Greenberg Keiko I, McAdams-DeMarco Mara A, Köttgen Anna, Appel Lawrence J, Coresh Josef, Grams Morgan E
Departments of Medicine and
Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Epidemiology, Johns Hopkins School of Public Health, Baltimore, Maryland;
Clin J Am Soc Nephrol. 2015 May 7;10(5):776-83. doi: 10.2215/CJN.05870614. Epub 2015 Feb 25.
Higher urate levels are associated with higher risk of CKD, but the association between urate and AKI is less established. This study evaluated the risk of hospitalized AKI associated with urate concentrations in a large population-based cohort. To explore whether urate itself causes kidney injury, the study also evaluated the relationship between a genetic urate score and AKI.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A total of 11,011 participants from the Atherosclerosis Risk in Communities study were followed from 1996-1998 (baseline) to 2010. The association between baseline plasma urate and risk of hospitalized AKI, adjusted for known AKI risk factors, was determined using Cox regression. Interactions of urate with gout and CKD were tested. Mendelian randomization was performed using a published genetic urate score among the participants with genetic data (n=7553).
During 12 years of follow-up, 823 participants were hospitalized with AKI. Overall, mean participant age was 63.3 years, mean eGFR was 86.3 ml/min per 1.73 m(2), and mean plasma urate was 5.6 mg/dl. In patients with plasma urate >5.0 mg/dl, there was a 16% higher risk of hospitalized AKI for each 1-mg/dl higher urate (adjusted hazard ratio, 1.16; 95% confidence interval, 1.10 to 1.23; P<0.001). When stratified by history of gout, the association between higher urate and AKI was significant only in participants without a history of gout (P for interaction=0.02). There was no interaction of CKD and urate with AKI, nor was there an association between genetic urate score and AKI.
Plasma urate >5.0 mg/dl was independently associated with risk of hospitalized AKI; however, Mendelian randomization did not provide evidence for a causal role of urate in AKI. Further research is needed to determine whether lowering plasma urate might reduce AKI risk.
较高的尿酸水平与慢性肾脏病(CKD)风险增加相关,但尿酸与急性肾损伤(AKI)之间的关联尚不明确。本研究在一个大型人群队列中评估了与尿酸浓度相关的住院AKI风险。为探究尿酸本身是否会导致肾损伤,该研究还评估了遗传尿酸评分与AKI之间的关系。
设计、地点、参与者及测量方法:共有11011名来自社区动脉粥样硬化风险研究的参与者从1996年至1998年(基线)随访至2010年。使用Cox回归确定经已知AKI风险因素校正后的基线血浆尿酸与住院AKI风险之间的关联。对尿酸与痛风和CKD的相互作用进行了检验。在有基因数据的参与者(n = 7553)中,使用已发表的遗传尿酸评分进行孟德尔随机化分析。
在12年的随访期间,823名参与者因AKI住院。总体而言,参与者的平均年龄为63.3岁,平均估算肾小球滤过率(eGFR)为每1.73平方米86.3毫升/分钟,平均血浆尿酸为5.6毫克/分升。在血浆尿酸>5.0毫克/分升的患者中,尿酸每升高1毫克/分升,住院AKI风险高16%(校正风险比,1.16;95%置信区间,1.10至1.23;P<0.001)。按痛风病史分层时,较高尿酸与AKI之间的关联仅在无痛风病史的参与者中显著(相互作用P值 = 0.02)。CKD和尿酸与AKI之间没有相互作用,遗传尿酸评分与AKI之间也没有关联。
血浆尿酸>5.0毫克/分升与住院AKI风险独立相关;然而,孟德尔随机化分析未提供尿酸在AKI中起因果作用的证据。需要进一步研究以确定降低血浆尿酸是否可能降低AKI风险。