Evidence map›Paper›PMID 42676544›Full record

ArticleJournal of clinical practice and research2026

Endothelial Biomarkers Predict Clinical Deterioration in Acute Pancreatitis.

Rauf Agayev, Aliniyaz Mammadov, Emil Iskandarov, Farajullah Idrisov

Abstract read
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Article in Journal of clinical practice and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Rauf AgayevDepartment of Surgery, Scientific Centre of Surgery, Baku, Azerbaijan.
Aliniyaz MammadovDepartment of Surgery, Scientific Centre of Surgery, Baku, Azerbaijan.
Emil IskandarovDepartment of Surgery Training Division, The Administration of Regional Medical Divisions, Baku, Azerbaijan.
Farajullah IdrisovDepartment of Surgery, Scientific Centre of Surgery, Baku, Azerbaijan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Endothelial dysfunction contributes to the severity of acute pancreatitis (AP), but the prognostic utility of endothelial biomarkers and their association with therapeutic interventions remain poorly defined. This study aimed to determine whether endothelial dysfunction biomarkers predict clinical deterioration in AP and whether plasmapheresis is associated with changes in these biomarkers and clinical outcomes. Materials and Methods: In this prospective cohort study of 100 patients with AP, serial endothelial biomarkers, including vascular endothelial growth factor (VEGF), von Willebrand factor (vWF), endothelin-1 (ET-1), and soluble E-selectin (sE-selectin), were measured on admission and on days 3 and 7. All patients received conventional therapy, and 68 additionally received adjunctive plasmapheresis through nonrandomized assignment. The conventional therapy cohort (n=32) was stratified into Worsened (n=17) and Improved (n=15) subgroups according to clinical course to establish prognostic biomarker cutoffs. Results: Endothelial marker levels at admission predicted subsequent clinical deterioration (p<0.001). Biomarker trajectories differed significantly between the Improved and Worsened subgroups. Patients who received plasmapheresis exhibited more favorable biomarker profiles, with levels resembling those of the Improved subgroup by day 7. This biomarker pattern was associated with a lower rate of the composite clinical deterioration endpoint than that observed in the Worsened subgroup (12% vs. 100%, p<0.001). Conclusion: Endothelial dysfunction biomarkers are early predictors of the clinical course of AP. Plasmapheresis was associated with favorable biomarker trajectories and improved clinical outcomes, suggesting that endothelial dysfunction may be a potential therapeutic target warranting investigation in randomized trials.

Indexed as

Acute pancreatitisbiomarkersendothelial dysfunctionplasmapheresisprognosis

Identifiers

PMID42676544
PMCPMC13526765

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