Suppr超能文献

非侵入性产前筛查中胎儿分数的富集降低了母体背景干扰。

Enrichment of the fetal fraction in non-invasive prenatal screening reduces maternal background interference.

机构信息

State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, MOE-LSB and MOE-LSC, Department of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.

Center for Reproduction and Genetics, The Affiliated Suzhou Hospital of Nanjing Medical University, 26 Daoqian Street, Suzhou, Jiangsu, 215002, China.

出版信息

Sci Rep. 2018 Dec 5;8(1):17675. doi: 10.1038/s41598-018-35738-0.

Abstract

Measurement of cell-free fetal DNA (cffDNA) is an indispensable process for non-invasive prenatal screening (NIPS). According to recent studies, cffDNA in maternal plasma can be enriched for various lengths of fragments, and a sufficient amount of cffDNA can effectively eliminate background interference on the part of maternal DNA. Therefore, we developed a simple and effective separation method, improved NIPS (iNIPS), that enriches the fetal fraction and improves the accuracy of NIPS for fetal aneuploid detection. We adopted a novel strategy to achieve enrichment of 125-135 bp cell-free DNA (cfDNA) by e-gel electrophoresis. To evaluate clinical performance, we compared NIPS and iNIPS results from 2153 retrospective clinical samples. Of the 22 samples with NIPS results of "no call", 17 samples were reclassified as "unaffected" (9 cases of chr13, 5 cases of chr18, and 3 cases of chr21); 2 samples remained classified as "no call" (1 case of chr18 and 1 case of chr21); and 3 samples were identified as T21 by iNIPS. The average increase in abundance of cfDNA fragments of 125-135 bp was 2.5 times, and the average decrease in maternal background interference was 1.3 times. On this basis, the detection of fetal aneuploidy was highly improved with the fetal fraction as low as 2%; iNIPS achieved 100% sensitivity and 99.90% specificity in retrospective samples.

摘要

检测游离胎儿 DNA(cffDNA)是无创性产前筛查(NIPS)不可或缺的过程。根据最近的研究,母体血浆中的 cffDNA 可以富集到各种长度的片段,并且足够量的 cffDNA 可以有效地消除母体 DNA 的背景干扰。因此,我们开发了一种简单有效的分离方法,即改良 NIPS(iNIPS),它可以富集胎儿分数并提高 NIPS 对胎儿非整倍体检测的准确性。我们采用了一种新的策略,通过 e-凝胶电泳实现了 125-135bp 游离 DNA(cfDNA)的富集。为了评估临床性能,我们比较了 2153 例回顾性临床样本中的 NIPS 和 iNIPS 结果。在 22 例 NIPS 结果为“无信号”的样本中,17 例被重新分类为“正常”(9 例为 13 号染色体,5 例为 18 号染色体,3 例为 21 号染色体);2 例仍被归类为“无信号”(1 例为 18 号染色体,1 例为 21 号染色体);3 例通过 iNIPS 被诊断为 T21。125-135bp 大小 cfDNA 片段的丰度平均增加了 2.5 倍,母体背景干扰平均降低了 1.3 倍。在此基础上,即使胎儿分数低至 2%,也能显著提高胎儿非整倍体的检测效果;iNIPS 在回顾性样本中实现了 100%的敏感性和 99.90%的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9a5/6281613/477ad4fb87c0/41598_2018_35738_Fig1_HTML.jpg

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