Evidence map›Paper›PMID 34791290›Full record

ArticleInflammatory bowel diseases2021

Current Trends in IBD-Development of Mucosal-Based Biomarkers and a Novel Minimally Invasive Recoverable Sampling System.

Yunki Y Yau, Valerie C Wasinger, Robert P Hirten, Emil Chuang, Merodean Huntsman, Jack Stylli, Jeff Shimizu, Vijay Yajnik, Jeffrey Smith, Shaoying N Lee and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2021. 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
1.2field-weighted citation impact, top 19% 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.

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, 14 citations in OpenAlex.

  1. Review
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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 7 institutions in 2 countries.

Yunki Y YauSchool of Medical Sciences, Faculty of Medicine, The University of New South Wales, Sydney, NSW, Australia.
Valerie C WasingerBioanalytical Mass Spectrometry Facility, Mark Wainwright Analytical Centre, The University of New South Wales, Sydney, NSW, Australia.
Robert P HirtenDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Merodean HuntsmanUniversity of Utah, School of Medicine, Salt Lake City, UT, USA.
Jack StylliGeorgetown University, School of Medicine, Washington D.C., USA.
Jeff ShimizuProgenity, Inc, San Diego, CA, USA.
Vijay YajnikTakeda Pharmaceuticals, Cambridge MA, USA.
Jeffrey SmithProgenity, Inc, San Diego, CA, USA.
Shaoying N LeeProgenity, Inc, San Diego, CA, USA.
Sharat SinghProgenity, Inc, San Diego, CA, USA.
Christopher WahlProgenity, Inc, San Diego, CA, USA.
Rupert W LeongSchool of Medical Sciences, Faculty of Medicine, The University of New South Wales, Sydney, NSW, Australia.
Bruce E SandsDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Progenity (United States) · USConcord Repatriation General Hospital · AUIcahn School of Medicine at Mount Sinai · USThe University of Sydney · AUGeorgetown University · USTakeda (United States) · USUniversity of Utah · US

Funding

Digital Biomarkers of Ulcerative Colitis FlareK23DK129835 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HIRTEN, ROBERT · 2021 to 2025
$812k
Crohn's & Colitis FoundationNIDDK NIH HHS K23 DK129835
6 · The paper itself

Abstract

Despite recent developments in therapy for inflammatory bowel diseases (IBDs), there have been limited advances in diagnostic tools available to aid in disease management. A growing body of evidence suggests that there are important host-microbe interactions at the mucosal interface that modulate the inflammatory response in patients with IBD. Additionally, the importance of mucosal integrity and its disruption appears to be important in the pathophysiology and perpetuation of the disease. The ability to characterize this interface may provide valuable information for both disease monitoring and identification of new treatment targets. Endoscopy remains the primary tool for disease monitoring, and mucosal healing is the primary therapeutic target in IBD treatment. However, establishing mucosal healing requires repetitive endoscopic procedures, and endoscopy is limited by factors such as invasiveness, cost, and risk of adverse events. Moreover, the use of a bowel preparation for colonoscopies alters the mucus layer and thus perturbs evaluation of the host-microbe interaction. Stool sampling may also be inaccurate because it reflects the end state of metabolites and proteins, failing to take into account the degradation or alteration of substrates of interest by bacterial proteases and other enzymes during passage through the colon. A novel sampling capsule, called the Recoverable Sampling System (RSS), is being developed as a complementary tool to colonoscopy. The RSS is intended to be a platform for noninvasive autonomous sampling, preservation, handling, and storage of analytes of interest found in the gastrointestinal fluids. A proprietary preservative contained within the chambers of the capsule has been developed to stabilize DNA and proteins for ex vivo microbiome and metabolomics analyses. Surrogate markers such as SPP24 and GUCA2a have been identified to correlate with gut health, intestinal permeability, and inflammation and could be locally sampled by the RSS. The potential clinical utility of an RSS device is broad and would likely be able to guide therapy by allowing for more frequent disease monitoring, aiding in disease characterization, and facilitating in the identification of novel therapeutic targets.

Indexed as

DysbiosisIntestinal MucosaBiomarkersColonColonoscopyHumansInflammatory Bowel DiseasesBiomarkersgut dysbiosisinflammatory bowel diseasemucosal biomarkersmucosal samplingnovel sampling technology

Identifiers

PMID34791290
PMCPMC9214562
OpenAlexW3212718676

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.