Evidence map›Paper›PMID 37632076›Full record

ArticleViruses2023

Burden of Chikungunya Virus Infection during an Outbreak in Myanmar.

Mya Myat Ngwe Tun, Aung Kyaw Kyaw, Khine Mya Nwe, Su Su Myaing, Ye Thu Win, Shingo Inoue, Yuki Takamatsu, Takeshi Urano, Hlaing Myat Thu, Saw Wutt Hmone and 2 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 4 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

12 authors at 5 institutions in 2 countries.

Mya Myat Ngwe TunDepartment of Tropical Viral Vaccine Development, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.
Aung Kyaw KyawDepartment of Medical Research, Ministry of Health, Yangon 11191, Myanmar.ORCID 0000-0002-1384-8030
Khine Mya NweDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.
Su Su MyaingDepartment of Medical Research, Ministry of Health, Yangon 11191, Myanmar.
Ye Thu Win550-Bedded Children Hospital (Mandalay), Department of Medical Services, Ministry of Health, Mandalay City 05021, Myanmar.
Shingo InoueKenya Research Station, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.
Yuki TakamatsuDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.
Takeshi UranoCenter for Vaccines and Therapeutic Antibodies for Emerging Infectious Diseases, Shimane University, Izumo 690-8504, Japan.
Hlaing Myat ThuDepartment of Medical Research, Ministry of Health, Yangon 11191, Myanmar.
Saw Wutt HmoneDepartment of Pathology, University of Medicine-1, Ministry of Health, Yangon 11131, Myanmar.
Kyaw Zin ThantMyanmar Academy of Medical Science, Yangon 11201, Myanmar.
Kouichi MoritaDepartment of Tropical Viral Vaccine Development, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.
Ministry of Health · MMNagasaki University · JPShimane University · JPMyanmar Oxford Clinical Research Unit · MMUniversity of Medicine Mandalay · MM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chikungunya virus (CHIKV) infection is a re-emerging arboviral disease with no approved vaccine, although numerous options are in development. Before vaccine implementation, disease burden, affected age group, and hospitalization rate information should be documented. In 2019, a sizeable outbreak of the East Central South African genotype of CHIKV occurred in Myanmar, and during this period, a cross-sectional study was conducted in two regions, Mandalay and Yangon, to examine the molecular and seropositivity rate of the CHIKV infection. The participants (1124) included dengue-suspected pediatric patients, blood donors, and healthy volunteers, who were assessed using molecular assays (quantitative real-time RT-PCR), serological tests (anti-CHIKV IgM capture and IgG indirect enzyme-linked immunosorbent assays), and neutralization tests. The tests confirmed the following positivity rates: 11.3% (127/1124) for the molecular assay, 12.4% (139/1124) for the anti-CHIKV IgM Ab, 44.5% (500/1124) for the anti-CHIKV IgG Ab, and 46.3% (520/1124) for the CHIKV neutralizing Ab. The highest rate for the molecular test occurred with the dengue-suspected pediatric patients. The seroprevalence rate through natural infection was higher in the healthy volunteers and blood donors than that in the pediatric patients. The results of this study will help stakeholders determine the criteria for choosing appropriate recipients when a CHIKV vaccine is introduced in Myanmar.

Indexed as

Chikungunya FeverChikungunya virusDengueAntibodies, ViralChildCross-Sectional StudiesDisease OutbreaksHumansImmunoglobulin GImmunoglobulin MMyanmarSeroepidemiologic StudiesAntibodies, ViralImmunoglobulin GImmunoglobulin Mchikungunya burdenmolecular detectionMyanmarseropositivity

Identifiers

PMID37632076
PMCPMC10459206
OpenAlexW4385805836

What OpenQuestion holds

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LicenceCC BY
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.