Development and application of a digital PCR-based assay for rapid diagnosis of common fetal chromosomal aneuploidies.
10.3760/cma.j.cn511374-20250402-00196
- Author:
Xuejiao CHEN
1
;
Yanfeng YANG
;
Yuanyuan YING
;
Feiyan PAN
;
Zhiqiang GU
;
Weimeng JIAO
;
Zehang HE
;
Huihui XU
Author Information
1. Central Laboratory of Taizhou Hospital Affiliated to Wenzhou Medical University, Linhai, Zhejiang 317000, China. xuhh@enzemed.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Female;
Pregnancy;
Aneuploidy;
Prenatal Diagnosis/methods*;
Karyotyping;
Retrospective Studies;
Polymerase Chain Reaction/methods*;
Chromosome Disorders/genetics*;
Adult;
Trisomy 13 Syndrome/diagnosis*;
Trisomy 18 Syndrome/genetics*;
Down Syndrome/genetics*
- From:
Chinese Journal of Medical Genetics
2025;42(5):592-596
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To assess the clinical value of digital PCR (dPCR) for the prenatal diagnosis of common fetal aneuploidies.
METHODS:A dPCR-based assay was developed for detecting trisomies 21, 18, and 13. A retrospective analysis was carried out on 173 amniotic fluid samples collected by the Prenatal Diagnosis Center of Taizhou Hospital between January 2017 and December 2023. By using chromosomal karyotyping as the gold standard, the diagnostic performance of the multiplex dPCR system was evaluated in a double-blind manner. This study has been approved by the Ethics Committee of Taizhou Hospital (Ethics No. K20250339).
RESULTS:Chromosomal karyotyping has identified 59 cases of trisomy 21, 5 cases of trisomy 18, 2 cases of trisomy 13, 6 cases with chromosomal structural abnormalities or mosaicisms, and 101 cases with a normal karyotype. The dPCR results (Z-score cutoff = 4.0, CI = 99.997%) showed full concordance with karyotyping (sensitivity = 100%, specificity = 100%, Kappa = 1). Among the 6 structurally abnormal or mosaicism samples, dPCR has accurately detected 4 cases, but mis-classified 2 cases of trisomy 21 with very low-level mosaicisms (3.3%, 6.9%, respectively) as normal.
CONCLUSION:The established multiplex dPCR system demonstrated high diagnostic accuracy for common chromosomal aneuploidies, with results available within 24 hours. It can serve as an efficient supplementary tool to conventional chromosomal karyotyping, providing reliable support for time-sensitive clinical decision-making in prenatal diagnosis.
