Evidence map›Paper›PMID 28189770›Full record

ArticleThe Journal of allergy and clinical immunology2017

The role of ST2 and ST2 genetic variants in schistosomiasis.

Xin Long, Michelle Daya, Jianping Zhao, Nicholas Rafaels, Huifang Liang, Joseph Potee, Monica Campbell, Bixiang Zhang, Maria Ilma Araujo, Ricardo R Oliveira and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. [Focus on schistosomiasis cirrhosis: disease burden, pathogenic characteristics, and research frontiers].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Article
  2. Article
  3. Article
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  5. Cellular Mechanisms of Liver Fibrosis.Frontiers in pharmacology · 2021
    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

19 authors at 8 institutions in 3 countries.

Xin LongHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinical Study Center of Liver Surgery in Hubei Province, Wuhan, China; Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Michelle DayaBiomedical Informatics and Personalized Medicine, University of Colorado School of Medicine, Aurora, Colo.
Jianping ZhaoHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinical Study Center of Liver Surgery in Hubei Province, Wuhan, China.
Nicholas RafaelsJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Huifang LiangHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinical Study Center of Liver Surgery in Hubei Province, Wuhan, China.
Joseph PoteeJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Monica CampbellJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Bixiang ZhangHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinical Study Center of Liver Surgery in Hubei Province, Wuhan, China.
Maria Ilma AraujoServico de Imunologia, Hospital Universitario Professor Edgard Santos, Salvador, Brazil.
Ricardo R OliveiraInstituto Goncalo Moniz, Fundacao Oswaldo Cruz - Bahia, Salvador, Brazil.
Rasika A MathiasJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Li GaoJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md.
Ingo RuczinskiBloomberg School of Public Health, The Johns Hopkins University, Baltimore, Md.
Steve N GeorasDepartment of Medicine, University of Rochester Medical Center, Rochester, NY.
Donata VercelliArizona Respiratory Center, University of Arizona, Tucson, Ariz.
Terri H BeatyBloomberg School of Public Health, The Johns Hopkins University, Baltimore, Md.
Kathleen C BarnesJohns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Md. Electronic address: Kathleen.Barnes@UCDenver.edu.
Xiaoping ChenHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinical Study Center of Liver Surgery in Hubei Province, Wuhan, China. Electronic address: chenxp@medmail.com.cn.
Qian ChenDivision of Gastroenterology and Hepatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Electronic address: chenqian201579@yahoo.com.
Johns Hopkins University · USHuazhong University of Science and Technology · CNJohns Hopkins Medicine · USComplexo Hospitalar Universitário Professor Edgard Santos · BRFundação Oswaldo Cruz · BRUniversity of Arizona · USUniversity of Colorado Denver · USUniversity of Rochester Medical Center · US

Funding

Functional impact of IL33 polymorphisms on asthma & other Th2-mediated diseasesR01HL112088 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BARNES, KATHLEEN C · 2012 to 2016
$3.6M
NHLBI NIH HHS R01 HL112088
6 · The paper itself

Abstract

backgroundChronic schistosomiasis and its severe complication, periportal fibrosis, are characterized by a predominant T

objectiveWe investigated the role of ST2 (a receptor for the T

methodsWe recruited 947 adult participants (339 with end-stage schistosomiasis and liver cirrhosis, 307 with chronic infections without liver fibrosis, and 301 health controls) from a S japonicum-endemic area (Hubei, China). Six ST2 single nucleotide polymorphisms were genotyped. Serum soluble ST2 (sST2) was measured by ELISA, and ST2 expression in normal liver tissues, Hepatitis B virus-induced fibrotic liver tissues, and S japonicum-induced fibrotic liver tissues was measured by immunohistochemistry.

resultsWe found sST2 levels were significantly higher in the end-stage group (36.04 [95% CI, 33.85-38.37]) compared with chronic cases and controls (22.7 [95% CI, 22.0-23.4], P < 1E-10). In addition, S japonicum-induced fibrotic liver tissues showed increased ST2 staining compared with normal liver tissues (P = .0001). Markers rs12712135, rs1420101, and rs6543119 were strongly associated with sST2 levels (P = 2E-10, 5E-05, and 6E-05, respectively), and these results were replicated in an independent cohort from Brazil living in a S mansoni endemic region.

conclusionsWe demonstrate for the first time that end-stage schistosomiasis is associated with elevated sST2 levels and show that ST2 genetic variants are associated with sST2 levels in patients with schistosomiasis.

Indexed as

Endemic DiseasesAdultAnimalsBrazilChinaChronic DiseaseCohort StudiesDisease ProgressionFemaleFibrosisGenotypeHumansInterleukin-1 Receptor-Like 1 ProteinInterleukin-33LiverLiver CirrhosisIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33liver cirrhosis immunohistochemistrySchistosoma japonicumsST2ST2

Identifiers

PMID28189770
PMCPMC5550370
OpenAlexW2587206612

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.