Evidence map›Paper›PMID 39449183›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2024

Type 2 Diabetes Subtypes and Their Role in Metabolic Liver Disease and Fibrosis Progression.

Froylan David Martínez-Sánchez, David Medina-Julio, Jacqueline Córdova-Gallardo, Maria Juliana Corredor Nassar, Nahum Méndez-Sánchez

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 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.

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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

5 authors.

Froylan David Martínez-SánchezFaculty of Medicine, National Autonomous University of Mexico, Copilco University, Mexico City, Mexico.ORCID 0000-0002-2719-1105
David Medina-JulioFaculty of Medicine, National Autonomous University of Mexico, Copilco University, Mexico City, Mexico.ORCID 0000-0002-3654-7521
Jacqueline Córdova-GallardoFaculty of Medicine, National Autonomous University of Mexico, Copilco University, Mexico City, Mexico.ORCID 0000-0002-4299-5400
Maria Juliana Corredor NassarDepartment of Internal Medicine, Hospital General "Dr. Manuel Gea González", Mexico City, Mexico.ORCID 0000-0002-1279-1618
Nahum Méndez-SánchezFaculty of Medicine, National Autonomous University of Mexico, Copilco University, Mexico City, Mexico.ORCID 0000-0001-5257-8048

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The relationship between different subgroups of type 2 diabetes (T2D) and the progression of metabolic dysfunction-associated steatotic liver disease (MASLD) and liver fibrosis has not been thoroughly studied. This study aims to determine the association between T2D subgroups and the risk of developing advanced liver fibrosis using the Fibrosis-4 (FIB-4) index, a non-invasive marker for assessing liver fibrosis risk. MATERIAL AND METHODS A total of 1205 patients with T2D were categorized into 4 distinct subgroups: severe insulin-deficient diabetes (SIDD), severe insulin-resistant diabetes (SIRD), mild obesity-related diabetes (MOD), and mild age-related diabetes (MARD). The FIB-4 index was calculated for each patient to estimate the degree of liver fibrosis, with the following cutoff points: <1.3 indicating no or mild fibrosis, 1.3-2.67 suggesting moderate fibrosis, and >2.67 indicating advanced fibrosis (F3-F4). Logistic regression was used to compare the odds of advanced fibrosis across these subgroups. RESULTS The SIRD subgroup exhibited significantly higher odds of advanced liver fibrosis (F3-F4), compared with the other subgroups, as indicated by elevated FIB-4 scores (P<0.05). In contrast, the SIDD and MOD subgroups had lower odds of advanced fibrosis, while the MARD subgroup showed an intermediate association. CONCLUSIONS The findings suggest that the FIB-4 index, as a noninvasive assessment tool, effectively stratifies liver fibrosis risk among different T2D subgroups. This stratification can inform more personalized management strategies for patients with MASLD, underscoring the importance of accounting for the heterogeneity within T2D in clinical assessments of liver fibrosis risk.

Indexed as

Diabetes Mellitus, Type 2Disease ProgressionLiver CirrhosisAdultAgedBiomarkersFemaleHumansInsulin ResistanceMaleMiddle AgedObesityRisk FactorsBiomarkers

Identifiers

PMID39449183
PMCPMC11520462

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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.