Epidemiology of pediatric astrovirus gastroenteritis in a Nicaraguan birth cohort

medRxiv : the preprint server for health sciences(2023)

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摘要
Abstract: Background: Astrovirus is a leading cause of acute gastroenteritis in children worldwide. However, few prospective studies have analyzed astrovirus in community-dwelling pediatric populations in low-and-middle-income countries. Methods: We assessed the incidence, risk factors, clinical characteristics, genotypes, viral coinfections and seasonality of astrovirus gastroenteritis in 443 healthy Nicaraguan children born in 2017-2018, followed for 36 months. Children were recruited from maternity hospitals and birth records in an economically-diverse neighborhood of Leon, the second-largest city in Nicaragua. Astrovirus-positive episodes and genotypes were identified from diarrheal specimens with reverse transcription quantitative polymerase chain reaction and Sanger sequencing. Results: Of 1708 total specimens tested, eighty children (18%) experienced at least 1 astrovirus episode, and 9 experienced repeat episodes, mostly during the rainy season (May-October). The incidence of astrovirus episodes was 7.8/100 child-years (95% CI: 6.2, 9.8). Genotype-specific incidence of astrovirus also exhibited seasonality. Median age of astrovirus episode onset was 16 months (IQR 9, 23). Initial astrovirus episodes were not associated with protection against future episodes during the age span studied. Astrovirus cases were exclusively breastfed for a shorter period than uninfected children, and the human milk oligosaccharide lacto-N-fucopentaose-I was more concentrated in mothers of these children. Home toilets appeared to protect against future astrovirus episodes (HR=0.19, 95% CI 0.04-0.91). Human astrovirus-5 episodes, comprising 15% of all typed episodes, were associated with longer diarrhea and more symptomatic rotavirus co-infections. Conclusion: Astrovirus was a common cause of gastroenteritis in this cohort, and future studies should clarify the role of astrovirus genotype in clinical infection severity. ### Competing Interest Statement The authors have declared no competing interest. ### Funding Statement Funding for the SAGE study and salary support for SBD, FB, CTR, LG, SV, NAV, YR, and FG were supported by the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), through Grant Award R01AI127845. An international research capacity building award from the Fogarty International Center (FIC), NIH D43TW010923 provided additional salary support for FG, YR, and LG. SV and SBD. were supported by K24AI141744 from the NIAID. RJR has been funded by the NIH in 2018 to 2020 (2 T32GM 8719), and from 2022 to present (5T32DK007634), as well as the UNC Graduate School, GlaxoSmithKline, and CERobs, LLC. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The Ethical Committee for Biomedical Research of the Universidad Nacional Autonoma de Nicaragua Leon, the Institutional Review Board of the University of North Carolina at Chapel Hill, and the Centers for Disease Control in Atlanta gave ethical approval for this work. I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
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关键词
pediatric astrovirus gastroenteritis,epidemiology
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