Increased brain natriuretic peptide secretion is a marker of disease progression in nonobstructive hypertrophic

Maurizio Pieroni1, Fulvio Bellocci, Tommaso Sanna

  • 1Cardiology Department, Catholic University, Rome, Italy.

Insights

Progression of hypertrophic cardiomyopathy (HCM) to dilated phase increases both plasma and myocardial brain natriuretic peptide (BNP). Serial plasma BNP may noninvasively detect hemodynamic decline in HCM patients.

Area of Science:

  • Cardiology
  • Biochemistry

Background:

  • Hypertrophic cardiomyopathy (HCM) is linked to elevated plasma brain natriuretic peptide (BNP).
  • Sequential assessment of plasma and myocardial BNP in stable and dilated HCM is not well-documented.

Purpose of the Study:

  • To investigate sequential changes in plasma and myocardial BNP in patients with hypertrophic cardiomyopathy (HCM) as they progress to the dilated phase.
  • To correlate these changes with hemodynamic parameters and assess the potential for noninvasive monitoring.

Main Methods:

  • Forty HCM patients underwent cardiac catheterization, angiography, and left ventricular (LV) endomyocardial biopsy.
  • Patients were followed for progression to dilated phase, with a second invasive study including LV biopsy for those who progressed.
  • Plasma BNP levels were measured at baseline and follow-up; biopsies were analyzed for BNP expression via immunohistochemistry.

Main Results:

  • Patients progressing to dilated HCM (Group 2) showed significantly increased plasma BNP and elevated LV/right ventricular end-diastolic pressures compared to stable patients (Group 1).
  • Immunohistochemistry revealed a significant increase in myocardial BNP-positive myocytes in follow-up biopsies of Group 2 patients.
  • Increased myocardial BNP strongly correlated with elevated LV end-diastolic pressure and plasma BNP levels.

Conclusions:

  • Progression to end-stage HCM is marked by increased myocardial and plasma BNP.
  • Serial plasma BNP measurements may serve as a noninvasive indicator of hemodynamic deterioration in HCM.
  • Prompt monitoring of plasma BNP could facilitate timely initiation of heart failure therapy.
Abstract

Related Concept Videos

Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers01:19

Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers

Cardiac biomarkers are critical in diagnosing, prognosing, and managing cardiovascular diseases. Routine measurement of specific biomarkers such as B-type natriuretic peptide (BNP), C-reactive protein (CRP), and homocysteine (Hcy) is common practice in clinical settings to evaluate heart function and predict cardiovascular events.
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
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...
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...