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Published on: June 3, 2018
The GH/IGF-1 axis in chronic heart failure
Michele Arcopinto1, Emanuele Bobbio, Eduardo Bossone
1Department of Internal Medicine, Cardiovascular Sciences and Clinical Immunology, University Federico II, Naples, Italy.
Growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels are often low in Chronic Heart Failure (CHF). GH therapy shows mixed results, possibly due to varying impairment levels in patients.
Area of Science:
- Endocrinology
- Cardiology
- Metabolic Research
Background:
- Chronic Heart Failure (CHF) is traditionally linked to neurohormonal overactivity.
- Emerging evidence suggests hormone down-regulation, including the Growth Hormone (GH)/Insulin-like Growth Factor-1 (IGF-1) axis, in CHF patients.
- The GH/IGF-1 axis is crucial for cardiac growth, contractility, and vascular function.
Purpose of the Study:
- To discuss the biological actions of GH and IGF-1.
- To explore the cardiovascular implications of GH deficiency and excess.
- To examine the relationship between the somatotrophic axis and CHF, including therapeutic strategies and evidence gaps.
Main Methods:
- Review of existing literature on the GH/IGF-1 axis in cardiovascular health and CHF.
- Analysis of findings from placebo-controlled trials investigating GH therapy in CHF patients.
- Discussion of factors influencing individual responsiveness to GH therapy.
Main Results:
- Impaired GH/IGF-1 axis activity, characterized by low IGF-1, GH deficiency (GHD), and GH resistance, is frequently observed in CHF.
- These abnormalities correlate with disease severity, poor clinical status, and adverse outcomes.
- Clinical trials of GH therapy in CHF have yielded conflicting results, suggesting that the degree of GH/IGF-1 impairment influences treatment efficacy.
Conclusions:
- The GH/IGF-1 axis plays a significant role in cardiovascular regulation and is dysregulated in CHF.
- GH therapy's effectiveness in CHF is variable and may depend on the specific profile of GH/IGF-1 axis impairment.
- Further research is needed to clarify therapeutic strategies, safety, and optimal patient selection for GH-based interventions in CHF.
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