The Enhanced liver fibrosis score is associated with clinical outcomes and disease progression in patients with chronic liver disease

被引:50
作者
Irvine, Katharine M. [1 ]
Wockner, Leesa F. [2 ]
Shanker, Mihir [1 ]
Fagan, Kevin J. [1 ,3 ]
Horsfall, Leigh U. [1 ,3 ]
Fletcher, Linda M. [3 ]
Ungerer, Jacobus P. J. [4 ]
Pretorius, Carel J. [4 ]
Miller, Gregory C. [1 ]
Clouston, Andrew D. [1 ]
Lampe, Guy [5 ]
Powell, Elizabeth E. [1 ,3 ]
机构
[1] Univ Queensland, Sch Med, Ctr Liver Dis Res, Brisbane, Qld, Australia
[2] QIMR Berghofer Med Res Inst, Stat Unit, Brisbane, Qld, Australia
[3] Princess Alexandra Hosp, Dept Gastroenterol & Hepatol, Brisbane, Qld 4102, Australia
[4] Pathol Queensland, Dept Chem Pathol, Brisbane, Qld, Australia
[5] Princess Alexandra Hosp, Pathol Queensland, Brisbane, Qld 4102, Australia
基金
英国医学研究理事会;
关键词
liver cirrhosis; decompensation; liver cancer; non-invasive biomarkers; prediction of clinical outcomes; SIMPLE NONINVASIVE INDEX; CHRONIC HEPATITIS-C; PREDICT; MORTALITY; BURDEN; BIOPSY;
D O I
10.1111/liv.12896
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimsCurrent tools for risk stratification of chronic liver disease subjects are limited. We aimed to determine whether the serum-based ELF (Enhanced Liver Fibrosis) test predicted liver-related clinical outcomes, or progression to advanced liver disease, and to compare the performance of ELF to liver biopsy and non-invasive algorithms. MethodsThree hundred patients with ELF scores assayed at the time of liver biopsy were followed up (median 6.1years) for liver-related clinical outcomes (n=16) and clear evidence of progression to advanced fibrosis (n=18), by review of medical records and clinical data. ResultsFourteen of 73 (19.2%) patients with ELF score indicative of advanced fibrosis (9.8, the manufacturer's cut-off) had a liver-related clinical outcome, compared to only two of 227 (<1%) patients with ELF score <9.8. In contrast, the simple scores APRI and FIB-4 would only have predicted subsequent decompensation in six and four patients respectively. A unit increase in ELF score was associated with a 2.53-fold increased risk of a liver-related event (adjusted for age and stage of fibrosis). In patients without advanced fibrosis on biopsy at recruitment, 55% (10/18) with an ELF score 9.8 showed clear evidence of progression to advanced fibrosis (after an average 6years), whereas only 3.5% of those with an ELF score <9.8 (8/207) progressed (average 14years). In these subjects, a unit increase in ELF score was associated with a 4.34-fold increased risk of progression. ConclusionsThe ELF score is a valuable tool for risk stratification of patients with chronic liver disease.
引用
收藏
页码:370 / 377
页数:8
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