Time-Dependent Changes in YKL-40 and Inflammatory Markers in Experimental Acute Mesenteric Ischemia

BACKGROUND: Early diagnosis of acute mesenteric ischemia (AMI) remains challenging due to the lack of reliable biomarkers. This study aimed to investigate the time-dependent changes in chitinase-3-like protein 1 (YKL-40) and selected inflammatory markers in an experimental AMI model. METHODS: A randomized controlled experimental study was conducted on 48 Wistar-Albino rats. Mesenteric ischemia was induced by ligation of the superior mesenteric artery. Blood and tissue samples were collected at 1, 3, and 6 hours. Serum YKL-40, interleukin-6 (IL-6), interleukin-10 (IL-10) and lactate levels were measured, and histopathological damage was assessed. RESULTS: IL-6 levels increased significantly as early as 1 hour (p = 0.010) and showed a progressive rise over time (p < 0.001), with a strong positive correlation with histopathological damage (r = 0.805). Lactate levels increased significantly at later time points. YKL-40 levels did not differ in the early phase but were significantly elevated at 6 hours (p < 0.001). IL-10 levels decreased significantly in advanced ischemia (p = 0.005). CONCLUSION: IL-6 showed an early increase and a strong association with histopathological damage, whereas YKL-40 appeared to be associated with later-stage inflammation rather than early ischemic injury. These findings highlight the importance of time-dependent biomarker interpretation and support further evaluation of combined biomarker strategies in AMI.

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Publication Details

Journal
Biomarkers
Published
2026-08-21
DOI
https://doi.org/10.1080/1354750x.2026.2723432
Primary Topic
Abdominal vascular conditions and treatments
Type
article
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article

Time-Dependent Changes in YKL-40 and Inflammatory Markers in Experimental Acute Mesenteric Ischemia

Muhammed Ali Akbulut, Mehmet Aykut Yıldırım, Rahim Kocabaş, Fahriye Kılınç et al.
Biomarkers
Abdominal vascular conditions and treatments
article

Time-Dependent Changes in YKL-40 and Inflammatory Markers in Experimental Acute Mesenteric Ischemia

Muhammed Ali Akbulut, Mehmet Aykut Yıldırım, Rahim Kocabaş, Fahriye Kılınç, Abdullah Gürhan Duyan
article en

Abstract

BACKGROUND: Early diagnosis of acute mesenteric ischemia (AMI) remains challenging due to the lack of reliable biomarkers. This study aimed to investigate the time-dependent changes in chitinase-3-like protein 1 (YKL-40) and selected inflammatory markers in an experimental AMI model. METHODS: A randomized controlled experimental study was conducted on 48 Wistar-Albino rats. Mesenteric ischemia was induced by ligation of the superior mesenteric artery. Blood and tissue samples were collected at 1, 3, and 6 hours. Serum YKL-40, interleukin-6 (IL-6), interleukin-10 (IL-10) and lactate levels were measured, and histopathological damage was assessed. RESULTS: IL-6 levels increased significantly as early as 1 hour (p = 0.010) and showed a progressive rise over time (p < 0.001), with a strong positive correlation with histopathological damage (r = 0.805). Lactate levels increased significantly at later time points. YKL-40 levels did not differ in the early phase but were significantly elevated at 6 hours (p < 0.001). IL-10 levels decreased significantly in advanced ischemia (p = 0.005). CONCLUSION: IL-6 showed an early increase and a strong association with histopathological damage, whereas YKL-40 appeared to be associated with later-stage inflammation rather than early ischemic injury. These findings highlight the importance of time-dependent biomarker interpretation and support further evaluation of combined biomarker strategies in AMI.

Biomarkers
Selçuk University (TR), Necmettin Erbakan University (TR), Konya Eğitim ve Araştırma Hastanesi (TR), Karamanoğlu Mehmetbey University (TR)
Good health and well-being
Openalex Percentile: Top 7%
Abdominal vascular conditions and treatments
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Time-Dependent Changes in YKL-40 and Inflammatory Markers in Experimental Acute Mesenteric Ischemia — Muhammed Ali Akbulut, Mehmet Aykut Yıldırım, et al. · Biomarkers (2026) | TGRS Research Map | TGRS