Evidence map›Paper›PMID 36846097›Full record

ArticleCrohn's & colitis 3602023

Nonalcoholic Fatty Liver Disease Increases Cardiovascular Risk in Inflammatory Bowel Diseases.

Dana Kablawi, Faisal Aljohani, Chiara Saroli Palumbo, Sophie Restellini, Alain Bitton, Gary Wild, Waqqas Afif, Peter L Lakatos, Talat Bessissow, Giada Sebastiani

Abstract read
In one paragraph

Article in Crohn's & colitis 360, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Observational
  3. Review
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.

Dana KablawiDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Faisal AljohaniDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Chiara Saroli PalumboDivision of Gastroenterology, Jewish General Hospital, Montreal, Quebec, Canada.
Sophie RestelliniGastroenterology Department, University Hospital of Geneva, Geneva, Switzerland.
Alain BittonDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Gary WildDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Waqqas AfifDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Peter L LakatosDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.
Talat BessissowDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0003-2610-1910
Giada SebastianiDivision of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0003-2655-8283

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nonalcoholic fatty liver disease (NAFLD) is strongly associated with cardiovascular disease in the general population. Both conditions seem more frequent in patients with inflammatory bowel disease (IBD). We aimed to assess the effect of NAFLD and liver fibrosis on intermediate-high cardiovascular risk in IBD. Methods: We prospectively included IBD patients undergoing a routine screening program for NAFLD by transient elastography (TE) with associated controlled attenuation parameter (CAP). NAFLD and significant liver fibrosis were defined as CAP ≥275 dB m Results: Of 405 patients with IBD included, 278 (68.6%), 23 (5.7%), 47 (11.6%), and 57 (14.1%) were categorized as at low, borderline, intermediate, and high ASCVD risk, respectively. NAFLD and significant liver fibrosis were found in 129 (31.9%) and 35 (8.6%) patients, respectively. After adjusting for disease activity, significant liver fibrosis and body mass index, predictors of intermediate-high ASCVD risk were NAFLD (adjusted odds ratio [aOR] 2.97, 95% CI, 1.56-5.68), IBD duration (aOR 1.55 per 10 years, 95% CI, 1.22-1.97), and ulcerative colitis (aOR 2.32, 95% CI, 1.35-3.98). Conclusions: Assessment of cardiovascular risk should be targeted in IBD patients with NAFLD, particularly if they have longer IBD duration and ulcerative colitis.

Indexed as

atherosclerotic cardiovascular disease riskcontrolled attenuation parameterIBD durationtransient elastographyulcerative colitis

Identifiers

PMID36846097
PMCPMC9951742

What OpenQuestion holds

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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.