Kabbany Mohammad Nasser, Conjeevaram Selvakumar Praveen Kumar, Guirguis John, Rivas John, Akras Zade, Lopez Rocio, Hanouneh Ibrahim, Eghtesad Bijan, Alkhouri Naim
From the Department of Pediatric Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, Ohio, USA.
Exp Clin Transplant. 2018 Oct;16(5):562-567. doi: 10.6002/ect.2016.0340. Epub 2017 Sep 26.
Several scoring systems have been developed to noninvasively predict the presence of advanced fibrosis in patients with chronic liver disease. Hepatitis C virus and nonalcoholic fatty liver disease are the 2 most common indications for orthotopic liver transplant and are associated with disease recurrence that can lead to fibrosis progression. Here, we evaluated the performance of commonly used fibrosis scores in assessing the presence of advanced fibrosis in patients after orthotopic liver transplant.
Our study consisted of consecutive patients with hepatitis C virus or nonalcoholic fatty liver disease who underwent a liver biopsy after transplant and had laboratory measurements within 1 week of biopsy. Graft fibrosis was determined by an experienced pathologist (stage F0-F4). Advanced fibrosis was defined as stage F3-F4. The following fibrosis scores were calculated for each patient: aspartate aminotransferase/alanine aminotransferase ratio, aspartate aminotransferase/platelet ratio index, and fibrosis-4 index.
We analyzed 93 patients with median age of 59 years (25th and 75th percentile of 53 and 64 y) and median body mass index of 31.8 kg/m² (25th and 75th percentile of 27 and 37.6 kg/m²). Of total patients, 41 (44%) were diabetic. Median time to liver biopsy posttransplant was 27.7 months (25th and 75 percentile of 10.8 and 59.9 mo). We found that 54 patients (58%) had no fibrosis, 15 (16.1%) had F1, 8 (8.6%) had F2, 7 (7.5%) had F3, and 9 (9.7%) had F4. Overall, advanced fibrosis (F3-F4) was present in 16 patients. Aspartate aminotransferase/alanine amino-transferase ratio, aspartate aminotransferase/platelet ratio index, and fibrosis-4 index were not significantly different between patients with and without advanced fibrosis (all P > .05). The calculated fibrosis scores had poor diagnostic accuracy for presence of advanced fibrosis posttransplant.
Commonly used liver fibrosis scores are not accurate in predicting the presence of advanced fibrosis in patients after liver transplant.
已开发出多种评分系统,用于无创预测慢性肝病患者是否存在晚期纤维化。丙型肝炎病毒和非酒精性脂肪性肝病是原位肝移植最常见的两个适应证,且与可导致纤维化进展的疾病复发相关。在此,我们评估了常用纤维化评分在评估原位肝移植患者晚期纤维化存在情况时的性能。
我们的研究纳入了连续的丙型肝炎病毒或非酒精性脂肪性肝病患者,这些患者在移植后接受了肝活检,并在活检后1周内进行了实验室检测。移植肝纤维化由一位经验丰富的病理学家判定(F0-F4期)。晚期纤维化定义为F3-F4期。为每位患者计算以下纤维化评分:天冬氨酸转氨酶/丙氨酸转氨酶比值、天冬氨酸转氨酶/血小板比值指数和纤维化-4指数。
我们分析了93例患者,中位年龄为59岁(第25和第75百分位数分别为53岁和64岁),中位体重指数为31.8kg/m²(第25和第75百分位数分别为27kg/m²和37.6kg/m²)。在所有患者中,41例(44%)患有糖尿病。移植后至肝活检的中位时间为27.7个月(第25和第75百分位数分别为10.8个月和59.9个月)。我们发现,54例患者(58%)无纤维化,15例(16.1%)为F1期,8例(8.6%)为F2期,7例(7.5%)为FIII期,9例(9.7%)为F4期。总体而言,16例患者存在晚期纤维化(F3-F4)。有和没有晚期纤维化的患者之间,天冬氨酸转氨酶/丙氨酸转氨酶比值、天冬氨酸转氨酶/血小板比值指数和纤维化-4指数均无显著差异(所有P>.05)。计算出的纤维化评分对移植后晚期纤维化存在情况的诊断准确性较差。
常用的肝纤维化评分在预测肝移植患者晚期纤维化的存在情况时并不准确。