Effect of sofosbuvir-based DAAs on changes in lower-density lipoprotein in HCV patients: a systematic review and meta-analysis

被引:1
|
作者
Wang, Ying-Wen [1 ,5 ]
Lee, Wei-Ping [2 ,3 ]
Huang, Yi-Hsiang [4 ,5 ,6 ]
Hou, Ming-Chih [4 ,5 ]
Lan, Keng-Hsin [4 ,5 ,7 ]
机构
[1] Taipei Vet Gen Hosp, Healthcare & Management Ctr, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Med Res, Taipei, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Coll Life Sci, Inst Biochem & Mol Biol, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol & Hepatol, 201,Sect 2,Shi Pai Rd, Taipei 112, Taiwan
[5] Natl Yang Ming ChiaoTung Univ, Coll Med, Sch Med, Taipei, Taiwan
[6] Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Clin Med, Taipei, Taiwan
[7] Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Pharmacol, Taipei, Taiwan
关键词
Direct-acting antivirals; Hepatitis C virus; Lipids; Low-density lipoprotein; Sofosbuvir; HEPATITIS-C VIRUS; SERUM-LIPID PROFILES; INFECTION; PREVALENCE; STEATOSIS;
D O I
10.1186/s12879-021-06657-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Previous studies reported worsened lipid profiles in patients infected with hepatitis C virus (HCV) during direct-acting antivirals (DAAs) treatment. This study aimed to investigate the effect of sofosbuvir (SOF)-based DAAs on changes in low-density lipoprotein (LDL) in HCV patients. Methods A systematic review of articles published before 31 May 2021 was conducted by searching MEDLINE, Cochrane Library, EMBASE, and CINAHL Plus. Eligible studies were those comparing SOF-based DAAs and non-SOF DAAs for HCV patients and providing numerical data for changes in LDL. Risk of Bias in Non-randomized Studies- of Interventions was used for assessing risk of bias, and meta-analysis was performed for changes in LDL. Results Six studies comprising 1248 patients were included, 848 patients treated with SOF-based DAAs and 400 patients with non-SOF DAAs vs. SOF-based DAAs group had significantly greater increases in LDL from baseline to week 4 than non-SOF DAAs group (P = 0.001). However, changes in LDL from baseline to the end of treatment (P = 0.060), to post-treatment week 12 (P = 0.263), and to post-treatment week 24 (P = 0.319) did not significantly differ between the two groups. Further comparison of SOF/ledipasvir with asunaprevir/daclatasvir revealed a similar trend in changes in LDL. Conclusions For HCV patients, SOF-based DAA regimens were associated with rapid and significant increases in LDL during the initial 4 weeks of treatment, and the changes did not sustain after the end of treatment. Potential mechanism might be related to the phosphoramidate side chain of SOF.
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页数:12
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