Inflammatory biomarkers for early prediction of severe acute pancreatitis: A systematic review and meta-analysis.

0 MEDICINE, RESEARCH & EXPERIMENTAL
Kexin Zhang, Bohao Liu, Guipeng Zhang, Ying Zhang, Junjie Liu
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Abstract

Acute pancreatitis (AP) can rapidly progress to severe disease, making accurate early risk stratification essential for timely treatment. This systematic review and meta-analysis evaluated the predictive performance of inflammatory biomarkers for AP severity. PubMed, Web of Science, the Cochrane Library, and Embase were searched from inception to November 5, 2025, for diagnostic accuracy studies in adults with AP. Study quality was assessed using the Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) tool, and diagnostic performance was pooled using bivariate or conventional random-effects models. Overall, 88 studies comprising 12,318 participants and evaluating 17 biomarkers were included. Polymorphonuclear neutrophil elastase (PMN-elastase) showed the strongest overall performance, with an area under the curve (AUC) of 0.96 within 1 day after admission and sensitivity and specificity of 0.93 and 0.94, respectively, at admission. Interleukin-6 (IL-6) also demonstrated strong early predictive performance, with an AUC of 0.93 within 1 day and sensitivity and specificity of 0.96 and 0.80, respectively, within 2 days. C-reactive protein (CRP) performed better during serial monitoring than during early assessment, reaching an AUC of 0.92 on day 5 and a diagnostic odds ratio (DOR) of 177.22 on day 6. The CRP-to-albumin ratio, procalcitonin, interleukin-8, carboxypeptidase B activation peptide, and neopterin showed moderate-to-high predictive performance. By contrast, the neutrophil-to-lymphocyte ratio and white blood cell count showed modest accuracy, whereas the platelet-to-lymphocyte ratio, erythrocyte sedimentation rate, and interleukin-10 had limited predictive value. PMN-elastase and IL-6 are promising biomarkers for early assessment of AP severity, whereas CRP is more suitable for dynamic monitoring. However, substantial methodological and clinical heterogeneity precludes direct ranking of biomarkers and highlights the need for standardized, prospective studies evaluating multimarker models.

早期预测严重急性胰腺炎的炎症生物标志物:系统回顾和荟萃分析。
急性胰腺炎(AP)可迅速发展为严重疾病,因此准确的早期风险分层对于及时治疗至关重要。本系统综述和荟萃分析评估了炎症生物标志物对AP严重程度的预测性能。检索PubMed、Web of Science、Cochrane Library和Embase,从成立到2025年11月5日,检索成人AP的诊断准确性研究。使用诊断准确性研究质量评估2 (QUADAS-2)工具评估研究质量,使用双变量或传统随机效应模型汇总诊断效果。总体而言,纳入了88项研究,包括12,318名参与者,评估了17种生物标志物。多形核中性粒细胞弹性酶(pmn -弹性酶)表现出最强的综合性能,入院后1天内的曲线下面积(AUC)为0.96,入院时的敏感性和特异性分别为0.93和0.94。白细胞介素-6 (IL-6)也表现出较强的早期预测能力,1天内AUC为0.93,2天内敏感性和特异性分别为0.96和0.80。c -反应蛋白(CRP)在连续监测期间的表现优于早期评估,第5天AUC达到0.92,第6天诊断优势比(DOR)为177.22。crp -白蛋白比、降钙素原、白介素-8、羧肽酶B激活肽和新天鹅蛋白显示出中等至高的预测性能。相比之下,中性粒细胞与淋巴细胞比率和白细胞计数显示出适度的准确性,而血小板与淋巴细胞比率、红细胞沉降率和白细胞介素-10的预测价值有限。pmn弹性蛋白酶和IL-6是早期评估AP严重程度的有希望的生物标志物,而CRP更适合动态监测。然而,大量的方法学和临床异质性排除了对生物标志物的直接排序,并强调了对多标志物模型进行标准化、前瞻性研究的必要性。
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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