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Cell-free fetal DNA testing and its correlation with prenatal indications.
Wang, Jing-Wei; Lyu, Yong-Nan; Qiao, Bin; Li, Yan; Zhang, Yan; Dhanyamraju, Pavan Kumar; Bamme, Yevgeniya; Yu, Michael D; Yang, Dongqin; Tong, Yong-Qing.
Afiliação
  • Wang JW; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China.
  • Lyu YN; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China.
  • Qiao B; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China.
  • Li Y; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China.
  • Zhang Y; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China.
  • Dhanyamraju PK; Pennsylvania State University College of Medicine and Hershey Medical center, Hershey, PA, 17033, USA.
  • Bamme Y; Pennsylvania State University College of Medicine and Hershey Medical center, Hershey, PA, 17033, USA.
  • Yu MD; Jefferson University Hospital, 1025 Walnut St, Philadelphia, PA19107, USA.
  • Yang D; Department of Digestive Diseases, Huashan Hospital, Fudan University, 12 Middle Wulumuqi Road, Shanghai, 200040, China. kobesakura@fudan.edu.cn.
  • Tong YQ; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, 99 Ziyang Road of Wuchang District, Wuhan, 430060, China. tytsing@whu.edu.cn.
BMC Pregnancy Childbirth ; 21(1): 585, 2021 Aug 24.
Article em En | MEDLINE | ID: mdl-34429082
ABSTRACT

BACKGROUND:

The prenatal test of cell-free fetal DNA (cffDNA) is also known as noninvasive prenatal testing (NIPT) with high sensitivity and specificity. This study is to evaluate the performance of NIPT and its clinical relevance with various clinical indications.

METHODS:

A retrospective analysis was conducted on 14,316 pregnant women with prenatal indications, including advanced maternal age (≥35 years), maternal serum screening abnormalities, the thickened nuchal translucency (≥2.5 mm) and other ultrasound abnormalities, twin pregnancy/IVF-ET pregnancy, etc. The whole-genome sequencing (WGS) of maternal plasma cffDNA was employed in this study.

RESULTS:

A total of 189 (1.32%) positive NIPT cases were identified, and 113/189 (59.79%)cases were confirmed by invasive prenatal testing. Abnormal serological screening (53.14%) was the most common indication, followed by elderly pregnancy (23.02%). The positive prediction value for T21, T18, T13, sex chromosome abnormalities, other autosomal aneuploidy abnormalities, and CNV abnormalities were 91.84, 68.75,37.50, 66.67, 14.29, and 6.45%, respectively. The positive rate and the true positive rate of nuchal translucency (NT) thickening were the highest (4.17 and 3.33%), followed by the voluntary requirement group (3.49 and 1.90%) in the various prenatal screening indications. The cffDNA concentration was linearly correlated with gestational age (≥10 weeks) and the positive NIPT group's Z-score values.

CONCLUSIONS:

whole-genome sequencing of cffDNA has extremely high sensitivity and specificity for T21, high sensitivity for T18, sex chromosome abnormalities, and T13. It also provides evidence for other abnormal chromosomal karyotypes (CNV and non-21/18/13 autosomal aneuploidy abnormalities). The cffDNA concentration is closely related to the gestational age and determines the specificity of NIPT. Our results highlight NIPT's clinical significance, which is an effective prenatal screening tool for high-quality care of pregnancy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Gravidez de Alto Risco / Transtornos Cromossômicos / Teste Pré-Natal não Invasivo Tipo de estudo: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy País/Região como assunto: Asia Idioma: En Revista: BMC Pregnancy Childbirth Assunto da revista: OBSTETRICIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Gravidez de Alto Risco / Transtornos Cromossômicos / Teste Pré-Natal não Invasivo Tipo de estudo: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy País/Região como assunto: Asia Idioma: En Revista: BMC Pregnancy Childbirth Assunto da revista: OBSTETRICIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China