Li Zhenyuan, Deng Yanghua, Liao Qiong
Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Department of Pediatrics, West China Second University Hospital, Sichuan University/, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, 610041, China.
BMC Pediatr. 2025 Aug 25;25(1):652. doi: 10.1186/s12887-025-06032-6.
Matrix metalloproteinase-7 (MMP-7) has emerged as a promising biomarker for the early detection of biliary atresia (BA), with potential to significantly improve diagnostic accuracy and patient outcomes. This meta-analysis evaluated the diagnostic performance of MMP-7 to determine its clinical utility in the identification of BA.
A comprehensive literature search was performed in PubMed, Embase, Web of Science, and the Cochrane Library for studies published through March 21, 2024. Study quality was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2 tool. Diagnostic parameters including sensitivity, specificity, likelihood ratios, and diagnostic odds ratios were pooled. Summary receiver operating characteristic curves were constructed to evaluate overall diagnostic performance.
9 studies comprising 710 patients were included in the analysis. MMP-7 demonstrated a pooled sensitivity of 0.80 (95% CI: 0.58-0.92) and specificity of 0.97 (95% CI: 0.90-0.99), with an area under the curve of 0.97 (95% CI: 0.95-0.98). Subgroup analyses by geographic sample size, study type and mean/median age revealed no significant differences in diagnostic performance. An inverse relationship was observed between cutoff values and sensitivity, with higher thresholds yielding lower sensitivity but improved specificity.
The sensitivity of MMP-7 is influenced by sample processing methods, sample handling time, and substantial variability in cutoff values. Therefore, it cannot serve as an independent diagnostic tool for BA, and BA diagnosis should continue to rely on the gold standard. However, MMP-7 may serve as a valuable tool for risk stratification in BA. Future research should investigate the diagnostic performance of MMP-7 across varying cutoff values, reflecting the observed variability across studies.
CRD42024532998.
基质金属蛋白酶-7(MMP-7)已成为早期诊断胆道闭锁(BA)的一种有前景的生物标志物,有可能显著提高诊断准确性和患者预后。这项荟萃分析评估了MMP-7的诊断性能,以确定其在BA诊断中的临床应用价值。
在PubMed、Embase、Web of Science和Cochrane图书馆中进行了全面的文献检索,以查找截至2024年3月21日发表的研究。使用诊断准确性研究质量评估-2工具评估研究质量。汇总了包括敏感性、特异性、似然比和诊断比值比在内的诊断参数。构建汇总的受试者工作特征曲线以评估总体诊断性能。
分析纳入了9项研究,共710例患者。MMP-7的汇总敏感性为0.80(95%CI:0.58-0.92),特异性为0.97(95%CI:0.90-0.99),曲线下面积为0.97(95%CI:0.95-0.98)。按地理样本量、研究类型和平均/中位数年龄进行的亚组分析显示,诊断性能无显著差异。观察到临界值与敏感性之间呈反比关系,较高的阈值导致较低的敏感性,但特异性提高。
MMP-7的敏感性受样本处理方法、样本处理时间和临界值的显著变异性影响。因此,它不能作为BA的独立诊断工具,BA诊断仍应依靠金标准。然而,MMP-7可能是BA风险分层的有价值工具。未来的研究应调查MMP-7在不同临界值下的诊断性能,以反映各研究中观察到的变异性。
PROSPERO注册号:CRD42024532998。