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




Epigenetic Biomarker Signature Predicts the Likelihood of Premature Birth

By LabMedica International staff writers
Posted on 07 Mar 2022

Researchers have identified an epigenetic biomarker signature for preterm birth that can be used in a clinical setting to predict the likelihood that a pregnant woman might deliver prematurely. More...

Preterm birth (earlier than 37 weeks) is the major cause of newborn and infant mortality affecting nearly one in every ten live births. Many premature infants face a number of health issues, including cognitive disabilities and cardiovascular problems. Preterm birth has been linked to risk factors such as a twin or multiple pregnancy and preclampsia. Yet, many early births are unexpected, and having a diagnostic test in the first-term of pregnancy could allow caregivers to take steps to delay or prevent a preterm birth.

A study carried out by investigators at Washington State University Pullman, USA) was designed to develop an epigenetic biomarker for susceptibility of preterm birth using buccal cells from the mother, father, and child (triads). An epigenome-wide association study (EWAS) was used to identify differential DNA methylation regions (DMRs) using a comparison of control term birth versus preterm birth triads.

Cheek swabs were obtained from two groups of mother-father-infant triads shortly after the babies were born. In one set of 19 triads, the infants were born prematurely and in another group of 21 triads, the babies were carried to full term. DNA was isolated from the buccal cell collections and analyzed with a methylated DNA immunoprecipitation (MeDIP) procedure to obtain methylated DNA for subsequent sequencing (Seq) for an MeDIP-Seq protocol. This procedure provides a genome-wide assessment of greater than 90% of the genome, compared to approximately 50–70% for bisulfite sequencing, or less than 1% for array analysis.

Epigenetic DMR associations with preterm birth were identified for both the mother and father that were distinct and suggested potential epigenetic contributions from both parents. The mother (165 DMRs) and female child (136 DMRs) had the highest number of DMRs and were highly similar, suggesting potential epigenetic inheritance of the epimutations. The male child had negligible DMR associations. Clearly the female infants’ epigenetic biomarker signature was not used to predict potential preterm birth, but could potentially be used to assess later life disease susceptibility in the individual.

"The signature we found was present in all the parents we analyzed," said senior author Dr. Michael Skinner, professor of biological sciences at Washington State University. "This is likely to lead eventually to a very useful test. We used buccal cells, which are collected by a cheek swab. It is very non-invasive and easy to do. Although we may not be able to fix the problem, if we know that it is going to develop because of these diagnostics, we can treat it. This could help with the transition from reactionary medicine to preventive medicine."

The study was published in the March 1, 2022, online edition of the journal Scientific Reports.

Related Links:
Washington State University 


Platinum Member
ADAMTS-13 Protease Activity Test
ATS-13 Activity Assay
Verification Panels for Assay Development & QC
Seroconversion Panels
POCT Fluorescent Immunoassay Analyzer
FIA Go
Gold Member
hCG Whole Blood Pregnancy Test
VEDALAB hCG-CHECK-1
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 © 2000-2026 Globetech Media. All rights reserved.