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. 2023 Jan 18;20(3):1728. doi: 10.3390/ijerph20031728

Table 2.

Associations between HUA and sUA at baseline with new-onset CKD.

N No of Events (%) Model 1 Model 2
HR (95% CI) p Value HR (95% CI) p Value
HUA at Baseline
Non-HUA 24,553 933 (3.80%) 1.00 1.00
HUA 3869 279 (7.21%) 1.70 (1.48–1.93) <0.001 1.28 (1.12–1.47) <0.001
sUA (μmol/L)
 Q1 (≤285) 7024 192 (2.73%) 1.00 1.00
 Q2 (266–318) 7087 260 (3.67%) 1.22 (1.01–1.47) 0.036 1.03 (0.85–1.25) 0.738
 Q3 (319–374) 7091 309 (4.36%) 1.46 (1.22–1.74) <0.001 1.04 (0.85–1.27) 0.705
 Q4 (≥375) 7220 451 (6.25%) 2.02 (1.70–2.39) <0.001 1.24 (1.01–1.51) 0.038
 p trend <0.001 <0.001

Model 1 was not adjusted for any covariates. Model 2 was adjusted for age (<45 years, 45–64 years, ≥65 years), gender (male, female), BMI (<24.0 kg·m−2, 24.0–27.9 kg·m−2, ≥28 kg·m−2), smoking status (non-smoker, smoker, ex-smoker), drinking status (non-drinker, drinker, ex-drinker), diabetes (no, yes), hypertension (no, yes), TG (≤1.20 mmol/L, 1.21–2.00 mmol/L, ≥2.01 mmol/L) at baseline. Q1–Q4 referred to the quartiles of serum uric acid grouped according to the quartiles of the non-CKD participants, respectively. The median of each group was included in the regression model as a continuous variable to calculate the p value for the test of trend. HUA, hyperuricemia; sUA, serum uric acid; SBP, systolic blood pressure; CKD, chronic kidney disease; HR, hazard ratio; CI, confidence interval.