Evidence map›Paper›PMID 35426515›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2022

Evaluation of fresh, frozen, and lyophilized fecal samples by SPME and derivatization methods using GC×GC-TOFMS.

Seo Lin Nam, Kieran Tarazona Carrillo, A Paulina de la Mata, Olle M de Bruin, Evgueni Doukhanine, James Harynuk

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Article in Metabolomics : Official journal of the Metabolomic Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Evaluation of solutions for stabilizing feces in metabolomics studies using GC × GC-TOFMS.Metabolomics : Official journal of the Metabolomic Society · 2025
    Article
  4. Evaluation of normalization strategies for GC-based metabolomics.Metabolomics : Official journal of the Metabolomic Society · 2024
    Article
  5. Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Seo Lin NamDepartment of Chemistry, University of Alberta, T6G 2G2, Edmonton, Alberta, Canada.
Kieran Tarazona CarrilloDepartment of Chemistry, University of Alberta, T6G 2G2, Edmonton, Alberta, Canada.
A Paulina de la MataDepartment of Chemistry, University of Alberta, T6G 2G2, Edmonton, Alberta, Canada.
Olle M de BruinDNA Genotek, Ottawa, Ontario, Canada.
Evgueni DoukhanineDNA Genotek, Ottawa, Ontario, Canada.
James HarynukDepartment of Chemistry, University of Alberta, T6G 2G2, Edmonton, Alberta, Canada. james.harynuk@ualberta.ca.ORCID 0000-0002-9627-5206

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFeces is a highly complex matrix containing thousands of metabolites. It also contains live bacteria and enzymes, and does not have a static chemistry. Consequently, proper control of pre-analytical parameters is critical to minimize unwanted variations in the samples. However, no consensus currently exists on how fecal samples should be stored/processed prior to analysis.

objectiveThe effects of sample handling conditions on fecal metabolite profiles and abundances were examined using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS).

methodsSolid-phase microextraction (SPME) and derivatization via trimethylsilylation (TMS) were employed as complementary techniques to evaluate fresh, frozen, and lyophilized fecal samples with expanded coverage of the fecal metabolome. The total number of detected peaks and the signal intensities were compared among the different handling conditions.

resultsOur analysis revealed that the metabolic profiles of fecal samples depend greatly on sample handling and processing conditions, which had a more pronounced effect on results obtained by SPME than by TMS derivatization. Overall, lyophilization resulted in a greater amount of total and class-specific metabolites, which may be attributed to cell lysis and/or membrane disintegration.

conclusionsA comprehensive comparison of the sample handling conditions provides a deeper understanding of the physicochemical changes that occur within the samples during freezing and lyophilization. Based on our results, snap-freezing at -80 °C would be preferred over lyophilization for handling samples in the field of fecal metabolomics as this imparts the least change from the fresh condition.

Indexed as

MetabolomicsSolid Phase MicroextractionFecesFreezingGas Chromatography-Mass SpectrometryderivatizationfecesGC×GC-TOFMSlyophilizationmetabolomicsmicrobiomeSPME

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.