Evidence map›Paper›PMID 34730107›Full record

ArticleGut and liver2022

Metabolic Dysfunction-Associated Fatty Liver Disease Better Predicts Incident Cardiovascular Disease.

Seogsong Jeong, Yun Hwan Oh, Seulggie Choi, Jooyoung Chang, Sung Min Kim, Joung Sik Son, Gyeongsil Lee, Won Kim, Sang Min Park

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Seogsong JeongDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul, Korea.ORCID 0000-0003-4646-8998
Yun Hwan OhDepartment of Family Medicine, Jeju National University School of Medicine, Jeju, Korea.ORCID 0000-0002-1627-7528
Seulggie ChoiDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul, Korea.ORCID 0000-0002-0581-165X
Jooyoung ChangDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul, Korea.ORCID 0000-0002-8586-0645
Sung Min KimDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul, Korea.ORCID 0000-0002-1957-2186
Joung Sik SonDepartment of Family Medicine, Korea University Guro Hospital, Seoul, Korea.ORCID 0000-0003-2460-3378
Gyeongsil LeeDepartment of Family Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0003-1910-9658
Won KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea.ORCID 0000-0002-2926-1007
Sang Min ParkDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul, Korea.ORCID 0000-0002-7498-4829
Seoul National University · KRJeju National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Metabolic dysfunction (MD)-associated fatty liver disease is a new positive diagnostic criterion based on hepatic steatosis and MD. However, a comprehensive evaluation on the association of MD and hepatic steatosis with incident cardiovascular disease (CVD) has yet to be performed. Methods: This retrospective cohort study included 333,389 participants from the Korean National Health Insurance Service database who received a health examination between 2009 and 2010. Hepatic steatosis was defined using the Korean National Health and Nutrition Examination Survey-derived nonalcoholic fatty liver disease scoring system. Cox proportional hazards regression was adopted to determine the adjusted hazard ratio (aHR) with 95% confidence interval (CI) for CVD according to the presence of hepatic steatosis and MD, as well as the composite term. Results: This study included 179,437 men and 153,952 women with a median age of 57 years. Hepatic steatosis with MD (aHR, 2.00; 95% CI, 1.89 to 2.13) and without MD (aHR, 1.30; 95% CI, 1.10 to 1.54) significantly increased the risk of CVD compared to no steatosis without MD (reference). However, steatosis revealed no significant difference in the risk of CVD compared to no steatosis among participants with one MD (aHR, 1.09; 95% CI, 0.91 to 1.30). In participants with steatosis, the presence of one and ≥2 MDs had aHR values of 1.25 (95% CI, 0.87 to 1.79) and 1.71 (95% CI, 1.22 to 2.41), respectively, compared to no MD. Conclusions: Combined consideration of hepatic steatosis and MD was significantly associated with increased CVD risk and showed better predictive performance for CVD than hepatic steatosis or MD alone.

Indexed as

Cardiovascular DiseasesNon-alcoholic Fatty Liver DiseaseFemaleHumansMaleMiddle AgedNutrition SurveysRetrospective StudiesRisk FactorsCardiometabolic risk factorsCardiovascular diseasesFatty liverLiver diseases

Identifiers

PMID34730107
PMCPMC9289825
OpenAlexW3209772013

What OpenQuestion holds

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LicenceCC BY-NC
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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.