Evidence map›Paper›PMID 28877980›Full record

ArticleGut2018

NAD metabolism fuels human and mouse intestinal inflammation.

Romana R Gerner, Victoria Klepsch, Sophie Macheiner, Kathrin Arnhard, Timon E Adolph, Christoph Grander, Verena Wieser, Alexandra Pfister, Patrizia Moser, Natascha Hermann-Kleiter and 4 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Gut, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05561738 (Nicotinamide Riboside in Ulcerative Colitis), which is not on this map. Cited by 132 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 5% of its field
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.

NCT05561738 naterminatednot on this mapstarted 2024, after this paper: background citation

Nicotinamide Riboside in Ulcerative Colitis

TypeinterventionalSponsorUniversity of PittsburghRan2024 to 2026Enrolled19ConditionsUlcerative ColitisArmsNicotinamide Riboside Chloride, Placebo, Standard of Care
3 · Its place in the literature

Who cites it

132 citing papers in PubMed, 1 synthesis or guideline pooled it, 185 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. NADAging cell · 2026
    Article
  6. Article
  7. Article
  8. Temporal transcriptomic profiling identifies core regulators in cytokine-induced gut barrier disruption in differentiated Caco-2 cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Disruption of Gut Microbiota-Mediated De Novo NADAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  18. Article
  19. Article
  20. Apoptotic Bodies Restore NAD and Mitochondrial Homeostasis in Fibroblasts.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article

72 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Romana R GernerDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.ORCID 0000-0003-2377-6509
Victoria KlepschDivision of Translational Cell Genetics, Department for Pharmacology and Genetics, Medical University Innsbruck, Innsbruck, Austria.
Sophie MacheinerDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Kathrin ArnhardInstitute of Legal Medicine and Core Facility Metabolomics, Medical University Innsbruck, Innsbruck, Austria.
Timon E AdolphDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Christoph GranderDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Verena WieserDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Alexandra PfisterDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Patrizia MoserDepartment of Pathology, Medical University Innsbruck, Innsbruck, Austria.
Natascha Hermann-KleiterDivision of Translational Cell Genetics, Department for Pharmacology and Genetics, Medical University Innsbruck, Innsbruck, Austria.ORCID 0000-0003-4389-9813
Gottfried Baier
Herbert OberacherInstitute of Legal Medicine and Core Facility Metabolomics, Medical University Innsbruck, Innsbruck, Austria.
Herbert TilgDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Alexander R MoschenDivision of Internal Medicine I, Department of Medicine, Medical University Innsbruck, Innsbruck, Austria.
Innsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveNicotinamide phosphoribosyltransferase (NAMPT, also referred to as pre-B cell colony-enhancing factor or visfatin) is critically required for the maintenance of cellular nicotinamide adenine dinucleotide (NAD) supply catalysing the rate-limiting step of the NAD

designWe investigated the impact of NAMPT inhibition by the small-molecule inhibitor FK866 in the dextran sulfate sodium (DSS) model of colitis and the azoxymethane/DSS model of colitis-associated cancer. The impact of NAD depletion on differentiation of mouse and human primary monocytes/macrophages was studied in vitro. Finally, we tested the efficacy of FK866 compared with dexamethasone and infliximab in lamina propria mononuclear cells (LPMNC) isolated from patients with IBD.

resultsFK866 ameliorated DSS-induced colitis and suppressed inflammation-associated tumorigenesis in mice. FK866 potently inhibited NAMPT activity as demonstrated by reduced mucosal NAD, resulting in reduced abundances and activities of NAD-dependent enzymes including PARP1, Sirt6 and CD38, reduced nuclear factor kappa B activation, and decreased cellular infiltration by inflammatory monocytes, macrophages and activated T cells. Remarkably, FK866 effectively supressed cytokine release from LPMNCs of patients with IBD. As FK866 was also effective in Rag1

conclusionOur data emphasise the importance of NAD immunometabolism for mucosal immunity and highlight FK866-mediated NAMPT blockade as a promising therapeutic approach in acute intestinal inflammation.

Indexed as

Colitis, UlcerativeColonic NeoplasmsAcrylamidesAnimalsCell DifferentiationDexamethasoneEnergy MetabolismGastrointestinal AgentsHumansInfliximabIntestinal MucosaMacrophagesMiceMonocytesNADNicotinamide PhosphoribosyltransferaseAcrylamidesDexamethasoneGastrointestinal AgentsInfliximabN-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamideNADNicotinamide PhosphoribosyltransferasePiperidinesColonic Mucosal MetabolismEnergy MetabolismGut InflammationIBD Basic ResearchInflammatory Bowel Disease

Identifiers

PMID28877980
PMCPMC6145287
OpenAlexW2753842728

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.