Hyperuricaemia in congenital heart disease patients

Efrén Martínez-Quintana1, Fayna Rodríguez-González2

  • 11Cardiology Service,Insular-Materno Infantil University Hospital,Las Palmas de Gran Canaria,Spain.

Insights

High serum uric acid in congenital heart disease patients correlates with increased cardiovascular risk factors like obesity and inflammation. However, this study found no significant difference in mortality rates between hyperuricemic and non-hyperuricemic patients.

Area of Science:

  • Cardiology
  • Metabolic Health
  • Congenital Heart Disease

Background:

  • Hyperuricemia is linked to cardiovascular risks, including type 2 diabetes and dyslipidemia, and is associated with higher mortality.
  • Congenital heart disease (CHD) patients represent a unique population where cardiovascular risk factors may be altered.

Purpose of the Study:

  • To investigate the relationship between serum uric acid levels and cardiovascular risk factors in patients with congenital heart disease.
  • To determine if serum uric acid levels impact survival rates in this patient cohort.

Main Methods:

  • A cohort of 329 congenital heart disease patients (190 male, 139 female) with available uric acid measurements were studied.
  • Patients were followed up to assess survival, with clinical and biochemical parameters analyzed based on serum uric acid concentrations.

Main Results:

  • In male CHD patients, high uric acid (>7 mg/dl) correlated with higher BMI, creatinine, cholesterol, LDL-C, triglycerides, and CRP.
  • In female CHD patients, high uric acid (>5.7 mg/dl) correlated with younger age, greater hypoxemia, obesity, and elevated CRP and NT-proBNP.
  • No significant difference in mortality was observed between CHD patients with high versus low serum uric acid levels during a median 90-month follow-up.

Conclusions:

  • Hyperuricemic CHD patients exhibit higher levels of hypoxemia, body mass index, and C-reactive protein.
  • Despite associations with adverse risk factors, elevated serum uric acid did not significantly affect mortality in this congenital heart disease cohort.
Abstract

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