Scriven Paul N
Genetics Laboratories, 5th Floor Tower Wing, Guy's Hospital, Great Maze Pond, London, SE1 9RT, UK.
Reprod Biol Endocrinol. 2017 Jun 30;15(1):49. doi: 10.1186/s12958-017-0269-y.
The aim of this theoretical study is to explore the cost-effectiveness of aneuploidy screening in a UK setting for every woman aged under the age of 40 years when fresh and vitrified-warmed embryos are transferred one at a time in a first full cycle of assisted conception.
It is envisaged that a 24-chromosome genetic test for aneuploidy could be used to exclude embryos with an abnormal test result from transfer, or used only to rank embryos with the highest potential to be viable; the effect on cumulative outcome is assessed. The cost associated with one additional live birth event and one clinical miscarriage avoided is estimated, and the time taken to complete a cycle considered. The numbers of individual woman for whom testing is likely to be beneficial or detrimental is also evaluated.
Adding aneuploidy screening to a first treatment cycle is unlikely to result in a higher chance of a live birth event, and can be detrimental for some women. Premature termination of a clinical trial is likely to be biased in favour of genetic testing. Testing is likely to be an expensive way of reducing the chance of clinical miscarriage and shortening treatment time without a substantial reduction in the cost of testing, and is likely to benefit a minority of women. Selecting out embryos is likely to reduce the treatment time for women whether or not they have a baby, whilst ranking embryos only to reduce the time for those that have a child and not for those who need another stimulated cycle.
Adding aneuploidy screening to IVF treatment for women under the age of 40 years is unlikely to be beneficial for most women. To achieve an unbiased assessment of the cost-effectiveness of genetic testing for aneuploidy, clinical trials need to take account of women who still have embryos available for transfer at the end of the study period. Specifying the proportions of women for whom testing is likely to be beneficial and detrimental may help better inform couples who might be considering adding aneuploidy screening to their treatment cycle.
本理论研究旨在探讨在英国,针对40岁以下的每位女性,在首次完整的辅助受孕周期中每次移植一枚新鲜胚胎或玻璃化冷冻复苏胚胎时,非整倍体筛查的成本效益。
设想使用一种针对24条染色体的非整倍体基因检测来排除检测结果异常的胚胎不进行移植,或者仅用于对最有可能存活的胚胎进行排序;评估其对累积结局的影响。估计与多一次活产事件和避免一次临床流产相关的成本,并考虑完成一个周期所需的时间。还评估了检测可能有益或有害的个体女性数量。
在首个治疗周期增加非整倍体筛查不太可能提高活产几率,且对部分女性可能有害。临床试验的提前终止可能偏向于基因检测。检测可能是一种昂贵的方式,虽能降低临床流产几率和缩短治疗时间,但检测成本不会大幅降低,且可能仅使少数女性受益。筛选胚胎可能会缩短女性的治疗时间,无论她们是否生育,而仅对胚胎进行排序只会缩短生育女性的治疗时间,对需要再次促排卵周期的女性则无效。
对40岁以下女性的体外受精治疗增加非整倍体筛查对大多数女性不太可能有益。为了对非整倍体基因检测的成本效益进行无偏评估,临床试验需要考虑在研究期结束时仍有胚胎可供移植的女性。明确检测可能有益和有害的女性比例,可能有助于更好地为考虑在治疗周期中增加非整倍体筛查的夫妇提供信息。