We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Study Validates Use of Noninvasive Test for Defective Fetal Chromosomes

By LabMedica International staff writers
Posted on 13 Dec 2015
A German biomedical company has reported the successful validation of its qPCR (quantitative real-time PCR)-based noninvasive test for fetal genetic abnormalities such as trisomy 21 (Down's syndrome).

LifeCodexx AG (Konstanz, Germany) recently announced that its qPCR-based PrenaTest had been successfully validated in a study of nearly 700 samples of maternal blood.

Starting from the ninth week of pregnancy, the PrenaTest is able to determine trisomy 21, trisomies 21, 18, and 13, as well as gonosomal aneuploidies (Turner, triple X, Klinefelter, and XYY syndromes), in blood samples from expectant mothers at risk for fetal aneuploidies. More...
If desired, the gender of the child may also be determined. This assay acts as a supplement to the noninvasive prenatal diagnostic techniques already in use, but—in comparison with invasive examination methods—it does not involve the risk of procedure-related miscarriage.

The test method of the PrenaTest is based on the analysis of cell-free DNA (cfDNA) in the pregnant woman’s blood. The cfDNA is present in fragments and freely circulates in the maternal blood. In addition to maternal cfDNA, the blood also contains approximately 2%–40% (on average approximately 10%) cell-free fetal DNA (cffDNA). The cffDNA essentially comes from the cytotrophoblast, that is, from placental cells of the growing embryo and is thus of extra-embryonic origin. It develops through apoptosis and necrosis of the trophoblast cells and is continually excreted into the pregnant woman’s bloodstream. The lifespan of the DNA fragments is about two hours. Within a few hours after birth of the child, the cffDNA is no longer detectable in the mother’s blood. With the PrenaTest, the cffDNA in the maternal blood is used to determine whether there is a chromosomal imbalance for a particular chromosome to thus determine a corresponding chromosomal disorder in the unborn child. Prenatal tests based on this method are known as noninvasive prenatal testing (NIPT).

The data generated by the clinical validation study was presented on the occasion of the FMF (Fetal Medicine Foundation) Advances Course held December 5-6, 2015, in London (United Kingdom).

“For the first time leading medical associations in Europe recently recommended that NIPT can now be used as primary screening for fetal trisomy 21 in all pregnant women of any age or risk,” said Dr. Wera Hofmann, CSO of LifeCodexx AG. “Due to its rapid turnaround time and low cost, our qPCR-based PrenaTest will be the ideal noninvasive prenatal test which will allow doctors to implement the new recommendations into their clinical routine.”

Related Links:

LifeCodexx AG



Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Neonatal Heel Incision Device
Tenderfoot
New
Fully Automated Urinalysis System
DxU 1800 Fully Automated Urinalysis System
Platinum Member
Integrated Biochemical & Immunological System
Biolumi CX Solution X10+C10
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image Credit: iStock

Prehospital Blood Test Could Reduce Emergency Transfers for Chest Pain

Chest pain leads to ambulance transport to an emergency department for about 95% of patients, although only a minority have a serious cardiac condition. Troponin testing helps assess heart muscle damage,... Read more

Immunology

view channel
Image: Aptiva utilizes particle-based multi-analyte technology (PMAT) (Photo courtesy of Werfen)

Werfen Expands Automated APS Testing with FDA-Cleared and CE-Marked IgA Reagent

Antiphospholipid syndrome (APS) is an autoimmune disorder associated with thrombosis and pregnancy complications, but its symptoms can overlap with those of other conditions, complicating diagnosis.... Read more

Microbiology

view channel
Image: RealTime Labs’ Mycotoxin Extensive Panel measures 31 mold-related toxins across seven toxin classes from a single urine sample (Photo courtesy of RealTime Labs)

New Urine Test Expands Mycotoxin Analysis to 31 Markers for Broader Exposure Assessment

Clinical evaluation of mold exposure increasingly relies on urinary mycotoxin testing, but limited marker coverage and metabolite masking can make results more difficult to interpret. Broader analysis... Read more

Technology

view channel
Image: ADLM recommends that emerging AI tools follow the same professional oversight, quality, validation, and monitoring standards as traditional clinical testing within CLIA’s existing framework (Image Credit: Adobe Stock)

ADLM Calls for CLIA Updates to Support Safe AI Use in Laboratory Medicine

Clinical laboratories increasingly use artificial intelligence to verify, interpret, and report results, but safeguards under the Clinical Laboratory Improvement Amendments (CLIA) were designed in 1992.... Read more

Industry

view channel
Image

Collaboration Combines AI Cognitive Assessment and RNA Blood Testing for Earlier Alzheimer’s Detection

Alzheimer’s disease is often identified only after substantial neurodegeneration, partly because current diagnostic pathways are fragmented and difficult to scale. As treatment shifts toward earlier intervention,... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.