IVF success rates in individuals accessing preimplantation genetic testing for monogenic conditions (PGT-M): a single centre retrospective cohort study of 572 IVF cycles

被引:0
作者
Poulton, Alice [1 ,2 ,3 ]
Menezes, Melody [2 ,3 ,4 ]
Hardy, Tristan [1 ,2 ]
Lewis, Sharon [2 ,3 ]
Hui, Lisa [2 ,3 ,5 ,6 ]
机构
[1] Monash IVF Grp Ltd, Level 1,510 Church St, Clayton, Vic 3121, Australia
[2] Univ Melbourne, Parkville, Vic, Australia
[3] Murdoch Childrens Res Inst, Parkville, Vic, Australia
[4] Victorian Clin Genet Serv, Parkville, Vic, Australia
[5] Mercy Hosp Women, Heidelberg, Vic, Australia
[6] Northern Hosp, Epping, Vic, Australia
关键词
Preimplantation genetic testing; Karyomapping; Single gene disorder; Monogenic disorder; 24-chromosome aneuploidy screening; PGT-M; DIAGNOSIS; THERAPY;
D O I
10.1007/s10815-025-03416-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose To evaluate live birth rates per embryo transfer where the primary indication for assisted reproduction was preimplantation genetic testing for monogenic conditions. Methods All oocytes were fertilized using intracytoplasmic sperm injection. On days 5-7, similar to 5 trophectoderm cells were biopsied. Whole genome amplification was performed on biopsy samples, followed by a karyomapping protocol. Embryos underwent concurrent 24-chromosome screening. Outcomes included the number of stimulated cycles resulting in embryo biopsy, monogenic and aneuploidy screening results, embryo transfers, and clinical pregnancies and live births. Generalized Estimating Equations were used to analyze the relationship between binary clinical outcomes and fertility covariates. Results Between 2015 and 2022, the laboratory biopsied and tested 2344 embryos for monogenic indications, from 527 stimulated cycles. Eight hundred forty-nine biopsied embryos were euploid and low probability of the condition of interest. Five hundred and thirteen embryos were transferred, resulting in 263 clinical pregnancies, and 230 live births. This translated to clinical pregnancy and live birth rates per embryo transfer of 51.3% (95% CI, 47.0-55.6%) and 44.8% (95% CI, 40.6-49.2%). Compared with patients undergoing preimplantation genetic testing without a subfertility factor, patients with a subfertility factor were 48% less likely to achieve a clinical pregnancy per embryo transfer (beta = - 0.4797474, p = 0.026) and 42% less likely to achieve a live birth (beta = - 0.4172361, p = 0.052). Conclusions Individuals accessing preimplantation genetic testing for monogenic conditions have higher clinical pregnancy and live birth rates than couples accessing in vitro fertilization for other indications such as subfertility. These findings confirm that preimplantation genetic testing is an effective reproductive option for Australian carrier individuals.
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收藏
页码:1567 / 1576
页数:10
相关论文
共 34 条
[1]  
Adamson GD, 2009, WOMENS HEALTH, V5, P351, DOI [10.2217/whe.09.28, 10.2217/WHE.09.28]
[2]   The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation [J].
Archibald, Alison D. ;
McClaren, Belinda J. ;
Caruana, Jade ;
Tutty, Erin ;
King, Emily A. ;
Halliday, Jane L. ;
Best, Stephanie ;
Kanga-Parabia, Anaita ;
Bennetts, Bruce H. ;
Cliffe, Corrina C. ;
Madelli, Evanthia O. ;
Ho, Gladys ;
Liebelt, Jan ;
Long, Janet C. ;
Braithwaite, Jeffrey ;
Kennedy, Jillian ;
Massie, John ;
Emery, Jon D. ;
McGaughran, Julie ;
Marum, Justine E. ;
Boggs, Kirsten ;
Barlow-Stewart, Kristine ;
Burnett, Leslie ;
Dive, Lisa ;
Freeman, Lucinda ;
Davis, Mark R. ;
Downes, Martin J. ;
Wallis, Mathew ;
Ferrie, Monica M. ;
Pachter, Nicholas ;
Scuffham, Paul A. ;
Casella, Rachael ;
Allcock, Richard J. N. ;
Ong, Royston ;
Edwards, Samantha ;
Righetti, Sarah ;
Lunke, Sebastian ;
Lewis, Sharon ;
Walker, Susan P. ;
Boughtwood, Tiffany F. ;
Hardy, Tristan ;
Newson, Ainsley J. ;
Kirk, Edwin P. ;
Laing, Nigel G. ;
Delatycki, Martin B. .
JOURNAL OF PERSONALIZED MEDICINE, 2022, 12 (11)
[3]   Effects of culture conditions on IVF outcome [J].
Behr, B ;
Wang, H .
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2004, 115 :S72-S76
[4]   Rare single gene disorders: estimating baseline prevalence and outcomes worldwide [J].
Blencowe H. ;
Moorthie S. ;
Petrou M. ;
Hamamy H. ;
Povey S. ;
Bittles A. ;
Gibbons S. ;
Darlison M. ;
Modell B. ;
Bittles A.H. ;
Christianson A. ;
Cousens S. ;
Darlison M. ;
Gibbons S. ;
Khoshnood B. ;
Howson C.P. ;
Lawn J.E. ;
Mastroiacovo P. ;
Morris J.K. ;
Mossey P.A. ;
Neville A.J. ;
Rankin J. ;
Schuler-Faccini L. ;
Wren C. ;
Yunis K.A. .
Journal of Community Genetics, 2018, 9 (4) :397-406
[5]   Anti-Mullerian hormone as a predictor of reproductive potential [J].
Bressler, Leah Hawkins ;
Steiner, Anne .
CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2018, 25 (06) :385-390
[6]   Public Awareness and Acceptability of PGT-M in Cancer Predisposition Syndromes [J].
Calosci, Davide ;
Passaglia, Lisa ;
Gabbiato, Ilaria ;
Cartisano, Francesca ;
Affuso, Rebecca ;
Sorrentino, Ugo ;
Zuccarello, Daniela .
GENES, 2023, 14 (11)
[7]   The economic impact of assisted reproductive technology: a review of selected developed countries [J].
Chambers, Georgina M. ;
Sullivan, Elizabeth A. ;
Ishihara, Osamu ;
Chapman, Michael G. ;
Adamson, G. David .
FERTILITY AND STERILITY, 2009, 91 (06) :2281-2294
[8]   Factors influencing patients' decision-making about preimplantation genetic testing for monogenic disorders [J].
Cheng, Lin ;
Meiser, Bettina ;
Kirk, Edwin ;
Kennedy, Debra ;
Barlow-Stewart, Kristine ;
Kaur, Rajneesh .
HUMAN REPRODUCTION, 2022, 37 (11) :2599-2610
[9]   Rare Monogenic Diseases: Molecular Pathophysiology and Novel Therapies [J].
Condo, Ivano .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (12)
[10]   Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening [J].
Dive, Lisa ;
Freeman, Lucinda ;
McEwen, Alison .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 (01) :5-6