Evidence map›Paper›PMID 41511994›Full record

ArticlePloS one2026

Fecal butyrate and deoxycholic acid quantitation for rapid assessment of the gut microbiome.

Michael W Mullowney, Angelica Moran, Antonio Hernandez, Mary McMillin, Amber R Rose, David Moran, Jessica Little, Ann B Nguyen, Bhakti K Patel, Christopher J Lehmann and 4 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Michael W MullowneyDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-2884-4307
Angelica MoranDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0003-4013-2182
Antonio HernandezDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-7883-4852
Mary McMillinDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Amber R RoseDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-1388-0305
David MoranDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Jessica LittleDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Ann B NguyenDepartment of Medicine, University of Chicago, Chicago, Illinois, United States of America.
Bhakti K PatelDepartment of Medicine, University of Chicago, Chicago, Illinois, United States of America.
Christopher J LehmannDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Matthew A OdenwaldDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Eric G PamerDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.
Kiang-Teck J YeoDepartment of Pathology, University of Chicago, Chicago, Illinois, United States of America.
Ashley M SidebottomDuchossois Family Institute, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-8670-9090

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intestinal microbiome is composed of myriad microbial species with impacts on host health that are mediated by the production of metabolites. While loss of bacterial species and beneficial metabolites from the fecal microbiome is associated with development of a range of diseases and medical complications, there are currently no clinical diagnostic tests that rapidly identify individuals with microbiome deficiencies. This method aims to rapidly quantify fecal concentrations of butyrate and deoxycholic acid, as depletion of these two metabolites are associated with adverse clinical outcomes and result from the loss of a subset of health-associated bacterial species. We present a rapid diagnostic screen based on 3-nitrophenylhydrazine derivatization and ultrahigh-performance liquid chromatography-mass spectrometry that measures fecal butyrate and deoxycholic acid concentrations as markers of microbiome function. A matrix-matched calibration curve was developed using a simulated fecal mixture to optimize accuracy and facilitate adherence to clinical laboratory regulations. The assay resulted in an analytical measurement range from 4.30-3030 µM (LLOQ = 3.71 µM) for butyrate and from 0.9-64.9 µM (LLOQ = 0.7 µM) for deoxycholic acid. Precision evaluation demonstrated a coefficient of variation <15% at all quality control levels tested. The rapid liquid chromatography-mass spectrometry screen can be performed in under an hour from extraction to provision of quantitative results, enabling the rapid identification of patients with defective microbiome function.

Indexed as

ButyratesDeoxycholic AcidFecesGastrointestinal MicrobiomeChromatography, High Pressure LiquidHumansLiquid Chromatography-Mass SpectrometryButyratesDeoxycholic Acid

Identifiers

PMID41511994
PMCPMC12788677

What OpenQuestion holds

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Registered trials

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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.