ReviewHormones (Athens, Greece)2026
Current management of MASLD in type 2 diabetes.
Review in Hormones (Athens, Greece), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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.
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.
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0 citing papers in PubMed.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Steatotic liver disease encompasses a wide range of disease states, from steatosis to steatohepatitis and ultimately cirrhosis. As these stages progress, several severe hepatic and non-hepatic issues are triggered. Patients with diabetes exhibit accelerated progression through the MASLD spectrum, with increased liver-related mortality. To recognize the close association between MASLD and type 2 diabetes (T2D), it must be understood that lipid and glucose metabolism are closely intertwined. Insulin resistance and obesity are central features of both MASLD and T2D and stem from multifactorial etiologies related to lifestyle, environmental, genetic, and epigenetic factors. Due to the shared physiopathological routes and the higher risk of disease progression attributed to MASLD and T2D, hepatic steatosis should be suspected and screened for in patients with T2D. Once the diagnosis of MASLD is established, lifestyle interventions, with close follow-up and strict metabolic control must be implemented. The presence of clinically significant fibrosis warrants management by an interdisciplinary team, including a gastroenterologist or hepatologist. Current pharmacotherapies that target metabolic dysfunction aim to prevent cardiovascular disease and MASH cirrhosis. This review discusses drugs approved for T2D treatment with liver-related benefits, as well as ongoing research for dual treatment strategies.
Indexed as
Identifiers
41888466What Socratic holds
Registered trials
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.