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Updated: Jul 4, 2026

Optimized Analysis of In Vivo and In Vitro Hepatic Steatosis
Published on: March 11, 2017
Dysregulated growth hormone-insulin-like growth factor-1 axis in adults with metabolic dysfunction-associated
Dario Messetti1, Alessandro Mantovani1, Riccardo Morandin1
1Department of Medicine, University of Verona, Verona, Italy; Metabolic Diseases Research Unit, IRCCS Sacro Cuore - Don Calabria Hospital, Negrar di Valpolicella, Italy.
Aim:
A dysregulated growth hormone (GH)-insulin-like growth factor-1 (IGF-1) axis may contribute to the development and progression of metabolic dysfunction-associated steatotic liver disease (MASLD). However, the available evidence remains inconsistent.
Data Synthesis:
We systematically searched PubMed and Scopus from database inception through 31 January 2026 to identify eligible observational studies assessing the association between circulating GH and IGF-1 levels and MASLD (diagnosed by liver biopsy or imaging). The primary outcome was the difference in circulating GH and IGF-1 levels between adults (age >18 years) with and without MASLD. Effect sizes were expressed as weighted mean differences (WMDs) with 95% confidence intervals (95%CI). A total of 18 observational studies were included. Fourteen studies (13,112 participants) measured circulating IGF-1 levels, five studies (7500 participants) measured circulating GH levels, and one study assessed both hormones. Individuals with MASLD had significantly lower circulating GH (random-effects WMD: -0.34 ng/ml; 95%CI, -0.61 to -0.07; I2 = 81.5%) and IGF-1 (random-effects WMD: -24.85 ng/ml; 95%CI, -37.88 to -11.81; I2 = 94.8%) levels than controls. Circulating IGF-1 levels were also lower in individuals with biopsy-confirmed metabolic dysfunction-associated steatohepatitis or advanced liver fibrosis (F2-F4 stages). Sensitivity analyses did not substantially alter these findings.
Conclusion:
Circulating GH and IGF-1 levels are inversely associated with the presence and severity of MASLD. Further studies are needed to better understand the complex but existing link between a dysregulated (suppressed) GH-IGF-1 axis and MASLD.
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