Weber Sabine, Allgeier Julian, Denk Gerald, Gerbes Alexander L
Department of Medicine II, Liver Centre Munich, LMU Klinikum Munich, Munich, Germany.
Visc Med. 2022 Jun;38(3):223-228. doi: 10.1159/000519752. Epub 2021 Nov 3.
Clinically significant drug-induced liver injury (DILI) is defined by elevations of alanine aminotransferase (ALT) ≥5 times the upper limit of normal (ULN), alkaline phosphatase (ALP) ≥2 × ULN, or ALT ≥3 × ULN and total bilirubin TBIL >2 × ULN. However, DILI might also occur in patients who do not reach those thresholds and still may benefit from discontinuation of medication.
Fifteen patients recruited for our prospective study on potentially hepatotoxic drugs were included. DILI diagnosis was based on RUCAM (Roussel Uclaf Causality Assessment Method) score and expert opinion and was supported by an in vitro test using monocyte-derived hepatocyte-like (MH) cells.
Median RUCAM score was 6 (range 4-8), indicating that DILI was possible or probable in all cases. The predominant types of liver injury were mixed (60%) and cholestatic (40%). While no elevation above 2 × ULN of ALP and TBIL was observed, gamma-glutamyltransferase (GGT) above 2 × ULN was identified in 8 of the patients. Six of the 15 patients did not achieve full remission and showed persistent elevation of GGT, which was significantly associated with peak GGT elevation above 2 × ULN ( = 0.005).
Here we present a case series of patients with liver enzyme elevation below the conventional thresholds who developed DILI with a predominant GGT elevation leading to drug withdrawal and/or chronic elevation of liver parameters, in particular of GGT. Thus, we propose that DILI should be considered in particular in cases with marked increase of GGT even if conventional DILI threshold levels are not reached, resulting in discontinuation of the causative drug and/or close monitoring of the patients.
具有临床意义的药物性肝损伤(DILI)定义为丙氨酸氨基转移酶(ALT)升高至正常上限(ULN)的5倍以上、碱性磷酸酶(ALP)升高至2×ULN以上,或ALT升高至3×ULN且总胆红素(TBIL)>2×ULN。然而,DILI也可能发生在未达到这些阈值的患者中,这些患者停药后仍可能受益。
纳入了15名参与我们关于潜在肝毒性药物的前瞻性研究的患者。DILI诊断基于RUCAM(赛诺菲因果关系评估方法)评分和专家意见,并通过使用单核细胞衍生的肝样(MH)细胞的体外试验得到支持。
RUCAM评分中位数为6(范围4 - 8),表明所有病例均可能或很可能为DILI。肝损伤的主要类型为混合型(60%)和胆汁淤积型(40%)。虽然未观察到ALP和TBIL升高超过2×ULN,但8名患者的γ-谷氨酰转移酶(GGT)高于2×ULN。15名患者中有6名未完全缓解,GGT持续升高,这与GGT峰值升高超过2×ULN显著相关(P = 0.005)。
在此,我们展示了一系列肝酶升高低于传统阈值的患者病例,这些患者发生了以GGT升高为主的DILI,导致停药和/或肝脏参数尤其是GGT的慢性升高。因此,我们建议,即使未达到传统的DILI阈值水平,但GGT显著升高的病例尤其应考虑DILI,应停用致病药物和/或密切监测患者。