Effect of serum MMP-7 on the diagnostic accuracy of biliary atresia: systematic review and meta-analysis.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2025-06-26 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1581053
Haojun Wang, Hui Liu, Wanfu Li, Ainiwaer Keranmu, Peng Liang, Yaqi Wang, Tao Zhang, Yeliaman Jiayilawu
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引用次数: 0

Abstract

Background: Biliary atresia (BA) is an obstructive fibrotic disorder that typically progresses to cirrhosis and, ultimately, death in children. Current gold standard diagnostics for BA include intraoperative cholangiography and liver biopsy, both invasive procedures with significant complication risks. Matrix metalloproteinase-7 (MMP-7) has emerged as a highly accurate noninvasive diagnostic biomarker for BA. This study therefore aimed to evaluate the diagnostic utility of serum MMP-7 for BA detection.

Methods: We performed a comprehensive search of English-language databases (PubMed, Web of Science, ScienceDirect) with literature from the inception of these databases through 30 November 2024. Study quality was assessed using the QUADAS-2 tool. Sensitivity, specificity, positive/negative likelihood ratios (PLR/NLR), and area under the receiver operating characteristic curve (AUC-ROC) were calculated using Meta-DiSc 1.4 and STATA 18.0.

Results: This systematic review and meta-analysis included 13 articles (17 studies) comprising 2,836 serum samples from pediatric subjects. Binary classification model analysis showed pooled sensitivity of 0.93 (95% CI: 0.92-0.94) and specificity of 0.85 (95% CI: 0.83-0.87) for MMP-7. Positive likelihood ratio (PLR) was 7.68 (95%CI: 5.04-11.72), the negative likelihood ratio (NLR) was 0.08 (95%CI: 0.05-0.14), and the diagnosis odds ratio (DOR) was 104.34 (95%CI: 55.97-194.51). AUC was 0.9628. Meta-regression analysis identified publication year as a significant heterogeneity source (p = 0.007). Sensitivity analysis confirmed the robust diagnostic stability of MMP-7 for BA. Significant heterogeneity was observed across studies (I2 = 78.6%). Subgroup analysis by publication year showed that heterogeneity primarily originated from studies published in or after 2023.

Conclusion: Serum MMP-7 represents a convenient, accurate, and reliable noninvasive biomarker for enhancing BA diagnostic efficiency. However, due to significant heterogeneity, further validation via large-scale, multicenter studies with standardized protocols is needed.

Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/recorddashboard, identifier CRD42024623643.

血清MMP-7对胆道闭锁诊断准确性的影响:系统回顾和荟萃分析。
背景:胆道闭锁(BA)是一种梗阻性纤维化疾病,通常进展为肝硬化,并最终导致儿童死亡。目前BA的金标准诊断包括术中胆管造影和肝活检,这两种侵入性手术都有明显的并发症风险。基质金属蛋白酶-7 (Matrix metalloproteinase-7, MMP-7)已成为一种高度准确、无创的BA诊断生物标志物。因此,本研究旨在评估血清MMP-7对BA检测的诊断价值。方法:我们对英文数据库(PubMed, Web of Science, ScienceDirect)进行了全面的检索,检索从这些数据库建立到2024年11月30日的文献。使用QUADAS-2工具评估研究质量。使用Meta-DiSc 1.4和STATA 18.0计算敏感性、特异性、阳性/阴性似然比(PLR/NLR)和受试者工作特征曲线下面积(AUC-ROC)。结果:本系统综述和荟萃分析纳入13篇文章(17项研究),包括2,836份儿科受试者血清样本。二元分类模型分析显示,MMP-7的敏感性为0.93 (95% CI: 0.92-0.94),特异性为0.85 (95% CI: 0.83-0.87)。阳性似然比(PLR)为7.68 (95%CI: 5.04 ~ 11.72),阴性似然比(NLR)为0.08 (95%CI: 0.05 ~ 0.14),诊断优势比(DOR)为104.34 (95%CI: 55.97 ~ 194.51)。AUC为0.9628。meta回归分析发现出版年份是显著的异质性来源(p = 0.007)。敏感性分析证实了MMP-7对BA的诊断稳定性。研究间存在显著的异质性(I2 = 78.6%)。按发表年份进行的亚组分析显示,异质性主要来自2023年或之后发表的研究。结论:血清MMP-7是一种方便、准确、可靠的无创生物标志物,可提高BA的诊断效率。然而,由于显著的异质性,需要通过大规模、多中心的标准化研究来进一步验证。系统综述注册:https://www.crd.york.ac.uk/PROSPERO/recorddashboard,标识符CRD42024623643。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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