Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, 1- 7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Department of Gastroenterology, Nagasaki Harbor Medical Center, Shinti 6-39, Nagasaki, 850-8555, Japan.
Sci Rep. 2024 Oct 23;14(1):25003. doi: 10.1038/s41598-024-76040-6.
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.
我们测量了肝硬化患者的肠脂肪酸结合蛋白(I-FABP)水平,这是一种评估小肠黏膜损伤的有用标志物,以确定其与肝功能和并发症的关系。这项横断面研究纳入了 71 例因肝硬化并发症或肝细胞癌(A 队列)而接受治疗的肝硬化患者和 104 例接受直接作用抗病毒治疗丙型肝炎病毒(HCV)的肝硬化患者(B 队列)。通过 ELISA 测量 I-FABP 水平,根据肝储备情况进行评估,并与非侵入性评分系统比较,以评估其在肝硬化并发症中的诊断性能。两个队列的 I-FABP 水平在肝储备降低的患者中均显著升高(CTP 分级 A/BC 队列 A,2.33/3.17ng/mL,p=0.032;队列 B,2.46/3.64ng/mL,p=0.008)和存在胃食管静脉曲张(GEV)的并发症患者(GEV(-)/(+)队列 A,1.66/3.67ng/mL,p<0.001;队列 B,2.32/3.36ng/mL,p=0.003)。此外,多变量逻辑回归分析确定 I-FABP 是两个队列中导致 GEV 存在的唯一因素,其在 GEV 诊断方面优于非侵入性评分系统(敏感性 84.6%;特异性 84.2%;敏感性 69.6%;特异性 63.8%)。总之,肝硬化患者小肠黏膜损伤增加与肝储备降低和 GEV 存在有关。I-FABP 水平反映门静脉高压,可能有助于肝硬化的管理。