Tanaka Atsushi, Hirohara Junko, Nakanuma Yasuni, Tsubouchi Hirohito, Takikawa Hajime
Department of Medicine, Teikyo University School of Medicine, 2-11-1, Kaga, Itabashi-ku, Tokyo, 173-8605, Japan,
J Gastroenterol. 2015 Jun;50(6):675-82. doi: 10.1007/s00535-014-0998-z. Epub 2014 Sep 20.
Bezafibrate is reported to have biochemical efficacy for patients with primary biliary cirrhosis (PBC) refractory to ursodeoxycholic acid (UDCA), yet the long-term effect is still unknown. In Japan, nationwide surveys of PBC have been performed since 1980. In the current study, we retrospectively examined whether response to bezafibrate treatment is associated with the long-term outcomes using this large-scale database.
Among 7,376 patients in the database, we enrolled patients who were treated with UDCA at 13-15 mg/kg per day and followed up for at least 2 years after diagnosis. Bezafibrate (400 mg/day) was administered in addition to UDCA when biochemical response to UDCA was not optimal. Response to bezafibrate treatment was determined by serum alanine transaminase (ALT) levels within 2-3 years or at the earliest point thereafter from the commencement of bezafibrate treatment.
We enrolled 1,121 PBC patients, and the observational period was 6.1 ± 3.4 years. Among the PBC patients, 835 were asymptomatic, defined as no liver-related symptoms at the baseline. In asymptomatic PBC patients, multivariate analysis indicated that ALT response to bezafibrate treatment was significantly associated with the presence of liver-related symptoms at the end of observation [hazard ratio 1.46 (95 % confidence interval 1.01-2.13), P = 0.048]. The cumulative liver-related-symptoms-free rate of patients treated with bezafibrate and who had a normal ALT level was significantly higher than that of those treated with bezafibrate and who had an elevated ALT level (P < 0.001), and was comparable to that of those who received UDCA monotherapy.
These results suggested that normalization of ALT levels with additional bezafibrate treatment significantly decreased the rate of occurrence of liver-related symptoms in asymptomatic PBC patients with suboptimal response to UDCA.
据报道,对于对熊去氧胆酸(UDCA)治疗无效的原发性胆汁性肝硬化(PBC)患者,苯扎贝特具有生化疗效,但其长期疗效仍不明确。在日本,自1980年以来已开展了全国性的PBC调查。在本研究中,我们利用这个大规模数据库回顾性研究了苯扎贝特治疗反应与长期预后之间的关联。
在数据库中的7376例患者中,我们纳入了每天接受13 - 15 mg/kg UDCA治疗且诊断后至少随访2年的患者。当对UDCA的生化反应不理想时,除UDCA外还给予苯扎贝特(400 mg/天)。苯扎贝特治疗反应通过开始苯扎贝特治疗后2 - 3年内或此后最早时间点的血清丙氨酸转氨酶(ALT)水平来确定。
我们纳入了1121例PBC患者,观察期为6.1±3.4年。在PBC患者中,835例无症状,定义为基线时无肝脏相关症状。在无症状PBC患者中,多因素分析表明,苯扎贝特治疗后ALT反应与观察结束时肝脏相关症状的存在显著相关[风险比1.46(95%置信区间1.01 - 2.13),P = 0.048]。接受苯扎贝特治疗且ALT水平正常的患者累积无肝脏相关症状发生率显著高于接受苯扎贝特治疗且ALT水平升高的患者(P < 0.001),且与接受UDCA单药治疗的患者相当。
这些结果表明,对于对UDCA反应欠佳的无症状PBC患者,额外使用苯扎贝特治疗使ALT水平正常化可显著降低肝脏相关症状的发生率。