Evidence map›Paper›PMID 19149774›Full record

ArticleParasite immunology2009

Hepatosplenomegaly associated with chronic malaria exposure: evidence for a pro-inflammatory mechanism exacerbated by schistosomiasis.

S Wilson, F M Jones, J K Mwatha, G Kimani, M Booth, H C Kariuki, B J Vennervald, J H Ouma, E Muchiri, D W Dunne

Open access · bronzeAbstract read
In one paragraph

Article in Parasite immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Clinical spectrum and complications ofMalariaWorld journal · 2025
    Article
  4. Article
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  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Human schistosomiasis: clinical perspective: review.Journal of advanced research · 2013
    Review
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

10 authors at 4 institutions in 3 countries.

S WilsonDepartment of Pathology, University of Cambridge, Cambridge, UK. sw320@cam.ac.uk
F M Jones
J K Mwatha
G Kimani
M Booth
H C Kariuki
B J Vennervald
J H Ouma
E Muchiri
D W Dunne
University of Cambridge · GBKenya Medical Research Institute · KEMinistry of Health · KEUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In sub-Saharan Africa, chronic hepatosplenomegaly, with palpable firm/hard organ consistency, is common, particularly among school-aged children. This morbidity can be caused by long-term exposure to malaria, or by Schistosoma mansoni, and it is exacerbated when these two occur together. Although immunological mechanisms probably underlie the pathogenic process, these mechanisms have not been identified, nor is it known whether the two parasites augment the same mechanisms or induce unrelated processes that nonetheless have additive or synergistic effects. Kenyan primary schoolchildren, living in a malaria/schistosomiasis co-transmission area, participated in cross-sectional parasitological and clinical studies in which circulating immune modulator levels were also measured. Plasma IL-12p70, sTNF-RII, IL-10 and IL-13 levels correlated with relative exposure to malaria, and with hepatosplenomegaly. Soluble-TNF-RII and IL-10 were higher in children infected with S. mansoni. Hepatosplenomegaly caused by chronic exposure to malaria was clearly associated with increased circulating levels of pro-inflammatory mediators, with higher levels of regulatory modulators, and with tissue repair cytokines, perhaps being required to control the inflammatory response. The higher levels of regulatory modulators amongst S. mansoni infected children, compared to those without detectable S. mansoni and malarial infections, but exposed to malaria, suggest that S. mansoni infection may augment the underlying inflammatory reaction.

Indexed as

AdolescentAnimalsChildChild, PreschoolChronic DiseaseCross-Sectional StudiesHepatomegalyHumansInflammationInterleukin-10Interleukin-12Interleukin-13KenyaLymphokinesMalaria, FalciparumReceptors, Tumor Necrosis Factor, Type IIInterleukin-10Interleukin-12Interleukin-13LymphokinesReceptors, Tumor Necrosis Factor, Type II

Identifiers

PMID19149774
PMCPMC2680340
OpenAlexW2050767470

What OpenQuestion holds

Textmetadata
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.