Evidence map›Paper›PMID 26671515›Full record

ArticleEuropean journal of gastroenterology & hepatology2016

Role of body composition and metabolic profile in Barrett's oesophagus and progression to cancer.

Simona Di Caro, Wui Hang Cheung, Lucia Fini, Margaret G Keane, Belinda Theis, Rehan Haidry, Laura Di Renzo, Antonino De Lorenzo, Laurence Lovat, Rachel L Batterham and 1 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of gastroenterology & hepatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Signaling pathways and targeted interventions for precancers.Signal transduction and targeted therapy · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. The effects of prehabilitation on body composition in patients undergoing multimodal therapy for esophageal cancer.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2023
    Article
  6. Neutrophil-Lymphocyte Ratio as a Marker of Progression from Non-Dysplastic Barrett's Esophagus to Esophageal Adenocarcinoma: a Cross-Sectional Retrospective Study.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2020
    Article
  7. Article
  8. Predictors of Progression in Barrett's Esophagus.Current treatment options in gastroenterology · 2019
    Review
  9. Review
  10. Observational
  11. Review
  12. Article
  13. Observational
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

11 authors at 3 institutions in 2 countries.

Simona Di CaroDepartments of aGastroenterology bMedicine, Centre for Obesity Research, University College London Hospital, London, UK cDepartment of Gastroenterology, Busto Arstizio Hospital, Milan dDepartment of Neuroscience, Tor Vergata University, Rome, Italy.
Wui Hang Cheung
Lucia Fini
Margaret G Keane
Belinda Theis
Rehan Haidry
Laura Di Renzo
Antonino De Lorenzo
Laurence Lovat
Rachel L Batterham
Matthew Banks
University College London · GBCreative Commons · USBank of England · GB

Funding

Department of Health RP-2015-06-005
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe aim of this study was to evaluate the risk for Barrett's oesophagus (BE) on the basis of body composition, metabolic pathways, adipokines and metabolic syndrome (MS), as well as their role in cancer progression.

methodsIn patients with and without BE at gastroscopy, data on MS, BMI, waist/hip ratio for abdominal obesity (AO) and body fat percentage by bioimpedance were obtained. Fasting plasma glucose, insulin, HbA1c, lipid, serum adiponectin and leptin levels were measured. The homoeostasis model assessment (HOMA-IR) was used to estimate insulin resistance. Histological findings for BE were correlated with the above parameters. Risk factors for BE identified using univariate analysis were entered into a multivariate logistic regression analysis.

resultsA total of 250 patients and 224 controls (F/M: 189/285, mean age 58.08±15.51 years) were enroled. In the BE and control groups, 39.6 versus 31.3% were overweight, 32 versus 22.8% were obese, 75.6 versus 51.3% had AO, and 28.1 versus 18.9% were metabolically obese, respectively. AO [odds ratio (OR) 3.08], increased body fat percentage (OR 2.29), and higher BMI (overweight: OR 2.04; obese: OR 2.26) were significantly associated with BE. A positive trend was found in Normal Weight Obese Syndrome (OR 1.69). MS was associated with BE (overweight: OR 3.05; obese: OR 5.2; AO: OR 8.08). Insulin levels (P=0.05) and HOMA-IR (P<0.001) were higher in BE. AO was the only independent risk factor associated with BE (OR 1.65; P=0.02) and high-grade dysplasia (OR 2.44) on multivariate analysis.

conclusionAO was strongly associated with BE and dysplasia. BE was associated with MS and higher insulin/HOMA-IR, suggesting the activation of specific metabolic pathways in patients with altered body composition.

Indexed as

AdiposityAdenocarcinomaAdipokinesAdultAgedBarrett EsophagusBiomarkersBlood GlucoseBody Mass IndexCase-Control StudiesChi-Square DistributionDisease ProgressionEsophageal NeoplasmsFemaleGastroscopyGlycated HemoglobinAdipokinesBiomarkersBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanInsulinLipids

Identifiers

PMID26671515
PMCPMC4739314
OpenAlexW2212727844

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Registered trials

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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.