Hatami Behzad, Abdi Saeed, Pourhoseingholi Mohamad Amin, Eghlimi Hesameddin, Rabbani Amir Hassan, Masoumi Maryam, Hajimohammadebrahim-Ketabforoush Melika
Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Teheran, Iran.
Department of Adult Gastroenterology and Hepatology, School of Medicine, Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Ayatollah Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Gastroenterol Hepatol Bed Bench. 2023;16(4):432-440. doi: 10.22037/ghfbb.v16i4.2443.
To evaluate the effects of N-acetylcysteine (NAC) supplementation in cirrhotic patients.
Chronic hepatic inflammation leads to fibrosis and cirrhosis through various mechanisms such as oxidative stress. NAC is one of the intracellular precursors of glutathione that can degrade most reactive oxygen species. Recently, the beneficial effects of NAC in animal and human studies on preventing liver injury progression and improving liver function have been examined. However, more studies on human subjects are still required.
Well-known cirrhotic patients with a specific etiology and aged 18 to 70 years who referred to the gastrointestinal clinic of Ayatollah Taleghani Hospital from December 2018 to December 2019 were enrolled in the present randomized double-blind controlled trial. Patients in the intervention group received NAC tablets at a dose of 600 mg daily, and the control group received a placebo. Demographic data, medical characteristics, and Child-Pugh and MELD scores evaluated at baseline and after 6 months.
Totally, 60 patients completed the present study (30 patients in the intervention group, and 30 patients in the control group). Hematological and biochemical parameters were normal in both groups with no significant differences at baseline and 6 months after intervention values. Moreover, the renal function indicators including serum creatinine (Cr) and urea (BUN) decreased significantly after intervention. Hepatic parameters also decreased significantly 6 months after intervention. Decreases in the renal and hepatic parameters 6 months after baseline in the control group were not statistically significant.
The results of this study showed that NAC improved hepatic and renal function by decreasing serum urea and creatinine levels but had no significant effect on hematological and biochemical parameters. Furthermore, NAC significantly improved hepatic profiles by decreasing ALT, AST, and ALP in the liver enzymes between the intervention and control groups. Moreover, NAC caused a significant decrease in Child-Pugh and MELD scores.
评估补充N-乙酰半胱氨酸(NAC)对肝硬化患者的影响。
慢性肝脏炎症通过氧化应激等多种机制导致纤维化和肝硬化。NAC是谷胱甘肽的细胞内前体之一,可降解大多数活性氧。最近,已对NAC在动物和人体研究中预防肝损伤进展和改善肝功能的有益作用进行了研究。然而,仍需要更多关于人类受试者的研究。
本随机双盲对照试验纳入了2018年12月至2019年12月转诊至阿亚图拉·塔莱加尼医院胃肠科的病因明确、年龄在18至70岁的著名肝硬化患者。干预组患者每日服用600毫克NAC片剂,对照组服用安慰剂。在基线和6个月后评估人口统计学数据、医学特征以及Child-Pugh和MELD评分。
共有60名患者完成了本研究(干预组30例,对照组30例)。两组的血液学和生化参数均正常,干预前后基线值和6个月后无显著差异。此外,干预后包括血清肌酐(Cr)和尿素(BUN)在内的肾功能指标显著下降。干预6个月后肝脏参数也显著下降。对照组基线后6个月肾脏和肝脏参数的下降无统计学意义。
本研究结果表明,NAC通过降低血清尿素和肌酐水平改善了肝肾功能,但对血液学和生化参数无显著影响。此外,NAC通过降低干预组和对照组之间肝酶中的ALT、AST和ALP显著改善了肝脏状况。此外,NAC使Child-Pugh和MELD评分显著降低。