Tada Toshifumi, Kumada Takashi, Toyoda Hidenori, Kiriyama Seiki, Tanikawa Makoto, Hisanaga Yasuhiro, Kanamori Akira, Kitabatake Shusuke, Yama Tsuyoki, Tanaka Junko
Department of Gastroenterology and Hepatology, Ogaki Municipal Hospital, 4-86 Minaminokawa, Ogaki, Gifu, 503-8502, Japan.
Department of Epidemiology, Infectious Disease Control, and Prevention, Hiroshima University Institute of Biomedical and Health Sciences, Hiroshima, Japan.
J Gastroenterol. 2016 Apr;51(4):380-9. doi: 10.1007/s00535-015-1117-5. Epub 2015 Sep 5.
Interferon (IFN)-based therapy has been reported to reduce the liver-related mortality rate in patients with chronic hepatitis C virus (HCV) infection. However, predictors of survival and causes of death, including non-liver-related causes, have not been sufficiently investigated in chronic HCV patients who have not received IFN-based therapy.
A total of 1723 patients with chronic HCV infection who were not treated with IFN-based therapy were enrolled. Survival from liver-related diseases and non-liver-related diseases and causes of death were analyzed on the basis of the fibrosis-4 (FIB-4) index, an index of liver fibrosis.
The median follow-up duration was 10.3 years. Of 465 patients who died during the follow-up period, 48.4 % died of liver-related diseases; of the remainder, 51.6 % died of non-liver-related diseases. On the basis of FIB-4 index, the liver-related mortality rate increased as the FIB-4 index increased: 16.1 % in the FIB-4 index < 1.45 group, 36.7 % in the 1.45 ≤ FIB-4 index ≤ 3.25 group, and 58.7 % in the FIB-4 index > 3.25 group (p < 0.001). Conversely, the non-liver-related mortality rate decreased as the FIB-4 index increased: 83.9, 63.3, and 41.3 %, respectively (p = 0.001). In the multivariate analysis, a FIB-4 index greater than 3.25 was identified as a risk factor independently associated with both liver-related death (hazard ratio 13.020; 95 % confidence interval 4.155-40.770) and non-liver-related death (hazard ratio 1.667; 95 % confidence interval 1.188-2.340).
Patients with chronic HCV infection and an elevated FIB-4 index may benefit from monitoring not only for the development of liver-related diseases but also for the development of non-liver-related diseases.
据报道,基于干扰素(IFN)的治疗可降低慢性丙型肝炎病毒(HCV)感染患者的肝脏相关死亡率。然而,在未接受基于IFN治疗的慢性HCV患者中,生存预测因素及死亡原因,包括非肝脏相关原因,尚未得到充分研究。
共纳入1723例未接受基于IFN治疗的慢性HCV感染患者。基于肝纤维化-4(FIB-4)指数(一种肝纤维化指标)分析肝脏相关疾病和非肝脏相关疾病的生存情况及死亡原因。
中位随访时间为10.3年。在随访期间死亡的465例患者中,48.4%死于肝脏相关疾病;其余患者中,51.6%死于非肝脏相关疾病。基于FIB-4指数,肝脏相关死亡率随FIB-4指数升高而增加:FIB-4指数<1.45组为16.1%,1.45≤FIB-4指数≤3.25组为36.7%,FIB-4指数>3.25组为58.7%(p<0.001)。相反,非肝脏相关死亡率随FIB-4指数升高而降低:分别为83.9%、63.3%和41.3%(p=0.001)。多变量分析中,FIB-4指数大于3.25被确定为与肝脏相关死亡(风险比13.020;95%置信区间4.155 - 40.770)和非肝脏相关死亡(风险比1.667;95%置信区间1.188 - 2.340)均独立相关的危险因素。
慢性HCV感染且FIB-4指数升高的患者不仅可能受益于对肝脏相关疾病发生情况的监测,还可能受益于对非肝脏相关疾病发生情况的监测。