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Hyperuricemia, urate-lowering therapy, and kidney outcomes: a systematic review and meta-analysis

机译:高尿酸血症,尿酸盐治疗和肾脏结果:系统审查和荟萃分析

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Background: Contradictory evidence exists for association of hyperuricemia and kidney function. To investigate the association of hyperuricemia and kidney function decline (hyperuricemia question) and effect of urate-lowering therapies (ULTs) on kidney function (ULT question), we performed a systematic review and meta-analysis. Methods: MEDLINE, Embase, Cochrane Central Register of Controlled Trials, and CINAHL were searched from inception to July 2020. We selected observational studies for the hyperuricemia question and controlled trials for the ULT question. Two investigators independently assessed study eligibility and abstracted the data. Risk of bias was assessed using the Newcastle–Ottawa Scale and Cochrane risk of bias tool. Meta-analysis was done using the inverse variance method and random effect model. We estimated odds ratio (OR), hazard ratio (HR), risk ratio (RR), and the mean difference (MD). Evidence certainty was evaluated using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system. Results: Of 12,037 studies screened, 131 studies with 3,414,226 patients were included. Hyperuricemia was associated with a significant risk of rapid estimated glomerula filtration rate (eGFR) decline ?3?ml/min per 1.73?m 2 per year (OR 1.38, 95% CI 1.20–1.59; low certainty), albuminuria (OR/HR 1.94, 95% CI 1.34–2.79; very low certainty), chronic kidney disease (OR/HR 2.13, 95% CI 1.74–2.61; very low certainty), and kidney failure (HR 1.53, 95% CI 1.18–1.99; very low certainty). Compared with control, ULT use for ?1?year was associated with significantly more improved eGFR (MD 1.81?ml/min per 1.73?m 2 , 95% CI 0.26–3.35; very low certainty), serum creatinine (MD ?0.33?mg/dl, 95% CI ?0.47 to ?0.19; low certainty), and proteinuria (MD ?5.44?mg/day, 95% CI ?8.49 to ?2.39; low certainty), but no difference in kidney failure. Conclusion: Hyperuricemia is associated with worsening eGFR, albuminuria, chronic kidney disease, and kidney failure. ULT use for ?1?year may improve kidney function. Registration: The protocol was registered at PROSPERO database, CRD42015013859.
机译:背景:矛盾血症和肾功能结合存在矛盾的证据。为了探讨高尿酸血症和肾功能下降(Heriuaricemia问题)的协会和对肾功能(ULT)对肾功能(ULT问题)的影响,我们进行了系统审查和荟萃分析。方法:从初始到2020年7月,搜查了受控试验的Medline,Embase,Cochrane中央登记,并从20020年7月搜索了Cinahl。我们选择了对ULT问题的高尿血症问题和对照试验的观察性研究。两位调查员独立评估了研究资格并抽象了数据。使用纽卡斯尔 - 渥太华规模和偏置工具的Cochrane风险评估偏见的风险。使用逆变异方法和随机效果模型进行META分析。我们估计了几率比(或),危险比(HR),风险比(RR)和平均差异(MD)。使用建议评估,开发和评估(等级)系统的评分评估证据确定性。结果:12,037项筛选研究,包括3,414,226名患者的131项研究。高尿酸血症与快速估计的肾小球过滤速率(EGFR)下降的显着风险有关?每年每年每年1.73毫升/分钟(或1.38,95%CI 1.20-1.59;低确定性),白蛋白尿(或/小时1.94,95%CI 1.34-2.79;非常低的确定性),慢性肾病(或/ HR 2.13,95%CI 1.74-2.61;非常低的确定性)和肾功能衰竭(HR 1.53,95%CI 1.18-1.99;非常低确定性)。与对照相比,ULT用于1?一年与更高的EGFR(MD 1.81?ml / min,每1.73×m 2,95%CI 0.26-3.35;非常低的确定性),血清肌酐(MD?0.33? Mg / DL,95%CI?0.47至0.19;低确定性)和蛋白尿(MD?5.44?MG /天,95%CI?8.49至?2.39;低确定性),但肾衰竭没有差异。结论:高尿酸血症与恶化EGFR,白蛋白尿,慢性肾病和肾功能衰竭有关。 ULT用于?1?一年可以改善肾功能。注册:该协议在Prospero数据库中注册,CRD42015013859。

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