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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >The impact of azathioprine on chronic viral hepatitis in renal transplantation: a long-term, single-center, prospective study on azathioprine withdrawal.
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The impact of azathioprine on chronic viral hepatitis in renal transplantation: a long-term, single-center, prospective study on azathioprine withdrawal.

机译:硫唑嘌呤对肾移植中慢性病毒性肝炎的影响:一项长期,单中心,前瞻性的硫唑嘌呤戒断研究。

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摘要

BACKGROUND: In transplanted patients, viral hepatitis progresses to chronic liver disease and patient's death after many years of transplantation. Also, it is well known that azathioprine (AZA) is harmful to the liver of these patients. However, it is unclear whether a low dose of AZA still represents a threat to the viral liver disease. METHODS: A total of 79 patients with hepatitis C, B, or both, transplanted between 1973 and 1990, were grouped according to whether they had AZA either withdrawn from the immunosuppressive regimen [group (G) I, n=45] or a dosage reduction only (group II, n=34). The decision to remove or to keep AZA was restricted to the patient's doctor. Patients records were reviewed by April 1997. RESULTS: After an equal time of follow-up, after the AZA changing (64+/-26 vs. 58+/-29 months), patients in GI showed a significant decrease in the serum liver parameters when compared to baseline [alanine aminotransferase (ALT): P=0.001; gamma-glutamyl transferase (gamma-GT): P=0.001 and total bilirubin: P=0.002], whereas in GII only ALT decreased (P=0.04) although gamma-GT and total bilirubin did not. Compared to baseline, serum creatinine (SCr) increased only in GI (P=0.001) but, at last follow-up, did not differ from GII. The intention-to-perform liver biopsies was equal in GI and GII (16 vs. 14) but the hystological findings of severe chronic liver disease (either chronic active hepatitis or cirrhosis) were more frequent in GII (P=0.004). Death with a functioning graft was much more frequent in GII than in GI (P=0.001). Infection and cirrhosis were more common as a cause of death in GII than in GI. CONCLUSIONS: The use AZA is harmful to renal transplantation patients with both chronic hepatitis C and B and, therefore, should be avoided. AZA withdrawal, but not dose adjustments, diminishes the serum liver enzymes and the progression rate of the chronic viral liver disease as well as the rate of death secondary to infection and cirrhosis.
机译:背景:在移植的患者中,病毒性肝炎会在移植多年后发展为慢性肝病,并导致患者死亡。同样,众所周知,硫唑嘌呤(AZA)对这些患者的肝脏有害。但是,目前尚不清楚低剂量的AZA是否仍对病毒性肝病构成威胁。方法:根据1973年至1990年间移植的79例丙型肝炎,乙型肝炎或两者兼有的患者,根据他们是否从免疫抑制方案中撤出了AZA(I组(G),n = 45)或剂量进行分组。仅减少(第二组,n = 34)。删除或保留AZA的决定仅限于患者的医生。患者记录在1997年4月之前进行了回顾。结果:在相等的随访时间之后,AZA改变(64 +/- 26与58 +/- 29个月)后,胃肠道患者的血清肝明显减少与基线相比的参数[丙氨酸转氨酶(ALT):P = 0.001; γ-谷氨酰转移酶(γ-GT):P = 0.001,总胆红素:P = 0.002],而在GII中,只有ALT降低(P = 0.04),尽管γ-GT和总胆红素没有。与基线相比,血清肌酐(SCr)仅在GI中升高(P = 0.001),但在最后一次随访中,与GII无差异。 GI和GII的有意图进行肝活检的人数相等(16比14),但GII中重度慢性肝病(慢性活动性肝炎或肝硬化)的体征学发现更为常见(P = 0.004)。 GII患者中,功能正常的移植物死亡比GI患者要高得多(P = 0.001)。感染和肝硬化是GII的死亡原因,而不是GI。结论:使用AZA对慢性丙型和乙型肝炎的肾移植患者均有害,因此应避免使用。停用AZA而不是调整剂量会减少血清肝酶和慢性病毒性肝病的进展速度,以及继发于感染和肝硬化的死亡率。

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