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Record W4414946281 · doi:10.1016/j.microc.2025.115623

Enhanced biomarker discovery through narrow-range data-dependent acquisition in untargeted metabolomics

2025· article· en· W4414946281 on OpenAlexafffund
Venus Baghalabadi, Andrew Leslie, J. Paul Fawcett, Devanand M. Pinto

Bibliographic record

VenueMicrochemical Journal · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicMetabolomics and Mass Spectrometry Studies
Canadian institutionsNational Research Council CanadaDalhousie University
FundersFaculty of Medicine, Dalhousie UniversityNational Research Council CanadaNational Research Council
KeywordsMetabolomicsBiomarker discoveryMetaboliteMass spectrometryData acquisitionMetabolomeBiomarkerProfiling (computer programming)

Abstract

fetched live from OpenAlex

Metabolomics involves the comprehensive analysis of small molecules in biological systems and is critical for clinical research and precision medicine. Liquid chromatography-mass spectrometry (LC-MS) is important in metabolomics due to its extensive metabolite coverage and high sensitivity. The increasing demand for disease biomarkers has increased LC-MS use, particularly untargeted metabolomics, which provides a complete view of the metabolome. However, the choice of MS acquisition method in untargeted metabolomics is crucial and challenging, as it impacts analysis coverage, sensitivity, and reproducibility. This work addresses the critical issue of selecting appropriate acquisition modes for untargeted metabolomics studies. We evaluated All Ion Fragmentation (AIF), Data-Dependent Acquisition (DDA), and Data-Independent Acquisition using Sequential Window Acquisition of All Theoretical Fragment Ion Spectra (DIA-SWATH) in untargeted metabolomics. Additionally, we introduced a novel modified DDA method with narrow mass ranges (DDA-NR). Using a standard mixture of 206 metabolites, we compared these methods in terms of metabolite identification, quantification, and spectra quality. Both DDA methods, particularly the modified DDA-NR, exhibited superior performance, identifying over 90 % of metabolites with high spectral quality and precision. We applied these methodologies to analysis of apheresis samples from CAR-T therapy patients, effectively identifying significant metabolic differences between complete response and progressive disease groups. The DDA-NR method particularly excelled in identifying metabolites at higher mass ranges, demonstrating its effectiveness in comprehensive metabolic profiling that can potentially inform and enhance therapeutic strategies. This study underscores the efficacy of DDA methods, particularly DDA-NR, in enhancing metabolite identification and spectral quality in untargeted metabolomics. These findings are significant for clinical applications, as they improve the reliability of metabolic profiling, aiding in better understanding and monitoring of metabolic changes in therapies such as CAR-T. This work contributes to establishing best practices in LC-MS-based metabolomics, facilitating advancements in analytical methodologies, and contributing to more effective and personalized cancer treatment strategies. • The modified DDA method with narrow mass ranges improved the coverage and spectral quality. • Method selection is important in capturing comprehensive metabolic signatures. • The DDA-NR approach has beneficial in detecting metabolites at higher mass ranges.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.025
Threshold uncertainty score0.880

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.289
Teacher spread0.273 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes2
Has abstractyes

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