Evidence map›Paper›PMID 33094451›Full record

ArticleDigestive diseases and sciences2021

Risk of Progression of Gastric Intestinal Metaplasia Is Significantly Greater When Detected in Both Antrum and Body.

Anthony O'Connor, Adam Bowden, Eoin Farrell, Joshua Weininger, Stephen Crowther, Deirdre McNamara, Paul Ridgway, Colm O'Morain

Abstract read
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Article in Digestive diseases and sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Cancer Progress and Priorities: Gastric Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
    Article
  3. Article
  4. 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

8 authors.

Anthony O'ConnorGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland. jpoconno@tcd.ie.ORCID 0000-0003-1722-4820
Adam BowdenGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland.
Eoin FarrellGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland.
Joshua WeiningerGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland.
Stephen CrowtherHistopathology Department, Trinity College Dublin, Tallaght University Hospital, Dublin, Ireland.
Deirdre McNamaraGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland.
Paul RidgwayUpper Gastrointestinal Surgery Department, Trinity College Dublin, Tallaght University Hospital, Dublin, Ireland.
Colm O'MorainGastroenterology Department, Trinity College Dublin, Tallaght University Hospital, Belgard Avenue, Tallaght, Dublin, D24 NR0A, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) is the fifth leading cause of cancer-related death worldwide. GC is usually preceded by a cascade of well-defined precursor lesions, set in place by an environmental trigger (H. pylori) including intestinal metaplasia (GIM) and dysplasia.

aimsTo investigate the rates of progression of GIM to dysplasia and GC in a region of low gastric cancer incidence.

methodsWe identified all patients diagnosed with GIM between January 1, 2008, and June 30, 2012. Any repeat upper endoscopy more than 1 year after index diagnosis and before December 31, 2018, was considered follow-up. Carcinomas the bulk of which were macroscopically located below the OGJ were considered primary gastric cancer.

resultsProgression to more advanced lesions was observed in six patients (0.6%). Four patients (three male) developed GC at median age 74 years (SD 6). Two patients progressed to dysplasia (one male) at median age 71 years (SD 4). Patients with GIM in both gastric antrum and body were significantly more likely to progress than those with GIM in only one location (3.1% vs. 0.4%) (p value 0.017). Fifty-eight patients who had H. pylori eradicated were followed up. No progression to dysplasia or GC was noted in this group, with 28 patients having persistent GIM at follow-up.

conclusionPatients with GIM in both antrum and body had a significantly increased risk of progression and warrant close attention. This is comparable to routinely followed premalignant conditions such as Barrett's esophagus and Colonic Polyps, and appropriate surveillance protocols should be followed in this group.

Indexed as

FemaleHumansMaleMetaplasiaMiddle AgedPrecancerous ConditionsStomachStomach NeoplasmsDysplasiaGastric cancerGastric intestinal metaplasiaH. pylori

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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.