanı. Annals of Health Sciences Research 3 2 49–53.
IEEE C. Ekici, “Preimplantasyon Genetik Tanı”, Ann Health Sci Res, c. 3, sy. 2, ss. 49–53, 2014.
ISNAD Ekici, Cemal. “Preimplantasyon Genetik Tanı”. Annals of Health Sciences Research 3/2 (Ekim 2014), 49-53.
JAMA Ekici C. Preimplantasyon Genetik Tanı. Ann Health Sci Res. 2014;3:49–53.
MLA Ekici, Cemal. “Preimplantasyon Genetik Tanı”. Annals of Health Sciences Research, c. 3, sy. 2, 2014, ss. 49-53.
Vancouver Ekici C. Preimplantasyon Genetik Tanı. Ann Health Sci Res. 2014;3(2):49-53.