Screening the population for left ventricular hypertrophy and left ventricular systolic dysfunction using natriuretic

James A de Lemos1, Darren K McGuire, Amit Khera

  • 1Donald W. Reynolds Cardiovascular Research Center, UT Southwestern Medical Center, Dallas, TX 75390-9047, USA. james.delemos@utsouthwestern.edu

Insights

Neither B-type natriuretic peptide (BNP) nor N-terminal pro-BNP (NT-proBNP) accurately identified left ventricular dysfunction in a general population. However, NT-proBNP showed slightly better screening performance in high-risk men.

Area of Science:

  • Cardiology
  • Biomarker Research
  • Diagnostic Imaging

Background:

  • Early identification of left ventricular systolic dysfunction (LVSD) and left ventricular hypertrophy (LVH) is crucial for timely treatment.
  • B-type natriuretic peptide (BNP) and N-terminal pro-BNP (NT-proBNP) are investigated as potential screening biomarkers.

Purpose of the Study:

  • To evaluate the screening performance of BNP and NT-proBNP for LVSD and LVH.
  • To compare the diagnostic accuracy of BNP and NT-proBNP in diverse demographic and clinical subgroups.

Main Methods:

  • A cohort of 2,429 subjects from the Dallas Heart Study without prior heart conditions were assessed.
  • Cardiovascular magnetic resonance imaging (CMR) was used to define LVSD (ejection fraction <55%) and LVH.
  • Serum levels of BNP and NT-proBNP were measured and correlated with CMR findings.

Main Results:

  • Both BNP and NT-proBNP showed significant associations with LVH and LVSD (P < .0001).
  • Neither biomarker demonstrated high discriminatory power for LVH or LVSD in the overall cohort (AUROC <0.7).
  • In men aged 50+ or with hypertension, NT-proBNP exhibited superior performance (AUROC 0.73-0.79) compared to BNP (AUROC 0.63-0.69).

Conclusions:

  • BNP and NT-proBNP are not sufficiently accurate for general population screening of LVH or LVSD.
  • NT-proBNP offers a marginal improvement over BNP for screening high-risk men, comparable to other established screening tests.
Abstract

Related Concept Videos

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...
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...
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,...
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...
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...