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The detection efficacy of noninvasive prenatal genetic testing (NIPT) for sex chromosome abnormalities and copy number variation and its differentiation in pregnant women of different ages.无创产前基因检测(NIPT)对性染色体异常和拷贝数变异的检测效能及其在不同年龄孕妇中的鉴别
Heliyon. 2024 Jan 7;10(2):e24155. doi: 10.1016/j.heliyon.2024.e24155. eCollection 2024 Jan 30.
3
Clinical value of positive CNVs results by NIPT without fetal ultrasonography-identified structural anomalies.NIPT 阳性结果而胎儿超声检查未见结构异常的临床价值。
Mol Genet Genomic Med. 2024 Jan;12(1):e2352. doi: 10.1002/mgg3.2352.
4
Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication.扩展型无创性产前检测在检测染色体非整倍体和微缺失/微重复中的临床应用价值评估。
Eur J Med Res. 2023 Aug 30;28(1):304. doi: 10.1186/s40001-023-01285-2.
5
Non-Invasive prenatal testing with rolling circle amplification: Real-world clinical experience in a non-molecular laboratory.滚环扩增的无创性产前检测:非分子实验室的真实临床经验。
J Clin Lab Anal. 2023 Mar;37(6):e24870. doi: 10.1002/jcla.24870. Epub 2023 Mar 27.
6
Factors affecting low fetal fraction in fetal screening with cell-free DNA in pregnant women: a systematic review and meta-analysis.影响孕妇游离胎儿 DNA 筛查中低胎儿分数的因素:系统评价和荟萃分析。
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Validity and Utility of Non-Invasive Prenatal Testing for Copy Number Variations and Microdeletions: A Systematic Review.无创产前检测拷贝数变异和微缺失的有效性及实用性:一项系统综述
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Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin, Number 226.筛查胎儿染色体异常:ACOG 实践公告,第 226 号。
Obstet Gynecol. 2020 Oct;136(4):e48-e69. doi: 10.1097/AOG.0000000000004084.

6-9 孕周的早期非侵入性产前检测。

Early Non-Invasive Prenatal Testing at 6-9 Weeks of Gestation.

机构信息

Obstetrics and Gynecology, University Hospital of Ioannina, 455 00 Ioannina, Greece.

Department of Molecular Genetics, Genomedica S.A., 185 37 Piraeus, Greece.

出版信息

Genes (Basel). 2024 Jul 8;15(7):895. doi: 10.3390/genes15070895.

DOI:10.3390/genes15070895
PMID:39062674
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11275238/
Abstract

Non-invasive prenatal testing (NIPT) is usually performed beyond 10 weeks of gestation, because earlier in pregnancy, the fetal fraction is low, resulting in failure to obtain reliable results. This study aimed to evaluate the clinical performance of NIPT earlier in pregnancy using a method for cell-free DNA (cfDNA) analysis that eliminates the need for polymerase chain reaction (PCR), DNA sequencing, or microarrays (Vanadis system, PerkinElmer, Waltham, MA, USA). Cell-free DNA was extracted from the maternal plasma of 30 singleton pregnancies at 6-9 weeks of gestation (group 1) and at 11-14 weeks of gestation of the same patients (group 2). The mean crown-rump length (CRL) and gestational age in group A was 16.12 mm and that in group B was 61.45 mm. In group A, results were obtained in all, but one, cases (97%). From the remaining pregnancies, one miscarried at 8 weeks and, therefore, the follow-up NIPT at 12 weeks could not be performed. The fetal sex was diagnosed correctly in the 28 cases that had a successful early test, and the results were in accordance with the examination at 12 weeks. There were no cases of aneuploidies and disomy was diagnosed correctly in all. The "Vanadis" prenatal NIPT assay can successfully be used early during the first trimester at 6-9 weeks of gestation (early NIPT) to identify the fetal sex. Further studies are needed to explore the diagnostic potential for aneuploidies.

摘要

无创性产前检测(NIPT)通常在妊娠 10 周后进行,因为在妊娠早期,胎儿游离 DNA (cfDNA)含量较低,导致无法获得可靠的结果。本研究旨在评估一种无需聚合酶链反应(PCR)、DNA 测序或微阵列(Vanadis 系统,PerkinElmer,马萨诸塞州沃尔瑟姆)即可分析 cfDNA 的方法,在妊娠早期进行 NIPT 的临床性能。从 30 例单胎妊娠的孕妇血浆中提取 cfDNA,分别在妊娠 6-9 周(第 1 组)和同一患者的妊娠 11-14 周(第 2 组)进行检测。第 1 组的平均头臀长(CRL)和妊娠年龄分别为 16.12mm 和 61.45mm。在第 1 组中,所有但一例(97%)患者获得了结果。在剩余的妊娠中,一例在 8 周时流产,因此无法进行 12 周的随访 NIPT。在 28 例成功进行早期检测的病例中,正确诊断了胎儿性别,结果与 12 周的检查结果一致。未发现非整倍体病例,且所有病例的三体均正确诊断。“Vanadis”产前 NIPT 检测可以在妊娠 6-9 周的早孕期(早期 NIPT)成功应用,以识别胎儿性别。需要进一步研究以探索非整倍体的诊断潜力。