Enterovirus genomic load and disease severity among children hospitalised with hand, foot and mouth disease

被引:23
作者
Song, Chunlan [1 ]
Zhou, Yonghong [2 ,4 ]
Li, Yu [3 ]
Liang, Lu [5 ,6 ]
Turtle, Lance [7 ,8 ]
Wang, Fang [1 ]
Wu, Peng [2 ]
Qiu, Qi [4 ]
Yang, Jianli [1 ]
Wang, Kai [4 ]
Cui, Peng [4 ]
Cheng, Yibing [1 ]
Zhang, Tianchen [3 ]
Guo, Chun [9 ]
Zeng, Mengyao [4 ,10 ]
Long, Lu [5 ,6 ]
Peiris, Malik [2 ]
Zhou, Chongchen [1 ]
Cowling, Benjamin J. [2 ]
Yu, Hongjie [4 ]
机构
[1] Zhengzhou Univ, Henan Childrens Hosp, Childrens Hosp, Zhengzhou, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, WHO Collaborating Ctr Infect Dis Epidemiol & Cont, Sch Publ Hlth, Hong Kong, Peoples R China
[3] Chinese Ctr Dis Control & Prevent, Key Lab Surveillance & Early Warning Infect Dis, Div Infect Dis, Beijing, Peoples R China
[4] Fudan Univ, Key Lab Publ Hlth Safety, Minist Educ, Sch Publ Hlth, Shanghai, Peoples R China
[5] Sichuan Univ, West China Sch Publ Hlth, Chengdu, Peoples R China
[6] Sichuan Univ, West China Fourth Hosp, Chengdu, Peoples R China
[7] Univ Liverpool, NIHR Hlth Protect Res Unit Emerging & Zoonot Infe, Liverpool, Merseyside, England
[8] Royal Liverpool Univ Hosp, Liverpool Hlth Partners, Trop & Infect Dis Unit, Liverpool, Merseyside, England
[9] Huazhong Univ Sci & Technol, Sch Publ Hlth, Wuhan, Peoples R China
[10] Fudan Univ, Shanghai Inst Planned Parenthood Res, NHC Key Lab Reprod Regulat, Shanghai, Peoples R China
来源
EBIOMEDICINE | 2020年 / 62卷
基金
英国惠康基金;
关键词
HFMD; Viral load; Viral genomic load; Enterovirus; Clinical severity; VIRAL REPLICATION; VIRUS;
D O I
10.1016/j.ebiom.2020.103078
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Examining associations between viral genomic loads of enteroviruses and clinical severity is important for promoting and improving development of antiviral drugs related to hand, foot and mouth disease (HFMD). Methods: Throat swabs were collected from HFMD cases at acute phase of illness using a standardized technique in a prospective study. The viral genomic load was categorized into low, medium, and high groups using parameters of real-time reverse transcription-polymerase chain reaction. The clinical severities were assessed with four indicators, respectively. Findings: We analysed 1109 HFMD cases, including 538 children with CV-A6, 231 with CV-A16, 156 with EV-A71, 78 with CV-A10, 59 with CV-A4, and 47 with CV-A2. EV-A71 genomic load categories were associated with risks of diagnoses of CNS complications (p = 0.016), requiring systemic corticosteroids or IVIG (p = 0.011), intensive care unit admission (p = 0.002) and length of hospital stay over 5 days (p = 0.048). In the multivariate analyses, point estimates of adjusted odds ratio (OR) tended to increase with viral genomic loads for all four severe outcomes and ORs of highest viral genomic load were all significantly larger than one for EV-A71. Interpretation: HFMD clinical severities positively associate with viral genomic loads of EV-A71 in throat swabs. Specific antiviral drugs should be developed to reduce enterovirus load and to alleviate the clinical severities for HFMD cases. (C) 2020 The Authors. Published by Elsevier B.V.
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页数:9
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