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胚胎植入前遗传学检测:美国妇产科医师学会委员会意见,799 号。

Preimplantation Genetic Testing: ACOG Committee Opinion, Number 799.

出版信息

Obstet Gynecol. 2020 Mar;135(3):e133-e137. doi: 10.1097/AOG.0000000000003714.

Abstract

Preimplantation genetic testing comprises a group of genetic assays used to evaluate embryos before transfer to the uterus. Preimplantation genetic testing-monogenic is targeted to single gene disorders, and preimplantation genetic testing-aneuploidy is a broader test that screens for aneuploidy in all chromosomes, including the 22 pairs of autosomes and the sex chromosomes X and Y. To test embryos that are at risk for chromosome gains and losses related to parental structural chromosomal abnormalities (eg, translocations, inversions, deletions, and insertions), preimplantation genetic testing-structural rearrangements is used. Independent of the preimplantation genetic testing modality employed, false-positive and false-negative results are possible. Patients and health care providers should be aware that a "normal" or negative preimplantation genetic test result is not a guarantee of a newborn without genetic abnormalities. Traditional diagnostic testing or screening for aneuploidy should be offered to all patients who have had preimplantation genetic testing-aneuploidy, in accordance with recommendations for all pregnant patients. It is especially important to offer diagnostic testing or screening for aneuploidy after preimplantation genetic testing-monogenic or preimplantation genetic testing-structural rearrangements if concurrent preimplantation genetic testing-aneuploidy is not performed. Many limitations exist to preimplantation genetic testing and include challenges in detecting microdeletions and microduplications, de novo variants, and imprinting disorders. An emerging problem has been detection of mosaicism during preimplantation genetic testing-aneuploidy. The clinical utility of preimplantation genetic testing-monogenic and preimplantation genetic testing-structural rearrangements is firmly established; however, the best use of preimplantation genetic testing-aneuploidy remains to be determined. Future research is necessary to establish the overall clinical utility for preimplantation genetic testing-aneuploidy, the subset of patients that may benefit from preimplantation genetic testing-aneuploidy, the clinical significance of mosaicism, and residual risk for aneuploidy in preimplantation genetic testing-aneuploidy screened embryos.

摘要

胚胎植入前遗传学检测包括一组用于在将胚胎转移到子宫之前对其进行评估的遗传检测。胚胎植入前遗传学检测-单基因疾病针对的是单基因疾病,而胚胎植入前遗传学检测-非整倍体是一种更广泛的检测方法,可筛查所有染色体的非整倍体,包括 22 对常染色体和性染色体 X 和 Y。为了检测与父母结构性染色体异常(例如易位、倒位、缺失和插入)相关的染色体增益和损失风险的胚胎,使用胚胎植入前遗传学检测-结构重排。无论使用何种胚胎植入前遗传学检测方式,都可能出现假阳性和假阴性结果。患者和医疗保健提供者应该意识到,“正常”或阴性的胚胎植入前遗传学检测结果并不能保证新生儿没有遗传异常。应根据所有孕妇的建议,向所有接受过胚胎植入前遗传学检测-非整倍体的患者提供传统的非整倍体诊断检测或筛查。如果未同时进行胚胎植入前遗传学检测-非整倍体,则在进行胚胎植入前遗传学检测-单基因疾病或胚胎植入前遗传学检测-结构重排之后,尤其需要提供非整倍体的诊断检测或筛查。胚胎植入前遗传学检测存在许多局限性,包括检测微缺失和微重复、新生变异和印迹障碍的挑战。胚胎植入前遗传学检测-非整倍体期间检测到镶嵌现象是一个新出现的问题。胚胎植入前遗传学检测-单基因疾病和胚胎植入前遗传学检测-结构重排的临床实用性已得到确立;然而,胚胎植入前遗传学检测-非整倍体的最佳用途仍有待确定。未来的研究有必要确定胚胎植入前遗传学检测-非整倍体的整体临床实用性、可能从胚胎植入前遗传学检测-非整倍体中受益的患者亚组、镶嵌现象的临床意义以及胚胎植入前遗传学检测-非整倍体筛查胚胎中非整倍体的残留风险。

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