Fontana Robert J, Hayashi Paul H, Barnhart Huiman, Kleiner David E, Reddy K Rajender, Chalasani Naga, Lee William M, Stolz Andrew, Phillips Thomas, Serrano Jose, Watkins Paul B
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
University of North Carolina, Chapel Hill, North Carolina, USA.
Am J Gastroenterol. 2015 Oct;110(10):1450-9. doi: 10.1038/ajg.2015.283. Epub 2015 Sep 8.
The long-term outcomes of patients with drug induced liver injury (DILI) are not well described. The aim of this study was to determine the frequency and severity of persistent liver biochemistry abnormalities in DILI patients followed over 2 years.
Subjects with evidence of liver injury at 6 months after DILI onset were offered a month 12 and 24 study visit.
Amongst the 99 patients with definite, probable, or very likely DILI and available laboratory data at 12 months after DILI onset, 74 (75%) had persistent liver injury (persisters) defined as a serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >1.5 × upper limit of normal (ULN) or an alkaline phosphatase >ULN, while 25 (25%) had resolved liver injury (resolvers). On multivariate analysis, month 12 persisters were significantly older (52.6 vs. 43.7 years, P=0.01) and more likely to have a cholestatic lab profile at DILI onset (54 vs. 20%, P<0.01) than resolvers. The month 12 persisters also had significantly poorer SF-36 physical summary scores at DILI onset and throughout follow-up compared with the resolvers (P<0.01). Amongst the 17 subjects with a liver biopsy obtained at a median of 387 days after DILI onset, 9 had chronic cholestasis, 3 had steatohepatitis, and 3 had chronic hepatitis.
In all, 75% of subjects with liver injury at 6 months after DILI onset have laboratory evidence of persistent liver injury during prolonged follow-up. Higher serum alkaline phosphatase levels at presentation and older patient age were independent predictors of persistent liver injury. Subjects with persistent liver injury at 12 months after DILI onset should be carefully monitored and assessed for liver disease progression.
药物性肝损伤(DILI)患者的长期预后尚无详尽描述。本研究旨在确定随访2年的DILI患者持续性肝生化异常的频率和严重程度。
DILI发病后6个月有肝损伤证据的受试者接受第12个月和第24个月的研究访视。
在99例确诊、很可能或极有可能患DILI且在DILI发病后12个月有可用实验室数据的患者中,74例(75%)存在持续性肝损伤(持续损伤者),定义为血清天冬氨酸氨基转移酶(AST)或丙氨酸氨基转移酶(ALT)>正常上限(ULN)的1.5倍或碱性磷酸酶>ULN,而25例(25%)肝损伤已缓解(缓解者)。多因素分析显示,与缓解者相比,第12个月时的持续损伤者年龄显著更大(52.6岁对43.7岁,P = 0.01),且在DILI发病时更有可能具有胆汁淤积性实验室检查结果(54%对20%,P < 0.01)。与缓解者相比,第12个月时的持续损伤者在DILI发病时及整个随访期间的SF - 36身体综合评分也显著更低(P < 0.01)。在DILI发病后中位387天进行肝活检的17例受试者中,9例有慢性胆汁淤积,3例有脂肪性肝炎,3例有慢性肝炎。
总体而言,DILI发病后6个月有肝损伤的受试者中,75%在长期随访期间有持续性肝损伤的实验室证据。就诊时血清碱性磷酸酶水平较高和患者年龄较大是持续性肝损伤的独立预测因素。DILI发病后12个月有持续性肝损伤的受试者应仔细监测并评估肝病进展情况。