Association Between Plasma Level of Galectin-9 and Survival of Patients With Drug-Induced Acute Liver Failure

被引:16
作者
Rosen, Hugo R. [1 ,2 ]
Biggins, Scott W. [1 ]
Niki, Toshiro [3 ,4 ]
Gralla, Jane [5 ,6 ]
Hillman, Holly [7 ]
Hirashima, Mitsuomi [3 ,4 ]
Schilsky, Michael [8 ,9 ,10 ,11 ]
Lee, William M. [12 ]
机构
[1] Univ Colorado, Dept Med, Div Gastroenterol & Hepatol, Aurora, CO USA
[2] Univ Colorado, Integrated Program Immunol, Aurora, CO USA
[3] Kagawa Univ, Dept Immunol, Kagawa, Japan
[4] GalPharma Co, Kagawa, Japan
[5] Univ Colorado Denver, Dept Pediat, Aurora, CO USA
[6] Univ Colorado Denver, Dept Biostat & Informat, Aurora, CO USA
[7] Med Univ S Carolina, Dept Publ Hlth Sci, Data Coordinat Unit, Charleston, SC 29425 USA
[8] Yale Univ, Med Ctr, Dept Med, Div Digest Dis, New Haven, CT USA
[9] Yale Univ, Med Ctr, Dept Med, Sect Transplantat & Immunol, New Haven, CT USA
[10] Yale Univ, Med Ctr, Dept Surg, Div Digest Dis, New Haven, CT USA
[11] Yale Univ, Med Ctr, Dept Surg, Sect Transplantat & Immunol, New Haven, CT USA
[12] Univ Texas SW Med Ctr Dallas, Div Digest & Liver Dis, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Innate Immune Responses; SIRS; Stratification; Prediction; FULMINANT HEPATIC-FAILURE; ACETAMINOPHEN HEPATOTOXICITY; INNATE IMMUNITY; KINGS-COLLEGE; KUPFFER CELL; GC-GLOBULIN; PROGNOSIS; CRITERIA; COHORT; TIM-3;
D O I
10.1016/j.cgh.2015.09.040
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Fewer than 50% of patients with acute liver failure (ALF) recover spontaneously, and ALF has high mortality without liver transplantation. Kupffer cells have been reported to mediate liver inflammation during drug-induced injury. Galectin-9 is produced by Kupffer cells and has diverse roles in regulating immunity. We investigated whether plasma levels of galectin-9 are associated with outcomes of patients with ALF. METHODS: We analyzed plasma samples (collected at time of hospital admission) and clinical data from 149 patients included in the Acute Liver Failure Study Group from July 2006 through November 2010 (110 had acetaminophen-induced hepatotoxicity and 39 had nonacetaminophen drug-induced liver injury). We compared data with those from all patients enrolled in the study (from July 1, 2006 through October 30, 2013), and from healthy individuals of similar ages with no evidence of liver disease (control subjects). Plasma levels of galectin-9 were measured using a polyclonal antibody and colorimetric assay. RESULTS: Patients with ALF had statistically higher plasma levels of galectin-9 than control subjects, but levels did not differ significantly between patients with acetaminophen-induced liver injury and drug-induced liver injury. A level of galectin-9 above 690 pg/mL was associated with a statistically significant increase in risk for mortality or liver transplantation caused by ALF. Competing risk analyses associated level of galectin-9 with transplant-free survival, independently of Model For End-Stage Liver Disease score or systemic inflammatory response syndrome. CONCLUSIONS: A one-time measurement of plasma galectin-9 level can be used to assign patients with ALF to high-, intermediate-, and low-risk groups. The combination of galectin-9 level and Model For End-Stage Liver Disease score was more closely associated with patient outcome than either value alone. These data might be used to determine patient prognoses and prioritize patients for liver transplantation.
引用
收藏
页码:606 / +
页数:10
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