Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study

被引:8
作者
Kim, Hyunjin [1 ]
Park, Ji Eun [1 ]
Kang, Kyung Min [1 ]
Jang, Hee Yeon [1 ]
Go, Minyeon [1 ,4 ]
Yang, So Hyun [1 ]
Kim, Jong Chul [1 ]
Lim, Seo Young [4 ]
Cha, Dong Hyun [1 ,2 ]
Choi, Jungah [3 ]
Shim, Sung Han [1 ,4 ]
机构
[1] CHA Biotech Inc, Ctr Genome Diagnost, Seoul 06125, South Korea
[2] CHA Univ, CHA Gangnam Med Ctr, Dept Obstet & Gynecol, Seoul 06135, South Korea
[3] CHA Univ, Coll Liberal Art, Pochon, Gyeonggi, South Korea
[4] CHA Univ, Coll Life Sci, Dept Biomed Sci, Seongnam 13488, South Korea
关键词
Noninvasive prenatal testing; Sex chromosome aneuploidies; Positive predictive value; Prenatal diagnosis; Genetic counseling; FREE FETAL DNA; CELL-FREE DNA; MATERNAL PLASMA; ASSOCIATION; MOSAICISM; BLOOD; AGE;
D O I
10.1186/s12884-024-06275-8
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundTo evaluate the clinical significance of noninvasive prenatal testing (NIPT) for detecting fetal sex chromosome aneuploidies (SCAs) in Korean pregnant women.MethodsWe retrospectively analyzed NIPT data from 9,176 women with singleton pregnancies referred to the CHA Biotech genome diagnostics center. Cell-free fetal DNA (cffDNA) was extracted from maternal peripheral blood, and high-throughput massively parallel sequencing was conducted. Subsequently, the positive NIPT results for SCA were validated via karyotype and chromosomal microarray analyses.ResultsOverall, 46 cases were SCA positive after NIPT, including 20, 12, 8, and 6 for Turner, triple X, Klinefelter, and Jacob syndromes, respectively. Among 37 women with invasive prenatal diagnosis, 19 had true positive NIPT results. The overall positive predictive value (PPV) of NIPT for detecting SCAs was 51.35%. The PPV was 18.75% for Turner, 88.89% for triple X, 71.43% for Klinefelter, and 60.00% for Jacob's syndromes. NIPT accuracy for detecting sex chromosome trisomies was higher than that for sex chromosome monosomy (P = 0.002). No significant correlation was observed between fetal SCA incidence and maternal age (P = 0.914), except for the borderline significance of Jacob's syndrome (P = 0.048). No significant differences were observed when comparing NIPT and karyotyping validation for fetal SCA according to pregnancy characteristics.ConclusionOur data suggest that NIPT can reliably screen for SCAs, and it performed better in predicting sex chromosome trisomies compared with monosomy X. No correlation was observed between maternal age and fetal SCA incidence, and no association was observed between different pregnancy characteristics. The accuracy of these findings requires improvements; however, our study provides an important reference for clinical genetic counseling and further management. Larger scale studies, considering confounding factors, are required for accurate evaluation.
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页数:9
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