Audu Rosemary Ajuma, Okwuraiwe Azuka Patrick, Ige Fehintola Anthonia, Adeleye Olufunke Oluwatosin, Onyekwere Charles Asabamaka, Lesi Olufunmilayo Adenike
Center for Human Virology and Genomics, Nigerian Institute of Medical Research, Lagos, Nigeria.
Department of Medicine, College of Medicine, Olabisi Onabanjo University Teaching Hospital, Lagos, Nigeria.
Pan Afr Med J. 2020 Dec 10;37:335. doi: 10.11604/pamj.2020.37.335.20299. eCollection 2020.
Hepatitis C Virus (HCV) is highly infectious with no currently available vaccine. Prior to treatment, it is recommended to confirm HCV infection with either quantitative or qualitative nucleic acid test. Access to these assays in Nigeria is limited but for effective management of patients, HCV viral load (VL) prior to therapy is required and genotype may be needed in some instances. This study aimed at reviewing the pattern of HCV viral load and genotype in the country, and its implication in patient management.
this was a retrospective study that involved data abstraction from an electronic database of an accredited laboratory between June 2013 and May 2017. De-linked data were abstracted from records of adult subjects with HCV VL and genotype results, these were analysed using Microsoft Excel 2010 and SPSS v20.
within the study period, 346 subjects had baseline VL and 134 (38.7%) had genotype results available. Of these, 202/346 (58.4%) had detectable VL results with higher prevalence in males (64.7%) and ≥51years (42.5%) age group. The median VL among 202 subjects was 407,430 (IQR: 96,388 - 1,357,012) IU/mL. Distribution of genotypes showed that genotypes 1 and 4 had prevalence of 63.2% and 16.8% respectively.
genotypes 1 and 4 have the highest prevalence. A greater proportion of subjects had VL values ≤800,000 IU/mL, an indication that they are more likely to respond well to available antiviral therapy hence, access to these antivirals will greatly improve management of HCV infection in Nigeria.
丙型肝炎病毒(HCV)具有高度传染性,目前尚无可用疫苗。在治疗前,建议通过定量或定性核酸检测来确认HCV感染。在尼日利亚,获得这些检测方法的途径有限,但为了有效管理患者,治疗前需要检测HCV病毒载量(VL),在某些情况下可能还需要检测基因型。本研究旨在回顾该国HCV病毒载量和基因型的模式及其对患者管理的意义。
这是一项回顾性研究,涉及从2013年6月至2017年5月期间一家认可实验室的电子数据库中提取数据。从成年受试者的HCV VL和基因型结果记录中提取去识别化数据,使用Microsoft Excel 2010和SPSS v20进行分析。
在研究期间,346名受试者有基线VL数据,134名(38.7%)有基因型结果。其中,202/346(58.4%)的VL结果可检测到,男性(64.7%)和≥51岁(42.5%)年龄组的患病率较高。202名受试者的VL中位数为407,430(四分位间距:96,388 - 1,357,012)IU/mL。基因型分布显示,基因型1和4的患病率分别为63.2%和16.8%。
基因型1和4的患病率最高。更大比例的受试者VL值≤800,000 IU/mL,这表明他们更有可能对现有的抗病毒治疗有良好反应,因此,获得这些抗病毒药物将大大改善尼日利亚HCV感染的管理。