Grønbaek Lisbet, Otete Harmony, Ban Lu, Crooks Colin, Card Timothy, Jepsen Peter, West Joe
Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus N, Denmark.
Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus N, Denmark.
Liver Int. 2020 Jul;40(7):1634-1644. doi: 10.1111/liv.14480. Epub 2020 May 2.
BACKGROUND & AIMS: There are few population-based studies of the incidence and mortality of autoimmune hepatitis. The burden of the disease and how it has changed over time have not been fully explored. We conducted a population-based cohort study on the incidence and mortality of autoimmune hepatitis in England, 1997-2015.
From the Clinical Practice Research Datalink we included 882 patients diagnosed with autoimmune hepatitis in England, 1997-2015. The patients were followed through 2015, and we calculated the sex- and age-standardized incidence and prevalence of autoimmune hepatitis. We examined variation in incidence by sex, age, calendar year, geographical region and socioeconomic status, and incidence rate ratios were calculated with Poisson regression. We calculated all-cause and cause-specific mortality.
The overall standardized incidence rate of autoimmune hepatitis was 2.08 (95% confidence interval 1.94-2.22) per 100,000 population per year, higher in women, higher in older age and independent of region and socioeconomic status. From 1997 to 2015 the incidence doubled from 1.27 (95% confidence interval 0.51-2.02) to 2.56 (95% confidence interval 1.79-3.33) per 100,000 population per year. The 10-year cumulative all-cause mortality was 31.9% (95% confidence interval 27.6-36.5), and the 10-year cumulative liver-related mortality, including hepatocellular carcinoma was ~10.5%.
This population-based study showed that the incidence of autoimmune hepatitis doubled over an eighteen-year period. The incidence was particularly high in older women and was similar across all regions of England and independent of socioeconomic status. Patients with autoimmune hepatitis had a high mortality.
基于人群的自身免疫性肝炎发病率和死亡率研究较少。该疾病的负担及其随时间的变化尚未得到充分探讨。我们对1997 - 2015年英格兰自身免疫性肝炎的发病率和死亡率进行了一项基于人群的队列研究。
从临床实践研究数据链中,我们纳入了1997 - 2015年在英格兰被诊断为自身免疫性肝炎的882例患者。对这些患者随访至2015年,我们计算了自身免疫性肝炎的性别和年龄标准化发病率及患病率。我们研究了发病率在性别、年龄、日历年、地理区域和社会经济地位方面的差异,并通过泊松回归计算发病率比。我们计算了全因死亡率和特定病因死亡率。
自身免疫性肝炎的总体标准化发病率为每年每10万人2.08(95%置信区间1.94 - 2.22),女性发病率更高,老年患者发病率更高,且与地区和社会经济地位无关。从1997年到2015年,发病率从每年每10万人1.27(95%置信区间0.51 - 2.02)翻倍至2.56(95%置信区间1.79 - 3.33)。10年累积全因死亡率为31.9%(95%置信区间27.6 - 36.5),10年累积肝脏相关死亡率(包括肝细胞癌)约为10.5%。
这项基于人群的研究表明,自身免疫性肝炎的发病率在18年期间翻倍。老年女性的发病率尤其高,在英格兰所有地区相似,且与社会经济地位无关。自身免疫性肝炎患者死亡率较高。