Evidence map›Paper›PMID 37607330›Full record

ArticleInflammatory bowel diseases2024

Inflammatory Bowel Disease Is an Independent Risk Factor for Metabolic Dysfunction-Associated Steatotic Liver Disease in Lean Individuals.

Samuel J Martínez-Domínguez, Sandra García-Mateo, Carla J Gargallo-Puyuelo, Beatriz Gallego-Llera, Pilar Callau, Carolina Mendi, María Teresa Arroyo-Villarino, Miguel Ángel Simón-Marco, Javier Ampuero, Fernando Gomollón

Open access · hybridAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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  18. Editorial: New Perspectives on Hepatic Steatosis.Journal of clinical and experimental hepatology
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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 3 institutions in 1 country.

Samuel J Martínez-DomínguezDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.ORCID 0000-0003-0857-8117
Sandra García-MateoDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.
Carla J Gargallo-PuyueloDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.
Beatriz Gallego-LleraDigestive Pathology Translational Research Group, Aragón Health Research Institute, Zaragoza, Spain.
Pilar CallauPrimary care center Delicias Sur, Zaragoza, Spain.
Carolina MendiPrimary care center Universitas, Zaragoza, Spain.
María Teresa Arroyo-VillarinoDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.
Miguel Ángel Simón-MarcoDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.
Javier AmpueroDepartment of Digestive Diseases, Virgen del Rocío University Hospital, Sevilla, Spain.
Fernando GomollónDepartment of Gastroenterology, Lozano Blesa University Hospital, Zaragoza, Spain.
Universidad de Zaragoza · ESCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESInstituto de Investigación Sanitaria Aragón · ES

Funding

Diputación General de Aragón DGACOVID-02
6 · The paper itself

Abstract

backgroundDespite classical association between metabolic dysfunction-associated steatotic liver disease (MASLD) and obesity, there is increasing evidence on the development of MASLD in lean individuals. The aim of the study was to assess the prevalence and risk factors of MASLD and significant liver fibrosis in lean participants with inflammatory bowel disease (IBD).

methodsThis was a cross-sectional, case-control study including 300 lean cases with IBD and 80 lean controls without IBD, matched by sex and age. All participants underwent a liver ultrasound, transient elastography, and laboratory tests.

resultsThe lean IBD group showed a significantly higher prevalence of MASLD compared with lean non-IBD group (21.3% vs 10%; P = .022), but no differences were observed in the prevalence of significant liver fibrosis (4.7% vs 0.0%; P = 1.000). No differences were found between the prevalence of MASLD in IBD and non-IBD participants who were overweight/obese (66.8% vs 70.8%; P = .442). In addition, the prevalence of MASLD was significantly higher in the overweight/obese IBD group compared with the lean IBD group (P < .001). IBD was an independent risk factor for MASLD in lean participants (odds ratio [OR], 2.71; 95% confidence interval [CI], 1.05-7.01; P = .04), after adjusting for classic metabolic risk factors and prior history of systemic steroid use. Nevertheless, no association between IBD related factors and MASLD was identified in lean IBD participants. When the overweight/obese and lean IBD groups with MASLD were compared, the overweight/obese IBD group with MASLD showed higher levels of the homeostatic model assessment of insulin resistance (OR, 1.49; 95% CI, 1.11-1.98; P = .007) and history of smoking (OR, 4.66; 95% CI, 1.17-18.49; P = .029).

conclusionsMASLD prevalence was higher in the lean IBD group compared with lean non-IBD group, independent of classic metabolic risk factors.

Indexed as

Inflammatory Bowel DiseasesAdultBody Mass IndexCase-Control StudiesCross-Sectional StudiesFemaleHumansLiver CirrhosisMaleMiddle AgedNon-alcoholic Fatty Liver DiseaseObesityPrevalenceRisk FactorsThinnessCrohn’s diseaseinflammatory bowel diseaselean MASLDliver fibrosisulcerative colitis

Identifiers

PMID37607330
PMCPMC11291618
OpenAlexW4386054741

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.