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
LGC Clinical Diagnostics

Download Mobile App




Blood Test Identifies Pregnant Women at Higher Risk of Preeclampsia

By LabMedica International staff writers
Posted on 30 Aug 2023

Preeclampsia, a serious pregnancy complication affecting 1 in 40 pregnant women, is characterized by elevated blood pressure. More...

Left untreated, it can lead to organ damage and, in rare instances, maternal or fetal death. As the exact cause remains uncertain, identifying high-risk patients is complex. Now, researchers have discovered that DNA analysis can identify women at higher risk of developing severe preeclampsia during later pregnancy stages. Detecting high-risk patients early will allow for administering preventive medication, significantly reducing the risk of severe preeclampsia.

Around 1 in 8 cases involve early-onset preeclampsia, manifesting between 20 and 34 weeks of pregnancy. Preterm births, often induced due to preeclampsia, require neonatal intensive care and can lead to serious complications. Promptly identifying women with an elevated risk of early preeclampsia is essential for initiating appropriate and preventive treatment, reducing both preeclampsia and potential premature birth risks. Current screening methods are often complex, time-consuming, and unreliable. In order to understand the pivotal role of the placenta, researchers from KU Leuven (Leuven, Belgium) compared placental DNA in 498 women with and without early preeclampsia.

Normal pregnancy brings changes in placental DNA structure through DNA methylation. However, the researchers found that women developing early preeclampsia exhibited a distinct DNA methylation pattern. While the cause of this difference remains unknown, it can allow physicians to identify high-risk women and initiate treatment before symptoms emerge. The new test offers a significant advantage: it can be conducted using DNA from a simple blood sample taken around the 12th week of pregnancy. Given that blood samples are routinely taken for non-invasive prenatal testing (NIPT) to identify fetal chromosomal abnormalities, additional placental samples or cells are not necessary.

"In time, our analysis can be carried out simultaneously with the NIPT test,” said Professor Bernard Thienpont who led the research. “But first, we will focus on implementing our new method on a larger scale, optimizing and validating it. We also want to investigate whether certain women would benefit more from preventive screening, for example, in the case of a first pregnancy."

Related Links:
KU Leuven 


Platinum Member
COVID-19 Rapid Test
OSOM COVID-19 Antigen Rapid Test
Verification Panels for Assay Development & QC
Seroconversion Panels
Anti-Cyclic Citrullinated Peptide Test
GPP-100 Anti-CCP Kit
Gold Member
Nasopharyngeal Applicator
CalgiSwab 5.5" Sterile Mini-tip Calcium Alginate Nasopharyngeal Swab w/Aluminum HDLE
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: QIP-MS could predict and detect myeloma relapse earlier compared to currently used techniques (Photo courtesy of Adobe Stock)

Mass Spectrometry-Based Monitoring Technique to Predict and Identify Early Myeloma Relapse

Myeloma, a type of cancer that affects the bone marrow, is currently incurable, though many patients can live for over 10 years after diagnosis. However, around 1 in 5 individuals with myeloma have a high-risk... Read more

Immunology

view channel
Image: The cancer stem cell test can accurately choose more effective treatments (Photo courtesy of University of Cincinnati)

Stem Cell Test Predicts Treatment Outcome for Patients with Platinum-Resistant Ovarian Cancer

Epithelial ovarian cancer frequently responds to chemotherapy initially, but eventually, the tumor develops resistance to the therapy, leading to regrowth. This resistance is partially due to the activation... Read more

Technology

view channel
Image: Ziyang Wang and Shengxi Huang have developed a tool that enables precise insights into viral proteins and brain disease markers (Photo courtesy of Jeff Fitlow/Rice University)

Light Signature Algorithm to Enable Faster and More Precise Medical Diagnoses

Every material or molecule interacts with light in a unique way, creating a distinct pattern, much like a fingerprint. Optical spectroscopy, which involves shining a laser on a material and observing how... Read more

Industry

view channel
Image: The collaboration aims to leverage Oxford Nanopore\'s sequencing platform and Cepheid\'s GeneXpert system to advance the field of sequencing for infectious diseases (Photo courtesy of Cepheid)

Cepheid and Oxford Nanopore Technologies Partner on Advancing Automated Sequencing-Based Solutions

Cepheid (Sunnyvale, CA, USA), a leading molecular diagnostics company, and Oxford Nanopore Technologies (Oxford, UK), the company behind a new generation of sequencing-based molecular analysis technologies,... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.