Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing
Authors
Bianchi, Diana W.Platt, Lawrence D.
Goldberg, James D.
Abuhamad, Alfred Z.
Sehnert, Amy J.
Rava, Richard P.
MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group
Moore Simas, Tiffany A.
UMass Chan Affiliations
Department of Obstetrics and GynecologyDocument Type
Journal ArticlePublication Date
2012-05-01Keywords
AdolescentAdult
*Aneuploidy
Case-Control Studies
Chromosome Disorders
Female
*High-Throughput Nucleotide Sequencing
Humans
Karyotyping
Male
Middle Aged
Pregnancy
Prenatal Diagnosis
Prospective Studies
Sensitivity and Specificity
*Sequence Analysis, DNA
Single-Blind Method
Young Adult
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetics and Genomics
Medical Genetics
Obstetrics and Gynecology
Metadata
Show full item recordAbstract
OBJECTIVE: To prospectively determine the diagnostic accuracy of massively parallel sequencing to detect whole chromosome fetal aneuploidy from maternal plasma. METHODS: Blood samples were collected in a prospective, blinded study from 2,882 women undergoing prenatal diagnostic procedures at 60 U.S. sites. An independent biostatistician selected all singleton pregnancies with any abnormal karyotype and a balanced number of randomly selected pregnancies with euploid karyotypes. Chromosome classifications were made for each sample by massively parallel sequencing and compared with fetal karyotype. RESULTS: Within an analysis cohort of 532 samples, the following were classified correctly: 89 of 89 trisomy 21 cases (sensitivity 100%, 95% [confidence interval] CI 95.9-100), 35 of 36 trisomy 18 cases (sensitivity 97.2%, 95% CI 85.5-99.9), 11 of 14 trisomy 13 cases (sensitivity 78.6%, 95% CI 49.2-95.3), [corrected] 232 of 233 females (sensitivity 99.6%, 95% CI 97.6 to more than 99.9), 184 of 184 males (sensitivity 100%, 95% CI 98.0-100), and 15 of 16 monosomy X cases (sensitivity 93.8%, 95% CI 69.8-99.8). There were no false-positive results for autosomal aneuploidies (100% specificity, 95% CI more than 98.5 to 100). In addition, fetuses with mosaicism for trisomy 21 (3/3), trisomy 18 (1/1), and monosomy X (2/7), three cases of translocation trisomy, two cases of other autosomal trisomies (20 and 16), and other sex chromosome aneuploidies (XXX, XXY, and XYY) were classified correctly. CONCLUSION: This prospective study demonstrates the efficacy of massively parallel sequencing of maternal plasma DNA to detect fetal aneuploidy for multiple chromosomes across the genome. The high sensitivity and specificity for the detection of trisomies 21, 18, 13, and monosomy X suggest that massively parallel sequencing can be incorporated into existing aneuploidy screening algorithms to reduce unnecessary invasive procedures. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT01122524. LEVEL OF EVIDENCE: II.Source
Obstet Gynecol. 2012 May;119(5):890-901. doi: 10.1097/AOG.0b013e31824fb482. Link to article on publisher's site
DOI
10.1097/AOG.0b013e31824fb482Permanent Link to this Item
http://hdl.handle.net/20.500.14038/42852PubMed ID
22362253Notes
Tiffany A. Moore Simas is a collaborator in the MELISSA Study Group.
Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1097/AOG.0b013e31824fb482