Fabbri Carlo, Jaboli M Francesca, Giovanelli Silvia, Azzaroli Francesco, Pezzoli Alessandro, Accogli Esterita, Liva Stefania, Nigro Giovanni, Miracolo Anna, Festi Davide, Colecchia Antonio, Montagnani Marco, Roda Enrico, Mazzella Giuseppe
Department of Internal Medicine and Gastroenterology, University of Bologna, Bologna, Italy.
World J Gastroenterol. 2003 Jul;9(7):1487-90. doi: 10.3748/wjg.v9.i7.1487.
To explore the prevalence of autoimmune gastritis in chronic hepatitis C virus (HCV) patients and the influence of alpha-interferon (IFN) treatment on autoimmune gastritis.
We performed a prospective study on 189 patients with positive anti-HCV and viral RNA enrolled in a 12-month IFN protocol. We evaluated: a) the baseline prevalence of autoimmune gastritis, b) the impact of IFN treatment on development of biochemical signs of autoimmune gastritis (at 3, 6 and 12 months), c) the evolution after IFN withdrawal (12 months) in terms of anti-gastric-parietal-cell antibodies (APCA), gastrin, anti-thyroid, and anti-non-organ-specific antibodies.
APCA positivity and 3-fold gastrin levels were detected in 3 (1.6 %) and 9 (5 %) patients, respectively, at baseline, in 25 (13 %) and 31 (16 %) patients at the end of treatment (both P<0.001, vs baseline), and in 7 (4 %) and 14 (7 %) patients 12 months after withdrawal (P=0.002 and P=0.01 respectively, vs baseline; P=not significant vs end of treatment). The development of autoimmune gastritis was strictly associated with the presence of autoimmune thyroiditis (P =0.0001), no relationship was found with other markers of autoimmunity.
In HCV patients, IFN frequently precipitates latent autoimmune gastritis, particularly in females. Following our 12-month protocol, the phenomenon generally regressed. Since APCA positivity and high gastrin levels are associated with the presence of antithyroid antibodies, development of autoimmune thyroiditis during IFN treatment may provide a surrogate preliminary indicator of possible autoimmune gastritis to limit the need for invasive examinations.
探讨慢性丙型肝炎病毒(HCV)患者自身免疫性胃炎的患病率以及α干扰素(IFN)治疗对自身免疫性胃炎的影响。
我们对189例抗HCV和病毒RNA阳性且参加为期12个月IFN治疗方案的患者进行了一项前瞻性研究。我们评估了:a)自身免疫性胃炎的基线患病率;b)IFN治疗对自身免疫性胃炎生化指标发展的影响(在3、6和12个月时);c)IFN停药后12个月时抗胃壁细胞抗体(APCA)、胃泌素、抗甲状腺抗体和抗非器官特异性抗体方面的变化。
基线时分别在3例(1.6%)和9例(5%)患者中检测到APCA阳性和胃泌素水平升高3倍;治疗结束时分别在25例(13%)和31例(16%)患者中检测到(与基线相比,P均<0.001);停药12个月后分别在7例(4%)和14例(7%)患者中检测到(与基线相比,P分别为0.002和0.01;与治疗结束时相比,P无统计学意义)。自身免疫性胃炎的发生与自身免疫性甲状腺炎密切相关(P =0.0001),与其他自身免疫标志物无相关性。
在HCV患者中,IFN常引发潜在的自身免疫性胃炎,尤其是在女性患者中。按照我们的12个月治疗方案,这种现象通常会消退。由于APCA阳性和高胃泌素水平与抗甲状腺抗体的存在相关,IFN治疗期间自身免疫性甲状腺炎的发生可能为可能的自身免疫性胃炎提供一个替代的初步指标,以减少侵入性检查的需求。