Evidence map›Paper›PMID 36303812›Full record

ArticleWorld journal of gastrointestinal endoscopy2022

Gastric intestinal metaplasia development in African American predominant United States population.

Akram I Ahmad, Arielle Lee, Claire Caplan, Colin Wikholm, Ioannis Pothoulakis, Zaynab Almothafer, Nishtha Raval, Samantha Marshall, Ankit Mishra, Nicole Hodgins and 14 more

Open access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal endoscopy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Gastric intestinal metaplasia regression in United States population: A retrospective longitudinal study.JGH open : an open access journal of gastroenterology and hepatology · 2024
    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 1 institution in 1 country.

Akram I AhmadDepartment of Internal Medicine, MedStar Washington Hospital Center, Washington, DC 20010, United States. akram.i.ahmad@medstar.net.
Arielle LeeDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Claire CaplanDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Colin WikholmDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Ioannis PothoulakisDepartment of Internal Medicine, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Zaynab AlmothaferDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Nishtha RavalDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Samantha MarshallDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Ankit MishraDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Nicole HodginsDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
In Guk KangDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Raymond K ChangDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Zachary DaileyDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Arvin DaneshmandDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Anjani KapadiaDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Jae Hak OhDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Brittney RodriguezDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Abhinav SehgalDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Matthew SweeneyDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Christopher B SwisherDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Daniel F ChildersDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Corinne O'ConnorDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Lynette M SequeiraDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
Won ChoDepartment of Internal Medicine, Georgetown University School of Medicine, Washington, DC 20007, United States.
MedStar Washington Hospital Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer significantly contributes to cancer mortality globally. Gastric intestinal metaplasia (GIM) is a stage in the Correa cascade and a premalignant lesion of gastric cancer. The natural history of GIM formation and progression over time is not fully understood. Currently, there are no clear guidelines on GIM surveillance or management in the United States.

aimTo investigate factors associated with GIM development over time in African American-predominant study population.

methodsThis is a retrospective longitudinal study in a single tertiary hospital in Washington DC. We retrieved upper esophagogastroduodenoscopies (EGDs) with gastric biopsies from the pathology department database from January 2015 to December 2020. Patients included in the study had undergone two or more EGDs with gastric biopsy. Patients with no GIM at baseline were followed up until they developed GIM or until the last available EGD. Exclusion criteria consisted of patients age < 18, pregnancy, previous diagnosis of gastric cancer, and missing data including pathology results or endoscopy reports. The study population was divided into two groups based on GIM status. Univariate and multivariate Cox regression was used to estimate the hazard induced by patient demographics, EGD findings, and

resultsOf 2375 patients who had at least 1 EGD with gastric biopsy, 579 patients were included in the study. 138 patients developed GIM during the study follow-up period of 1087 d on average, compared to 857 d in patients without GIM (

conclusionAn increase in age and non-Caucasian race/ethnicity are associated with an increased risk of GIM formation. The effect of

Indexed as

African American populationEsophagogastroduodenoscopyGastric cancerGastric intestinal metaplasiaHelicobacter pyloriRetrospective longitudinal study

Identifiers

PMID36303812
PMCPMC9593516
OpenAlexW4304592616

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.