Pharmaceutical Care Department, Virology Research Center, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Eur J Gastroenterol Hepatol. 2010 Oct;22(10):1235-8. doi: 10.1097/MEG.0b013e32833aa11b.
Isoniazid, rifampicin, and pyrazinamide, the first-line antituberculosis (anti-TB) drugs, are associated with hepatotoxicity.
To study the hepatoprotective effect of N-acetylcysteine (NAC) on liver injury induced by anti-TB drugs.
A randomized clinical trial was conducted on 60 new TB patients who were aged 60 years or more. Patients were randomized into two groups. In group I (n=32), drug regimen included daily doses of isoniazid, rifampicin, pyrazinamide, and ethambutol. Patients in group II (n=28) were treated with the same regimen and NAC. The patients were followed up for 2 weeks. Liver enzymes and bilirubins were measured at baseline, after 1 and 2 weeks of treatment, and whenever the patients presented with clinical symptoms of hepatotoxicity.
The mean+/-SD values of aspartate aminotransferase and alanine aminotransferase were significantly higher in group I than in group II after 1 and 2 weeks of treatment. Hepatotoxicity occurred in 12 patients with (37.5%) group I and none in group II. The mean duration of treatment before the onset of hepatotoxicity was 4.67+/-4.58 days.
NAC protects against anti-TB drug-induced hepatotoxicity.
异烟肼、利福平、吡嗪酰胺是一线抗结核(抗 TB)药物,与肝毒性有关。
研究 N-乙酰半胱氨酸(NAC)对抗结核药物引起的肝损伤的保护作用。
对 60 名年龄在 60 岁及以上的新结核患者进行了一项随机临床试验。患者被随机分为两组。在 I 组(n=32)中,药物方案包括异烟肼、利福平、吡嗪酰胺和乙胺丁醇的每日剂量。II 组(n=28)的患者接受相同的方案和 NAC 治疗。患者随访 2 周。在基线、治疗后 1 周和 2 周以及出现肝毒性临床症状时测量肝酶和胆红素。
治疗 1 周和 2 周后,I 组的天冬氨酸转氨酶和丙氨酸转氨酶的平均值+/-SD 值明显高于 II 组。I 组有 12 名患者(37.5%)发生肝毒性,而 II 组无患者发生肝毒性。肝毒性发生前的平均治疗时间为 4.67+/-4.58 天。
NAC 可预防抗结核药物引起的肝毒性。