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Establishing and validating noninvasive prenatal testing procedure for fetal aneuploidies in Vietnam

Phan M.-D. Gene Solutions, Ho Chi Minh City, Viet Nam|
Nguyen H.-N. | Giang H. | Truong K.D. | Hoang T.T.D. Medical Genetics Institute, Ho Chi Minh City, Viet Nam| Do T.T.T. Hai Phong University of Medicine and Pharmacy, Hai Phong City, Viet Nam| Nguyen T.T.Q. Gia Dinh Hospital, Ho Chi Minh City, Viet Nam| Nguyen N.H. Graduate Program of Genetics, University of Science, Ho Chi Minh City, Viet Nam| Nguyen T.M. Center for Molecular Medicine, University of Medicine and Pharmacy, Ho Chi Minh City, Viet Nam| Vo B.T. Tu Du Hospital, Ho Chi Minh City, Viet Nam| Trinh H.N.T. Hung Vuong Hospital, Ho Chi Minh City, Viet Nam| Nguyen T.V. School of Chemistry and Molecular Biosciences, the University of Queensland, Brisbane, Australia|

Journal of Maternal-Fetal and Neonatal Medicine Số 23, năm 2019 (Tập 32, trang 4009-4015)

DOI: 10.1080/14767058.2018.1481032

Tài liệu thuộc danh mục: ISI, Scopus

J. Matern.-Fetal Neonatal Med.

English

Từ khóa: adult; algorithm; amnion fluid analysis; aneuploidy; Article; calculation; chromosome 13; chromosome 18; chromosome 21; diagnostic accuracy; diagnostic test; female; high risk pregnancy; human; mathematical analysis; noninvasive prenatal testing; population research; prenatal diagnosis; priority journal; sensitivity and specificity; trisomy; trisomy 13; trisomy 21; validity; Viet Nam; aneuploidy; blood; case control study; DNA sequence; genetics; high throughput sequencing; middle aged; pregnancy; procedures; trisomy; young adult; cell free nucleic acid; Adult; Algorithms; Aneuploidy; Case-Control Studies; Cell-Free Nucleic Acids; Chromosomes, Human, Pair 13; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 21; Female; High-Throughput Nucleotide Sequencing; Humans; Middle Aged; Noninvasive Prenatal Testing; Pregnancy; Sequence Analysis, DNA; Trisomy; Vietnam; Young Adult
Tóm tắt tiếng anh
Objective: Noninvasive prenatal testing (NIPT) for fetal aneuploidies has been widely adopted in developed countries. Despite the sharp decrease in the cost of massively parallel sequencing, the technical know-how and skilled personnel are still one of the major limiting factors for applying this technology to NIPT in low-income settings. Here, we present the establishment and validation of our NIPT procedure called triSure for detection of fetal aneuploidies. Methods: We established the triSure algorithm based on the difference in proportion of fetal and maternal fragments from the target chromosome to all chromosomes. Our algorithm was validated using a published data set and an in-house data set obtained from high-risk pregnant women in Vietnam who have undergone amniotic testing. Several other aneuploidy calling methods were also applied to the same data set to benchmark triSure performance. Results: The triSure algorithm showed similar accuracy to size-based method when comparing them using published data set. Using our in-house data set from 130 consecutive samples, we showed that triSure correctly identified the most samples (overall sensitivity and specificity of 0.983 and 0.986, respectively) compared to other methods tested including count-based, sized-based, RAPIDR and NIPTeR. Conclusions: We have demonstrated that our triSure NIPT procedure can be applied to pregnant women in low-income settings such as Vietnam, providing low-risk screening option to reduce the need for invasive diagnostic tests. � 2018, � 2018 Informa UK Limited, trading as Taylor & Francis Group.

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