【植入前基因检测联合第三代测序阻断遗传性痉挛性截瘫的成功应用】。

Q Qi, Z Zhou, J Ma, B Yao, L Chen
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引用次数: 0

摘要

目的:报道应用第三代测序(TGS)联合胚胎植入前基因检测(PGT)成功预防由SPAST基因突变引起的遗传性痉挛性截瘫(HSP)的病例,并评估PGT- m和TGS在遗传性痉挛性截瘫治疗中的价值。方法:对一个HSP家族进行全外显子测序(WES),鉴定出SPAST基因c.1699G>T突变。先证者突变位点通过Sanger测序确定。选择SPAST基因突变侧的单核苷酸多态性(SNP)位点作为遗传连锁标记,构建携带突变基因的SNP单倍型。使用拮抗剂方案进行卵巢刺激以获取卵母细胞,随后进行胞浆内单精子注射(ICSI)和胚胎培养。对胚泡滋养外胚层细胞进行活组织检查,进行单基因疾病(PGT-M)的着床前基因检测,以便选择无疾病的胚胎进行移植。结果:本周期共取出卵母细胞20个,其中18个成功受精,12个囊胚符合活检条件。基因检测显示12个囊胚均成功扩增,并证实为整倍体。其中8个囊胚不携带父本突变,选择一个优质的整倍体胚胎进行冷冻胚胎移植(FET)。怀孕期间的羊水检测证实胎儿没有父系突变,因此生下了一个健康的女婴。结论:对于家系资料缺失的遗传病,应用第三代测序和PGT-M技术可有效阻断SPAST基因突变向子代的垂直遗传,避免非整倍体胚胎妊娠,帮助常染色体显性HSP家庭获得健康后代。
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[Successful application of preimplantation genetic testing combined with thirdgeneration sequencing for blocking hereditary spastic paraplegia].

Objective: We report a case of application of third-generation sequencing (TGS) combined with preimplantation genetic testing (PGT) for successful prevention of hereditary spastic paraplegia (HSP) caused by SPAST gene mutations and assess the value of PGT-M and TGS in managing hereditary spastic paraplegia.

Methods: A family affected by HSP underwent whole exon sequencing (WES), and a c.1699G>T mutation in the SPAST gene was identified. The mutation site in the proband was confirmed through Sanger sequencing. A single nucleotide polymorphism (SNP) site flanking the SPAST gene mutation was selected as the genetic linkage marker, and a SNP haplotype carrying the mutated gene was constructed. Ovarian stimulation using an antagonist regimen was performed for oocyte retrieval, followed by intracytoplasmic sperm injection (ICSI) and embryo culture. Blastocyst trophectoderm cells were biopsied for preimplantation genetic testing for monogenic disorders (PGT-M) to allow the selection of disease-free embryos for transfer.

Results: In this cycle, a total of 20 oocytes were retrieved, among which 18 were successfully fertilized to result in 12 blastocysts eligible for biopsy. Genetic testing revealed that all the 12 blastocysts were successfully amplified and confirmed as euploidy. Among them, 8 blastocysts did not carry paternal mutations, and a high-quality euploid embryo was selected for frozen embryo transfer (FET). Subsequent amniotic fluid testing during pregnancy confirmed the absence of paternal mutations in the fetus, resulting in the birth of a healthy baby girl.

Conclusion: For cases of genetic diseases with missing pedigree data, the application of third-generation sequencing and PGT-M technique can effectively block vertical transmission of SPAST gene mutation to the offspring, avoid pregnancy with an aneuploid embryo, and help families with autosomal dominant HSP obtain healthy offsprings.

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南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
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