Human enterovirus 71 disease in Sarawak, Malaysia: A prospective clinical, virological, and molecular epidemiological study

被引:161
作者
Ooi, Mong How
Wong, See Chang
Podin, Yuwana
Akin, Winnie
del Sel, Syvia
Mohan, Anand
Chieng, Chae Hee
Perera, David
Clear, Daniela
Wong, Darin
Blake, Emma
Cardosa, Jane
Solomon, Tom
机构
[1] Univ Liverpool, Viral Brain Infect Grp, Div Med Microbiol, Liverpool L69 3GA, Merseyside, England
[2] Univ Liverpool, Viral Brain Infect Grp, Div Neurol Surg, Liverpool L69 3GA, Merseyside, England
[3] Univ Malaysia Sarawak, Inst Hlth & Community Med, Samarahan, Malaysia
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1086/511073
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Human enterovirus (HEV)-71 causes large outbreaks of hand-foot-and-mouth disease with central nervous system (CNS) complications, but the role of HEV-71 genogroups or dual infection with other viruses in causing severe disease is unclear. Methods. We prospectively studied children with suspected HEV-71 (i.e., hand-foot-and-mouth disease, CNS disease, or both) over 3.5 years, using detailed virological investigation and genogroup analysis of all isolates. Results. Seven hundred seventy-three children were recruited, 277 of whom were infected with HEV-71, including 28 who were coinfected with other viruses. Risk factors for CNS disease in HEV-71 included young age, fever, vomiting, mouth ulcers, breathlessness, cold limbs, and poor urine output. Genogroup analysis for the HEV-71-infected patients revealed that 168 were infected with genogroup B4, 68 with C1, and 41 with a newly emerged genogroup, B5. Children with HEV-71 genogroup B4 were less likely to have CNS complications than those with other genogroups (26 [15%] of 168 vs. 30 [28%] of 109; odds ratio [OR], 0.48; 95% confidence interval [CI], 0.26 - 0.91; P = .0223) and less likely to be part of a family cluster (12 [7%] of 168 vs. 29 [27%] of 109; OR, 0.21; 95% CI, 0.10 - 0.46; P < .0001); children with HEV-71 genogroup B5 were more likely to be part of a family cluster (OR, 6.26; 95% CI, 2.77 - 14.18; P < .0001). Children with HEV-71 and coinfected with another enterovirus or adenovirus were no more likely to have CNS disease. Conclusions. Genogroups of HEV-71 may differ with regard to the risk of causing CNS disease and the association with family clusters. Dual infections are common, and all possible causes should be excluded before accepting that the first virus identified is the causal agent.
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页码:646 / 656
页数:11
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