Evidence map›Paper›PMID 39008030›Full record

ArticleHepatology international2024

NAFLD and MAFLD independently increase the risk of major adverse cardiovascular events (MACE): a 20-year longitudinal follow-up study from regional Australia.

Karl Vaz, William Kemp, Ammar Majeed, John Lubel, Dianna J Magliano, Kristen M Glenister, Lisa Bourke, David Simmons, Stuart K Roberts

Abstract read
In one paragraph

Article in Hepatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

9 authors.

Karl VazDepartment of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre 55 Commercial Road, VIC 3004, Melbourne, Australia. k.vaz@alfred.org.au.ORCID http://orcid.org/0000-0002-6427-6140
William KempDepartment of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre 55 Commercial Road, VIC 3004, Melbourne, Australia.
Ammar MajeedDepartment of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre 55 Commercial Road, VIC 3004, Melbourne, Australia.
John LubelDepartment of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre 55 Commercial Road, VIC 3004, Melbourne, Australia.
Dianna J MaglianoDiabetes and Population Health, Baker Heart and Diabetes Institute, Melbourne, Australia.
Kristen M GlenisterDepartment of Rural Health, University of Melbourne, Melbourne, Australia.
Lisa BourkeDepartment of Rural Health, University of Melbourne, Melbourne, Australia.
David Simmons *Department of Rural Health, University of Melbourne, Melbourne, Australia.
Stuart K Roberts *Department of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre 55 Commercial Road, VIC 3004, Melbourne, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe association between fatty liver disease (FLD) and cardiovascular disease (CVD) in an Australian context has yet to be defined. The primary aim of this study was to investigate the association between FLD and 3-point major adverse cardiovascular events (MACE).

methodsThis was a longitudinal follow-up study of a randomly sampled adult cohort from regional Australia between 2001 and 2003. Baseline covariates included demographic details, anthropometry, health and lifestyle data, and laboratory tests. Non-alcoholic fatty liver disease (NAFLD) and metabolic-(dysfunction) associated fatty liver disease (MAFLD) were diagnosed in participants with fatty liver index (FLI) ≥ 60 and meeting other standard criteria. ICD-10 codes were used to define clinical outcomes linked to hospitalisations. Three-point MACE defined as non-fatal myocardial infarction (MI) and cerebrovascular accident (CVA) and CVD death.

resultsIn total, 1324 and 1444 participants met inclusion criteria for NAFLD and MAFLD analysis, respectively. Over 23,577 and 25,469 person-years follow-up, NAFLD and MAFLD were independent predictors for 3-point MACE, adjusting for demographic covariates and known cardiometabolic risk factors, whilst considering non-CVD death as a competing event (NAFLD: sub-hazard ratio [sHR] 1.56, 95% confidence interval [CI 1.12-2.19]; MAFLD: sHR 1.51, 95% CI 1.11-2.06). The results held true on several sensitivity analyses.

conclusionsBoth forms of FLD increase the risk for CVD independent of traditional cardiometabolic risk factors.

Indexed as

Cardiovascular DiseasesNon-alcoholic Fatty Liver DiseaseAdultAgedAustraliaFatty LiverFemaleFollow-Up StudiesHumansLongitudinal StudiesMaleMiddle AgedRisk FactorsAtrial fibrillationCardiovascular diseaseMACEMAFLDNAFLD

Identifiers

PMID39008030
PMCPMC11297804

What Socratic 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 Socratic graph.