Evidence map›Paper›PMID 40411534›Full record

ArticleArchives of dermatological research2025

Decreased gut short-chain fatty acids in cutaneous T-cell lymphoma: a novel insight.

Zachary O Thomas, JoJo Holm, Morgan McCarthy, William Nguyen, Yanzhen Pang, Lauren P Chrisman, Joan Guitart, Michael B Burns, Xiaolong Alan Zhou

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Archives of dermatological research, 2025. 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. Review
  2. Review
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

9 authors.

Zachary O ThomasDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
JoJo HolmDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
Morgan McCarthyDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
William NguyenDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
Yanzhen PangDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
Lauren P ChrismanDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
Joan GuitartDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA.
Michael B BurnsDepartment of Biology, Loyola University Chicago, Chicago, IL, USA.
Xiaolong Alan ZhouDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St Suite 1600, Chicago, IL, 60611, USA. alan.zhou@northwestern.edu.

Funding

NIH HHS 5KL2TR001424
6 · The paper itself

Abstract

Short-chain fatty acids (SCFAs) are critical metabolites produced by gut microbiota that play a key role in modulating inflammation and regulating systemic immunity, including against cancer. Decreases in SCFAs can foster a permissive tumor immune environment. Recent studies have shown that cutaneous T-cell lymphoma (CTCL) patients exhibit increasing gut dysbiosis and loss of bacteria predicted to produce SCFAs with increasing disease severity. To investigate this functional connection, we collected stool swab samples from 15 individuals- 8 mycosis fungoides (MF) patients and 7 matched healthy controls (HC)- and quantified concentrations of four SCFAs (acetate, propionate, isovalerate, butyrate) via liquid chromatography-mass spectrometry. Our results demonstrated significantly reduced acetate and propionate concentrations in MF patients when compared to HC (both p = 0.027). Total measured SCFA concentrations were on average lower in MF versus HC, but did not achieve statistical significance (p = 0.063). Both propionate and acetate have been previously demonstrated to promote tumor apoptosis, inhibit tumor proliferation, and enhance antitumor immunity. Thus, dysbiosis-associated reductions in SCFAs may be another contributive factor in the immune dysfunction observed in CTCL. Our pilot findings add to the growing body of knowledge implicating the gut microbiota-SCFA axis in CTCL pathogenesis and offer potential new avenues for therapeutic intervention.

Indexed as

DysbiosisFatty Acids, VolatileGastrointestinal MicrobiomeMycosis FungoidesSkin NeoplasmsAdultAgedCase-Control StudiesFecesFemaleHumansMaleMiddle AgedPilot ProjectsPropionatesFatty Acids, VolatilePropionatesCutaneous T-cell lymphomaGut microbiomeShort-chain fatty acidsStool metabolites

Identifiers

PMID40411534

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.