Literature DB >> 32621537

Cumulative outcome of pre-implantation genetic diagnosis for sickle cell disease: a 5-year review.

Saaliha Vali1, Sunbal Mukhtar1, Anupa Nandi1, Kieren Wilson1, Laura Oakley2, Tarek El-Toukhy1, Eugene Oteng-Ntim1.   

Abstract

To review the cumulative outcome of pre-implantation genetic diagnosis (PGD) cycles performed for prevention of sickle cell disease (SCD). Couples referred for PGD for SCD between April 2012 and October 2017 were included. Ovarian stimulation was performed using a short gonadotrophin-releasing hormone (GnRH) antagonist protocol and follicle-stimulating hormone injections. The GnRH agonist was used to trigger oocyte maturation. Oocytes were fertilised using intracytoplasmic sperm injection. Trophectoderm biopsy was performed on day 5 or 6 followed by vitrification. Genetic testing was done using pre-implantation genetic haplotyping. A total of 60 couples started 70 fresh PGD cycles (mean 1·2 cycles/couple) and underwent a total of 74 frozen-embryo-transfer (FET) cycles (mean 1·3 FET/couple). The mean (SD) female age was 33 (4·4) years and the mean (SD) anti-müllerian hormone level was 22·9 (2·8) pmol/l. The cumulative live-birth rate was 54%/PGD cycle started and 63%/couple embarking on PGD. The rate of multiple births was 8%. The cumulative outcome of PGD treatment for prevention of SCD transmission is high and PGD treatment should be offered to all at-risk couples.
© 2020 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

Entities:  

Keywords:  in vitro fertilisation (IVF); pre-implantation genetic diagnosis (PGD); reproduction; sickle cell disease (SCD); single-gene disorder

Mesh:

Year:  2020        PMID: 32621537     DOI: 10.1111/bjh.16930

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  2 in total

1.  Acceptable, hopeful, and useful: development and mixed-method evaluation of an educational tool about reproductive options for people with sickle cell disease or trait.

Authors:  Isabel V Lake; Jake A Ruddy; James A Saba; Sajya M Singh; Macy L Early; Rachel J Strodel; Sophie Lanzkron; Jennifer W Mack; Emily R Meier; Mindy S Christianson; Lydia H Pecker
Journal:  J Assist Reprod Genet       Date:  2021-11-22       Impact factor: 3.412

Review 2.  Knowledge gaps in reproductive and sexual health in girls and women with sickle cell disease.

Authors:  Lydia H Pecker; Deva Sharma; Alecia Nero; Michael J Paidas; Russell E Ware; Andra H James; Kim Smith-Whitley
Journal:  Br J Haematol       Date:  2021-07-07       Impact factor: 8.615

  2 in total

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