Evidence map›Paper›PMID 25240172›Full record

ReviewThe Journal of infectious diseases2015

New research tools for urogenital schistosomiasis.

Gabriel Rinaldi, Neil D Young, Jared D Honeycutt, Paul J Brindley, Robin B Gasser, Michael H Hsieh

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 27 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

6 authors at 4 institutions in 3 countries.

Gabriel RinaldiDepartment of Microbiology, Immunology, and Tropical Medicine Research Center for Neglected Diseases of Poverty, School of Medicine and Health Sciences, George Washington University, Washington, D.C.
Neil D YoungFaculty of Veterinary and Agricultural Sciences, University of Melbourne, Australia.
Jared D HoneycuttStanford Immunology, Stanford University, California.
Paul J BrindleyDepartment of Microbiology, Immunology, and Tropical Medicine Research Center for Neglected Diseases of Poverty, School of Medicine and Health Sciences, George Washington University, Washington, D.C.
Robin B GasserFaculty of Veterinary and Agricultural Sciences, University of Melbourne, Australia Institute of Parasitology and Tropical Veterinary Medicine, Berlin, Germany.
Michael H HsiehBiomedical Research Institute, Rockville, Maryland Children's National Health System, Washington, D.C.
George Washington University · USUniversity of Melbourne · AUBiomedical Research Institute · USStanford University · US

Funding

Transduction of Schistosoma mansoni by pseudotyped retrovirusR01AI072773 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI BRINDLEY, PAUL J · 2007 to 2011
$2.5M
Estrogenic Modulation of Genitourinary Epithelial-Probiotic Cross-TalkK08DK087895 · NIDDK · STANFORD UNIVERSITY · PI HSIEH, MICHAEL HARRISON · 2010 to 2014
$902k
Antibiotic selection for schistosome transgenesisR21AI109532 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BRINDLEY, PAUL J, RINALDI, JOSE GABRIEL · 2014 to 2015
$436k
NIAID NIH HHS R01 AI072773NIAID NIH HHS R01AI072773NIAID NIH HHS R21 AI109532NIDDK NIH HHS K08 DK087895
6 · The paper itself

Abstract

Approximately 200,000,000 people have schistosomiasis (schistosome infection). Among the schistosomes, Schistosoma haematobium is responsible for the most infections, which are present in 110 million people globally, mostly in sub-Saharan Africa. This pathogen causes an astonishing breadth of sequelae: hematuria, anemia, dysuria, stunting, uremia, bladder cancer, urosepsis, and human immunodeficiency virus coinfection. Refined estimates of the impact of schistosomiasis on quality of life suggest that it rivals malaria. Despite S. haematobium's importance, relevant research has lagged. Here, we review advances that will deepen knowledge of S. haematobium. Three sets of breakthroughs will accelerate discoveries in the pathogenesis of urogenital schistosomiasis (UGS): (1) comparative genomics, (2) the development of functional genomic tools, and (3) the use of animal models to explore S. haematobium-host interactions. Comparative genomics for S. haematobium is feasible, given the sequencing of multiple schistosome genomes. Features of the S. haematobium genome that are conserved among platyhelminth species and others that are unique to S. haematobium may provide novel diagnostic and drug targets for UGS. Although there are technical hurdles, the integrated use of these approaches can elucidate host-pathogen interactions during this infection and can inform the development of techniques for investigating schistosomes in their human and snail hosts and the development of therapeutics and vaccines for the control of UGS.

Indexed as

AnimalsDisease Models, AnimalGenes, HelminthGenomicsHumansMolecular Sequence AnnotationSchistosoma haematobiumSchistosomiasis haematobiabladdergenomicsSchistosomaSchistosoma haematobiumSchistosomiasisurogenital schistosomiasis

Identifiers

PMID25240172
PMCPMC4416124
OpenAlexW2166932814

What OpenQuestion holds

Textmetadata
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.