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Meta-Analysis
. 2016 Jan 18;6(1):e010002.
doi: 10.1136/bmjopen-2015-010002.

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis

Sian Taylor-Phillips et al. BMJ Open. .

Abstract

Objective: To measure test accuracy of non-invasive prenatal testing (NIPT) for Down, Edwards and Patau syndromes using cell-free fetal DNA and identify factors affecting accuracy.

Design: Systematic review and meta-analysis of published studies.

Data sources: PubMed, Ovid Medline, Ovid Embase and the Cochrane Library published from 1997 to 9 February 2015, followed by weekly autoalerts until 1 April 2015.

Eligibility criteria for selecting studies: English language journal articles describing case-control studies with ≥ 15 trisomy cases or cohort studies with ≥ 50 pregnant women who had been given NIPT and a reference standard.

Results: 41, 37 and 30 studies of 2012 publications retrieved were included in the review for Down, Edwards and Patau syndromes. Quality appraisal identified high risk of bias in included studies, funnel plots showed evidence of publication bias. Pooled sensitivity was 99.3% (95% CI 98.9% to 99.6%) for Down, 97.4% (95.8% to 98.4%) for Edwards, and 97.4% (86.1% to 99.6%) for Patau syndrome. The pooled specificity was 99.9% (99.9% to 100%) for all three trisomies. In 100,000 pregnancies in the general obstetric population we would expect 417, 89 and 40 cases of Downs, Edwards and Patau syndromes to be detected by NIPT, with 94, 154 and 42 false positive results. Sensitivity was lower in twin than singleton pregnancies, reduced by 9% for Down, 28% for Edwards and 22% for Patau syndrome. Pooled sensitivity was also lower in the first trimester of pregnancy, in studies in the general obstetric population, and in cohort studies with consecutive enrolment.

Conclusions: NIPT using cell-free fetal DNA has very high sensitivity and specificity for Down syndrome, with slightly lower sensitivity for Edwards and Patau syndrome. However, it is not 100% accurate and should not be used as a final diagnosis for positive cases.

Trial registration number: CRD42014014947.

Keywords: REPRODUCTIVE MEDICINE.

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Figures

Figure 1
Figure 1
Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow chart of included articles.
Figure 2
Figure 2
Proportion of studies with low, high or unclear risk of bias using QUADAS 2.
Figure 3
Figure 3
Proportion of studies with low, high and unclear concerns regarding applicability using QUADAS 2.
Figure 4
Figure 4
Deeks’ funnel plot for Down (left) Edwards (centre) and Patau (right) syndromes. A vertical pattern would indicate no bias, slope is associated with publication bias.
Figure 5
Figure 5
Individual and pooled sensitivity and specificity for non-invasive prenatal testing (NIPT) for the detection of a. Down syndrome b. Edwards syndrome and c. Patau syndrome.

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