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改善1型自身免疫性肝炎中皮质类固醇疗法的终点以降低复发频率。

Improving the end point of corticosteroid therapy in type 1 autoimmune hepatitis to reduce the frequency of relapse.

作者信息

Montano-Loza Aldo J, Carpenter Herschel A, Czaja Albert J

机构信息

Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

出版信息

Am J Gastroenterol. 2007 May;102(5):1005-12. doi: 10.1111/j.1572-0241.2007.01153.x. Epub 2007 Feb 23.

DOI:10.1111/j.1572-0241.2007.01153.x
PMID:17319926
Abstract

OBJECTIVE

Relapse of autoimmune hepatitis may reflect incomplete suppression of disease activity prior to corticosteroid withdrawal, and liver tissue examination prior to the termination of therapy may be insufficient to predict subsequent course. Our goal was to refine treatment end point criteria so as to reduce the frequency of relapse after drug withdrawal.

METHODS

One hundred thirty-two patients with definite type 1 autoimmune hepatitis who fulfilled clinical, laboratory, and histological criteria for remission were evaluated. The degree of laboratory improvement at the termination of treatment was correlated with subsequent clinical course in patients who had improved to normal or near-normal histological findings during corticosteroid therapy.

RESULTS

Serum aspartate aminotransferase (AST) levels at the end of treatment were higher in patients who subsequently relapsed than in those who sustained remission (32 +/- 2 U/L vs 25 +/- 2 U/L, P= 0.04). Serum gamma-globulin (1.4 +/- 0.1 g/dL vs 1.2 +/- 0.1 g/dL, P=0.03) and immunoglobulin G (IgG) (1,416 +/- 55 mg/dL vs 1,079 +/- 57 mg/dL, P=0.001) levels were also higher in these patients prior to termination of therapy. The frequencies of abnormal serum AST (40%vs 13%, P=0.008), gamma-globulin (25%vs 3%, P=0.009), and IgG levels (36%vs 4%, P=0.001) at treatment withdrawal were also greater in the patients who subsequently relapsed.

CONCLUSIONS

Patients who are treated to normal serum AST, gamma-globulin, and IgG levels have a lower frequency of relapse than others despite comparable histological findings.

摘要

目的

自身免疫性肝炎复发可能反映出在停用皮质类固醇之前疾病活动未得到完全抑制,且治疗终止前的肝组织检查可能不足以预测后续病程。我们的目标是完善治疗终点标准,以降低停药后复发频率。

方法

对132例符合临床、实验室及组织学缓解标准的明确1型自身免疫性肝炎患者进行评估。在皮质类固醇治疗期间组织学检查结果改善至正常或接近正常的患者中,治疗终止时实验室指标的改善程度与后续临床病程相关。

结果

随后复发的患者治疗结束时血清天冬氨酸转氨酶(AST)水平高于持续缓解的患者(32±2 U/L对25±2 U/L,P = 0.04)。这些患者在治疗终止前血清γ-球蛋白(1.4±0.1 g/dL对1.2±0.1 g/dL,P = 0.03)和免疫球蛋白G(IgG)(1416±55 mg/dL对1079±57 mg/dL,P = 0.001)水平也更高。停药时血清AST异常(40%对13%,P = 0.008)、γ-球蛋白异常(25%对3%,P = 0.009)及IgG水平异常(36%对4%,P = 0.001)的频率在随后复发的患者中也更高。

结论

尽管组织学检查结果相当,但血清AST、γ-球蛋白和IgG水平恢复正常的患者复发频率低于其他患者。

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