Evidence map›Paper›PMID 24166958›Full record

ArticleInfection and immunity2014

Maternal infection with Schistosoma japonicum induces a profibrotic response in neonates.

Emily A McDonald, Ling Cheng, Blanca Jarilla, Marianne J Sagliba, Annaliza Gonzal, Amabelle J Amoylen, Remigio Olveda, Luz Acosta, David Baylink, Eric S White and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. 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
1.6field-weighted citation impact, top 20% 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, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Ghrelin regulating liver activity and its potential effects on liver fibrosis andFrontiers in cellular and infection microbiology · 2023
    Review
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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

12 authors at 5 institutions in 2 countries.

Emily A McDonaldCenter for International Health Research, Rhode Island Hospital, Providence, Rhode Island, USA.
Ling Cheng
Blanca Jarilla
Marianne J Sagliba
Annaliza Gonzal
Amabelle J Amoylen
Remigio Olveda
Luz Acosta
David Baylink
Eric S White
Jennifer F Friedman
Jonathan D Kurtis
Research Institute for Tropical Medicine · PHBrown University · USRhode Island Hospital · USLoma Linda University · USUniversity of Michigan–Ann Arbor · US

Funding

S.japonicum and pregnancy outcomes: an RCTU01AI066050 · NIAID · RHODE ISLAND HOSPITAL · PI FRIEDMAN, JENNIFER F · 2006 to 2012
$4.7M
Puberty, Immunity and Malnutrition in S. JaponicumR01AI048123 · NIAID · RHODE ISLAND HOSPITAL · PI KURTIS, JONATHAN D. · 2001 to 2005
$3.0M
Targeted Vaccine Development for Pediatric Falciparum MalariaR01AI076353 · NIAID · RHODE ISLAND HOSPITAL · PI KURTIS, JONATHAN D. · 2008 to 2011
$2.4M
Matrix biomarkers and compartmentalization in IPFR01HL109118 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WHITE, ERIC S · 2012 to 2015
$1.8M
TLR Mediated Trophoblast Injury and Poor Pregnancy Outcomes in S. japonicaF32AI093043 · NIAID · RHODE ISLAND HOSPITAL · PI MCDONALD, EMILY A · 2011 to 2013
$156k
NHLBI NIH HHS HL109118-01A1NHLBI NIH HHS R01 HL109118NIAID NIH HHS 1F32AI093043NIAID NIH HHS 1R01AI076353NIAID NIH HHS F32 AI093043NIAID NIH HHS R01 AI048123NIAID NIH HHS R01 AI076353NIAID NIH HHS R01AI48123NIAID NIH HHS U01 AI066050NIAID NIH HHS U01AI066050
6 · The paper itself

Abstract

The global burden of schistosomiasis is significant, with fibrosis a major associated morbidity and the primary cause of mortality. We have previously shown that schistosomiasis during pregnancy upregulates proinflammatory cytokines in the cord blood. In this study, we extend these findings to include a large panel of fibrosis-associated markers. We developed a multiplex bead-based assay to measure the levels of 35 proteins associated with fibrosis. Cord blood from 109 neonates born to mothers residing in an area of Schistosoma japonicum endemicity was assessed for these molecules. Ten mediators were elevated in the cord blood from schistosome-infected pregnancies, including insulin-like growth factor 1 (IGF-1), tumor growth factor β1 (TGF-β1), connective tissue growth factor (CTGF), procollagen I carboxy-terminal propeptide (PICP), amino-telopeptide of type 1 collagen (ICTP), collagen VI, desmosine, matrix metalloproteinase 2 (MMP-2), tissue inhibitor of metalloproteinases 1 (TIMP-1), and TIMP-4. Many of these were also positively correlated with preterm birth (PICP, ICTP, MMP-2, TGF-β1, desmosine, CTGF, TIMP-1). In addition, birth weight was 168 g lower for infants with detectable levels of CTGF than for those with CTGF levels below the level of detection. Maternal schistosomiasis results in upregulation of fibrosis-associated proteins in the cord blood of the neonate, a subset of which are also associated with adverse birth outcomes. As the first report of fibrosis-associated molecules altered in the newborn of infected mothers, this study has broad implications for the health of the fetus, stretching from gestation to adulthood.

Indexed as

AnimalsBiomarkersBirth WeightCohort StudiesFemaleFetal BloodHumansInfant, NewbornIntercellular Signaling Peptides and ProteinsLiver CirrhosisPhilippinesPregnancyPregnancy Complications, ParasiticPremature BirthSchistosoma japonicumSchistosomiasis japonicaBiomarkersIntercellular Signaling Peptides and Proteins

Identifiers

PMID24166958
PMCPMC3911825
OpenAlexW2009741081

What OpenQuestion holds

Textmetadata
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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.