Application of Digital Polymerase Chain Reaction (dPCR) in Non-Invasive Prenatal Testing (NIPT)

被引:0
|
作者
Guo, Ying [1 ,2 ]
Charoenkwan, Pimlak [3 ,4 ]
Traisrisilp, Kuntharee [1 ]
Piyamongkol, Wirawit [1 ]
Tongprasert, Fuanglada [1 ]
机构
[1] Chiang Mai Univ, Fac Med, Dept Obstet & Gynaecol, Chiang Mai 50200, Thailand
[2] Dali Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Dali 671000, Peoples R China
[3] Chiang Mai Univ, Fac Med, Dept Pediat, Chiang Mai 50200, Thailand
[4] Chiang Mai Univ, Fac Med, Thalassemia & Hematol Ctr, Chiang Mai 50200, Thailand
关键词
digital PCR (dPCR); non-invasive prenatal testing (NIPT); chromosomal aneuploidy; chromosomal microdeletions and microduplications; monogenic disease; CELL-FREE DNA; MOLECULAR-WEIGHT HEPARIN; FREE FETAL DNA; MATERNAL PLASMA; FETOPLACENTAL MOSAICISM; PCR SYSTEM; DIAGNOSIS; DUPLICATION; HEMOPHILIA; ANEUPLOIDY;
D O I
10.3390/biom15030360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This article reviews the current applications of the digital polymerase chain reaction (dPCR) in non-invasive prenatal testing (NIPT) and explores its potential to complement or surpass the capabilities of Next-Generation Sequencing (NGS) in prenatal testing. The growing incidence of genetic disorders in maternal-fetal medicine has intensified the demand for precise and accessible NIPT options, which aim to minimize the need for invasive prenatal diagnostic procedures. Cell-free fetal DNA (cffDNA), the core analyte in NIPT, is influenced by numerous factors such as maternal DNA contamination, placental health, and fragment degradation. dPCR, with its inherent precision and ability to detect low-abundance targets, demonstrates robustness against these interferences. Although NGS remains the gold standard due to its comprehensive diagnostic capabilities, its high costs limit widespread use, particularly in resource-limited settings. In contrast, dPCR provides comparable accuracy with lower complexity and expense, making it a promising alternative for prenatal testing.
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页数:33
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