Dalekos George N, Azariadis Kalliopi, Lygoura Vasiliki, Arvaniti Pinelopi, Gampeta Stella, Gatselis Nikolaos K
Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa, Larissa, Greece.
Institute of Internal Medicine and Hepatology, Larissa, Greece.
Liver Int. 2021 Jul;41(7):1592-1599. doi: 10.1111/liv.14900. Epub 2021 May 11.
BACKGROUND & AIMS: Autoimmune hepatitis (AIH) affects both sexes and all age groups. However, very few studies have focused specifically on the characteristics and outcome of AIH in patients aged 70 y or older.
25/234 patients with well-established AIH and disease onset at ≥70-y (median: 73-y) were analysed and compared to the rest patients (median: 47 y). Treatment response was assessed in all patients from both groups who were eligible for treatment (n = 202).
Disease presentation was mainly insidious in both groups (19/25, 76% vs. 134/209, 64.1%; P = .313). At diagnosis, older patients had lower alaninoaminotrasferase (101[433] vs. 199[441] IU/L, P < .05) but were more frequently cirrhotic (12/25, 48% vs. 57/209, 27.3%; P = .03). Importantly, similar rates of on-treatment response (16/18, 89% vs. 154/184, 84%; P = .565), corticosteroid withdrawal (10/16, 62.5% vs. 113/154, 73.4%; P = .355) and complete withdrawal of immunosuppression (1/16, 6.3% vs. 40/154, 26%; P = .122) were achieved in both groups. Treatment-related adverse events were evenly observed between groups (6/18, 33% vs. 54/184, 29%; P = .724). In treated patients, the age ≥70 y was only associated with the overall mortality (HR 8.3 [95% CI: 2.1-36.4], P = .003), but not with the liver-related mortality (HR 3.4 [95% CI: 0.4-30.0], P = .268).
AIH should be seriously considered in patients ≥70 y with unexplained impaired liver function tests as the disease is not infrequent in this group and seems to bear an increased risk for advanced disease stage at diagnosis. However, if immunosuppression is started promptly, it seems as safe and effective as in younger patients.
自身免疫性肝炎(AIH)可累及所有性别和年龄组。然而,很少有研究专门关注70岁及以上AIH患者的特征和预后。
分析25例确诊为AIH且发病年龄≥70岁(中位年龄:73岁)的患者,并与其余患者(中位年龄:47岁)进行比较。对两组中所有符合治疗条件的患者(n = 202)评估治疗反应。
两组疾病表现主要为隐匿性(19/25,76% 对134/209,64.1%;P = 0.313)。诊断时,老年患者丙氨酸转氨酶水平较低(101[433]对199[441]IU/L,P < 0.05),但肝硬化发生率更高(12/25,48% 对57/209,27.3%;P = 0.03)。重要的是,两组治疗反应率(16/18,89% 对154/184,84%;P = 0.565)、停用皮质类固醇率(10/16,6 in both groups. Treatment-related adverse events were evenly observed between groups (6/18, 33% vs. 54/184, 29%; P = 0.724). In treated patients, the age ≥70 y was only associated with the overall mortality (HR 8.3 [95% CI: 2.1-36.4], P = 0.003), but not with the liver-related mortality (HR 3.4 [95% CI: 0.4-30.0], P = 0.268).
对于70岁及以上肝功能检查不明原因异常的患者,应认真考虑AIH,因为该疾病在该组中并不罕见,且诊断时晚期疾病风险似乎增加。然而,如果及时开始免疫抑制治疗,其安全性和有效性似乎与年轻患者相当。 2.5% 对113/154,73.4%;P = 0.355)和完全停用免疫抑制剂率(1/16,6.3% 对40/154,26%;P = 0.122)相似。两组治疗相关不良事件发生率相近(6/18, 33% 对54/184,29%;P = 0.724)。在接受治疗的患者中,年龄≥70岁仅与总死亡率相关(HR 8.3 [95% CI:2.1 - 36.4],P = 0.003),而与肝脏相关死亡率无关(HR 3.4 [95% CI:0.4 - 30.0],P = 0.268)。
对于70岁及以上肝功能检查不明原因异常的患者,应认真考虑AIH,因为该疾病在该组中并不罕见,且诊断时晚期疾病风险似乎增加。然而,如果及时开始免疫抑制治疗,其安全性和有效性似乎与年轻患者相当。