From the Department of Neurology (R.A.P., A.B., K.J., S.M.P., T.F.T., M.A., L.D.), University of Pennsylvania, Philadelphia; and Sarepta Therapeutics (T.B.), Cambridge, MA.
Neurology. 2023 Nov 7;101(19):836-841. doi: 10.1212/WNL.0000000000207736. Epub 2023 Aug 18.
Preimplantation genetic testing for monogenic conditions (PGT-M), formerly called preimplantation genetic diagnosis, is a specialized assisted reproduction technique that aims to reduce the risk of a pregnancy inheriting a monogenic condition. Despite calls to increase awareness and prepare neurologists for discussing PGT-M with patients and their families, no guidelines currently exist. When introducing PGT-M to those who may be interested in using it, there are major factors for discussion, including (1) genetic considerations (e.g., requirement for a confirmed genetic diagnosis; timing of genetic test results); (2) practical considerations (e.g., access to PGT-M and genetic services); (3) technical considerations (e.g., factors that can affect the success rate of PGT-M); and (4) psychosocial and ethical considerations (e.g., predictive testing for asymptomatic family members; family dynamics and values). Here, our team of neurologists and specialized genetic counselors discusses the current state of genetic characterization in adult-onset neurodegenerative conditions and highlights the major factors that should be considered when discussing PGT-M with families.
针对单基因疾病的胚胎植入前遗传学检测(PGT-M),前称胚胎植入前遗传学诊断,是一种旨在降低单基因疾病妊娠遗传风险的专业辅助生殖技术。尽管人们呼吁提高认识,并让神经科医生为与患者及其家属讨论 PGT-M 做好准备,但目前尚无相关指南。在向可能有兴趣使用 PGT-M 的人介绍该技术时,有几个主要的讨论因素,包括(1)遗传因素(例如,需要明确的遗传诊断;遗传检测结果的时间);(2)实际因素(例如,PGT-M 和遗传服务的可及性);(3)技术因素(例如,可能影响 PGT-M 成功率的因素);和(4)心理社会和伦理因素(例如,对无症状家庭成员的预测性检测;家庭动态和价值观)。在此,我们的神经科医生和专业遗传咨询师团队讨论了成人发病的神经退行性疾病的遗传特征现状,并强调了在与家庭讨论 PGT-M 时应考虑的主要因素。