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生长激素治疗失代偿性肝硬化的疗效观察 被引量:1

Clinical Study on the Effcacy of Recombinant Human Growth Hormone in Treating Patients with Decompensated Liver Cirrhosis
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摘要 目的:观察重组人生长激素(rhGH)对失代偿性肝硬化(DLC)的疗效及其作用机制。方法:32例失代偿性肝硬化患者随机分为2组,对照组17例,给予一般对症治疗;治疗组15例,在对症治疗基础上加用重组人生长激素(rhGH)8 IU皮下注射,1次/d,连用10 d为1个疗程,休息1周后再用1疗程。分别在治疗前、后观察肝功能、胰岛素样生长因子-1(IGF-1)、胰岛素样生长因子结合蛋白(IGFBP-3)、白细胞介素-4(IL-4)和γ干扰素(IFNγ)的变化;肝功能用生化法检测,IGF-1与IGFBP-3用IRMA检测,IL-4与IFNγ用放免法检测。结果:治疗组临床症状改善较快,腹水消退明显,凝血酶元时间(PT)显著缩短,血浆白蛋白显著增加,IGF-1I、GFBP-3和IFNγ有升高倾向,血清IL-4水平略有下降;而对照组上述指标均无明显改善。结论:rhGH能克服GH抵抗,改善GH/IGF-1轴的功能,促进白蛋白合成,并能调节免疫,适用于失代偿性肝硬化病人。 Objective: To evaluate the therapeutic efficacy of recombinant human growth hormone (rhGH)in patients with decompensated liver cirrhosis (DLC) and its possible mechanism. Methods:Thirty-two cases were divided into two groups, one(rhGH group)received subcutaneous injection of rhGH 8 IU daily for 10 days in addition to symptomatic therapy,with one week interT val,then received another course of rhGH; while the other(control group) received symptomatic treatment alone. Liver function, insulin-like growth factor-1(IGF-1) , IGF binding protein-3 (IGFBP-3), interleukin-4(IL-4) and interferon gamma(IFN-γ) were serially detected before and after therapy by biochemistry,IRMA and RIA methods respectively. Results:Compared with control group,patients received rhGH improved more rapidly in appetite, fatigue, flatulence ,ascites and prothrombin time(PT) . Besides, there was a remarkable increase in plasma albumin level, and serum IGF-1,IGFBP-3 and IFNyconcentrations tend towards rise, serum IL-4 level decreased slightly which was not found in control group. Conclusion: recombinant human growth hormone would be able to overcome GH resistance,improve the function of GH/IGF-1 axis,promote protein synthesis, regulate immune function, and hence, may be good to decompensated cirrhotic patients.
出处 《实用临床医学(江西)》 CAS 2006年第1期29-32,共4页 Practical Clinical Medicine
关键词 失代偿性肝硬化 生长激素 胰岛素样生长因子-1 白细胞介素-4 Γ干扰素 flecompensated liver cirrhosis growth hormone insulin-like growth factor-l interleukin-4 interferon-γ
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