Evidence map›Paper›PMID 40323353›Full record

ArticleCanadian journal of public health = Revue canadienne de sante publique2026

Sex differences in the prevalence and cardiometabolic risk profiles of steatotic liver disease: A Canadian Longitudinal Study on Aging analysis.

Jessica Burnside, Felice Cinque, Giada Sebastiani, Alnoor Ramji, Keyur Patel, Mark Swain, Sahar Saeed

Abstract read
In one paragraph

Article in Canadian journal of public health = Revue canadienne de sante publique, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Time-Varying Impact of Steatosis and Alcohol on Mortality: A Marginal Structural Model of the Canadian Longitudinal Study on Aging.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  3. Association of Systemic Inflammatory Indices with Metabolic Dysfunction-Associated Steatotic Liver Disease and Liver Fibrosis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Sex Hormones and Metabolic Dysfunction-Associated Steatotic Liver Disease.International journal of molecular sciences · 2025
    Review
  8. Article
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

7 authors.

Jessica BurnsidePublic Health Sciences, Queen's University, Kingston, ON, Canada.
Felice CinqueMcGill University Health Centre, Montreal, QC, Canada.
Giada SebastianiMcGill University Health Centre, Montreal, QC, Canada.
Alnoor RamjiDivision of Gastroenterology, University of British Columbia, Vancouver, BC, Canada.
Keyur PatelDivision of Gastroenterology and Hepatology, University Health Network Toronto, Toronto, ON, Canada.
Mark SwainCalgary Liver Unit, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Sahar SaeedPublic Health Sciences, Queen's University, Kingston, ON, Canada. sahar.saeed@queensu.ca.ORCID http://orcid.org/0000-0002-0224-379X

Funding

Cal Wenzel Family Foundation Endowed Chair in HepatologyFonds de Recherche du Québec - Santé 296306Government of Ontario Ontario Graduate ScholarshipQueen's University (CA) Research Initiation Grant
6 · The paper itself

Abstract

objectiveSteatotic liver disease (SLD) is absent from global public health agendas. Our study is the first to comprehensively examine SLD prevalence in Canada, focusing on sex differences.

methodsWe used data from the Canadian Longitudinal Study on Aging between 2012 and 2018. Steatosis was identified using the validated NAFLD Ridge Score. Using the most recent diagnostic criteria, we defined metabolic (dysfunction)-associated steatotic liver disease (MASLD), metabolic dysfunction-associated alcohol-associated liver disease (MetALD), and alcohol-associated liver disease (ALD) and estimated prevalences by sociodemographic factors. Survey-weighted adjusted prevalence ratios (aPR) for MASLD (sex-stratified) and MetALD were estimated using Poisson regression with robust standard errors.

resultsA total of 24,888 people (51.4% female; median age 58 years) were included. The most common subtype of SLD was MASLD, 35% (95%CI, 34-36), followed by MetALD 2.6% (2.3-2.9), and ALD 0.8% (0.6-1.0). Overall, the prevalences for MASLD and MetALD were significantly higher among males at 46% (45-48) and 3.7% (3.2-4.2) compared to females at 24% (23-26) and 1.6% (1.2‒2.1), respectively. Lower household incomes were associated with higher MASLD prevalence in females (aPR, 2.9, 2.4-3.5) and males (aPR, 1.1, 1.0-1.3). Multimorbidity was high among the MASLD group; 31 unique MASLD phenotypes based on cardiometabolic characteristics were identified. Females with MASLD were also more likely to have more cardiometabolic conditions compared to males with MASLD.

conclusionIn this large Canadian cohort, we found significant sex differences in SLD burden and cardiometabolic features. Epidemiological assessments are necessary to improve preparedness for the significant projected increase in advanced liver disease.

Indexed as

AgingCardiometabolic Risk FactorsFatty LiverAdultAgedCanadaFemaleHumansLongitudinal StudiesMaleMiddle AgedPrevalenceSex FactorsCLSAGenderMASLDMetALDPrevalenceSex

Identifiers

PMID40323353
PMCPMC13001155

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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.