Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 213

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Clinical‐histological associations in gastroparesis: results from the Gastroparesis Clinical Research Consortium

Open access
Grover, M., Bernard, C. E., Pasricha, P. J., Lurken, M. S., Faussone‐Pellegrini, M. S., Smyrk, T. C., Parkman, H. P., Abell, T. L., Snape, W. J., Hasler, W. L., McCallum, R. W., Nguyen, L., Koch, K. L., Calles, J., Lee, L., Tonascia, J., Ünalp‐Arida, A., Hamilton, F. A., Farrugia, G., on behalf the NIDDK Gastroparesis Clinical Research Consortium (GpCRC)·2012·Neurogastroenterology & Motility

Abstract

Background Cellular changes associated with diabetic (DG) and idiopathic gastroparesis (IG) have recently been described from patients enrolled in the Gastroparesis Clinical Research Consortium. The association of these cellular changes with gastroparesis symptoms and gastric emptying is unknown. The aim of this study was to relate cellular changes to symptoms and gastric emptying in patients with gastroparesis. Methods Earlier, using full thickness gastric body biopsies from 20 DG, 20 IG, and 20 matched controls, we found decreased interstitial cells of Cajal (ICC) and enteric nerves and an increase in immune cells in both DG and IG. Here, demographic, symptoms [gastroparesis cardinal symptom index score (GCSI)], and gastric emptying were related to cellular alterations using Pearson’s correlation coefficients. Key Results Interstitial cells of Cajal counts inversely correlated with 4 h gastric retention in DG but not in IG (r = −0.6, P = 0.008, DG, r = 0.2, P = 0.4, IG). There was also a significant correlation between loss of ICC and enteric nerves in DG but not in IG (r = 0.5, P = 0.03 for DG, r = 0.3, P = 0.16, IG). Idiopathic gastroparesis with a myenteric immune infiltrate scored higher on the average GCSI (3.6 ± 0.7 vs 2.7 ± 0.9, P = 0.05) and nausea score (3.8 ± 0.9 vs 2.6 ± 1.0, P = 0.02) as compared to those without an infiltrate. Conclusions & Inferences In DG, loss of ICC is associated with delayed gastric emptying. Interstitial cells of Cajal or enteric nerve loss did not correlate with symptom severity. Overall clinical severity and nausea in IG is associated with a myenteric immune infiltrate. Thus, full thickness gastric biopsies can help define specific cellular abnormalities in gastroparesis, some of which are associated with physiological and clinical characteristics of gastroparesis.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/j.1365-2982.2012.01894.x

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 5 references

Cited by

See all 213

Metadata

Authors
Grover, M., Bernard, C. E., Pasricha, P. J., Lurken, M. S., Faussone‐Pellegrini, M. S., Smyrk, T. C., Parkman, H. P., Abell, T. L., Snape, W. J., Hasler, W. L., McCallum, R. W., Nguyen, L., Koch, K. L., Calles, J., Lee, L., Tonascia, J., Ünalp‐Arida, A., Hamilton, F. A., Farrugia, G., & on behalf the NIDDK Gastroparesis Clinical Research Consortium (GpCRC)
Venue
Neurogastroenterology & Motility
Publisher
Wiley
Published
2012-02-17
Volume
24
Issue
6
Pages
531
ISSN
  • 1350-1925 (ISSN-L)
  • 1365-2982
OpenAlex
W1830718785
Cited by
213
References
5
FWCI
11.63
Type
journal article
Language
en
Open access
green

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Clinical‐histological associations in gastroparesis: results from the Gastroparesis Clinical Research Consortium. https://app.cochat.ai/papers/10.1111/j.1365-2982.2012.01894.x
The paper
Grover, M., Bernard, C. E., Pasricha, P. J., Lurken, M. S., Faussone‐Pellegrini, M. S., Smyrk, T. C., Parkman, H. P., Abell, T. L., Snape, W. J., Hasler, W. L., McCallum, R. W., Nguyen, L., Koch, K. L., Calles, J., Lee, L., Tonascia, J., Ünalp‐Arida, A., Hamilton, F. A., Farrugia, G., & on behalf the NIDDK Gastroparesis Clinical Research Consortium (GpCRC). (2012). Clinical‐histological associations in gastroparesis: results from the Gastroparesis Clinical Research Consortium. Neurogastroenterology & Motility. https://doi.org/10.1111/j.1365-2982.2012.01894.x

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.