Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory for Hepatitis C and Immunologic Liver Disease, Beijing, China.
Yamanashi Prefectural Hospital Organization, Yamanashi, Japan.
Antiviral Res. 2018 Oct;158:178-184. doi: 10.1016/j.antiviral.2018.08.001. Epub 2018 Aug 16.
BACKGROUND & AIMS: Resistance associated substitutions (RAS) can reduce the efficacy of some direct-acting antiviral HCV regimens. Here, prevalence of RAS in genotype (GT) 1b, 2, 3, and 6 HCV-infected patients from Asian counties, North America and Europe are described and compared.
Pretreatment HCV RAS were assessed with 15% cutoff from patients enrolled in clinical trials of sofosbuvir-containing regimens in Mainland China, Japan, Korea, and India. Phylogenetic analyses were performed to investigating subtype diversity.
In GT1b patients, the prevalence of NS5A RAS, including Y93H, was similar across Asian countries (18-21%), and North America (15%) or Europe (19%). The prevalence of NS5B NI RAS, including L159F, was lower in Asian countries (1-5%) compared to North America (4%) or Europe (20%). The prevalence of NS3 RAS in patients from China (22%) and North America (28%) were lower than in Europe (40%). For GT2 patients in China, 100% had GT2a subtype with high prevalence of NS5A L31M. For GT3, the prevalence of GT3b was substantially higher in China (54%) than in North America or Europe (<1%); 99% of GT3b patients in China had NS5A RAS A30K+L31M, which confers high levels of resistance to NS5A inhibitors. In GT3a patients in China, the prevalence of NS5A RAS was lower (5%) than in North America and Europe (14-16%). Prevalence of NS5B NI RAS in GT2 and GT3 patients was rare across regions (<2%).
Differences in the prevalence of GT2 and GT3 subtypes and NS5A RAS were observed between Asian and Western countries.
耐药相关突变(RAS)可降低某些直接作用抗病毒 HCV 方案的疗效。本研究旨在描述并比较亚洲、北美和欧洲 HCV 基因型(GT)1b、2、3 和 6 感染患者中 RAS 的流行率。
采用 15%的临界值,对中国大陆、日本、韩国和印度索磷布韦含药方案临床试验中入组患者的 HCV RAS 进行检测。采用系统进化分析方法对亚群多样性进行研究。
在 GT1b 患者中,包括 Y93H 在内的 NS5A RAS 在亚洲国家(18-21%)、北美(15%)或欧洲(19%)的流行率相似。与北美(4%)或欧洲(20%)相比,亚洲国家(1-5%)的 NS5B NI RAS 包括 L159F 在内的流行率较低。中国(22%)和北美的 NS3 RAS 流行率(28%)低于欧洲(40%)。中国 GT2 患者 100%为 GT2a 亚型,其 NS5A L31M 突变率较高。GT3 中,中国的 GT3b 流行率明显高于北美或欧洲(<1%);中国 99%的 GT3b 患者均存在 NS5A RAS A30K+L31M,对 NS5A 抑制剂具有高度耐药性。中国 GT3a 患者中 NS5A RAS 的流行率(5%)低于北美和欧洲(14-16%)。GT2 和 GT3 患者中 NS5B NI RAS 的流行率在各地区均较低(<2%)。
亚洲和西方国家在 GT2 和 GT3 亚型以及 NS5A RAS 的流行率方面存在差异。