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Uric acid, left ventricular mass index, and risk of cardiovascular disease in essential hypertension
Yoshio Iwashima1, Takeshi Horio, Kei Kamide
1Department of Geriatric Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.
Insights
Elevated serum uric acid (UA) is linked to increased left ventricular mass index (LVMI) in hypertension patients. This combination independently predicts cardiovascular disease (CVD) events, suggesting a direct association.
Area of Science:
- Cardiology
- Nephrology
- Hypertension Research
Background:
- Elevated serum uric acid (UA) is common in hypertension.
- The causal link between UA and cardiovascular events is unclear.
- Left ventricular mass index (LVMI) is a marker of cardiac remodeling.
Purpose of the Study:
- To examine the association between serum UA and LVMI in essential hypertension.
- To prospectively investigate if combined UA and LVMI predict cardiovascular disease (CVD) incidence.
- To determine if UA is an independent predictor of CVD events in this population.
Main Methods:
- Prospective study of 619 asymptomatic essential hypertension patients without prior CVD.
- Assessed serum UA and LVMI, using sex-specific medians for grouping.
- Utilized multiple regression, Kaplan-Meier survival analysis, and Cox proportional hazards models.
Main Results:
- A significant association was confirmed between serum UA and LVMI in both sexes.
- Higher UA and LVMI levels were associated with significantly poorer CVD-free survival.
- The combination of higher UA and LVMI independently predicted CVD events (HR, 2.38; P<0.03).
Conclusions:
- Serum UA is independently associated with LVMI in essential hypertension.
- Hyperuricemia combined with left ventricular hypertrophy is a powerful, independent predictor of CVD.
- The association between UA and CVD events may be partly mediated by LVMI.
Abstract:
Elevated serum uric acid (UA) is frequently encountered in individuals with hypertension, but whether the relationship between UA and cardiovascular events is circumstantial or causal remains to be answered. We examined the association between serum UA and left ventricular mass index (LVMI) and investigated prospectively whether the combination of UA and LVMI can predict the incidence of cardiovascular disease (CVD) in asymptomatic subjects with essential hypertension. A total of 619 subjects (mean age, 61 years; 52% female) free of prior CVD were included in this study. A significant association between UA and LVMI was also confirmed in multiple regression analysis (male: F=4.29, P<0.04; female: F=4.24, P<0.05). During follow-up (mean, 34 months), 28 subjects (14 female) developed CVD including myocardial infarction, angina pectoris, congestive heart failure, cerebral infarction, and transient cerebral ischemia. Sex-specific median values were used to separate the higher group from the lower group of UA and LVMI. Kaplan-Meier curves showed a significantly poorer survival rate in the group with higher UA and LVMI (LVMI, male: >126.9, female: >112.0 g/m2; UA, male: >374.7, female: >303.3 micromol/L; log-rank chi2=13.18; P<0.01). Multivariate Cox regression analysis showed that the combination of higher UA and LVMI was an independent predictor for CVD events (hazard ratio, 2.38; P<0.03). Our findings demonstrate that UA is independently associated with LVMI and suggest that the combination of hyperuricemia combined with left ventricular hypertrophy is an independent and powerful predictor for CVD. The association between UA and CVD events may be introduced in part because of a direct association of UA with LVMI.
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