Evidence map›Paper›PMID 35265726›Full record

ArticleOpen forum infectious diseases2022

Association of Lower Exposure Risk With Paucisymptomatic/Asymptomatic Infection, Less Severe Disease, and Unrecognized Ebola Virus Disease: A Seroepidemiological Study.

J Daniel Kelly, Raphael G Frankfurter, Jacqueline M Tavs, Mohamed Bailor Barrie, Timothy McGinnis, Mohamed Kamara, Adams Freeman, Komba Quiwah, Michelle C Davidson, Bonnie Dighero-Kemp and 9 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 2 countries.

J Daniel KellyDepartment of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.ORCID https://orcid.org/0000-0002-7616-0321
Raphael G FrankfurterSchool of Medicine, University of California, San Francisco, California, USA.
Jacqueline M TavsF. I. Proctor Foundation, University of California, San Francisco, California, USA.
Mohamed Bailor BarrieDepartment of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
Timothy McGinnisDepartment of Global Health and Social Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Mohamed KamaraPartners In Health, Freetown, Sierra Leone.
Adams FreemanPartners In Health, Freetown, Sierra Leone.
Komba QuiwahPartners In Health, Freetown, Sierra Leone.
Michelle C DavidsonSchool of Medicine, University of California, San Francisco, California, USA.
Bonnie Dighero-KempIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Harrison GichiniIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Elizabeth ElliottIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Cavan ReillyDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota, USA.
Lisa E HensleyIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
H Clifford LaneIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Sheri D WeiserDivision of HIV, Infectious Disease, and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.ORCID https://orcid.org/0000-0002-7807-4072
Travis C PorcoDepartment of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
George W RutherfordDepartment of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
Eugene T RichardsonPartners In Health, Freetown, Sierra Leone.
University of California, San Francisco · USNational Institute of Allergy and Infectious Diseases · USSierra Leone Urban Research Centre · SLBrigham and Women's Hospital · USHarvard University · USUniversity of Minnesota · US

Funding

Medical Scientist Training Program (T32 NRSA Training Grant)T32GM141323 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Aimee Kao · 2021 to 2026
$10.5M
Ebola modeling: behavior, asymptomatic infection, and contacts (2019-nCoV Admin Supplement)R01GM130900 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PORCO, TRAVIS CHRISTIAN · 2019 to 2022
$1.6M
Social Epidemiology of Ebola Virus DiseaseK08AI139361 · NIAID · HARVARD MEDICAL SCHOOL · PI RICHARDSON, EUGENE THOMAS · 2019 to 2022
$751k
Understanding the epidemiology and natural history of unrecognized Ebola virus infectionK23AI146268 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KELLY, JOHN DANIEL · 2019 to 2022
$748k
NIAID NIH HHS K08 AI139361NIAID NIH HHS K23 AI146268NIAID NIH HHS L30 AI126521NIGMS NIH HHS R01 GM130900NIGMS NIH HHS T32 GM141323
6 · The paper itself

Abstract

Background: It remains unclear if there is a dose-dependent relationship between exposure risk to Ebola virus (EBOV) and severity of illness. Methods: From September 2016 to July 2017, we conducted a cross-sectional, community-based study of Ebola virus disease (EVD) cases and household contacts of several transmission chains in Kono District, Sierra Leone. We analyzed 154 quarantined households, comprising both reported EVD cases and their close contacts. We used epidemiological surveys and blood samples to define severity of illness as no infection, pauci-/asymptomatic infection, unrecognized EVD, reported EVD cases who survived, or reported EVD decedents. We determine seropositivity with the Filovirus Animal Nonclinical Group EBOV glycoprotein immunoglobulin G antibody test. We defined levels of exposure risk from 8 questions and considered contact with body fluid as maximum exposure risk. Results: Our analysis included 76 reported EVD cases (both decedents and survivors) and 421 close contacts. Among these contacts, 40 were seropositive (22 paucisymptomatic and 18 unrecognized EVD), accounting for 34% of the total 116 EBOV infections. Higher exposure risks were associated with having had EBOV infection (maximum risk: adjusted odds ratio [AOR], 12.1 [95% confidence interval {CI}, 5.8-25.4; trend test: Conclusions: This community-based study of EVD cases and contacts provides epidemiological evidence of a dose-dependent relationship between exposure risk and severity of illness, which may partially explain why pauci-/asymptomatic EBOV infection, less severe disease, and unrecognized EVD occurs.

Indexed as

Ebola virusepidemiologyexposure riskpublic healthtransmission

Identifiers

PMID35265726
PMCPMC8900924
OpenAlexW4220864915

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.