Information contained on this page is provided by an independent third-party content provider. WorldNow and this Station make no warranties or representations in connection therewith. If you have any questions or comments about this page please contact email@example.com.
SOURCE Ariosa Diagnostics, Inc.
Largest published clinical dataset in twins of any company offering NIPT
SAN JOSE, Calif., Dec. 19, 2013 /PRNewswire/ -- Ariosa Diagnostics, Inc., maker of the Harmony™ Prenatal Test, announced today the publication of two clinical studies involving twin pregnancies in Fetal Diagnosis and Therapy. The two studies provide information on how to consider use of non-invasive prenatal testing (NIPT) with cell-free DNA (cfDNA) in identical (monozygotic) and fraternal (dizygotic) twin pregnancies. Previous studies in singleton pregnancies demonstrated the accuracy of the Harmony test in assessing the risk of fetal trisomy 21, which causes Down syndrome, and other chromosome conditions.
Entitled "Fetal Fraction Estimate in Twin Pregnancies Using Directed Cell-Free DNA Analysis," the first study highlights the importance of estimating the percentage of fetal fraction (FF) in analyzing twin pregnancies with NIPT. Using NIPT in twin pregnancies is more complex than in singleton pregnancies because the two fetuses can be either monozygotic, meaning both fetuses are genetically identical, or dizygotic, in which case only one fetus is likely to have a trisomy when present. The study concluded that with the Harmony test algorithm, use of the fetal fraction in the analysis of FF for one of the twins will allow for more accurate testing. The full text of this study is available at http://www.karger.com/Article/Pdf/355653.
The second study, entitled "Cell-free DNA Analysis for Trisomy Risk Assessment in First-Trimester Twin Pregnancies," was conducted by Professor Kypros Nicolaides from the Harris Birthright Research Centre of Fetal Medicine in London. Among 192 total twin pregnancies as part of a blinded study, the Harmony test correctly classified 9 of 10 pregnancies with fetal trisomy 21, 1 of 1 pregnancies with fetal trisomy 13, and no false positives. Actual clinical implementation of Harmony in twin pregnancies identified 2 trisomy 21 and 1 trisomy 18 affected pregnancies, as well. An abstract of the study is available at http://www.karger.com/Article/FullText/356495.
"We continue our commitment to the publication of peer-reviewed clinical studies demonstrating the value of the Harmony test for trisomy risk assessment. Our innovative technology offers an accurate and safe screening option to physicians caring for patients with twins," says Thomas Musci, MD, Chief Medical Officer of Ariosa Diagnostics.
The Harmony test is a blood test for pregnant women that can be used as early as 10 weeks in pregnancy. By evaluating cfDNA from the fetus found in maternal circulation, the test can assess the risk of Down syndrome with greater than 99% accuracy and provide fetal sex information. Compared to current prenatal screening tests that have up to a 20% error rate, the Harmony test with its much higher accuracy, represents a significant advance in prenatal testing.
About Ariosa Diagnostics
Ariosa Diagnostics, Inc. is a molecular diagnostics company committed to innovating together to improve patient care. The flagship product, the HarmonyTM Prenatal Test, is a safe, highly accurate and affordable prenatal test for maternal and fetal health. Led by an experienced team, Ariosa is using its proprietary technology to perform a directed analysis of cell-free DNA in blood. The HarmonyTM Prenatal Test equips pregnant women and their healthcare providers with reliable information to make decisions regarding their health, without creating unnecessary stress or anxiety.
The company began operations in 2010 and is headquartered in San Jose, Calif. For more information, visit www.ariosadx.com. Follow us on Twitter @HarmonyPrenatal and on Facebook at Harmony Prenatal for Healthy Pregnancy.
©2012 PR Newswire. All Rights Reserved.