Suppr超能文献

多重置换扩增的脊髓性肌萎缩症单基因疾病的胚胎植入前遗传学检测:11 例未受影响的活产。

Preimplantation Genetic Testing for Monogenic Disease of Spinal Muscular Atrophy by Multiple Displacement Amplification: 11 unaffected livebirths.

机构信息

Reproductive Medicine Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China, 510080.

Guangdong Provincial Key Laboratory of Reproductive Medicine, Guangzhou, China, 510080.

出版信息

Int J Med Sci. 2019 Sep 7;16(9):1313-1319. doi: 10.7150/ijms.32319. eCollection 2019.

Abstract

: Preimplantation genetic testing for monogenic disease (PGT-M) has become an effective method for providing couples with the opportunity of a pregnancy with a baby free of spinal muscular atrophy (SMA). Multiple displacement amplification (MDA) overcomes the innate dilemma of very limited genetic material available for PGT-M. : To evaluate the use of MDA, combined with haplotype analysis and mutation amplification, in PGT-M for families with SMA. : MDA was used to amplify the whole genome from single blastomeres or trophectoderm (TE) cells. Exon 7 of the survival motor neuron gene 1 (SMN1) and eleven STRs markers flanking the SMN1 gene were incorporated into singleplex polymerase chain reaction (PCR) assays on MDA products. : Sixteen cycles (19 ovum pick-up cycles) of PGT-M were initiated in 12 couples. A total of 141 embryos were tested: 90 embryos were biopsied at the cleavage stage and 51 embryos were biopsied at the blastocyst stage. MDA was successful on 94.44% (85/90) of the single blastomeres and on 92.16% (47/51) of the TE cells. And the PCR efficiency were 98.4% (561/570) and 100% (182/182), respectively. In addition, the average allele drop-out (ADO) rates were 13.3% (60/392) and 9.8% (11/112), respectively. The results for SMN1 exon 7 were all matched with haplotype analysis, which allowed an accurate diagnosis of 93.62% (132/141) embryos. Twelve families had unaffected embryos available for transfer and a total of 38 embryos were transferred in 20 embryo transfer cycles. Eight transfers were successful, resulting in a clinical pregnancy rate of 40% (8/20) and an implantation rate of 28.95% (11/38). Finally, 11 healthy babies were born. Among them, 5 SMA carriers were singleton live births and 3 SMA carriers had twin births. : Careful handling during the MDA procedure can improve subsequent PCR efficiency and reduce the ADO rate. We suggest that this protocol is reliable for increasing the accuracy of the PGT-M for SMA.

摘要

胚胎植入前遗传学检测用于单基因疾病(PGT-M)已成为为夫妇提供机会,使他们能够怀上不患有脊肌萎缩症(SMA)的婴儿。多重置换扩增(MDA)克服了用于 PGT-M 的遗传物质非常有限的固有困境。评估 MDA 与单体型分析和突变扩增相结合在 SMA 家族中的 PGT-M 中的应用。MDA 用于扩增单个卵裂球或滋养外胚层(TE)细胞的全基因组。生存运动神经元基因 1(SMN1)的外显子 7 和 SMN1 基因侧翼的 11 个 STR 标记被纳入 MDA 产物的单重聚合酶链反应(PCR)检测中。12 对夫妇开始了 16 个周期(19 个卵母细胞采集周期)的 PGT-M。共检测了 141 个胚胎:90 个胚胎在卵裂期进行活检,51 个胚胎在囊胚期进行活检。MDA 在 94.44%(90/90)的单个卵裂球和 92.16%(47/51)的 TE 细胞上成功。PCR 效率分别为 98.4%(561/570)和 100%(182/182)。此外,平均等位基因缺失(ADO)率分别为 13.3%(60/392)和 9.8%(11/112)。SMN1 外显子 7 的结果均与单体型分析相匹配,这使得 93.62%(132/141)的胚胎能够进行准确诊断。12 个家庭有未受影响的胚胎可供转移,共进行了 20 次胚胎转移周期,转移了 38 个胚胎。8 次转移成功,临床妊娠率为 40%(8/20),着床率为 28.95%(11/38)。最终,11 名健康婴儿出生。其中,5 名 SMA 携带者为单胎活产,3 名 SMA 携带者为双胞胎出生。MDA 过程中的仔细处理可以提高后续 PCR 效率并降低 ADO 率。我们建议该方案可用于提高 SMA 的 PGT-M 准确性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验