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Circulating Cell-Free DNA for Brain Abscess Diagnosis: A Pilot Study

Assessment of Circulating Cell-Free DNA for the Microbiological Diagnosis of Brain Abscesses: A Pilot Proof-of-Concept Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07479225
Acronym
METABCES-PoC
Enrollment
15
Registered
2026-03-18
Start date
2026-04-01
Completion date
2028-03-31
Last updated
2026-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Abscess

Keywords

Brain Abscess, Cell-Free DNA, Metagenomics

Brief summary

Brain abscess is a severe intracranial infection associated with significant morbidity and mortality. Standard management combines neurosurgical intervention, when feasible, with prolonged intravenous antibiotic therapy. Neurosurgical procedures, such as surgical drainage or stereotactic aspiration, play a key role in reducing intracranial pressure, decreasing the infectious burden, and obtaining samples for microbiological identification. However, neurosurgical intervention is not always possible due to technical limitations or patien related contrindications. In these situations, microbiological documentation becomes particularly challenging. Conventional diagnostic methods have limited sensitivity, with blood cultures and lumbar puncture yielding positive results in only about 25% of brain abscess cases. Recent advances in infectious disease diagnostics have introduced metagenomic approaches that may improve pathogen detection. Studies have shown that metagenomic analysis of operative samples can provide more comprehensive microbiological documentation than conventional culture-based methods. In addition, next-generation sequencing (NGS) of circulating microbial cell-free DNA in blood enables the detection of short microbial DNA fragments with a short half-life, reflecting active infection. This technology has already demonstrated promising results in clinical situations where microbiological documentation is difficult, such as febrile neutropenia. The present study aims to evaluate the performance of this approach in patients with brain abscess.

Detailed description

Brain abscess is a rare but severe intracranial infection, with an estimated incidence of approximately 0.8 cases per 100,000 individuals and a reported mortality rate ranging from 10% to 20%. Current management relies on a combination of neurosurgical intervention and prolonged intravenous antimicrobial therapy. When feasible, surgical drainage or stereotactic aspiration is performed to reduce intracranial pressure, decrease the infectious burden, and obtain biological samples for microbiological identification of the causative pathogen, enabling targeted antimicrobial treatment. However, neurosurgical intervention is not always feasible. Technical factors such as small abscess size or deep anatomical location may prevent access to the lesion, and some patients may present contraindications to neurosurgical procedures. In these situations, microbiological documentation becomes particularly challenging. Conventional diagnostic methods, including blood cultures and cerebrospinal fluid analysis, have limited sensitivity in brain abscess and frequently fail to identify the causative pathogen. Recent advances in molecular diagnostics have led to the development of metagenomic sequencing approaches for pathogen detection. Metagenomic analysis enables the unbiased identification of microbial DNA directly from clinical samples and may provide broader pathogen detection than traditional culture-based techniques. In neurosurgical infections, metagenomic sequencing performed on operative samples has shown promising results and may improve microbiological documentation compared with standard diagnostic methods. In parallel, sequencing of circulating microbial cell-free DNA (cfDNA) in peripheral blood using next-generation sequencing represents an innovative and minimally invasive diagnostic approach. This technology detects short fragments of microbial DNA released into the bloodstream during active infection and may provide clinically relevant diagnostic information. This study aims to evaluate the diagnostic performance of circulating microbial cfDNA metagenomic sequencing in patients with brain abscess and to compare its performance with metagenomic sequencing and conventional microbiological cultures performed on intraoperative samples when available. This pilot study is designed to provide proof-of-concept data on the diagnostic performance of circulating microbial cfDNA sequencing in brain abscess. The results may help define the role of this diagnostic approach in improving microbiological documentation and guiding targeted antimicrobial therapy, particularly when neurosurgical sampling is not feasible.

Interventions

DIAGNOSTIC_TESTPlasma Microbial Cell-Free DNA Metagenomic Sequencing

A 20 mL peripheral blood sample will be collected prior to neurosurgical intervention for metagenomic next-generation sequencing (mNGS) analysis of circulating microbial cell-free DNA. Results will be compared with metagenomic analysis and conventional culture of intraoperative brain abscess specimens, which serve as the reference standard for microbiological identification.

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant ≥ 18 years of age. * Participant presenting with a brain abscess requiring neurosurgical * Signed Informed Consent * Covered by health insurance

Exclusion criteria

* Participant in exclusion period for another study * Participant referred to in articles L1121-5 to L1121-8 of the CSP (corresponding to all protected persons : pregnant woman, parturient, breastfeeding mother, person deprived of liberty by judicial or administrative decision, persons undergoing psychiatric care under articles L.3212-1 and L.3213-1 who do not fall under article L.1121-8, persons admitted to a healthcare or social institution for purposes other than research, minors, person under legal protection or unable to express consent). * Staff members with a hierarchical relationship to the principal investigator

Design outcomes

Primary

MeasureTime frameDescription
Blood and Brain Abscess Metagenomic ConcordanceDay 0Comparison of bacterial species identified by metagenomic next-generation sequencing of cell-free DNA (cfDNA) from blood samples versus metagenomic analysis of per-operative brain abscess samples.

Secondary

MeasureTime frameDescription
Metagenomic Next-Generation Sequencing vs. Culture ConcordanceDay 0Evaluation of bacterial species identification using metagenomic next-generation sequencing compared to gold-standard culture techniques on per-operative brain abscess samples.
Plasma Cell-Free DNA vs. Abscess Culture CorrelationDay 0Comparison of bacterial species identified by metagenomic analysis of circulating cell-free DNA (cfDNA) from blood samples versus species identified by conventional culture of per-operative brain abscess samples.
Potential Clinical Impact on Antimicrobial TreatmentAt 1 MonthAssessment of potential therapeutic modifications or antibiotic optimization induced by metagenomic next-generation sequencing results compared to standard culture-based diagnosis.

Countries

France

Contacts

CONTACTMarion LE MARECHAL, MD,PhD
MLemarechal@chu-grenoble.fr04 76 76 52 91
CONTACTSaber touati, PhD
stouati1@chu-grenoble.fr04 76 76 58 05

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026