Evidence map›Paper›PMID 30086735›Full record

ArticleBMC medical genomics2018

Transcriptomic signatures reveal immune dysregulation in human diabetic and idiopathic gastroparesis.

Madhusudan Grover, Simon J Gibbons, Asha A Nair, Cheryl E Bernard, Adeel S Zubair, Seth T Eisenman, Laura A Wilson, Laura Miriel, Pankaj J Pasricha, Henry P Parkman and 14 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05981300 (GpCRC Pediatric Gastroparesis Registry 2), which is not on this map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 4% 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.

NCT05981300 recruitingnot on this mapstarted 2024, after this paper: background citation

GpCRC Pediatric Gastroparesis Registry 2: Characterization and Clinical Course of Symptoms and Gastric Emptying in Pediatric, Adolescent, and Young Adult Participants With Symptoms of Gastroparesis

Typeobservational_patient_registrySponsorJohns Hopkins Bloomberg School of Public HealthRan2024 to 2027Enrolled216ConditionsGastroparesis, Gastroparesis-like Syndrome
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. A pilot genome-wide association study meta-analysis of gastroparesis.United European gastroenterology journal · 2023
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Common Pathophysiological Mechanisms and Treatment of Diabetic Gastroparesis.Journal of neurogastroenterology and motility · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Ten controversies in gastroparesis and a look to the future.Neurogastroenterology and motility · 2023
    Review
  13. Progress in Gastroparesis - A Narrative Review of the Work of the Gastroparesis Clinical Research Consortium.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2022
    Review
  14. Review
  15. Review
  16. Gastroparesis.Gastroenterology · 2022
    Review
  17. Review
  18. Review
  19. Observational
  20. 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

24 authors at 12 institutions in 1 country.

Madhusudan GroverEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA. Grover.madhusudan@mayo.edu.
Simon J GibbonsEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA.
Asha A NairBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
Cheryl E BernardEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA.
Adeel S ZubairEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA.
Seth T EisenmanEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA.
Laura A WilsonJohns Hopkins University Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Laura MirielJohns Hopkins University Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Pankaj J PasrichaJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Henry P ParkmanTemple University, Philadelphia, PA, USA.
Irene SarosiekTexas Tech University, El Paso, TX, USA.
Richard W McCallumTexas Tech University, El Paso, TX, USA.
Kenneth L KochWake Forest University, Winston-Salem, NC, USA.
Thomas L AbellUniversity of Louisville, Louisville, KY, USA.
William J SnapeCalifornia Pacific Medical Center, San Francisco, CA, USA.
Braden KuoMassachusetts General Hospital, Boston, MA, USA.
Robert J ShulmanBaylor College of Medicine, Houston, TX, USA.
Travis J McKenzieDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Todd A KelloggDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Michael L KendrickDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
James TonasciaJohns Hopkins University Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Frank A HamiltonNational Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA.
Gianrico FarrugiaEnteric NeuroScience Program, Division of Gastroenterology & Hepatology, Mayo Clinic, 200 1st Street SW, Rochester, MN, 55905, USA. Farrugia.gianrico@mayo.edu.ORCID 0000-0003-3473-5235
NIDDK Gastroparesis Clinical Research Consortium (GpCRC)
Mayo Clinic · USJohns Hopkins University · USMayo Clinic in Arizona · USTexas Tech University · USBaylor College of Medicine · USCalifornia Pacific Medical Center · USMassachusetts General Hospital · USMayo Clinic in Florida · USNational Institute of Diabetes and Digestive and Kidney Diseases · USTemple University · USUniversity of Louisville · USWake Forest University · US

Funding

Physiological Characterization and Data Integration CoreP01DK068055 · NIDDK · MAYO CLINIC ROCHESTER · PI BHARUCHA, ADIL E. · 2004 to 2019
$23.8M
Gastroparesis Consortium Continuation-Data Coordinating CenterU01DK074008 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI TONASCIA, JAMES A · 2006 to 2015
$17.4M
PGpR2 Year 4 Supplement for the Scientific Data Research Center (SDRC) of the GpCRC 4U24DK074008 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI David M Shade · 2017 to 2026
$11.7M
Subtypes of GastroparesisU01DK073974 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Baharak Moshiree · 2006 to 2026
$7.4M
Temple University Gastroparesis Clinical CenterU01DK073975 · NIDDK · TEMPLE UNIV OF THE COMMONWEALTH · PI HENRY PAUL PARKMAN · 2006 to 2026
$7.4M
U of L Clinical Center to Investigate the Pathogenesis, Etiology, and Treatment of Gastroparesis through the NIDDK Gastroparesis ConsortiumU01DK074007 · NIDDK · UNIVERSITY OF MISSISSIPPI MED CTR · PI Thomas Lyman Abell · 2006 to 2026
$7.0M
Advancing Clinical Science in Pediatric GastroparesisU01DK112194 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Bruno Pedro Chumpitazi, Geoffrey A Preidis · 2016 to 2026
$5.3M
"Barrier function alterations in post-infectious irritable bowel syndrome"K23DK103911 · NIDDK · MAYO CLINIC ROCHESTER · PI GROVER, MADHUSUDAN · 2015 to 2019
$804k
NIDDK NIH HHS K23 DK103911NIDDK NIH HHS K23DK103911NIDDK NIH HHS P01 DK068055NIDDK NIH HHS U01 DK073974NIDDK NIH HHS U01DK073974NIDDK NIH HHS U01 DK073975NIDDK NIH HHS U01DK073975NIDDK NIH HHS U01 DK074007NIDDK NIH HHS U01DK074007NIDDK NIH HHS U01 DK074008NIDDK NIH HHS U01 DK112194NIDDK NIH HHS U24 DK074008
6 · The paper itself

Abstract

backgroundCellular changes described in human gastroparesis have revealed a role for immune dysregulation, however, a mechanistic understanding of human gastroparesis and the signaling pathways involved are still unclear.

methodsDiabetic gastroparetics, diabetic non-gastroparetic controls, idiopathic gastroparetics and non-diabetic non-gastroparetic controls underwent full-thickness gastric body biopsies. Deep RNA sequencing was performed and pathway analysis of differentially expressed transcripts was done using Ingenuity®. A subset of differentially expressed genes in diabetic gastroparesis was validated in a separate cohort using QT-PCR.

results111 genes were differentially expressed in diabetic gastroparesis and 181 in idiopathic gastroparesis with a log

conclusionsDiabetic and idiopathic gastroparesis have both unique and overlapping transcriptomic signatures. Innate immune signaling likely plays a central role in pathogenesis of human gastroparesis.

Indexed as

Gene Expression ProfilingAdultDiabetes ComplicationsFemaleGastroparesisHumansMaleMiddle AgedSignal TransductionYoung AdultDiabetes mellitusMacrophagesNext generation sequencingRNASignaling

Identifiers

PMID30086735
PMCPMC6081936
OpenAlexW2886446104

What OpenQuestion holds

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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.