The current clinical applications of preimplantation genetic testing (PGT): acknowledging the limitations of biology and technology.

IF 3.9 3区 医学 Q1 PATHOLOGY Expert Review of Molecular Diagnostics Pub Date : 2024-08-11 DOI:10.1080/14737159.2024.2390187
Georgia Kakourou, Christalena Sofocleous, Thalia Mamas, Christina Vrettou, Joanne Traeger-Synodinos
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Abstract

Introduction: Preimplantation Genetic Testing (PGT) is a cutting-edge test used to detect genetic abnormalities in embryos fertilized through Medically Assisted Reproduction (MAR). PGT aims to ensure that embryos selected for transfer are free of specific genetic conditions or chromosome abnormalities, thereby reducing chances for unsuccessful MAR cycles, complicated pregnancies, and genetic diseases in future children.

Areas covered: In PGT, genetics, embryology, and technology progress and evolve together. Biological and technological limitations are described and addressed to highlight complexity and knowledge constraints and draw attention to concerns regarding safety of procedures, clinical validity, and utility, extent of applications and overall ethical implications for future families and society.

Expert opinion: Understanding the genetic basis of diseases along with advanced technologies applied in embryology and genetics contribute to faster, cost-effective, and more efficient PGT. Next Generation Sequencing-based techniques, enhanced by improved bioinformatics, are expected to upgrade diagnostic accuracy. Complicating findings such as mosaicism, mt-DNA variants, variants of unknown significance, or variants related to late-onset or polygenic diseases will however need further appraisal. Emphasis on monitoring such emerging data is crucial for evidence-based counseling while standardized protocols and guidelines are essential to ensure clinical value and respect of Ethical, Legal and Societal Issues.

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植入前基因检测(PGT)的当前临床应用:承认生物学和技术的局限性。
导言:胚胎植入前基因检测(PGT)是用于检测通过医学辅助生殖(MAR)受精的胚胎是否存在基因异常的尖端检测方法。PGT 的目的是确保被选中进行移植的胚胎没有特定的遗传病或染色体异常,从而减少医学辅助生殖周期不成功、复杂妊娠和未来孩子患遗传病的几率:在 PGT 中,遗传学、胚胎学和技术共同进步和发展。对生物学和技术的局限性进行了描述和论述,以突出复杂性和知识限制,并提请人们关注程序的安全性、临床有效性和实用性、应用范围以及对未来家庭和社会的总体伦理影响:专家意见:对疾病遗传基础的了解以及在胚胎学和遗传学中应用的先进技术,有助于更快、更经济、更有效地进行 PGT。以下一代测序为基础的技术,再加上生物信息学的改进,有望提高诊断的准确性。然而,马赛克现象、mt-DNA 变异、意义不明的变异或与晚发性或多基因疾病相关的变异等复杂结果还需要进一步评估。重视监测这些新出现的数据对于循证咨询至关重要,而标准化的方案和指南对于确保临床价值和尊重伦理、法律和社会问题也至关重要。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
71
审稿时长
1 months
期刊介绍: Expert Review of Molecular Diagnostics (ISSN 1473-7159) publishes expert reviews of the latest advancements in the field of molecular diagnostics including the detection and monitoring of the molecular causes of disease that are being translated into groundbreaking diagnostic and prognostic technologies to be used in the clinical diagnostic setting. Each issue of Expert Review of Molecular Diagnostics contains leading reviews on current and emerging topics relating to molecular diagnostics, subject to a rigorous peer review process; editorials discussing contentious issues in the field; diagnostic profiles featuring independent, expert evaluations of diagnostic tests; meeting reports of recent molecular diagnostics conferences and key paper evaluations featuring assessments of significant, recently published articles from specialists in molecular diagnostic therapy. Expert Review of Molecular Diagnostics provides the forum for reporting the critical advances being made in this ever-expanding field, as well as the major challenges ahead in their clinical implementation. The journal delivers this information in concise, at-a-glance article formats: invaluable to a time-constrained community.
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