Rodenbach Kyle E, Schneider Michael F, Furth Susan L, Moxey-Mims Marva M, Mitsnefes Mark M, Weaver Donald J, Warady Bradley A, Schwartz George J
University of Rochester Medical Center, Rochester, NY.
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Am J Kidney Dis. 2015 Dec;66(6):984-92. doi: 10.1053/j.ajkd.2015.06.015. Epub 2015 Jul 21.
Hyperuricemia is associated with essential hypertension in children. No previous studies have evaluated the effect of hyperuricemia on progression of chronic kidney disease (CKD) in children.
Prospective observational cohort study.
SETTING & PARTICIPANTS: Children and adolescents (n=678 cross-sectional; n=627 longitudinal) with a median age of 12.3 (IQR, 8.6-15.6) years enrolled at 52 North American sites of the CKiD (CKD in Children) Study.
Serum uric acid level (<5.5, 5.5-7.5, and >7.5mg/dL).
Composite end point of either >30% decline in glomerular filtration rate (GFR) or initiation of renal replacement therapy.
Age, sex, race, blood pressure status, GFR, CKD cause, urine protein-creatinine ratio (<0.5, 0.5-<2.0, and ≥2.0mg/mg), age- and sex-specific body mass index > 95th percentile, use of diuretics, and serum uric acid level.
Older age, male sex, lower GFR, and body mass index > 95th percentile were associated with higher uric acid levels. 162, 294, and 171 participants had initial uric acid levels < 5.5, 5.5 to 7.5, or >7.5 mg/dL, respectively. We observed 225 instances of the composite end point over 5 years. In a multivariable parametric time-to-event analysis, compared with participants with initial uric acid levels < 5.5mg/dL, those with uric acid levels of 5.5 to 7.5 or >7.5mg/dL had 17% shorter (relative time, 0.83; 95% CI, 0.62-1.11) or 38% shorter (relative time, 0.62; 95% CI, 0.45-0.85) times to event, respectively. Hypertension, lower GFR, glomerular CKD cause, and elevated urine protein-creatinine ratio were also associated with faster times to the composite end point.
The study lacked sufficient data to examine how use of specific medications might influence serum uric acid levels and CKD progression.
Hyperuricemia is a previously undescribed independent risk factor for faster progression of CKD in children and adolescents. It is possible that treatment of children and adolescents with CKD with urate-lowering therapy could slow disease progression.
高尿酸血症与儿童原发性高血压相关。既往尚无研究评估高尿酸血症对儿童慢性肾脏病(CKD)进展的影响。
前瞻性观察队列研究。
北美52个CKiD(儿童慢性肾脏病)研究站点招募的儿童及青少年(横断面研究n = 678;纵向研究n = 627),中位年龄12.3岁(四分位间距,8.6 - 15.6岁)。
血清尿酸水平(<5.5、5.5 - 7.5及>7.5mg/dL)。
肾小球滤过率(GFR)下降>30%或开始肾脏替代治疗的复合终点。
年龄、性别、种族、血压状况、GFR、CKD病因、尿蛋白肌酐比值(<0.5、0.5 - <2.0及≥2.0mg/mg)、年龄和性别特异性体重指数>第95百分位数、利尿剂使用情况及血清尿酸水平。
年龄较大、男性、较低的GFR及体重指数>第95百分位数与较高的尿酸水平相关。162、294和171名参与者的初始尿酸水平分别<5.5、5.5至7.5或>7.5mg/dL。5年期间我们观察到225例复合终点事件。在多变量参数化事件发生时间分析中,与初始尿酸水平<5.5mg/dL的参与者相比,尿酸水平为5.5至7.5或>7.5mg/dL的参与者事件发生时间分别缩短17%(相对时间,0.83;95%CI,0.62 - 1.11)或38%(相对时间,0.62;95%CI,0.45 - 0.85)。高血压、较低的GFR、肾小球CKD病因及升高的尿蛋白肌酐比值也与复合终点事件发生时间较快相关。
该研究缺乏足够数据来检验特定药物的使用如何影响血清尿酸水平及CKD进展。
高尿酸血症是儿童及青少年CKD进展加快的一个此前未被描述的独立危险因素。对患有CKD的儿童及青少年进行降尿酸治疗有可能减缓疾病进展。