Khare Shivam, Arora Anil, Sharma Praveen, Dhawan Shashi, Bansal Naresh, Singla Vikas, Kumar Ashish
Institute of Liver, Gastroenterology & Pancreatico-Biliary Sciences, Sir Ganga Ram Hospital, New Delhi, India.
Department of Histopathology, Sir Ganga Ram Hospital, New Delhi, India.
J Clin Transl Hepatol. 2020 Jun 28;8(2):143-149. doi: 10.14218/JCTH.2020.00002. Epub 2020 May 29.
Evaluation of significant liver fibrosis is important for treatment decision and treatment response evaluation in patients with chronic hepatitis B. Since liver biopsy is invasive and transient elastography (TE) has limited availability, various non-invasive blood parameters need evaluation for their capabilities for detection of significant fibrosis. In this retrospective study, records of patients who had undergone liver biopsy for treatment-naïve chronic hepatitis B were evaluated to obtain various non-invasive blood parameters (aspartate aminotransferase-to-platelet ratio index [referred to as APRI], Fibrosis-4 score [referred to as FIB-4], gamma-glutamyl transpeptidase-to-platelet ratio [referred to as GPR], and gamma-glutamyl transpeptidase-to-albumin ratio [referred to as GAR]), in addition to TE, to assess significant liver fibrosis and compare these to fibrosis stage in liver biopsy. A total of 113 patients were included in the study (median age 33 [interquartile range: 11-82 years], 74% males). Most (75%) patients were HBeAg-negative. The liver biopsy revealed significant fibrosis (Ishak ≥3) in 13% of the patients and nil or mild fibrosis (Ishak <3) in 87% of the patients. TE findings were available for 85 patients, APRI and FIB-4 for 95 patients, GPR for 79 patients, and GAR for 78 patients. The median values of all the parameters were significantly higher in patients with significant fibrosis, as compared to patients with non-significant fibrosis, and all the blood parameters as well as TE were able to identify patients with significant fibrosis significantly well (<0.05). All non-invasive parameters had low positive predictive value but negative predictive value above 92%. Compared to TE, all the non-invasive blood parameters had similar area under the curve for detecting significant fibrosis, with excellent negative predictive value (≥93%). Non-invasive blood parameters (APRI, FIB-4, GPR, and GAR) with negative predictive values above 93% are excellent parameters for ruling-out significant fibrosis in patients with chronic hepatitis B. These can be used at bedside in place of TE.
评估显著肝纤维化对于慢性乙型肝炎患者的治疗决策和治疗反应评估至关重要。由于肝活检具有侵入性且瞬时弹性成像(TE)的可及性有限,因此需要评估各种非侵入性血液参数检测显著纤维化的能力。在这项回顾性研究中,对未经治疗的慢性乙型肝炎患者进行肝活检的记录进行评估,以获取各种非侵入性血液参数(天冬氨酸转氨酶与血小板比值指数[称为APRI]、Fibrosis-4评分[称为FIB-4]、γ-谷氨酰转肽酶与血小板比值[称为GPR]以及γ-谷氨酰转肽酶与白蛋白比值[称为GAR]),此外还包括TE,以评估显著肝纤维化,并将这些结果与肝活检中的纤维化分期进行比较。该研究共纳入113例患者(中位年龄33岁[四分位间距:11 - 82岁],74%为男性)。大多数(75%)患者HBeAg阴性。肝活检显示,13%的患者有显著纤维化(Ishak≥3),87%的患者无或轻度纤维化(Ishak<3)。85例患者有TE结果,95例患者有APRI和FIB-4结果,79例患者有GPR结果,78例患者有GAR结果。与非显著纤维化患者相比,显著纤维化患者所有参数的中位值均显著更高,并且所有血液参数以及TE均能很好地识别出显著纤维化患者(P<0.05)。所有非侵入性参数的阳性预测值较低,但阴性预测值均高于92%。与TE相比,所有非侵入性血液参数在检测显著纤维化方面的曲线下面积相似,具有出色的阴性预测值(≥93%)。阴性预测值高于93%的非侵入性血液参数(APRI、FIB-4、GPR和GAR)是排除慢性乙型肝炎患者显著纤维化的优秀参数。这些参数可在床边使用以替代TE。