Dysregulated growth hormone-insulin-like growth factor-1 axis in adults with metabolic dysfunction-associated steatotic liver disease: a meta-analysis.

Nutr Metab Cardiovasc DisJun 24, 2026 (epub)

Dario Messetti, Alessandro Mantovani, Riccardo Morandin et al.

✦ AI-curated · Sources linked

In 30 seconds

This systematic review and meta-analysis examined observational evidence on circulating growth hormone (GH) and insulin-like growth factor-1 (IGF-1) in adults with and without metabolic dysfunction-associated steatotic liver disease (MASLD). Across 18 studies, MASLD was associated with lower levels of both hormones than in controls: GH weighted mean difference (WMD) −0.34 ng/ml (95% CI, −0.61 to −0.07) and IGF-1 WMD −24.85 ng/ml (95% CI, −37.88 to −11.81). IGF-1 was also lower with biopsy-confirmed steatohepatitis or advanced fibrosis. These observational findings indicate association, not causation.

Key findings

  • Across five studies measuring GH, MASLD was associated with lower levels than controls (WMD: −0.34 ng/ml; 95% CI, −0.61 to −0.07; I² = 81.5%).
  • Across 14 studies measuring IGF-1, levels were lower in MASLD (WMD: −24.85 ng/ml; 95% CI, −37.88 to −11.81; I² = 94.8%).
  • IGF-1 levels were also lower in participants with biopsy-confirmed steatohepatitis or advanced liver fibrosis (F2–F4).

Why it matters

The findings link a suppressed GH–IGF-1 axis with MASLD presence and, for IGF-1, with more severe liver disease. This may help frame questions about endocrine and metabolic features accompanying MASLD, while the substantial between-study heterogeneity and observational evidence mean the results do not establish whether hormonal changes contribute to disease or result from it.

What to keep in mind

The evidence is observational, and heterogeneity was high for both GH and IGF-1 estimates (I² = 81.5% and 94.8%, respectively), limiting causal interpretation and consistency.

Source

Published in Nutr Metab Cardiovasc Dis. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Gastroenterology

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.