To the Editor: We read with great interest the article by Yatsenko et al.,1 “Maternal Cell-Free DNA–Based Screening for Fetal Microdeletion and the Importance of Careful Diagnostic Follow-Up,” describing a single prenatal case identified by noninvasive prenatal screening as harboring a deletion at 22q11.2. Upon diagnostic postnatal testing, however, a smaller, noncritical deletion at 22q11.21 was identified. As stated by the authors, noninvasive prenatal screening (also referred to as noninvasive prenatal testing (NIPT)) has emerged as a powerful tool in screening for fetal aneuploidies. Major providers of this technology have expanded their test offerings to include screening for common microdeletion syndromes. Despite high sensitivity and specificity for common trisomies, the recent literature suggests a need for extreme caution in interpreting NIPT because of false-positive rates higher than previously reported when compared with invasive testing as well as concerns regarding the potential for overrepresentation of the positive predictive value for specific aneuploidies.1,2
We wanted to make an important and substantial addition to the observation by Yatsenko et al.3 based on our analysis of cases evaluated by NIPT over the past year and subsequently referred to our laboratory for diagnostic testing by chromosomal microarrays and/or karyotype analysis. From our analysis of 287 consecutive samples, NIPT results were available for 278 cases, and diagnostic testing results were available for 277 of these cases. Of the 88 cases with normal NIPT results, diagnostic testing was concordant (normal chromosomal microarrays and/or karyotype) in 79 cases; discordant in 4 (2 cases with gender discordance, 1 case with monosomy X, and 1 case with two large duplications at 1q42.13q44 and 22q11.1q12.3); and concordant but with a structural variation in 5 cases (1 case with inversion 7, 3 cases with a small deletion or duplication, 1 case with a deletion and a duplication). For 162 cases with NIPT suggestive of a whole-chromosome aneuploidy, diagnostic testing was concordant in 69.8% cases, with the highest true-positive rate for trisomy 21 (88.4%) and the lowest for monosomy X (28%). Results were discordant in 23.5% of cases, with the highest discordant rates for trisomy 13 and monosomy X (47 and 72%, respectively). In 11 cases (6.7%), diagnostic testing revealed results that were only partially concordant with NIPT.
The most significant and recent observation we wish to highlight in this letter is 25 cases for which NIPT results suggested a microdeletion or a segmental aneuploidy (Table 1). The false-positive rates were uniformly high for the common microdeletions tested for by some providers using expanded versions of NIPT. Notably, diagnostic testing revealed false-positive NIPT results in five of seven cases with 22q11.21 deletion, five of six cases with 5p deletion, three of four cases with 1p36 deletion, and one of one case with 4p deletion. Diagnostic testing results were concordant for a single case each where NIPT results identified a 15q deletion, a 9p duplication (confirmed to be an isodicentric (9p) duplication), and a 13 q deletion, respectively. In one case where NIPT was suggestive of both 18p and 18q terminal deletions, diagnostic testing revealed only a deletion of 14 Mb at 18p11.32p11.21. In a single case with NIPT suggestive of trisomy 18q, diagnostic testing showed a duplication of 18p11.21q23 that was further characterized as a translocation of the duplicated segment to the p-arm of one chromosome 13, resulting in trisomy for the 18p11.21q23 segment. In one case where NIPT results indicated a “partial deletion of 21q,” diagnostic testing revealed a 9.2-Mb duplication at 21q11.2-q21.1 that was inserted at 14p11.2. In a single case where NIPT results were inconclusive for chromosome 13, chromosomal microarrays showed a large region of allelic homozygosity for chromosome 13.
In conclusion, our results suggest an overall concordance rate between NIPT and invasive/diagnostic testing of ~69%, a discordance rate of 20%, and a partial concordance rate of 11%. The frequency of structural abnormalities that may not be defined or are poorly defined by NIPT is substantial. In addition, the ambiguous and nonspecific nature of NIPT results introduces a significant degree of confusion for clinicians and patients alike. The cases listed in this report and those from recent publications warrant additional large studies to determine the sensitivity and specificity of current NIPT technologies to detect microdeletions, with an explicit definition of breakpoints. Until now, identification of clinically relevant unbalanced genomic alterations, specifically microdeletions and microduplications, has been driven primarily by diagnostic testing and has been precluded from any screening tests. With the multiple layers of complexity associated with pathogenic copy-number alterations, such as variability in size, gene content, variable penetrance and expressivity, and genetic and phenotypic heterogeneity, it would be extremely prudent to take a much more cautious approach to expanding NIPT/noninvasive prenatal screening for microdeletions. It is our belief that, unlike whole-chromosome aneuploidies, biological causes such as confined placental mosaicism may not play as large a role in contributing to the high false-positive rates for microdeletions/microduplications. As has been recommended, extensive pretest genetic counseling with a complete discussion of the benefits and limitations of NIPT versus diagnostic testing must occur, specifically for low-risk patients with abnormal NIPT and high-risk patients with normal NIPT.
The authors are employees of CombiMatrix Diagnostics and T.S., K.H., and N.D. own stock in the company.
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Genetics in Medicine (2016)