Division of Hepatogastroenterology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
PLoS One. 2019 Jan 9;14(1):e0208858. doi: 10.1371/journal.pone.0208858. eCollection 2019.
Previous studies have reported that sustained virological response (SVR) to interferon-based treatment reduces the risk of mortality in chronic hepatitis C (CHC) patients, mainly in cirrhotic patients. A population-based study reported that metabolic risk factors increase the risk of mortality in CHC patients. We aim to investigate the association between SVR, metabolic risk factors and mortality in CHC patients with and without advanced fibrosis.
We collected data from 1452 CHC patients who underwent interferon-based therapy. All patients underwent liver biopsy prior to therapy. Mild fibrosis was defined as a modified Knodell score of 0-2, while advanced fibrosis was defined as a score of 3-4.
1452 patients were followed up for a median (IQR) of 6.6 (4.2-9.4) years, 1124 patients (77.4%) achieved SVR, 619 patients (42.6%) were advanced fibrosis. 14 patients with mild fibrosis and 55 patients with advanced fibrosis died during follow-up period. According to multivariate Cox regression analyses, SVR reduced the risks of all-cause mortality (HR, 0.21; 95% CI, 0.12-0.37; P<0.001), liver-related mortality (HR, 0.19; 95% CI, 0.10-0.38; P < .001), and non-liver-related mortality (HR, 0.26; 95% CI, 0.10-0.71; P = 0.009) in the patients with advanced fibrosis. SVR also reduced the risk of liver-related mortality (HR, 0.09; 95% CI, 0.01-0.60; P = 0.013) in the patients with mild fibrosis. Anti-hypertensive treatment increased the risks of all-cause mortality (HR, 6.1; 95% CI: 1.66-22.54; P = 0.006) and liver-related mortality (HR, 12.3; 95% CI: 1.4-108.5; P = 0.02) in the patients with mild fibrosis.
SVR and metabolic risk factors are associated with mortality in CHC patients given interferon-based treatment.
既往研究报道,基于干扰素的治疗获得持续病毒学应答(SVR)可降低慢性丙型肝炎(CHC)患者的死亡率,主要是在肝硬化患者中。一项基于人群的研究报道,代谢危险因素增加了 CHC 患者的死亡风险。我们旨在研究 SVR、代谢危险因素与有无晚期纤维化的 CHC 患者的死亡率之间的关系。
我们收集了 1452 例接受基于干扰素治疗的 CHC 患者的数据。所有患者在治疗前均进行了肝活检。轻度纤维化定义为改良 Knodell 评分 0-2,而晚期纤维化定义为评分 3-4。
1452 例患者中位(IQR)随访 6.6(4.2-9.4)年,1124 例(77.4%)患者获得 SVR,619 例(42.6%)患者为晚期纤维化。14 例轻度纤维化患者和 55 例晚期纤维化患者在随访期间死亡。根据多变量 Cox 回归分析,SVR 降低了所有原因死亡率(HR,0.21;95%CI,0.12-0.37;P<0.001)、肝相关死亡率(HR,0.19;95%CI,0.10-0.38;P <.001)和非肝相关死亡率(HR,0.26;95%CI,0.10-0.71;P = 0.009)的风险在晚期纤维化患者中。SVR 还降低了轻度纤维化患者的肝相关死亡率(HR,0.09;95%CI,0.01-0.60;P = 0.013)的风险。抗高血压治疗增加了轻度纤维化患者的全因死亡率(HR,6.1;95%CI:1.66-22.54;P = 0.006)和肝相关死亡率(HR,12.3;95%CI:1.4-108.5;P = 0.02)的风险。
基于干扰素的治疗的 CHC 患者的 SVR 和代谢危险因素与死亡率相关。