Scientific Reports (Oct 2024)

Elevated intestinal fatty acid-binding protein levels as a marker of portal hypertension and gastroesophageal varices in cirrhosis

  • Satoshi Miuma,
  • Hisamitsu Miyaaki,
  • Naota Taura,
  • Yasuko Kanda,
  • Satoshi Matsuo,
  • Kazuaki Tajima,
  • Kosuke Takahashi,
  • Yasuhiko Nakao,
  • Masanori Fukushima,
  • Masafumi Haraguchi,
  • Ryu Sasaki,
  • Eisuke Ozawa,
  • Tatsuki Ichikawa,
  • Kazuhiko Nakao

DOI
https://doi.org/10.1038/s41598-024-76040-6
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 12

Abstract

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Abstract We measured intestinal fatty acid-binding protein (I-FABP) levels, a useful marker of small intestinal mucosal injury, in patients with cirrhosis to determine their relationship with liver function and complications. This cross-sectional study included 71 patients with cirrhosis admitted for treatment of cirrhotic complications or hepatocellular carcinoma (cohort A) and 104 patients with cirrhosis who received direct-acting antiviral therapy for HCV (cohort B). I-FABP levels, measured by ELISA, were evaluated relative to hepatic reserve and compared with non-invasive scoring systems for diagnostic performance in cirrhotic complications. The median I-FABP level in both cohorts were significantly elevated in patients with reduced hepatic reserve (CTP grade A/BC cohort A, 2.33/3.17 ng/mL, p = 0.032; cohort B, 2.46/3.64 ng/mL, p = 0.008) and complications with gastroesophageal varices (GEV; GEV (-)/(+) cohort A, 1.66/3.67 ng/mL, p < 0.001; cohort B, 2.32/3.36 ng/mL; p = 0.003). Further, multiple logistic regression analysis identified I-FABP as the only factor contributing to GEV presence in both cohorts, which outperformed non-invasive scoring systems for GEV diagnosis (sensitivity 84.6%; specificity 84.2%; sensitivity 69.6%; specificity 63.8%, respectively). In conclusion, elevated small-intestinal mucosal injury in patients with cirrhosis was related to reduced hepatic reserve and GEV presence. I-FABP levels reflect portal hypertension and may be useful in cirrhosis management.