Serum thrombospondin 2 is a novel predictor for the severity in the patients with NAFLD

纤维化 内科学 胃肠病学 医学 血栓反应素 血栓反应蛋白 血栓反应蛋白1 肝活检 肝硬化 病理 活检 血管生成 金属蛋白酶 基质金属蛋白酶
作者
Takefumi Kimura,Naoki Tanaka,Naoyuki Fujimori,Tomoo Yamazaki,Takahito Katsuyama,Yuichi Iwashita,Jonathan Pham,Satoru Joshita,Sai P. Pydi,Takeji Umemura
出处
期刊:Liver International [Wiley]
卷期号:41 (3): 505-514 被引量:32
标识
DOI:10.1111/liv.14776
摘要

Abstract Aim Thrombospondins are a family of multidomain and secretory glycoproteins. Among them, thrombospondin 2 (TSP2) encoded by TSP2 gene has been reported to be involved in various functions such as collagen/fibrin formation, maintenance of normal blood vessel density and cell adhesion properties. Microarray analyses ranked TSP2 as one of the most highly up‐regulated genes in the fibrotic liver in patients with non‐alcoholic fatty liver disease (NAFLD). Since TSP2 possesses unique properties as a secretory protein, we hypothesized that hepatic TSP2 gene expression levels would be reflected in serum TSP2 levels. In this study, we examined the relationship between serum TSP2 concentrations and clinicopathological findings in NAFLD patients. Methods One hundred and thirty NAFLD patients who had undergone liver biopsy between 2009 and 2015 were retrospectively enrolled. Serum samples were collected at the time of biopsy, and TSP2 was measured by enzyme immunoassays. Results Serum TSP2 levels moderately correlated with ballooning (r = 0.56, P < .001) and fibrosis stage (r = 0.53, P < .001). The AUC values of TSP2 for predicting mild fibrosis (≧F1), moderate fibrosis (≧F2) and severe fibrosis (≧F3) were 0.73, 0.76 and 0.82 respectively. Additionally, NAFLD activity score (NAS) correlated best with TSP2 (r = 0.52, P < .001) compared to conventional NAFLD‐related biomarkers, such as cytokeratin 18 M30, hyaluronic acid, type IV collagen 7S, APRI and FIB‐4 index. Conclusion Serum TSP2 levels reflected hepatocyte ballooning, fibrosis and NAS in NAFLD patients. For clinical application of serum TSP2 as a predictor of NAFLD histological activity, additional validation and mechanistic investigations are required.
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