Published in:
Open Access
01-12-2015 | Original Article
Serum uric acid and the incidence of CKD and hypertension
Authors:
Satoru Kuriyama, Yukio Maruyama, Shinichiro Nishio, Yasuhito Takahashi, Satoshi Kidoguchi, Chisa Kobayashi, Daisuke Takahashi, Naoki Sugano, Tatsuo Hosoya, Takashi Yokoo
Published in:
Clinical and Experimental Nephrology
|
Issue 6/2015
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Abstract
Background
Uric acid (UA) levels correlate positively with the prevalence of chronic kidney disease (CKD) and/or hypertension. We tested the hypothesis that UA may also have a link to a new incidence of CKD and hypertension.
Methods
Study design is a cohort study and the predictor is UA levels. Of the 15,470 screened cases, 8223 participants without CKD were eligible for the analysis of the incidence of CKD. Among these CKD candidates, 7569 participants were eligible for the analysis of the new development of hypertension. The observation period was 4 years.
Results
Relationship of UA with new cases of CKD. Higher UA levels had a closer association with the new development of CKD; 1.1 % (UA < 5 mg/dL), 1.5 % (5.0–5.9 mg/dL), 1.7 % (6.0–6.9 mg/dL), and 3.4 % (≧7 mg/dL), respectively (p < 0.001 by the Chi-square test). Cox proportional hazard analysis showed that the estimates of the CKD development were eGFR [Hazard Ratio (HR) 0.816, 95 % confidence intervals (CI) 0.791–0.840] and male gender (HR 0.562, 95 % CI 0.322–0.982). UA levels and new development of hypertension. Higher UA levels had a closer association with the new development of hypertension; 5.0 % (UA < 5 mg/dL), 8.9 % (5.0–5.9 mg/dL), 10.6 % (6.0–6.9 mg/dL), and 11.8 % (≧7 mg/dL), respectively (p < 0.001 by the Chi-square test). Cox proportional hazard analysis showed that the estimates of the hypertension development were BMI (HR 1.190, 95 % CI 1.155–1.226), age (HR 1.021, 95 % CI 1.010–1.032), HDL-cholesterol (HR 1.013, 95 % CI 1.007–1.019), male gender (HR 1.791, 95 % CI 1.338–2.395), UA level (HR 1.112, 95 % CI 1.024–1.207), and eGFR (HR 1008, 95 % CI 1.002–1.013). Furthermore, the logistic analysis showed that the odds ratio (OR) to estimate hypertension in the high UA group (UA ≧ 7 mg/dL; OR 1.33, 95 % CI 1.01–1.80) was greater than that in the low UA group (UA < 5 mg/dL). Kaplan–Meier analysis also confirmed the finding that the higher the UA levels the greater the hypertension development (p < 0.001 by the Log-rank test and Cox proportional hazard analysis).
Conclusion
High UA levels are associated with the new development of hypertension, but not with the incidence of CKD.