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
Vicotex

Download Mobile App




Non‐Invasive Prenatal Diagnosis of Spinal Muscular Atrophy Validated

By LabMedica International staff writers
Posted on 08 Oct 2019
The discovery of cell‐free DNA (cfDNA) in maternal plasma has enhanced the development of non‐invasive prenatal testing (NIPT). More...
Although NIPT for fetal aneuploidies has already been clinically applied, non‐invasive prenatal diagnosis for many single‐gene disorders remains on the developing stage.

Droplet digital PCR is a technology with high sensitivity, specificity, and accuracy to detect and analyze low-abundance nucleic acids. Its high resolution is guaranteed by millions of oil droplets generated per test. Utilizing digital PCR, the feasibility of non‐invasive prenatal diagnosis (NIPD) for fetal monogenic disorders has been proved in several studies analyzing cfDNA.

Medical Geneticists at the Central South University (Changsha, China) recruited pregnant women seeking Spinal Muscular Atrophy (SMA) prenatal diagnosis on 16 ~ 22 weeks of gestation for a study. All of the pregnancies had undergone non‐invasive prenatal screening for fetal aneuploidies by next‐generation sequencing (NGS).

The scientists extracted cell‐free DNA from maternal plasma using the QIAamp Circulating Nucleic Acid Kit and the concentrations of cfDNA samples were tested on Qubit. Amniotic fluid was obtained by amniocentesis, from which fetal genomic DNA was extracted by the phenol‐chloroform method. RainDrop droplet digital PCR was performed following standard protocols. SMN1/SMN2 copy numbers of all participants and fetuses were quantified by the multiplex ligation‐dependent probe amplification (MLPA) analysis using SALSA MLPA Kit.

The team reported that the concordance rate with the results of MLPA testing of amniocyte DNA was 94.12% in one test set and 90% in another set of participants. For all tests with a classifiable result, the percent of agreement with the results of MLPA testing of amniocyte DNA was up to 100% (25/25). The authors concluded that they had developed a direct, rapid, and low‐cost technique, which has a potential to be utilized for first‐trimester non‐invasive prenatal diagnosis and screening for spinal muscular atrophy with considerable reliability and feasibility. The study was published on September 25, 2019, in the Journal of Clinical Laboratory Analysis.

Related Links:
Central South University


Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Flocked Fiber Swabs
Puritan® Patented HydraFlock®
New
MR-proADM Test
B•R•A•H•M•S MR-proADM KRYPTOR test
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: Using a finger-prick blood sample, the new test can deliver accurate results at the point of care in 15 minutes. (Photo courtesy of Walter and Eliza Hall Institute of Medical Research)

Rapid Ferritin Test Enables Iron Deficiency Detection at the Point of Care

Iron deficiency is one of the world’s most common nutritional disorders and can be difficult to diagnose where access to laboratories and trained personnel is limited. Women and children in low-resource... Read more

Pathology

view channel
Image: Adrenal gland tumor stained with hematoxylin and eosin (top) and CYP11B2 (bottom) (Photo courtesy of Christofer Juhlin)

Simple Immunohistochemical Size Ratio Improves Classification of Primary Aldosteronism

Primary aldosteronism is a common but underdiagnosed cause of hypertension, in which excess aldosterone promotes salt retention and raises blood pressure. Identifying the dominant source of hormone overproduction... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.