Scholarlink

Background <p>Early and accurate detection of acute kidney injury (AKI)&#xa0;in children is difficult because serum creatinine rises late and lacks sensitivity. Serum cystatin C has been proposed as an earlier biomarker, but pediatric evidence has been inconsistent.</p> Methods <p>We performed a systematic review and meta-analysis of studies evaluating serum cystatin C for pediatric acute kidney injury. PubMed, Cochrane Library, Scopus, and Web of Science were searched from inception through June 2025. Eligible studies compared cystatin C against standardized AKI definitions (KDIGO, pRIFLE, or AKIN) and reported sufficient diagnostic accuracy data. Two reviewers independently screened, extracted, and assessed study quality using QUADAS-2. Pooled estimates of sensitivity and specificity were calculated using a bivariate random effects model with hierarchical summary receiver operating characteristic curves. Subgroup and meta-regression analyses explored sources of heterogeneity. Certainty of evidence was assessed with GRADE-DTA. The review was registered with PROSPERO (CRD420251104342).</p> Results <p>Twenty-six studies comprising 3742 pediatric patients were included. Pooled sensitivity was 78.2% (95% CI 72.6–82.9) and specificity was 79.5% (95% CI 73.5–84.5), with an area under the curve of 0.854, reflecting good overall discriminatory power. Predictive values varied with disease prevalence: at 10% prevalence, the negative predictive value reached 97.0%, while at 40% prevalence, the positive predictive value increased to 71.8%. Bayesian meta-regression identified clinical setting as a significant effect modifier, with higher accuracy in ward-based studies compared with pediatric intensive care unit cohorts. Sensitivity analyses confirmed robustness, and no evidence of publication bias was detected. Certainty of evidence was rated moderate for sensitivity and specificity and high for area under the curve.</p> Conclusions <p>Serum cystatin C is a reliable biomarker for early pediatric AKI detection, offering superior performance to creatinine and particularly strong rule-out value in lower-prevalence settings. Its clinical utility would be enhanced by standardized cut-offs, cost-effectiveness evaluation, and integration into biomarker panels.</p> Graphical abstract <p></p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Diagnostic accuracy of serum cystatin C for pediatric acute kidney injury: a systematic review and meta-analysis

  • 期刊论文

  • 发表日期：

    2026年2月4日

查看全文
  • Mohammed Alsabri,
  • Mohamed Amr Elkarargy,
  • Amira A. Aboali,
  • Salma S. Alrawa,
  • Mohamed Nabil Galal,
  • Eslam Abady,
  • Noha S. Shaban,
  • Sarah C. Urbon

摘要

Background

Early and accurate detection of acute kidney injury (AKI) in children is difficult because serum creatinine rises late and lacks sensitivity. Serum cystatin C has been proposed as an earlier biomarker, but pediatric evidence has been inconsistent.

Methods

We performed a systematic review and meta-analysis of studies evaluating serum cystatin C for pediatric acute kidney injury. PubMed, Cochrane Library, Scopus, and Web of Science were searched from inception through June 2025. Eligible studies compared cystatin C against standardized AKI definitions (KDIGO, pRIFLE, or AKIN) and reported sufficient diagnostic accuracy data. Two reviewers independently screened, extracted, and assessed study quality using QUADAS-2. Pooled estimates of sensitivity and specificity were calculated using a bivariate random effects model with hierarchical summary receiver operating characteristic curves. Subgroup and meta-regression analyses explored sources of heterogeneity. Certainty of evidence was assessed with GRADE-DTA. The review was registered with PROSPERO (CRD420251104342).

Results

Twenty-six studies comprising 3742 pediatric patients were included. Pooled sensitivity was 78.2% (95% CI 72.6–82.9) and specificity was 79.5% (95% CI 73.5–84.5), with an area under the curve of 0.854, reflecting good overall discriminatory power. Predictive values varied with disease prevalence: at 10% prevalence, the negative predictive value reached 97.0%, while at 40% prevalence, the positive predictive value increased to 71.8%. Bayesian meta-regression identified clinical setting as a significant effect modifier, with higher accuracy in ward-based studies compared with pediatric intensive care unit cohorts. Sensitivity analyses confirmed robustness, and no evidence of publication bias was detected. Certainty of evidence was rated moderate for sensitivity and specificity and high for area under the curve.

Conclusions

Serum cystatin C is a reliable biomarker for early pediatric AKI detection, offering superior performance to creatinine and particularly strong rule-out value in lower-prevalence settings. Its clinical utility would be enhanced by standardized cut-offs, cost-effectiveness evaluation, and integration into biomarker panels.

Graphical abstract