ReviewEndocrine2025
Repurposing levothyroxine for managing metabolic dysfunction-associated steatotic liver disease.
Review in Endocrine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Hypothyroidism and Metabolic Dysfunction-Associated Steatotic Liver Disease: Mechanisms, Clinical Links, and Therapeutic Implications.Current obesity reports · 2026Review
Corrections and comments
- Erratum issued
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeMetabolic dysfunction-associated steatotic liver disease (MASLD) is an entity closely linked to obesity and/or insulin resistance, projected to affect about half of the global adult population by 2040. New therapeutic strategies that are both effective and affordable are needed to address this impending public health crisis.
methodsA narrative review was conducted to identify studies supporting the use of levothyroxine and thyroid hormone analogs in treating MASLD and metabolic dysfunction-associated steatohepatitis (MASH).
resultsClinical studies have identified clear pathophysiological links between low (or low-normal) thyroid function and increased risk of hepatic steatosis. Of the two main thyroid hormone receptor (THR) isoforms, THRα and THRβ, the latter primarily mediates the metabolic effects of thyroid hormones in the liver, which could greatly benefit patients with MASLD. Recently, selective analogs of hepatic THRβ receptors have been developed to treat MASLD, with early clinical data demonstrating an effective profile. However, due to the increasing prevalence of MASLD in both developed and developing countries, the high cost of branded drugs may hinder their widespread use.
conclusionsAlthough the development of thyromimetics mainly aims to prevent activation of THRα in other tissues, there is evidence supporting the efficacy and safety of low-dose levothyroxine (LT4) therapy for treating MASLD. This review aims to systematically explore the potential of LT4 therapy as an alternative approach to managing MASLD.
Indexed as
Identifiers
What 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.