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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Risk Factors and Clinical Course for Liver Steatosis or Nonalcoholic Steatohepatitis After Living Donor Liver Transplantation
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Risk Factors and Clinical Course for Liver Steatosis or Nonalcoholic Steatohepatitis After Living Donor Liver Transplantation

机译:肝硬化危险因素和临床疗程,肝脏肝脏移植后肝硬化或非醇胫骨肝炎

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Background Posttransplant liver steatosis occurs frequently and can affect patient outcome. Our aim was to clarify the risk factors for steatosis or steatohepatitis after living donor liver transplantation (LT) through a retrospective examination of recent 100 living donor LT recipients and their liver donors. Methods Liver biopsy was performed at 1 year after LT and each year, thereafter, or as needed due to abnormal liver enzyme levels, with a median follow-up of 4 years (2-10 years). Results Liver steatosis (= 5%) was identified in 33 cases, with steatohepatitis identified in 9 of 33 patients with liver steatosis. Recipients with liver steatosis were younger than those without steatosis (53.4 +/- 9.5 years vs 57.6 +/- 9.9 years, respectively; P = 0.045). Of note, the prevalence of steatosis was significantly higher among LT recipients who received a graft from a donor with steatosis than without (60% vs 23%, respectively; P = 0.001). Donor steatosis was also associated with steatohepatitis in recipients after LT (steatohepatitis/simple steatosis, 88%:50%). On multivariate analysis, younger recipient age (P = 0.023) and donor steatosis (P = 0.005) were independent risk factors of liver steatosis after LT. Among the 33 recipients in our study group, 26 were assessed by serial liver biopsies, with 6 showing progression of the nonalcoholic fatty liver disease activity score. An increase in body weight was predictive of steatosis progression after LT (P = 0.005). Conclusions Age and donor steatosis influence the risk of liver steatosis and steatohepatitis in recipients after LT. The clinical course of steatosis is relatively benign, with only 19% developing nonalcoholic fatty liver disease activity score and 7.6% significant fibrosis.
机译:背景技术后翻盖肝脏脂肪变性经常发生并且会影响患者结果。我们的目标是通过回顾性检查最近的100个活体供体LT受者及其肝脏供体,阐明生活患者肝移植(LT)后扼杀脂肪变性或胫骨肝炎的危险因素。方法在LT和每年后1年进行肝活检,此后,由于肝酶水平异常,每年或根据需要,中值随访4岁(2-10岁)。结果在33例中鉴定了肝脏脂肪变性(& = 5%),患有胫骨肝炎中的9例患者肝脏脂肪变性中的9例。具有肝脏脂肪变性的受者比没有脂肪变性的人更年轻(53.4 +/- 9.5岁,分别为57.6 +/- 9.9岁; P = 0.045)。值得注意的是,在LT的受者之间,脂肪变性的患病率显着高于施主患者的接枝,而不是没有(60%与23%; p = 0.001)。在LT(STEATOHPOATISITIS / SIMPLISISION,88%:50%)之后,供体脂肪变性也与受体中的脂肪性肝炎有关。在多变量分析中,年轻受体年龄(P = 0.023)和供体脂肪变性(P = 0.005)是肝脏脂肪变性的独立危险因素。在我们的研究组中的33名受者中,通过连续肝活组织检查评估了26例,其中6例显示非酒精性脂肪肝病活动评分的进展。体重的增加是在LT(p = 0.005)后的脂肪变性进展的预测性。结论年龄和供体脂肪变性在LT中影响受者肝脏脂肪变性和胫骨肝炎的风险。脂肪变性的临床课程相对良性,仅培养非酒精性脂肪肝疾病活动评分和7.6%的显着纤维化。

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    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

    Nagasaki Univ Grad Sch Biomed Sci Dept Surg Nagasaki Japan;

    Nagasaki Univ Grad Sch Biomed Sci Dept Surg Nagasaki Japan;

    Nagasaki Univ Grad Sch Biomed Sci Dept Surg Nagasaki Japan;

    Nagasaki Univ Grad Sch Biomed Sci Dept Surg Nagasaki Japan;

    Nagasaki Univ Grad Sch Biomed Sci Dept Gastroenterol &

    Hepatol 1-7-1 Sakamoto Nagasaki 8528501;

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  • 中图分类 器官移植术 ;
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