Evidence map›Paper›PMID 26990869›Full record

ArticlePloS one2016

Further Evidence of Increasing Diversity of Plasmodium vivax in the Republic of Korea in Recent Years.

Jung-Yeon Kim, Youn-Kyoung Goo, Young-Gun Zo, So-Young Ji, Hidayat Trimarsanto, Sheren To, Taane G Clark, Ric N Price, Sarah Auburn

Abstract read
In one paragraph

Article in PloS one, 2016. 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
–field-weighted citation impact
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.

  1. Molecular Surveillance ofPathogens (Basel, Switzerland) · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. PCR-RFLP for Rapid Subtyping ofThe Korean journal of parasitology · 2017
    Article
  9. Diversity ofThe Korean journal of parasitology · 2017
    Article
  10. Article
  11. Article
  12. Article
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

9 authors.

Jung-Yeon KimDivision of Malaria and Parasitic Diseases, National Institute of Health, Korea CDC, Osong Saeng-myeong, 2 ro, Osong Health Technology Administration, Osong, Republic of Korea.
Youn-Kyoung GooDivision of Malaria and Parasitic Diseases, National Institute of Health, Korea CDC, Osong Saeng-myeong, 2 ro, Osong Health Technology Administration, Osong, Republic of Korea.
Young-Gun ZoDepartment of Molecular Parasitology, Sungkyunkwan University School of Medicine and Center for Molecular Medicine, Samsung Biomedical Research Institute, Suwon, Gyeonggi-do 440-746, Republic of Korea.
So-Young JiDivision of Malaria and Parasitic Diseases, National Institute of Health, Korea CDC, Osong Saeng-myeong, 2 ro, Osong Health Technology Administration, Osong, Republic of Korea.
Hidayat TrimarsantoEijkman Institute for Molecular Biology, Jl. Diponegoro 69, Jakarta Pusat, 10430, Indonesia.
Sheren ToGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, NT 0810, Australia.
Taane G ClarkFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, United Kingdom.
Ric N PriceGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, NT 0810, Australia.
Sarah AuburnGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, NT 0810, Australia.

Funding

Medical Research Council MR/K000551/1Medical Research Council MR/M01360X/1Wellcome TrustWellcome Trust 091625
6 · The paper itself

Abstract

backgroundVivax malaria was successfully eliminated from the Republic of Korea (ROK) in the late 1970s but re-emerged in 1993. Two decades later as the ROK enters the final stages of malaria elimination, dedicated surveillance of the local P. vivax population is critical. We apply a population genetic approach to gauge P. vivax transmission dynamics in the ROK between 2010 and 2012. METHODOLOGY/PRINCIPAL

findingsP. vivax positive blood samples from 98 autochthonous cases were collected from patients attending health centers in the ROK in 2010 (n = 27), 2011 (n = 48) and 2012 (n = 23). Parasite genotyping was undertaken at 9 tandem repeat markers. Although not reaching significance, a trend of increasing population diversity was observed from 2010 (HE = 0.50 ± 0.11) to 2011 (HE = 0.56 ± 0.08) and 2012 (HE = 0.60 ± 0.06). Conversely, linkage disequilibrium declined during the same period: IAS = 0.15 in 2010 (P = 0.010), 0.09 in 2011 (P = 0.010) and 0.05 in 2012 (P = 0.010). In combination with data from other ROK studies undertaken between 1994 and 2007, our results are consistent with increasing parasite divergence since re-emergence. Polyclonal infections were rare (3% infections) suggesting that local out-crossing alone was unlikely to explain the increased divergence. Cases introduced from an external reservoir may therefore have contributed to the increased diversity. Aside from one isolate, all infections carried a short MS20 allele (142 or 149 bp), not observed in other studies in tropical endemic countries despite high diversity, inferring that these regions are unlikely reservoirs.

conclusionsWhilst a number of factors may explain the observed population genetic trends, the available evidence suggests that an external geographic reservoir with moderate diversity sustains the majority of P. vivax infection in the ROK, with important implications for malaria elimination.

Indexed as

Genetic VariationAdolescentAdultAgedChildFemaleGenetics, PopulationHumansLinkage DisequilibriumMalaria, VivaxMaleMicrosatellite RepeatsMiddle AgedPlasmodium vivaxRepublic of KoreaYoung Adult

Identifiers

PMID26990869
PMCPMC4798397

What OpenQuestion holds

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Registered trials

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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.