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泰国扩大和优化全国丙型肝炎病毒筛查的目标人群,以制定公共卫生政策。

Birth-cohort HCV screening target in Thailand to expand and optimize the national HCV screening for public health policy.

机构信息

Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Chumpare Hospital, Chum Phae, Khon Kaen, Thailand.

出版信息

PLoS One. 2018 Aug 23;13(8):e0202991. doi: 10.1371/journal.pone.0202991. eCollection 2018.

DOI:10.1371/journal.pone.0202991
PMID:30138441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6107264/
Abstract

The World Health Organization aims to eliminate HCV infection worldwide by 2030. A targeted HCV screening policy is currently unavailable in Thailand, but a decrease in HCV infection has been observed in the country. However, a previous study showed that there was a higher HCV seroprevalence in adults aged between 30-64 years in the Phetchabun province (15.5%), as compared to the Khon Kaen province (3.6%). It was hypothesized that young adults had a lower rate of HCV seropositivity; this was determined by the age distribution of anti-HCV in Phetchabun and with the identification of high seroprevalence birth cohorts. In order to compare the provincial findings to the national level, anti-HCV birth cohorts were further analyzed in Khon Kaen (averaged-HCV prevalence) as well as the Thai data set that was derived from the previous literature. Thai individuals aged between 18-30 years residing in Phetchabun (n = 1453) were recruited, tested for the presence of anti-HCV antibodies and viral RNA and completed questionnaires that were designed to identify HCV exposure risks. Data was collected and compiled from previously published articles (n = 1667, age 30-64 years). The HCV seropositivity in Phetchabun by age group (18-64, at 5-year intervals) and the birth year were tabulated parallel to the Khon Kaen data set (n = 2233) in conjunction with data from the national survey 2014 (n = 5964) representing the Thai population. Factors such as age, male gender, agricultural work, blood transfusion, intravenous drug use and having a tattoo were associated with anti-HCV positivity in Phetchabun. HCV seroprevalence was less than 4.0% (ranging from 0.0-3.5%) from the age of 18-34 years. A dramatic increase of 15.1% was found in adults aged greater than or equal to 35 years, whereas, the age group in Khon Kaen and the national population with increasing prevalence of HCV were older (≥40). The HCV seropositivity cohort accumulated for those born between 1951-1982 accounted for 71.4-100.0% of all seropositive individuals. Subsequently, new cases occurred sporadically. This finding provides evidence that there is a disproportionately high HCV seroprevalence among people born before 1983 (or aged ≥35). This cohort should be targeted for priority screening as part of the national HCV screening policy. Incorporating this birth cohort with other risk factors could improve HCV diagnostic rates, resulting in overall improvements in parallel to those given by novel antiviral treatment.

摘要

世界卫生组织的目标是到 2030 年在全球消除 HCV 感染。目前,泰国没有针对 HCV 的靶向筛查政策,但该国的 HCV 感染率有所下降。然而,之前的一项研究表明,在披集府(15.5%),30-64 岁的成年人 HCV 血清阳性率高于孔敬府(3.6%)。据推测,年轻人 HCV 血清阳性率较低;这是通过披集府抗 HCV 的年龄分布以及确定高血清流行出生队列来确定的。为了将省级发现与国家水平进行比较,进一步分析了孔敬府的抗 HCV 出生队列(平均 HCV 患病率)以及源自之前文献的泰国数据集。在披集府招募了年龄在 18-30 岁之间的泰国人(n = 1453),检测他们是否存在抗 HCV 抗体和病毒 RNA,并完成了旨在确定 HCV 暴露风险的问卷。数据来自之前发表的文章(n = 1667,年龄 30-64 岁)。按照与孔敬府数据(n = 2233)以及代表泰国人口的 2014 年全国调查(n = 5964)相结合的方式,按年龄组(18-64 岁,每 5 年一次)和出生年份列出披集府的 HCV 血清阳性率。年龄、男性、农业工作、输血、静脉注射药物和纹身等因素与披集府的抗 HCV 阳性有关。18-34 岁时 HCV 血清流行率低于 4.0%(0.0-3.5%)。35 岁及以上的成年人 HCV 血清流行率显著增加 15.1%,而孔敬府和全国 HCV 流行率不断增加的年龄组则更大(≥40 岁)。1951-1982 年出生的 HCV 血清阳性者累积率占所有血清阳性者的 71.4-100.0%。随后,新病例偶有发生。这一发现表明,1983 年以前(或 35 岁及以上)出生的人群 HCV 血清阳性率过高。该人群应作为国家 HCV 筛查政策的优先筛查对象。将这一出生队列与其他危险因素结合起来,可以提高 HCV 的诊断率,从而与新型抗病毒治疗一起取得整体改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/122a8df855ab/pone.0202991.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/931a616f8426/pone.0202991.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/cd5e6291dcd0/pone.0202991.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/122a8df855ab/pone.0202991.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/931a616f8426/pone.0202991.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/cd5e6291dcd0/pone.0202991.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ce/6107264/122a8df855ab/pone.0202991.g003.jpg

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