Evidence map›Paper›PMID 39607105›Full record

ArticleCadernos de saude publica2024

Comparing diabetes prediction based on metabolic dysfunction-associated steatotic liver disease and nonalcoholic fatty liver disease: the ELSA-Brasil study.

Gabriela Wünsch Lopes, Scheine Leite Canhada, Rodrigo Citton Padilha Dos Reis, Maria de Fátima Haueisen Sander Diniz, Alessandra Carvalho Goulart, Luciana Costa Faria, Rosane Harter Griep, Hugo Perazzo, Bruce Bartholow Duncan, Maria Inês Schmidt

Abstract readComparative Study
In one paragraph

Article in Cadernos de saude publica, 2024. 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. Review
  3. 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

10 authors.

Gabriela Wünsch LopesPrograma de Pós-graduação em Epidemiologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brasil.ORCID 0000-0002-6862-0914
Scheine Leite CanhadaPrograma de Pós-graduação em Epidemiologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brasil.ORCID 0000-0002-4324-9848
Rodrigo Citton Padilha Dos ReisPrograma de Pós-graduação em Epidemiologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brasil.ORCID 0000-0003-1766-0964
Maria de Fátima Haueisen Sander DinizFaculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brasil.ORCID 0000-0001-9146-5003
Alessandra Carvalho GoulartHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brasil.ORCID 0000-0003-1076-5210
Luciana Costa FariaFaculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brasil.ORCID 0000-0002-0226-3491
Rosane Harter GriepInstituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.ORCID 0000-0002-6250-2036
Hugo PerazzoInstituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.ORCID 0000-0003-0931-6418
Bruce Bartholow DuncanPrograma de Pós-graduação em Epidemiologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brasil.ORCID 0000-0002-7491-2630
Maria Inês SchmidtPrograma de Pós-graduação em Epidemiologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brasil.ORCID 0000-0002-3837-0731

Funding

Research Support, Non-US Gov’t
6 · The paper itself

Abstract

We aimed to compare nonalcoholic fatty liver disease (NAFLD) and metabolic dysfunction-associated steatotic liver disease (MASLD) definitions concerning diabetes prediction in a large sample of Brazilian adults. As a secondary objective, we compared associations between NAFLD/MASLD and diabetes across self-declared race/skin color groups. The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil) is a prospective cohort study of Brazilian civil servants (35-74 years) enrolled from 2008 to 2010 and followed up from 2012-2014 and 2017-2019. We ascertained type 2 diabetes mellitus at baseline as well as follow-up visits based on self-reported diagnosis, medication use, and glycemic tests (fasting and 2h post-OGTT glucose and HbA1c). We excluded individuals with heavy alcohol consumption or self-reported cirrhosis/hepatitis. We analyzed 7,073 subjects. NAFLD was defined by ultrasound-based steatosis. Participants with steatosis and at least one cardiometabolic factor were considered as having MASLD. Cox proportional hazards models were performed to evaluate the association between NAFLD/MASLD and the incidence of type 2 diabetes mellitus. At baseline, 33.9% of individuals presented NAFLD and 32.5% presented MASLD. Over 9.4 years of follow-up, the relative increase in the incidence of diabetes was 78% for NAFLD (HR = 1.78; 95%CI: 1.58-2.01) and 88% for MASLD (HR = 1.88; 95%CI: 1.67-2.12). Associations did not differ significantly among race/skin color groups (p for interaction = 0.10 for MASLD and 0.08 for NAFLD). In this large cohort of middle-aged and older Brazilian adults, the relative incidence of diabetes was similar for NAFLD and MASLD definitions, with similar associations in all ethnic groups.

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseAdultAgedBrazilFemaleHumansIncidenceLongitudinal StudiesMaleMiddle AgedProspective StudiesRisk Factors

Identifiers

PMID39607105
PMCPMC11654101

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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.