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胱抑素 C 作为先天性神经性膀胱患儿早期肾功能不全的标志物。

Cystatin C as a marker of early renal insufficiency in children with congenital neuropathic bladder.

机构信息

Division of Pediatric Urology, Department of Urology, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania; Naval Medical Center Portsmouth, Portsmouth, Virginia.

Division of Pediatric Urology, Department of Urology, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

出版信息

J Urol. 2014 May;191(5 Suppl):1602-7. doi: 10.1016/j.juro.2013.09.093. Epub 2014 Mar 26.

Abstract

PURPOSE

Due to decreased muscle mass in children with congenital neuropathic bladder there may be significant inaccuracy when using the creatinine based estimated glomerular filtration rate. Cystatin C is highly sensitive and specific for measuring changes in the glomerular filtration rate in children and in patients with muscle wasting conditions. We hypothesized that a cystatin C calculated glomerular filtration rate would be more sensitive than the standard creatinine based modified Schwartz equation to detect renal insufficiency in children with congenital neuropathic bladder.

MATERIALS AND METHODS

We prospectively identified children with congenital neuropathic bladder at a multidisciplinary spina bifida clinic who underwent serum creatinine and serum cystatin C testing. Clinical history and anthropomorphic variables at the time of laboratory testing were catalogued. The creatinine based glomerular filtration rate was estimated using the modified (bedside) Schwartz formula and the cystatin C based rate was calculated using the Zappitelli cystatin C formula.

RESULTS

Dual estimated glomerular filtration rate calculation was done in 69 children at a total of 74 patient encounters. Absolute creatinine was within age range normal limits in each patient, including 1 with chronic kidney disease stage 3A. The median creatinine based estimated glomerular filtration rate was 123 ml per minute/1.73 m(2) (range 58 to 229). The median cystatin C based estimated rate was 103 ml per minute/1.73 m(2) (range 47 to 144) for an absolute median rate reduction of 15.4%. Using cystatin C estimates chronic kidney disease stage was upgraded from stage 1 to 2 in 13 patients (18.8%).

CONCLUSIONS

In children with neuropathic bladder the cystatin C estimated glomerular filtration rate is a better screening test for early renal insufficiency that is not detected by creatinine based rate calculations. To our knowledge it remains to be determined whether the cystatin C estimated glomerular filtration rate can ultimately improve the clinical outcome in this population.

摘要

目的

由于患有先天性神经源性膀胱的儿童肌肉量减少,使用基于肌酐的估算肾小球滤过率可能会出现显著的不准确。胱抑素 C 高度敏感和特异,可用于测量儿童和肌肉消耗疾病患者肾小球滤过率的变化。我们假设胱抑素 C 计算的肾小球滤过率比基于肌酐的改良 Schwartz 方程更敏感,能够检测到先天性神经源性膀胱儿童的肾功能不全。

材料和方法

我们前瞻性地在多学科脊柱裂诊所确定了患有先天性神经源性膀胱的儿童,他们接受了血清肌酐和血清胱抑素 C 检测。在进行实验室检测时,记录了临床病史和人体测量学变量。使用改良(床边)Schwartz 公式估算基于肌酐的肾小球滤过率,使用 Zappitelli 胱抑素 C 公式计算基于胱抑素 C 的滤过率。

结果

在总共 74 次患者就诊中,对 69 名儿童进行了双重估计肾小球滤过率计算。每位患者的绝对肌酐均在年龄范围内正常,包括 1 例慢性肾脏病 3A 期患者。基于肌酐的估算肾小球滤过率中位数为 123ml/分钟/1.73m²(范围为 58 至 229)。基于胱抑素 C 的估算率中位数为 103ml/分钟/1.73m²(范围为 47 至 144),绝对中位数降低了 15.4%。使用胱抑素 C 估计,慢性肾脏病分期在 13 名患者(18.8%)中从 1 期升级为 2 期。

结论

在患有神经源性膀胱的儿童中,胱抑素 C 估算的肾小球滤过率是一种更好的早期肾功能不全筛查试验,而基于肌酐的滤过率计算则无法检测到。据我们所知,胱抑素 C 估算的肾小球滤过率是否最终能改善该人群的临床结局仍有待确定。

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