Evidence map›Paper›PMID 24945801›Full record

ArticlePLoS neglected tropical diseases2014

Cystic echinococcoses in Mongolia: molecular identification, serology and risk factors.

Akira Ito, Temuulen Dorjsuren, Anu Davaasuren, Tetsuya Yanagida, Yasuhito Sako, Kazuhiro Nakaya, Minoru Nakao, Oyun-Erdene Bat-Ochir, Tsendjav Ayushkhuu, Narantuya Bazarragchaa and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  9. Genetic survey of cystic echinococcosis in farm animals in Oman.Tropical animal health and production · 2020
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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

16 authors at 3 institutions in 3 countries.

Akira ItoDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan.
Temuulen DorjsurenDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Department of Medical Biology and Histology, School of Biomedicine, Health Sciences University of Mongolia, Ulaanbaatar, Mongolia.
Anu DavaasurenDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; National Center for Communicable Diseases, Ulaanbaatar, Mongolia.
Tetsuya YanagidaDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan.
Yasuhito SakoDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan.
Kazuhiro NakayaDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan.
Minoru NakaoDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan.
Oyun-Erdene Bat-OchirNational Center of Pathology, Ulaanbaatar, Mongolia.
Tsendjav AyushkhuuNational Center for Maternal and Child Health, Ulaanbaatar, Mongolia.
Narantuya BazarragchaaDepartment of Surgery, State Central First Hospital, Ulaanbaatar, Mongolia.
Nyamkhuu GonchigsengeeDepartment of Surgery, State Central First Hospital, Ulaanbaatar, Mongolia.
Tiaoying LiDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Institute of Parasitic Diseases, Sichuan Centers for Disease Control and Prevention, Chengdu, China.
Gurbadam AgvaandaramDepartment of Medical Biology and Histology, School of Biomedicine, Health Sciences University of Mongolia, Ulaanbaatar, Mongolia.
Abmed DavaajavDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; National Center for Communicable Diseases, Ulaanbaatar, Mongolia.
Chinchuluun BoldbaatarDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Institute of Veterinary Medicine, Ulaanbaatar, Mongolia.
Gantigmaa ChuluunbaatarDepartment of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Mongolian Academy of Science, Ulaanbaatar, Mongolia.
Asahikawa Medical University · JPNational Center for Communicable Diseases · MNNational University of Mongolia · MN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCystic echinococcosis (CE) is a globally distributed cestode zoonosis that causes hepatic cysts. Although Echinococcus granulosus sensu stricto (s.s.) is the major causative agent of CE worldwide, recent molecular epidemiological studies have revealed that E. canadensis is common in countries where camels are present. One such country is Mongolia. METHODOLOGY/PRINCIPAL

findingsForty-three human hepatic CE cases that were confirmed histopathologically at the National Center of Pathology (NCP) in Ulaanbaatar (UB) were identified by analysis of mitochondrial cox 1 gene as being caused by either E. canadensis (n=31, 72.1%) or E. granulosus s.s. (n=12, 27.9%). The majority of the E. canadensis cases were strain G6/7 (29/31, 93.5%). Twenty three haplotypes were identified. Sixteen of 39 CE cases with data on age, sex and province of residence were citizens of UB (41.0%), with 13 of the 16 cases from UB caused by E. canadensis (G6/7) (81.3%). Among these 13 cases, nine were children (69.2%). All pediatric cases (n  =  18) were due to E. canadensis with 17 of the 18 cases (94.4%) due to strain G6/7. Serum samples were available for 31 of the 43 CE cases, with 22 (71.0%) samples positive by ELISA to recombinant Antigen B8/1 (rAgB). Nine of 10 CE cases caused by E. granulosus s.s. (90.0%) and 13 of 20 CE cases by E. canadensis (G6/7) (65.0%) were seropositive. The one CE case caused by E. canadensis (G10) was seronegative. CE cases caused by E. granulosus s.s. showed higher absorbance values (median value 1.131) than those caused by E. canadensis (G6/7) (median value 0.106) (p  =  0.0137). CONCLUSION/SIGNIFICANCE: The main species/strains in the study population were E. canadenis and E. granulossus s.s. with E. canadensis the predominant species identified in children. The reason why E. canadensis appears to be so common in children is unknown.

Indexed as

AdolescentAdultAgedAnimalsAntibodies, HelminthChildChild, PreschoolEchinococcosis, HepaticEchinococcusElectron Transport Complex IVFemaleHaplotypesHumansMaleMiddle AgedMolecular EpidemiologyAntibodies, HelminthElectron Transport Complex IV

Identifiers

PMID24945801
PMCPMC4063745
OpenAlexW2086680455

What OpenQuestion holds

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LicenceCC BY
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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.