Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Department of Comprehensive Community Care Systems, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Intern Med. 2021;60(2):191-199. doi: 10.2169/internalmedicine.5563-20. Epub 2021 Jan 15.
Objective The low-density lipoprotein cholesterol (LDL) level is known to increase following the treatment of hepatitis C virus (HCV) infection using direct-acting antiviral agents (DAAs). This study aimed to investigate the changes in the lipid profiles, including small-dense LDL cholesterol (sdLDL), in HCV patients treated with DAAs. Patients We retrospectively assessed 67 HCV patients who achieved sustained virological response with DAA administration and were observed for more than 2 years, of whom 32 were on daclatasvir/asunaprevir, 14 were on sofosbuvir/ledipasvir, and 21 were on sofosbuvir/ribavirin. Methods We evaluated the lipid profiles, including sdLDL, every 6 months until 2 years after the start of treatment and analyzed the factors related to changes in the sdLDL level. Results The median sdLDL value at baseline was 12.8 mg/dL, which increased to 19.5 mg/dL at 6 months (p<0.001) and remained elevated at 25.4 mg/dL at 2 years later (p<0.001). The Kaplan-Meier curve indicated that patients with high values of LDL, albumin, muscle attenuation and visceral to subcutaneous adipose tissue area ratio were at increased risk for elevation of sdLDL over 35 mg/dL (log-rank test: p<0.001; p=0.008, p=0.002 and p=0.042, respectively). A multivariate analysis performed on the factors contributing to elevation of sdLDL 2 years after DAA treatment (≥35.0 mg/dL) revealed pretreatment LDL (≥91.0 mg/dL) and muscle attenuation (≥33.7 HU) as significant factors (p=0.007 and p=0.032, respectively). Conclusion SdLDL increased continuously after DAA treatment, and high LDL levels and low intramuscular fat deposition before treatment contributed to elevated sdLDL levels after treatment.
目的 已知直接作用抗病毒药物(DAAs)治疗丙型肝炎病毒(HCV)感染后,低密度脂蛋白胆固醇(LDL)水平会升高。本研究旨在探讨 HCV 患者接受 DAA 治疗后血脂谱的变化,包括小而密 LDL 胆固醇(sdLDL)。
患者 我们回顾性评估了 67 例接受 DAA 治疗并观察超过 2 年实现持续病毒学应答的 HCV 患者,其中 32 例接受达卡他韦/阿舒瑞韦治疗,14 例接受索非布韦/雷迪帕韦治疗,21 例接受索非布韦/利巴韦林治疗。
方法 我们每 6 个月评估一次血脂谱,包括 sdLDL,直至治疗开始后 2 年,并分析与 sdLDL 水平变化相关的因素。
结果 基线时 sdLDL 值的中位数为 12.8mg/dL,治疗 6 个月时升高至 19.5mg/dL(p<0.001),2 年后仍维持在 25.4mg/dL (p<0.001)。Kaplan-Meier 曲线表明,LDL、白蛋白、肌肉衰减和内脏到皮下脂肪组织面积比高的患者发生 sdLDL 升高超过 35mg/dL 的风险增加(对数秩检验:p<0.001;p=0.008、p=0.002 和 p=0.042)。对 DAA 治疗 2 年后 sdLDL 升高(≥35.0mg/dL)的相关因素进行多因素分析,结果显示治疗前 LDL(≥91.0mg/dL)和肌肉衰减(≥33.7HU)是显著因素(p=0.007 和 p=0.032)。
结论 DAA 治疗后 sdLDL 持续升高,治疗前 LDL 水平高和肌肉内脂肪沉积低与治疗后 sdLDL 水平升高有关。