Antenatal screening for fetal trisomies using microarray-based cell-free DNA testing: A systematic review and meta-analysis

Prenat Diagn. 2020 Mar;40(4):454-462. doi: 10.1002/pd.5621. Epub 2019 Dec 21.

Abstract

Objective: To evaluate the test accuracy of non-invasive prenatal testing (NIPT) for fetal trisomy 21, 18, and 13 using cell-free (cf) DNA analysis in maternal plasma with microarray quantitation.

Method: Systematic review and meta-analysis. Searches in MEDLINE, Pre-MEDLINE, EMBASE, Web of Science, and the Cochrane Library to 09.07.2018.

Results: Five studies analyzing 3074 samples, including 187 trisomy 21, 43 trisomy 18, and 19 trisomy 13 cases, were identified. Risk of bias was high in all studies, introduced particularly by exclusions from analysis and by the role of the sponsor. Sensitivity of microarray-based cfDNA testing was 99.5% (95%CI 96.3%-99.9%) for trisomy 21, 97.7% (95%CI 87.9%-99.6%) for trisomy 18, and 100% (95%CI 83.2%-100%) for trisomy 13. Specificity was 100% (95% CI 99.87%-100%) for trisomy 21, 99.97% (95%CI 99.81%-99.99%) for trisomy 18, and 99.97% (95%CI 99.81%-99.99%) for trisomy 13. Pooled test failure rate was 1.1%. A direct comparison of microarray- and sequencing-based cfDNA found equivalent test accuracy.

Conclusion: Included studies suggest that NIPT using microarray-based cfDNA testing has high sensitivity and specificity for detecting fetal trisomy 21, 18, and 13. However, the evidence base is small and at high risk of bias.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Cell-Free Nucleic Acids / analysis*
  • Down Syndrome / diagnosis*
  • Female
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Microarray Analysis
  • Noninvasive Prenatal Testing / methods*
  • Pregnancy
  • Sensitivity and Specificity
  • Sequence Analysis, DNA
  • Trisomy 13 Syndrome / diagnosis*
  • Trisomy 18 Syndrome / diagnosis*

Substances

  • Cell-Free Nucleic Acids