Evidence map›Paper›PMID 17786437›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2008

High and typical 18F-FDG bowel uptake in patients treated with metformin.

Eric Gontier, Emmanuelle Fourme, Myriam Wartski, Cyrille Blondet, Gerald Bonardel, Elise Le Stanc, Marina Mantzarides, Herve Foehrenbach, Alain-Paul Pecking, Jean-Louis Alberini

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in European journal of nuclear medicine and molecular imaging, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 4 pooled it
2.0field-weighted citation impact, top 14% 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

77 citing papers in PubMed, 4 syntheses or guidelines pooled it, 192 citations in OpenAlex.

  1. Pooled it
  2. EANM/SNMMI guideline/procedure standard for [European journal of nuclear medicine and molecular imaging · 2025
    Guideline
  3. Pooled it
  4. Risk of fatal and nonfatal lactic acidosis with metformin use in type 2 diabetes mellitus.The Cochrane database of systematic reviews · 2010 · on this map
    Pooled it
  5. Trial
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  11. Impact of biguanide therapy on hepaticAnnals of nuclear medicine · 2026
    Article
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  14. Review
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  17. Multi-Organ metabolic profiling with [European journal of nuclear medicine and molecular imaging · 2025
    Article
  18. Article
  19. Article
  20. [Classical Sweet syndrome with multiple organ lesions byBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article

17 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 1 country.

Eric GontierDepartment of Nuclear Medicine, Military Hospital Val-de-Grâce, 74, Bd de Port Royal, 75230, Paris, cedex 05, France. gontierweb@hotmail.fr
Emmanuelle Fourme
Myriam Wartski
Cyrille Blondet
Gerald Bonardel
Elise Le Stanc
Marina Mantzarides
Herve Foehrenbach
Alain-Paul Pecking
Jean-Louis Alberini
HIA du Val-de-Grâce à Paris · FRHôpital René Huguenin · FRHôpital Foch · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis prospective and bi-centric study was conducted in order to determine the impact of antidiabetic treatments (AD) on (18)F-FDG bowel uptake in type 2 diabetic patients.

methodsFifty-five patients with previously diagnosed and treated type 2 diabetes mellitus (group 1) were divided in two subgroups: AD treatment including metformin (n=32; group 1a) and AD treatment excluding metformin (n=23; group 1b). The 95 patients without diabetes mellitus made up controls (group 2). (18)F-FDG uptake in small intestine and colon was visually graded and semi-quantitatively measured using the maximum standardized uptake value.

results(18)F-FDG bowel uptake was significantly increased in AD patients (group 1) as compared to controls (group 2) (p<0.001). Bowel uptake was significantly higher in AD patients including metformin (group 1a) as compared to AD patients excluding metformin (group 1b) (p<0.01), whose bowel uptake was not significantly different from controls (group 2). A metformin treatment was predictive of an increased bowel uptake in the small intestine (odds ratio OR=16.9, p<0.0001) and in the colon (OR=95.3, p<0.0001), independently of the other factors considered in the multivariate analysis. Bowel uptake pattern in the patients treated with metformin was typically intense, diffuse and continuous along the bowel, strongly predominant in the colon, in both the digestive wall and lumen.

conclusionThis study emphasizes that metformin significantly increases (18)F-FDG uptake in colon and, to a lesser extent, in small intestine. It raises the question of stopping metformin treatment before an (18)F-FDG PET/CT scan is performed for intra-abdominal neoplasic lesion assessment.

Indexed as

Case-Control StudiesColonDiabetes Mellitus, Type 2Fluorodeoxyglucose F18HumansHypoglycemic AgentsIntestinal MucosaIntestinesIntestine, SmallMetforminTissue DistributionFluorodeoxyglucose F18Hypoglycemic AgentsMetformin

Identifiers

PMID17786437
OpenAlexW2037851717

What OpenQuestion holds

Texttitle and abstract
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.