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银屑病患者中氨甲蝶呤的肝毒性:来自新斯科舍省的104例患者报告,以及长期随访期间肥胖、糖尿病和饮酒风险分析

Methotrexate hepatotoxicity in psoriatics: report of 104 patients from Nova Scotia, with analysis of risks from obesity, diabetes and alcohol consumption during long term follow-up.

作者信息

Malatjalian D A, Ross J B, Williams C N, Colwell S J, Eastwood B J

机构信息

Department of Community Health and Epidemiology, Dalhousie University, Halifax, Nova Scotia.

出版信息

Can J Gastroenterol. 1996 Oct;10(6):369-75. doi: 10.1155/1996/213596.

Abstract

BACKGROUND AND DESIGN

Methotrexate (MTX) hepatotoxicity in psoriatic patients is well recognized, but there are discrepancies in the reported incidence and associated risk factors. This retrospective study describes 104 Nova Scotian patients with psoriasis seen between 1979 and 1990. Patients received MTX over one to 11 years (mean 3.38), with baseline and annual follow-up liver biopsies. Clinical data were obtained by chart review. Statistical analysis evaluated the risks associated with obesity, diabetes, alcohol consumption and duration of therapy, with the histological grade of liver biopsies.

RESULTS

Of the 104 patients, 35 were obese, 10 were diabetic and 37 occasionally consumed alcohol. At the end of the study, 21 patients had developed severe hepatic fibrosis (grade IIIB), and three developed liver cirrhosis (grade IV). Significant risk of severe hepatotoxicity is related to diabetes (P = 0.02) but not to obesity (P = 0.12) or alcohol consumption (P = 0.12). All patients with cirrhosis took MTX for two years in standard doses of 20 to 25 mg/week.

CONCLUSIONS

In this first Canadian study evaluating MTX hepatotoxicity in psoriatics, the incidence of severe hepatotoxicity is high: 23.1% (24 of 104 patients). This study shows that diabetic patients are particularly at increased risk of MTX hepatotoxicity. Occasional alcohol consumption is not associated with increased risk. Three patients who developed cirrhosis over two years of standard MTX therapy may represent a subset of psoriatics with increased hepatic susceptibility to MTX. Another three patients whose severe hepatic fibrosis had regressed upon discontinuation of MTX, but who developed accelerated recurrence of the severe hepatic fibrosis upon resumption of MTX therapy, also suggest the possibility of unusual sensitivity to the drug. These cases emphasize the need for continuing surveillance, with regular liver biopsies, of psoriatic patients on MTX.

摘要

背景与设计

甲氨蝶呤(MTX)对银屑病患者的肝毒性已得到充分认识,但报告的发病率及相关危险因素存在差异。这项回顾性研究描述了1979年至1990年间在新斯科舍省就诊的104例银屑病患者。患者接受MTX治疗1至11年(平均3.38年),并在基线和每年随访时进行肝脏活检。通过查阅病历获取临床数据。统计分析评估了肥胖、糖尿病、饮酒及治疗持续时间与肝脏活检组织学分级相关的风险。

结果

104例患者中,35例肥胖,10例糖尿病,37例偶尔饮酒。研究结束时,21例患者出现严重肝纤维化(IIIB级),3例发展为肝硬化(IV级)。严重肝毒性的显著风险与糖尿病相关(P = 0.02),但与肥胖(P = 0.12)或饮酒(P = 0.12)无关。所有肝硬化患者均以20至25毫克/周的标准剂量服用MTX两年。

结论

在这项加拿大首次评估MTX对银屑病患者肝毒性的研究中,严重肝毒性的发生率很高:23.1%(104例患者中的24例)。本研究表明,糖尿病患者发生MTX肝毒性的风险尤其增加。偶尔饮酒与风险增加无关。在标准MTX治疗两年后出现肝硬化的3例患者可能代表了对MTX肝易感性增加的银屑病患者亚组。另外3例患者在停用MTX后严重肝纤维化消退,但在恢复MTX治疗后严重肝纤维化加速复发,这也提示了对该药物异常敏感的可能性。这些病例强调了对接受MTX治疗的银屑病患者进行持续监测并定期进行肝脏活检的必要性。

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