Growth Hormone Replacement Therapy in Heart Failure With Reduced Ejection Fraction: A Randomized, Double-Blind,

Alberto Maria Marra1, Roberta D'Assante2, Mariarosaria De Luca3

  • 1Department of Translational Medical Sciences, "Federico II" University, Naples, Italy; Interdepartmental Center for Gender Medicine Research "GENESIS," Federico II University, Naples, Italy.

JACC. Heart Failure
|March 6, 2025
PubMed

Insights

Growth hormone (GH) replacement therapy significantly improved exercise capacity and cardiac function in patients with heart failure and reduced ejection fraction (HFrEF) who also had GH deficiency (GHD). This treatment enhanced quality of life and clinical status in these patients.

Area of Science:

  • Cardiology
  • Endocrinology
  • Exercise Physiology

Background:

  • Reduced activity of the growth hormone (GH)/insulin-like growth factor (IGF)-1 axis is common in heart failure (HF) and linked to poor outcomes.
  • Preliminary studies suggest GH replacement may improve quality of life, cardiac function, and cardiovascular performance in HF patients.

Purpose of the Study:

  • To evaluate the cardiovascular effects of 1-year GH replacement therapy in patients with heart failure and reduced ejection fraction (HFrEF) and concomitant GH deficiency (GHD).

Main Methods:

  • A double-blind, randomized, placebo-controlled trial involving HFrEF patients (NYHA class I/II/III) with GHD.
  • Patients received either GH or placebo for 1 year, alongside standard background therapy.
  • Primary endpoint was peak oxygen consumption (VO2); secondary endpoints included hospitalizations, cardiac volumes, NT-proBNP, quality of life, and muscle strength.

Main Results:

  • GH therapy significantly improved peak VO2 (P < 0.01) and other cardiopulmonary exercise parameters (P < 0.05).
  • Improvements were observed in 6-minute walking distance (P < 0.05), handgrip strength (P < 0.01), and right ventricular function (P < 0.01).
  • GH treatment led to amelioration of clinical status (NYHA class, P < 0.05), improved quality of life (P < 0.05), and reduced NT-proBNP levels (P < 0.05).

Conclusions:

  • GH replacement therapy is effective in improving exercise performance in HFrEF patients with GHD.
  • The therapy enhances both left and right ventricular structure and function, leading to better clinical status and quality of life.
  • This study supports GH therapy as a beneficial treatment for HFrEF patients with GHD.
Abstract

Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
360
Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
1.4K
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
488
Heart Failure Drugs: &#946;-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
303
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
318
Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
136