Humphreys Jenny H, Warner Alexander, Costello Ruth, Lunt Mark, Verstappen Suzanne M M, Dixon William G
Arthritis Research UK Centre for Epidemiology, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Ann Rheum Dis. 2017 Sep;76(9):1509-1514. doi: 10.1136/annrheumdis-2016-210629. Epub 2017 Mar 23.
Patients with rheumatoid arthritis (RA) who take methotrexate (MTX) are advised to limit their alcohol intake due to potential combined hepatotoxicity. However, data are limited to support this. The aim of this study was to quantify the risk of developing abnormal liver blood tests at different levels of alcohol consumption, using routinely collected data from primary care.
Patients with RA in the Clinical Practice Research Datalink starting MTX between 1987 and 2016 were included. Hepatotoxicity was defined as transaminitis: alanine transaminase or aspartate aminotransferase more than three times the upper limit of normal. Crude rates of transaminitis were calculated per 1000 person-years, categorised by weekly alcohol consumption in units. Cox proportional hazard models tested the association between alcohol consumption and transaminitis univariately, then age and gender adjusted.
11 839 patients were included, with 530 episodes of transaminitis occurring in 47 090 person-years follow-up. Increased weekly alcohol consumption as a continuous variable was associated with increased risk of transaminitis, adjusted HR (95% CI) per unit consumed 1.01 (1.00 to 1.02); consuming between 15 and 21 units was associated with a possible increased risk of hepatotoxicity, while drinking >21 units per week significantly increased rates of transaminitis, adjusted HR (95% CI) 1.85 (1.17 to 2.93).
Weekly alcohol consumption of <14 units per week does not appear to be associated with an increased risk of transaminitis.
由于潜在的联合肝毒性,建议服用甲氨蝶呤(MTX)的类风湿性关节炎(RA)患者限制饮酒。然而,支持这一建议的数据有限。本研究的目的是利用从初级保健中常规收集的数据,量化不同饮酒水平下出现肝脏血液检查异常的风险。
纳入1987年至2016年间在临床实践研究数据链中开始服用MTX的RA患者。肝毒性定义为转氨酶升高:丙氨酸转氨酶或天冬氨酸转氨酶超过正常上限的三倍。按每1000人年计算转氨酶升高的粗发病率,并按每周饮酒量(单位)进行分类。Cox比例风险模型单变量检验饮酒与转氨酶升高之间的关联,然后对年龄和性别进行调整。
共纳入11839例患者,在47090人年的随访中发生了530次转氨酶升高事件。每周饮酒量作为连续变量增加与转氨酶升高风险增加相关,每摄入一个单位调整后的风险比(95%可信区间)为1.01(1.00至1.02);每周饮酒15至21个单位可能与肝毒性风险增加相关,而每周饮酒超过21个单位显著增加转氨酶升高率,调整后的风险比(95%可信区间)为1.85(1.17至2.93)。
每周饮酒量<14个单位似乎与转氨酶升高风险增加无关。