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

Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological ... read more Featured Products: More products

Download Mobile App




Noninvasive Blood Test Predicts Rejection After Heart Transplant

By LabMedica International staff writers
Posted on 06 Jun 2022

Heart transplantation (HTx) is the definitive treatment option for patients with advanced heart failure. More...

Despite continued advances in post-transplant outcomes, allograft rejection and allograft injury remain impediments to post-transplant survival.

Endomyocardial biopsy and histopathology remain the principal surveillance tools for rejection after heart transplant since they were developed decades ago. However, endomyocardial biopsy is invasive and expensive, and histopathology reads are prone to inter-observer variability.

Physicians at UC San Diego Health (San Diego, CA, USA) and their colleagues examined the performance characteristics of a novel test for detecting acute rejection (AR) in adult HTx recipients. Plasma samples with contemporaneous endomyocardial biopsies (EMBs) were obtained from HTx recipients. A total of 811 samples from 223 patients with dd-cfDNA testing and contemporaneous EMB were eligible for the study.

A clinically available SNP-based massively multiplexed-PCR dd-cfDNA assay was used to measure dd-cfDNA fraction. dd-cfDNA fractions were compared with EMB-defined rejection status and test performance was assessed by constructing ROC curves and calculating accuracy measures. Laboratory testing involved cfDNA extraction and library preparation using the Prospera test (Natera Inc., Austin, TX, USA). This was followed by cfDNA amplification using massively multiplexed-PCR, targeting over 13,000 single nucleotide polymorphisms designed to maximize the number of informative SNPs across ethnicities and next-generation sequencing of the resultant amplicons, with sequencing performed on the NextSeq500 (Illumina, San Diego, USA) on rapid run with an average of 14 to 15 million reads per sample.

The scientists reported that AR was observed in 49 biopsy matched samples from 35 patients while 762 samples from 210 patients did not show AR. Median dd-cfDNA fraction was significantly higher in samples with a matched biopsy showing AR (median 0.58%, IQR, 0.13%-1.68%) compared to samples where matched biopsies did not show AR. ROC analysis produced an area under the curve (AUC-ROC) of 0.86. Defining samples with dd-cfDNA fraction ≥0.15% as AR yielded 78.5% sensitivity and 76.9% specificity. Positive and negative predictive values were 25.1% and 97.3% respectively, calculated using the cohort AR prevalence of 9.0% with adjustment for repeat samples.

The authors concluded that their study affirms an association between elevated levels of dd-cfDNA and histologic evidence of rejection after heart transplant, and extends previous findings showing that dd-cfDNA is a valuable biomarker of allograft health. The study was published originally published on April 9, 2022 in the Journal of Heart and Lung Transplantation.

Related Links:
UC San Diego Health 
Natera Inc 
Illumina 

 

 


Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Fully-auto Specific Protein (Nephelometry) Analyzer
PA240
Platinum Member
Integrated Biochemical & Immunological System
Biolumi CX Solution X10+C10
New
Nucleic Acid Purification Instrument
QIAsymphony Connect
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: LVOne uses blood-based biomarkers to detect stroke and identify large vessel occlusion before hospital arrival, providing objective results earlier than traditional assessments. (Photo courtesy of UpFront Diagnostics)

First-of-Its-Kind Rapid Blood Test Gains CE Mark to Support Prehospital Stroke Triage

Rapid stroke identification before hospital arrival is critical because treatment efficacy declines with every minute of delay. However, definitive assessment typically requires hospital-based imaging,... 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 cognitive assessment, blood testing, phlebotomy, and MRI to support faster diagnosis across the UK (Image Credt: Adobe Stock)

New UK Collaboration Expands Access to Integrated Alzheimer’s Diagnostic Testing

C2N Diagnostics and Cambridge Cognition have partnered with The Alzheimer’s Trust to create an integrated pathway aimed at supporting earlier and more accurate diagnosis of Alzheimer’s disease and related dementias.... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.