Centre for Digestive Diseases, Division of Hepatology, Karolinska University Hospital, Stockholm, Sweden; Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden; Clinical Epidemiology Unit, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden.
Department of Gastroenterology and Hepatology, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
J Hepatol. 2017 Dec;67(6):1265-1273. doi: 10.1016/j.jhep.2017.07.027. Epub 2017 Aug 10.
BACKGROUND & AIMS: Non-alcoholic fatty liver disease (NAFLD) is very common in the general population, but identifying patients with increased risk of mortality and liver-specific morbidity remains a challenge. Non-alcoholic steatohepatitis (NASH) is thought to enhance this risk; therefore, resolution of NASH is a major endpoint in current pharmacologic studies. Herein, we aim to investigate the long-term prognosis of a large cohort of NAFLD patients, and to study the specific effect of NASH and fibrosis stage on prognosis. METHODS: We conducted a retrospective cohort study of 646 biopsy-proven NAFLD patients. Each case was matched for age, sex and municipality to ten controls. Outcomes on mortality and severe liver disease, defined as cirrhosis, liver decompensation/failure or hepatocellular carcinoma, were evaluated using population-based registers. Cox regression models adjusted for age, sex and type 2 diabetes were used to examine the long-term risk according to fibrosis stage. Likelihood ratio tests were used to assess whether adding NASH to these models increased the predictive capacity. Laplace regression was used to estimate the time to severe liver disease according to stage of fibrosis. RESULTS: During a follow-up of mean 20years (range 0-40) equivalent to 139,163 person-years, 12% of NAFLD patients and 2.2% of controls developed severe liver disease (p<0.001). Compared to controls, the risk of severe liver disease increased per stage of fibrosis (hazard ratio ranging from 1.9 in F0 to 104.9 in F4). Accounting for the presence of NASH did not change these estimates significantly (likelihood ratio test >0.05 for all stages of fibrosis). Similar results were seen for overall mortality. The lower end of the 95% confidence interval for the 10 percentile of time to development of severe liver disease was 22-26years in F0-1, 9.3years in F2, 2.3years in F3, and 0.9years to liver decompensation in F4. CONCLUSIONS: In this, the largest ever study of biopsy-proven NAFLD, the presence of NASH did not increase the risk of liver-specific morbidity or overall mortality. Knowledge of time to development of severe liver disease according to fibrosis stage can be used in individual patient counselling and for public health decisions. LAY SUMMARY: Non-alcoholic fatty liver disease (NAFLD) is very common in the general population, but reaching an accurate prognosis remains challenging. We investigate the long-term prognosis of a large cohort of NAFLD patients. In this, the largest ever study of biopsy-proven NAFLD, the presence of NASH did not increase the risk of liver-specific morbidity or overall mortality. Knowledge of time to development of severe liver disease according to fibrosis stage can be used in individual patient counselling and for public health decisions.
背景与目的:非酒精性脂肪性肝病(NAFLD)在普通人群中非常常见,但识别具有更高死亡率和肝脏特异性发病率风险的患者仍然是一个挑战。非酒精性脂肪性肝炎(NASH)被认为会增加这种风险;因此,NASH 的缓解是当前药物研究的主要终点。在此,我们旨在研究大量 NAFLD 患者的长期预后,并研究 NASH 和纤维化分期对预后的具体影响。
方法:我们对 646 例经活检证实的 NAFLD 患者进行了回顾性队列研究。每个病例均按年龄、性别和市与 10 个对照相匹配。使用基于人群的登记册评估死亡率和严重肝脏疾病(定义为肝硬化、肝功能失代偿/衰竭或肝细胞癌)的结局。使用 Cox 回归模型调整年龄、性别和 2 型糖尿病,以检查根据纤维化分期的长期风险。似然比检验用于评估将 NASH 纳入这些模型是否增加了预测能力。拉普拉斯回归用于根据纤维化分期估计严重肝脏疾病的时间。
结果:在平均 20 年(范围 0-40)的随访期间(相当于 139,163 人年),12%的 NAFLD 患者和 2.2%的对照组发生严重肝脏疾病(p<0.001)。与对照组相比,纤维化分期每增加一个阶段,严重肝脏疾病的风险就会增加(风险比范围从 F0 中的 1.9 到 F4 中的 104.9)。考虑到 NASH 的存在,这些估计值并没有显著改变(所有纤维化分期的似然比检验>0.05)。总体死亡率也出现了类似的结果。在 F0-1 中,发展为严重肝脏疾病的第 10 百分位数的时间的 95%置信区间的下限为 22-26 年,F2 为 9.3 年,F3 为 2.3 年,F4 为肝功能失代偿的 0.9 年。
结论:在这项迄今为止最大的经活检证实的 NAFLD 研究中,NASH 的存在并未增加肝脏特异性发病率或总体死亡率的风险。根据纤维化分期了解严重肝脏疾病发展的时间,可以用于个体患者咨询和公共卫生决策。
N Engl J Med. 2021-10-21
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