Schröder Torsten, Schmidt Klaus J, Olsen Vera, Möller Steffen, Mackenroth Tilo, Sina Christian, Lehnert Hendrik, Fellermann Klaus, Büning Jürgen
Departments of aMedicine I bDermatology, University Hospital Schleswig-Holstein, Campus Lübeck cGastroenterology Practice, Lübeck, Germany.
Eur J Gastroenterol Hepatol. 2015 Jun;27(6):698-704. doi: 10.1097/MEG.0000000000000350.
In inflammatory bowel disease (IBD), hepatic disorders are frequently due to nonalcoholic fatty liver disease and drug-induced hepatotoxicity. Immunosuppressive treatment is known to exert hepatotoxic side effects by a still unknown mode. The relevance of liver steatosis for the development of drug-related hepatotoxicity in IBD is unknown.
The charts of 259 patients with IBD under immunosuppression with either azathioprine, 6-mercaptopurine, or methotrexate were reviewed. The prevalence of liver steatosis was assessed by means of ultrasound reports. Aspartate transaminase and alanine transaminase above the normal range were used to indicate liver abnormalities.
Liver steatosis on the basis of ultrasound criteria was observed in 73 patients (28.2%). In patients with liver steatosis, the presence of elevated liver enzymes (ELE) was found to be significantly more prevalent (28.8 vs. 14.5%, P=0.0095). The finding of liver steatosis was associated with higher age (44.1 vs. 34.5 years, P<0.0001) and body weight (BMI 26.7 vs. 23.4 kg/m, P<0.0001). Development of ELE under immunosuppression was seen in 50 patients (19.3%). Of the patients who developed ELE, 44.0% (vs. 24.4%, P=0.0095) showed liver steatosis. Logistic regression analysis revealed that male individuals showed an increased likelihood of developing ELE associated with steatosis (P=0.0118, odds ratio=3.93) and that patients who received steroids less often developed ELE in association with liver steatosis (P=0.0414, odds ratio=0.31).
This study suggests that fatty liver represents a risk factor for hepatotoxicity in patients with IBD under immunosuppressive treatment and should be routinely considered in treatment strategies.
在炎症性肠病(IBD)中,肝脏疾病常由非酒精性脂肪性肝病和药物性肝毒性引起。已知免疫抑制治疗会通过一种尚不清楚的方式产生肝毒性副作用。IBD中肝脂肪变性与药物相关肝毒性发生的相关性尚不清楚。
回顾了259例接受硫唑嘌呤、6-巯基嘌呤或甲氨蝶呤免疫抑制治疗的IBD患者的病历。通过超声报告评估肝脂肪变性的患病率。使用高于正常范围的天冬氨酸转氨酶和丙氨酸转氨酶来表明肝脏异常。
根据超声标准,73例患者(28.2%)存在肝脂肪变性。在肝脂肪变性患者中,发现肝酶升高(ELE)更为普遍(28.8%对14.5%,P = 0.0095)。肝脂肪变性的发现与年龄较大(44.1岁对34.5岁,P < 0.0001)和体重较高(BMI 26.7对23.4kg/m²,P < 0.0001)有关。50例患者(19.