医学
内科学
胃肠病学
炎症
队列
丙氨酸转氨酶
天冬氨酸转氨酶
HBeAg
肝活检
慢性肝炎
丙氨酸转氨酶
乙型肝炎
转氨酶
活检
免疫学
乙型肝炎病毒
乙型肝炎表面抗原
病毒
生物化学
化学
酶
碱性磷酸酶
作者
Jia Wang,Juan Xia,R. Zhang,Xiaomin Yan,Yongfeng Yang,Xiang‐An Zhao,Haiyan Chang,G. Wang,Gang Chen,Y. Liu,Yuxin Chen,Bin Jia,Z. Zhang,Weimao Ding,Rui Huang,Chao Wu
摘要
Summary Identifying the degree of liver inflammation is critical for therapeutic judgement of patients with chronic hepatitis B ( CHB ). However, we lack indexes which can accurately predict significant liver inflammation in patients with CHB . This study aimed to develop a simple predictive index for liver inflammation in CHB using routine clinical parameters. A total of 519 patients with CHB who underwent liver biopsy were enrolled and randomly divided into training (n = 346) and validation cohorts (n = 173). Based on routine clinical parameters, gamma‐glutamyl transpeptidase ( GGT ; P = 0.031) and platelets ( PLT ; P < 0.001) were identified as independent predictors of significant inflammation by multivariable analysis in the training cohort. Accordingly, the GGT to PLT ratio ( GPR ) was developed to amplify the opposing effects for predicting liver inflammation. In the training cohort, the AUC s of GPR in predicting significant inflammation were 0.791 (95% CI : 0.742‐0.839), 0.783 (95% CI : 0.717‐0.849) and 0.791 (95% CI : 0.716‐0.867) in the entire patients with CHB , HB eAg‐positive CHB patients and HB eAg‐negative CHB patients, respectively. The diagnostic performance of GPR for significant inflammation was significantly superior to that of alanine aminotransferase ( ALT ), aspartate transaminase ( AST ) and GGT in all patients with CHB and HB eAg‐positive CHB patients, but was comparable with ALT , AST and GGT in HB eAg‐negative CHB patients. In the validation cohort, the diagnostic performance of GPR in assessing significant liver inflammation was also superior to other indexes in all patients with CHB and HB eAg‐positive CHB patients, but was comparable with GGT in HB eAg‐negative CHB patients. Thus, GPR can be a novel and simple index for predicting significant liver inflammation in CHB , especially for HB eAg‐positive CHB .
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