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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.
Insights
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.
Abstract:
The classic model of Chronic Heart Failure (CHF) is rooted in the overexpression of neurohormonal molecules. To complement this paradigm, increasing evidence indicates that a variety of hormones may be down-regulated in CHF patients. The list includes growth hormone (GH) and its tissue effector insulin-like growth factor-1 (IGF-1). The GH/IGF-1 axis regulates cardiac growth, stimulates myocardial contractility, and influences the vascular system. The relationship between the GH/IGF-1 axis and the cardiovascular system has been extensively demonstrated in numerous studies in animals models and confirmed by the cardiac derangements secondary to both GH excess and deficiency in humans. Impaired activity of the GH/IGF-1 axis in CHF has been described by several independent groups and includes a wide array of abnormalities, including low IGF-1 levels, GH deficiency (GHD), and GH resistance that may be related to the severity of heart disease. According to several observations, these derangements are associated with poor clinical status and outcome. Since the first study of GH therapy in CHF in 1996, several placebo-controlled trials have been conducted with conflicting results. These discordant findings are likely explained by the degree of CHF-associated GH/IGF-1 impairment that may impact on individual responsiveness to GH administration. Biological actions of GH and IGF-1, cardiovascular implication of GH deficiency and GH excess, relation between somatotrophic axis and CHF are discussed. Results from trials of GH therapy, emerging therapeutic strategies, safety issues, and lack in evidence are also reported.
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