Preimplantation Testing for Polygenic Disease (PGT-P): Brave New World or Mad Pursuit?

D. Griffin, A. Gordon
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Abstract

In preimplantation testing for monogenic disease (PGT-M), we are used to specific and directed diagnoses. Preimplantation testing for polygenic disease (PGT-P), however, represents a further level of complexity in that multiple genes are tested for with an associated polygenic risk score (PRS), usually established by a genome-wide association study (GWAS). PGT-P has a series of pros and cons and, like many areas of genetics in reproductive medicine, there are vocal proponents and opponents on both sides. As with all things, the question needs to be asked, how much benefit does PGT-P provide in comparison to the risks involved? For each disease, a case will need to be made for PGT-P, as will a justification that the family involved will actually benefit; the worry is that this might be more work than the cost justifies.
多基因疾病植入前检测(PGT-P):勇敢的新世界还是疯狂的追求?
在单基因疾病(PGT-M)的植入前测试中,我们习惯于特定和直接的诊断。然而,多基因疾病植入前检测(PGT-P)代表了更高的复杂性,因为多个基因的检测具有相关的多基因风险评分(PRS),通常由全基因组关联研究(GWAS)建立。PGT-P有一系列的利弊,就像生殖医学遗传学的许多领域一样,双方都有强烈的支持者和反对者。与所有事情一样,需要问的问题是,与所涉及的风险相比,PGT-P提供了多少好处?对于每种疾病,都需要为PGT-P提供一个病例,以及相关家庭将实际受益的理由;令人担忧的是,这可能比成本合理的工作量更多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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