Simon Tracey G, Henson Jacqueline, Osganian Stephanie, Masia Ricard, Chan Andrew T, Chung Raymond T, Corey Kathleen E
Liver Center, Division of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Boston Massachusetts; Department of Medicine, Massachusetts General Hospital, Boston Massachusetts; Harvard Medical School, Boston Massachusetts; Clinical and Translational Epidemiology Unit (CTEU), Massachusetts General Hospital, Boston Massachusetts.
Department of Medicine, Massachusetts General Hospital, Boston Massachusetts; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston Massachusetts.
Clin Gastroenterol Hepatol. 2019 Dec;17(13):2776-2784.e4. doi: 10.1016/j.cgh.2019.04.061. Epub 2019 May 9.
BACKGROUND & AIMS: There are few data from prospective studies on the effects of aspirin on fibrosis in patients with nonalcoholic fatty liver disease (NAFLD).
We performed a prospective cohort study of 361 adults with biopsy-confirmed NAFLD, from 2006 through 2015, examined every 3-12 months for incident advanced fibrosis defined using serial measurements of validated indices (the Fibrosis-4, NAFLD fibrosis score, and aspartate aminotransferase to platelet ratio indices). Histologic analyses of liver biopsies collected at baseline were performed by a blinded pathologist. Information collected at baseline and at each examination included frequency and duration of aspirin and nonsteroidal anti-inflammatory drug (NSAID) use. Using multivariable-adjusted logistic regression, we estimated the association of aspirin use with prevalent steatohepatitis (NASH) and fibrosis. Using multivariable-adjusted Cox proportional hazards modeling, we estimated the association between aspirin use and risk for fibrosis progression.
At enrollment, 151 subjects used aspirin daily. Compared with non-regular use, daily aspirin use was associated with significantly lower odds of NASH (adjusted odds ratio, 0.68; 95% CI, 0.37-0.89) and fibrosis (adjusted odds ratio, 0.54; 95% CI, 0.31-0.82). Among individuals with baseline F0-F2 fibrosis (n = 317), 86 developed advanced fibrosis over 3692 person-years. Daily aspirin users had significantly lower risk for developing incident advanced fibrosis vs non-regular users (adjusted hazard ratio [aHR], 0.63; 95% CI, 0.43-0.85). This relationship appeared to be duration dependent (adjusted P trend=.026), with the greatest benefit found with at least 4 years or more of aspirin use (aHR, 0.50; 95% CI, 0.35-0.73). Conversely, use of nonaspirin NSAIDs was not associated with risk for advanced fibrosis (aHR, 0.93; 95% CI, 0.81-1.05).
In a prospective study of patients with biopsy-proven NAFLD, daily aspirin use was associated with less severe histologic features of NAFLD and NASH, and lower risk for progression to advanced fibrosis with time.
关于阿司匹林对非酒精性脂肪性肝病(NAFLD)患者纤维化影响的前瞻性研究数据较少。
我们对361例经活检确诊为NAFLD的成年人进行了一项前瞻性队列研究,研究时间为2006年至2015年,每3 - 12个月进行一次检查,通过对有效指标(Fibrosis - 4、NAFLD纤维化评分和天冬氨酸转氨酶与血小板比值指数)的系列测量来定义新发的晚期纤维化。由一位盲法病理学家对基线时采集的肝活检组织进行组织学分析。在基线和每次检查时收集的信息包括阿司匹林和非甾体抗炎药(NSAID)的使用频率和持续时间。使用多变量调整的逻辑回归,我们估计了阿司匹林使用与现患脂肪性肝炎(NASH)和纤维化之间的关联。使用多变量调整的Cox比例风险模型,我们估计了阿司匹林使用与纤维化进展风险之间的关联。
入组时,151名受试者每天使用阿司匹林。与非规律使用相比,每天使用阿司匹林与NASH的显著较低几率(调整后的优势比,0.68;95%置信区间,0.37 - 0.89)和纤维化(调整后的优势比,0.54;95%置信区间,0.31 - 0.82)相关。在基线F0 - F2纤维化的个体(n = 317)中,86人在3692人年中发展为晚期纤维化。与非规律使用者相比,每天使用阿司匹林者发生新发晚期纤维化的风险显著较低(调整后的风险比[aHR],0.63;95%置信区间,0.43 - 0.85)。这种关系似乎依赖于使用持续时间(调整后的P趋势 = 0.026),使用阿司匹林至少4年或更长时间时获益最大(aHR,0.50;95%置信区间,0.35 - 0.73)。相反,使用非阿司匹林类NSAIDs与晚期纤维化风险无关(aHR,0.93;95%置信区间,0.81 - 1.05)。
在一项对经活检证实的NAFLD患者的前瞻性研究中,每天使用阿司匹林与NAFLD和NASH较轻的组织学特征相关,并且随着时间推移进展为晚期纤维化的风险较低。