State Key Laboratory for Diagnosis and Treatment of Infectious Diseases; National Clinical Research Center for Infectious Diseases; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases; The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
J Clin Invest. 2020 Apr 1;130(4):2069-2080. doi: 10.1172/JCI130197.
BACKGROUNDHBV-related acute-on-chronic liver failure (HBV-ACLF) is hallmarked by high short-term mortality rates, calling for accurate prognostic biomarkers for initial risk stratification.METHODSThree tandem mass tag-labeled (TMT-labeled) quantitative proteomic studies were performed on 10 patients with HBV-related acute hepatic decompensation and on 20 patients with HBV-ACLF. Candidate biomarkers were preliminarily verified in a cross-sectional cohort (n = 144) and further confirmed in 2 prospective cohorts (n = 207 and n = 148).RESULTSPlasminogen, a potential prognostic biomarker for HBV-ACLF, was identified by TMT quantitative proteomics and preliminarily verified in the cross-sectional cohort. Further validation with a prospective cohort (n = 207) showed that plasminogen levels at admission were significantly lower (P < 0.001) in HBV-ACLF nonsurvivors than in survivors. The cumulative survival duration of patients with high plasminogen levels was significantly longer (P < 0.001) than that of patients with low plasminogen levels. During hospitalization, plasminogen levels significantly decreased (P = 0.008) in the deterioration group but significantly increased (P < 0.001) in the improvement group. Additionally, plasminogen levels gradually increased in survivors but gradually decreased in nonsurvivors. The P5 score, a prognostic panel incorporating plasminogen levels, hepatic encephalopathy occurrence, age, international normalized ratio (INR), and total bilirubin, was significantly superior to the Child-Pugh, Model for End-stage Liver Disease (MELD), Chronic Liver Failure Consortium ACLF (CLIF-C ACLF), Chinese Group on the Study of Severe Hepatitis B (COSSH), and HINT (a prognostic score based on hepatic encephalopathy occurrence, INR, neutrophil count, and thyroid-stimulating hormone) scores (all P < 0.05). The performances of the plasminogen level and P5 score were validated in a second multicenter, prospective cohort (n = 148).CONCLUSIONSPlasminogen is a promising prognostic biomarker for HBV-ACLF, and sequential plasminogen measurements could profile the clinical course of HBV-ACLF. P5 is a high-performance prognostic score for HBV-ACLF.FUNDINGThe National Key Research and Development Program (2017YFC1200204); the National Natural Science Foundation of China (81400589, 81600497); the Foundation for Innovative Research Groups of the National Natural Science Foundation of China (81121002); the Chinese High-Tech Research and Development Programs (2012AA020204); the National S&T Major Project (2012ZX10002004); and the Zhejiang Provincial Medicine and Health Science and Technology Project (2016147735).
HBV 相关的慢加急性肝衰竭(HBV-ACLF)的特点是短期死亡率高,因此需要准确的预后生物标志物进行初始风险分层。
对 10 例 HBV 相关急性肝失代偿患者和 20 例 HBV-ACLF 患者进行了三个串联质量标签(TMT 标记)定量蛋白质组学研究。候选生物标志物在横断面队列(n=144)中进行了初步验证,并在两个前瞻性队列(n=207 和 n=148)中进一步确认。
纤溶酶原是 HBV-ACLF 的一种潜在预后生物标志物,通过 TMT 定量蛋白质组学鉴定,并在横断面队列中进行了初步验证。进一步在前瞻性队列(n=207)中的验证显示,HBV-ACLF 非幸存者入院时的纤溶酶原水平明显低于幸存者(P<0.001)。纤溶酶原水平较高的患者的累积生存时间明显长于纤溶酶原水平较低的患者(P<0.001)。在住院期间,恶化组的纤溶酶原水平显著降低(P=0.008),而改善组的纤溶酶原水平显著升高(P<0.001)。此外,纤溶酶原水平在幸存者中逐渐升高,而在非幸存者中逐渐降低。包含纤溶酶原水平、肝性脑病发生、年龄、国际标准化比值(INR)和总胆红素的 P5 评分显著优于 Child-Pugh、终末期肝病模型(MELD)、慢性肝衰竭联盟 ACLF(CLIF-C ACLF)、中国重症乙型肝炎研究组(COSSH)和 HINT(基于肝性脑病发生、INR、中性粒细胞计数和促甲状腺激素的预后评分)评分(均 P<0.05)。纤溶酶原水平和 P5 评分的性能在第二个多中心前瞻性队列(n=148)中得到验证。
纤溶酶原是 HBV-ACLF 的一种有前途的预后生物标志物,连续纤溶酶原测量可以描绘 HBV-ACLF 的临床过程。P5 是一种用于 HBV-ACLF 的高性能预后评分。
国家重点研发计划(2017YFC1200204);国家自然科学基金(81400589、81600497);国家自然科学基金创新研究群体科学基金(81121002);国家高技术研究发展计划(2012AA020204);国家科技重大专项(2012ZX10002004);浙江省医药卫生科技计划项目(2016147735)。