Department of Gastroenterology, G B Pant Hospital, New Delhi, India.
Department of Gastroenterology, G B Pant Hospital, New Delhi, India.
Clin Gastroenterol Hepatol. 2014 Jun;12(6):1003-8.e1. doi: 10.1016/j.cgh.2013.11.006. Epub 2013 Nov 15.
BACKGROUND & AIMS: Hepatic encephalopathy (HE) is associated with a poor prognosis in patients with advanced liver disease. Probiotics alter the intestinal microbiota with non-urease-producing organisms that reduce production of ammonia. We investigated the efficacy of probiotics for the primary prophylaxis of HE.
We conducted a prospective trial at a tertiary care referral institute in New Delhi, India, from January 2012 through March 2013, of patients with cirrhosis without overt HE (age, 48.6 ± 11.1 y; 96 men and 64 women); 25 were Child-Turcotte-Pugh (CTP) class A, 51 were CTP class B, and 84 were CTP class C. Subjects were assigned randomly to groups given probiotics (1 × 10(8) colony-forming units, 3 times daily; n = 86, 42 with minimal HE) or no test article (control, n = 74; 33 with minimal HE). All subjects underwent psychometric analyses, critical flicker fusion (CFF) threshold assessments, glucose hydrogen breath tests to identify small intestinal bacterial overgrowth (SIBO), and lactulose hydrogen breath tests to measure orocecal transit time (OCTT). The primary end point was the development of overt HE.
At baseline, subjects in each group had comparable CTP score, model for end-stage liver disease scores, CFF assessments, psychometric hepatic encephalopathy scores, and OCTT. After a mean follow-up period of 38.6 ± 8.80 weeks for patients given probiotics and 40.3 ± 9.8 weeks for controls, 6 patients given probiotics and 7 controls died (P = .81). Three months of probiotic administration significantly reduced levels of arterial ammonia, SIBO, and OCTT; increased psychometric hepatic encephalopathy scores; and increased CFF thresholds, compared with baseline. Seven subjects in the probiotic group and 14 controls developed overt HE (P < .05; hazard ratio for controls vs probiotic group, 2.1; 95% confidence interval, 1.31-6.53). Psychometric hepatic encephalopathy scores, CTP scores, and SIBO correlated with the development of overt HE.
In a prospective, randomized controlled trial, probiotics were found to be effective in preventing HE in patients with cirrhosis. Trial registration No: CTRI/2012/07/002807.
肝性脑病(HE)与晚期肝病患者的预后不良有关。益生菌通过产生非尿素酶的生物体改变肠道微生物群,从而减少氨的产生。我们研究了益生菌用于原发性 HE 预防的效果。
我们在印度新德里的一家三级医疗转诊机构进行了一项前瞻性试验,纳入了无显性 HE 的肝硬化患者(年龄 48.6±11.1 岁;96 名男性和 64 名女性);25 名患者为 Child-Turcotte-Pugh(CTP)A级,51 名患者为 CTP B 级,84 名患者为 CTP C 级。受试者随机分为给予益生菌(1×10^8 个菌落形成单位,每日 3 次;n=86,42 名患者有轻微 HE)或不给予试验药物(对照组,n=74;33 名患者有轻微 HE)。所有受试者均接受心理测量分析、临界闪烁融合(CFF)阈值评估、葡萄糖氢呼气试验以识别小肠细菌过度生长(SIBO)以及乳果糖氢呼气试验以测量口盲传输时间(OCTT)。主要终点是显性 HE 的发生。
在基线时,每组患者的 CTP 评分、终末期肝病模型评分、CFF 评估、心理测量性肝性脑病评分和 OCTT 均相似。接受益生菌治疗的患者平均随访 38.6±8.80 周,对照组为 40.3±9.8 周后,6 名接受益生菌治疗的患者和 7 名对照组患者死亡(P=0.81)。与基线相比,益生菌治疗 3 个月可显著降低动脉血氨、SIBO 和 OCTT 水平;增加心理测量性肝性脑病评分;并增加 CFF 阈值。益生菌组有 7 名患者和对照组有 14 名患者发生显性 HE(P<0.05;对照组与益生菌组的危险比为 2.1;95%置信区间为 1.31-6.53)。心理测量性肝性脑病评分、CTP 评分和 SIBO 与显性 HE 的发生相关。
在一项前瞻性、随机对照试验中,益生菌被发现可有效预防肝硬化患者的 HE。试验注册号:CTRI/2012/07/002807。