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Published on: January 14, 2014
Plasma Uric Acid as a Prognostic Marker in Patients With Hypertrophic Cardiomyopathy
Ling Zhu1, Jizheng Wang2, Yilu Wang2
1Department of Cardiovascular Medicine, First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, Shanxi, People's Republic of China.
Insights
High uric acid (UA) levels are linked to worse outcomes in hypertrophic cardiomyopathy (HCM) patients. This study shows UA is an independent predictor of cardiovascular death, mortality, and cardiac events in HCM.
Area of Science:
- Cardiology
- Biochemistry
- Clinical Medicine
Background:
- Uric acid (UA) is a known risk factor for cardiovascular diseases.
- The prognostic significance of UA in hypertrophic cardiomyopathy (HCM) has not been previously evaluated.
Purpose of the Study:
- To investigate the clinical implications of plasma UA levels on the prognosis of patients diagnosed with HCM.
Main Methods:
- A cohort of 588 adult HCM patients was enrolled between 1999 and 2011.
- Plasma UA levels were measured at enrollment, and patients were followed until 2014.
Main Results:
- Higher UA levels (highest tertile) were associated with increased risks of cardiovascular death (HR 3.10), all-cause mortality (HR 2.33), cardiac events (HR 4.20), heart failure (HR 3.46), and arrhythmias (HR 9.19).
- Each 1 mg/dL increase in UA concentration independently predicted worse outcomes, including cardiovascular death (HR 1.29) and cardiac events (HR 1.27).
Conclusions:
- Plasma uric acid levels serve as an independent predictor of adverse outcomes in patients with hypertrophic cardiomyopathy.
- Elevated UA may indicate a higher risk for mortality and cardiac events in HCM patients.
Background:
Uric acid (UA) has been shown to be an independent risk factor for various cardiovascular diseases. However, its significance in hypertrophic cardiomyopathy (HCM) has not yet been evaluated. The objective of the present study was to evaluate clinical implications of plasma UA levels on the prognosis of patients with HCM.
Methods:
A total of 588 adult patients with HCM were enrolled at FuWai Hospital from 1999-2011 and followed until 2014. The plasma levels of UA were measured at enrollment.
Results:
During the follow-up of 5.2 ± 2.4 years, 44 (7.5%) patients had cardiovascular-related deaths, and 100 (17.0%) patients had cardiac events. Compared with the first tertile of UA concentration (< 284.6 μmol/L), patients in the highest tertile (> 358.7 μmol/L) had a higher risk for the development of adverse events: cardiovascular death (adjusted hazard ratio [HR], 3.10; 95% confidence interval [CI], 1.37-7.04; P = 0.007), all-cause mortality (adjusted HR, 2.33; 95% CI, 1.11-4.89; P = 0.025), cardiac events (adjusted HR, 4.20, 95% CI, 2.38-7.42; P < 0.001), heart failure events (adjusted HR, 3.46; 95% CI, 1.86-6.45; P < 0.001), and arrhythmic events (adjusted HR, 9.19; 95% CI, 2.40-35.25; P = 0.001). Similarly, the continuous variable of UA (for every 1 mg/dL higher concentration) was also an independent predictor for adverse outcomes: cardiovascular death (adjusted HR, 1.29; 95% CI, 1.11-1.49; P = 0.001), all-cause mortality (adjusted HR, 1.23; 95% CI, 1.07-1.41; P = 0.004), cardiac events (adjusted HR, 1.27; 95% CI, 1.15-1.41; P < 0.001), heart failure events (adjusted HR, 1.19; 95% CI, 1.06-1.33; P = 0.003), and arrhythmic events (adjusted HR, 1.60; 95% CI, 1.30-1.98; P < 0.001).
Conclusions:
Our results indicate that UA is an independent predictor of adverse outcomes in patients with HCM.
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