Related Experiment Video
Updated: Aug 10, 2026

08:01
In utero Measurement of Heart Rate in Mouse by Noninvasive M-mode Echocardiography
Published on: November 22, 2013
Hyperuricemia in congenital heart disease
American Journal of Diseases of Children (1960)
|September 1, 1978
Summary
Hyperuricemia is common in patients with cyanotic congenital heart disease, often linked to polycythemia. Many may develop subclinical kidney damage due to high uric acid levels.
Area of Science:
- Cardiology
- Nephrology
- Genetics
Background:
- Gout is infrequently associated with secondary polycythemia.
- Congenital heart disease, particularly cyanotic types, can cause profound polycythemia.
- The relationship between polycythemia in congenital heart disease and hyperuricemia is not well-established.
Purpose of the Study:
- To determine the incidence of hyperuricemia in patients with congenital heart disease.
- To investigate the correlation between serum uric acid levels and the degree of polycythemia.
- To assess the potential risk of uric acid nephropathy in this patient population.
Main Methods:
- Retrospective study of 81 patients with congenital heart disease.
- Serum uric acid levels were measured.
- Correlation analysis was performed between uric acid levels and polycythemia severity.
Main Results:
- Twenty of 46 patients (43%) with cyanotic congenital heart disease exhibited hyperuricemia (serum uric acid > 8 mg/dl).
- Hyperuricemia was more prevalent in older cyanotic males (81% in those >15 years).
- Serum uric acid levels showed a direct correlation with the degree of polycythemia (r = .44, P < .02).
Conclusions:
- Hyperuricemia is a significant clinical issue in cyanotic congenital heart disease.
- The degree of polycythemia is directly associated with elevated uric acid levels.
- A substantial number of these patients may be at risk for subclinical uric acid nephropathy.
Related Concept Videos
Rheumatic Heart Disease I: Introduction
Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies
The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
Rheumatic Heart Disease III: Medical Management
Rheumatic heart disease (RHD) management can be divided into two main strategies: prevention and long-term management.Primary PreventionPrimary prevention focuses on timely diagnosis and management of group A streptococcal pharyngitis to prevent acute rheumatic fever. The most widely used antibiotic for treating this condition is intramuscular benzathine penicillin G.Acute Rheumatic Fever TreatmentThe primary treatment goal for a patient diagnosed with acute rheumatic fever is to suppress the...
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...
Urinary Tract Calculi I: Introduction
Renal calculi, or kidney stones, are solid deposits of minerals and salts formed inside the kidneys. In medical terminology, "calculus" refers to the stone itself, while "lithiasis" describes the process of stone formation. Depending on their location within the urinary system, these stones may be classified as either urolithiasis, when situated within the urinary tract, or nephrolithiasis, when located within the kidneys. Each term signifies the specific impact of the stone.Predisposition...
Jaundice
Jaundice, or icterus, is the yellow discoloration of the skin, sclerae, and mucous membranes. It happens when plasma bilirubin levels rise above 2.5-3 mg/dL, leading to bilirubin deposition in tissue.Bilirubin is a byproduct of hemoglobin degradation. In macrophages, hemoglobin breaks down into globin and heme. Globin is converted into amino acids, while heme is turned into biliverdin by heme oxygenase, which is then reduced to unconjugated bilirubin by biliverdin reductase.Unconjugated...

