Huang Yi-Wen, Lee Chia-Long, Yang Sien-Sing, Fu Szu-Chieh, Chen Yun-Yi, Wang Ting-Chuan, Hu Jui-Ting, Chen Ding-Shinn
Liver Center, Cathay General Hospital Medical Center, Taipei, Taiwan.
School of Medicine, Taipei Medical University College of Medicine, Taipei, Taiwan.
Am J Gastroenterol. 2016 Jul;111(7):976-85. doi: 10.1038/ajg.2016.179. Epub 2016 May 10.
The protective effect of statins in cirrhosis and its decompensation in chronic hepatitis B (CHB) patients remains unknown.
We conducted a population-based cohort study using data from the Taiwanese National Health Insurance Research Database from 1997 to 2009. A total of 298,761 CHB patients were identified. CHB patients using statins (n=6,543; defined as ≥28 cumulative defined daily doses (cDDD)) and a 1:1 ratio propensity score and inception point (the date of first use of statins)-matched non-statins (<28 cDDD) were followed up from the inception point until the development of cirrhosis or its decompensation or until withdrawal from insurance or December 2009.
After adjustment for competing mortality, CHB patients using statins had a significantly lower cumulative incidence of cirrhosis (relative risk)=0.433; 95% confidence interval (CI)=0.344-0.515; modified log-rank test, P<0.001) and decompensated cirrhosis (relative risk=0.468; 95% CI=0.344-0.637; P<0.001) compared with patients not using statins. After adjustment for age, gender, comorbidity index, hypertension, diabetes, hyperlipidemia, hepatocellular carcinoma, obesity, non-alcoholic fatty liver disease, aspirin use, diabetes medication, CHB treatment, non-statin lipid-lowering drugs, and triglyceride lipid-lowering drugs using the Cox proportional hazard model, statins were still an independent protector against cirrhosis (adjusted hazard ratio (AHR)=0.512; 95% CI=0.413-0.634; P<0.001) and its decompensation (AHR=0.534; 95% CI=0.433-0.659; P<0.001). The AHRs for cirrhosis were 0.467 and 0.200, and the AHRs for decompensated cirrhosis were 0.611 and 0.231 with 91-365 and >365 cDDD of statins, respectively.
CHB patients who receive statin therapy have a dose-dependent reduction in the risk of cirrhosis and its decompensation.
他汀类药物对慢性乙型肝炎(CHB)患者肝硬化及其失代偿的保护作用尚不清楚。
我们利用1997年至2009年台湾国民健康保险研究数据库的数据进行了一项基于人群的队列研究。共确定了298,761例CHB患者。使用他汀类药物的CHB患者(n = 6,543;定义为累积规定日剂量(cDDD)≥28)与1:1比例倾向评分和起始点(首次使用他汀类药物的日期)匹配的未使用他汀类药物患者(<28 cDDD)从起始点开始随访,直至发生肝硬化或其失代偿,或直至退出保险或2009年12月。
在调整了竞争死亡率后,使用他汀类药物的CHB患者肝硬化的累积发病率显著较低(相对风险=0.433;95%置信区间(CI)=0.344 - 0.515;改良对数秩检验,P<0.001),失代偿期肝硬化的累积发病率也显著较低(相对风险=0.468;95% CI = 0.344 - 0.637;P<0.001),与未使用他汀类药物的患者相比。在使用Cox比例风险模型调整年龄、性别、合并症指数、高血压、糖尿病、高脂血症、肝细胞癌、肥胖、非酒精性脂肪性肝病、阿司匹林使用、糖尿病药物治疗、CHB治疗、非他汀类降脂药物和甘油三酯降脂药物后,他汀类药物仍然是预防肝硬化(调整后风险比(AHR)=0.512;95% CI = 0.413 - 0.634;P<0.001)及其失代偿(AHR = 0.534;95% CI = 0.433 - 0.659;P<0.001)的独立保护因素。他汀类药物cDDD为91 - 365和>365时,肝硬化的AHR分别为0.467和0.200,失代偿期肝硬化的AHR分别为0.611和0.231。
接受他汀类药物治疗的CHB患者发生肝硬化及其失代偿的风险呈剂量依赖性降低。