Evidence map›Paper›PMID 21199883›Full record

ArticleThe Journal of infectious diseases2011

Tissue inhibitor of matrix-metalloprotease-1 predicts risk of hepatic fibrosis in human Schistosoma japonicum infection.

Valeria Fabre, Haiwei Wu, Sunthorn PondTor, Hannah Coutinho, Luz Acosta, Mario Jiz, Remigio Olveda, Ling Cheng, Eric S White, Blanca Jarilla and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  15. Resolvin E1 reduces hepatic fibrosis in mice withExperimental and therapeutic medicine · 2014
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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

13 authors at 5 institutions in 2 countries.

Valeria FabreDepartment of Medicine, Memorial Hospital of Rhode Island, Brown University Medical School, Providence, RI, USA. valeria_fabre@brown.edu
Haiwei Wu
Sunthorn PondTor
Hannah Coutinho
Luz Acosta
Mario Jiz
Remigio Olveda
Ling Cheng
Eric S White
Blanca Jarilla
Stephen T McGarvey
Jennifer F Friedman
Jonathan D Kurtis
Rhode Island Hospital · USBrown University · USMemorial Hospital of Rhode Island · USResearch Institute for Tropical Medicine · PHUniversity of Michigan–Ann Arbor · US

Funding

Puberty, Immunity and Malnutrition in S. JaponicumR01AI048123 · NIAID · RHODE ISLAND HOSPITAL · PI KURTIS, JONATHAN D. · 2001 to 2005
$3.0M
Matrix biomarkers and compartmentalization in IPFR01HL109118 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WHITE, ERIC S · 2012 to 2015
$1.8M
S. japonicum morbidity and pro-inflammatory cytokinesK23AI052125 · NIAID · RHODE ISLAND HOSPITAL · PI FRIEDMAN, JENNIFER F · 2002 to 2006
$624k
NHLBI NIH HHS R01 HL109118NIAID NIH HHS K23 AI052125NIAID NIH HHS K23AI52125NIAID NIH HHS R01 AI048123NIAID NIH HHS R01AI48123
6 · The paper itself

Abstract

backgroundSchistosomes infect 200 million individuals annually and cause significant hepatic fibrosis in up to 20%. Little is known regarding the mechanisms of schistosome-associated hepatic fibrosis in humans, and few biomarkers for risk of fibrosis have been identified.

methodsWe treated 611 Schistosoma japonicum-infected Filipinos with praziquantel (PZQ) and performed ultrasound to quantify hepatic fibrosis at baseline and 12 months after PZQ treatment. We developed a multiplexed assay (FibroPlex) that quantifies predictors and effect modifiers of fibrosis. We measured FibroPlex analytes produced by peripheral blood mononuclear cells stimulated with schistosome egg antigen 4 weeks after PZQ treatment and related these levels to risk of fibrosis 1 year after PZQ treatment.

resultsAfter adjusting for potential confounders, including baseline grade of fibrosis, individuals with detectable tissue inhibitor of matrix-metalloprotease-1 (TIMP-1) had a 3.5-fold greater risk of fibrosis 1 year after PZQ treatment, compared with individuals with undetectable levels (odds ratio, 3.48; 95% confidence interval, 1.41-8.43; P = .007). DISCUSSION: Because TIMP-1 inhibits most matrix metalloproteases, which are responsible for collagen degradation, these data suggest that schistosome-associated hepatic fibrosis results, in part, from excessive inhibition of collagen remodeling. These data further suggest that TIMP-1 is a promising biomarker for assessing risk of hepatic fibrosis in schistosomiasis and, potentially, other infectious and noninfectious causes of liver disease.

Indexed as

AdolescentAdultAnimalsAnthelminticsBiomarkersChildCohort StudiesCollagenFecesFemaleHumansLiver CirrhosisMalePhilippinesPraziquantelPrognosisAnthelminticsBiomarkersCollagenPraziquantelTissue Inhibitor of Metalloproteinase-1

Identifiers

PMID21199883
PMCPMC3072733
OpenAlexW2103875294

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.