Woolbright Benjamin L, Bridges Brian W, Dunn Winston, Olson Jody C, Weinman Steven A, Jaeschke Hartmut
Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS, USA.
Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Gene Expr. 2017 Nov 27;17(4):301-312. doi: 10.3727/105221617X15016197658871. Epub 2017 Aug 3.
Alcoholic liver disease encompasses the progressive stages of liver dysfunction that culminates in alcoholic cirrhosis (AC) and in severe cases alcoholic hepatitis (AH). Currently, prognostic scores have limited specificity and sensitivity. Plasma keratin-18 (K18) levels are elevated during liver disease and may be biomarkers of outcome. The objective of this study was to determine if total K18 (M65) or caspase-cleaved K18 (M30) levels were different between AC and AH patients. M65 and M30 levels were measured in the plasma of consented healthy controls and patients with AC and AH. Cell death was assessed by TUNEL staining and caspase activity. M65 and M30 values were significantly higher in AC patients compared to healthy controls and further increased in AH patients. The M65 values and the M30/M65 ratios of nonsurviving AH patients were significantly elevated above their surviving counterparts and healthy controls. Statistical analysis indicated that M30/M65 ratios outperformed current indices for accurately distinguishing the prognosis of AH patients. These scores occurred with minimal increase in plasma cell death markers such as ALT and AST. Serum caspase activity, TUNEL staining, and M30 immunohistochemistry in biopsies indicated that serum and tissue values may not correlate well with overall cell death. In conclusion, both M65 and M30 differentiate AH from AC patients, and M65 values and the M30/M65 ratio are capable of predicting early stage mortality; however, they may not accurately reflect pure hepatocyte cell death in these populations, as they do not strongly correlate with traditional cell death markers.
酒精性肝病包括肝功能障碍的进展阶段,最终导致酒精性肝硬化(AC),严重时会引发酒精性肝炎(AH)。目前,预后评分的特异性和敏感性有限。血浆角蛋白-18(K18)水平在肝病期间会升高,可能是预后的生物标志物。本研究的目的是确定AC患者和AH患者的总K18(M65)或半胱天冬酶切割的K18(M30)水平是否存在差异。在获得同意的健康对照者以及AC和AH患者的血浆中测量M65和M30水平。通过TUNEL染色和半胱天冬酶活性评估细胞死亡情况。与健康对照者相比,AC患者的M65和M30值显著更高,而AH患者的这些值进一步升高。未存活的AH患者的M65值和M30/M65比值显著高于其存活的对应患者以及健康对照者。统计分析表明,M30/M65比值在准确区分AH患者的预后方面优于当前指标。这些评分出现时,血浆细胞死亡标志物如ALT和AST的升高幅度最小。活检中的血清半胱天冬酶活性、TUNEL染色和M30免疫组化表明,血清和组织值可能与总体细胞死亡情况相关性不佳。总之,M65和M30均可区分AH患者和AC患者,M65值和M30/M65比值能够预测早期死亡率;然而,它们可能无法准确反映这些人群中单纯的肝细胞死亡情况,因为它们与传统细胞死亡标志物的相关性不强。