Evidence mapPaperPMID 41220583Full record

ReviewFrontiers in endocrinology2025

Metabolic dysfunction associated fatty liver disease and type 2 diabetes: pathophysiological links, epidemiological trends, and clinical implications.

Mohammad Sarif Mohiuddin, Noushin Tabassum Neha, Jawad Ul Karim Mahir, Fardin Al Fahad Shakib, Md Ashraful Alam, Md Wahiduzzaman, Rashu Barua, Shakila Jahan Shimu, Mahbubur Rahman, Md Rafin Hossain and 3 more

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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

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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

13 authors.

Mohammad Sarif MohiuddinDepartment of Foundations of Medicine, New York University Grossman Long Island School of Medicine, Mineola, NY, United States.
Noushin Tabassum NehaDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Jawad Ul Karim MahirDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Fardin Al Fahad ShakibDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Md Ashraful AlamDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Md WahiduzzamanDepartment of Foundations of Medicine, New York University Grossman Long Island School of Medicine, Mineola, NY, United States.
Rashu BaruaDepartment of Foundations of Medicine, New York University Grossman Long Island School of Medicine, Mineola, NY, United States.
Shakila Jahan ShimuDepartment of Health Informatics, Harrisburg University of Science and Technology, Harrisburg, PA, United States.
Mahbubur RahmanDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Md Rafin HossainDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Mohammad Hossain ShariareDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Mohammad Mohabbulla MohibDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Mohammad Borhan UddinDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty liver disease (NAFLD), has recently been recognized as a public health issue because it is closely linked to metabolic disorders, including type 2 diabetes mellitus (T2DM). This review aims to discuss the bidirectional relationship between MASLD and T2DM and the similarities in their pathophysiology, which include insulin resistance (IR), lipogenesis, inflammation, and alterations in the gut microbiota. The incidence of MASLD has increased concomitantly with the obesity and diabetes pandemic, and more than 60% of individuals with T2DM have liver steatosis. The metabolic dysfunction is followed by adipokines, inflammatory mediators like TNF-α, IL-6, and oxidative stress, which worsen NAFLD and lead to T2DM. Since MASLD is usually asymptomatic in its early stages, it is important to screen high-risk populations such as obese and metabolic syndrome patients to enable them to start treatment early. Lifestyle changes, including changes in diet, weight loss, and increased physical activity, are currently the mainstay of treatment for MASLD; however, the potential of new pharmacological approaches that act on insulin signaling, hepatic lipid metabolism, and inflammation to improve treatment is encouraging. Although the role of MASLD in the pathogenesis of T2DM has been well-documented, there are issues with standardizing the diagnostic criteria and the availability of effective treatments. This is because the multidisciplinary management of metabolic diseases needs hepatology, endocrinology, and public health measures to prevent a global epidemic. More studies are required to fully understand the underlying molecular mechanisms of MASLD-T2DM and search for specific treatment for high-risk patients.

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseAnimalsHumansInsulin ResistanceObesityadipokineshepatic steatosisinflammationinsulin resistance (IR)lipotoxicitymetabolic dysfunction-associated fatty liver disease (MASLD)non-alcoholic fatty liver disease (NAFLD)type 2 diabetes mellitus (T2DM)

Identifiers

PMID41220583
PMCPMC12597808

What Socratic holds

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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.