Evidence map›Paper›PMID 25743242›Full record

ArticleCytokine2015

Application of multiplex arrays for cytokine and chemokine profiling of bile.

Troy J Kemp, Felipe A Castro, Yu-Tang Gao, Allan Hildesheim, Leticia Nogueira, Bing-Sheng Wang, Lu Sun, Gloriana Shelton, Ruth M Pfeiffer, Ann W Hsing and 2 more

Abstract read
In one paragraph

Article in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. The impact of environmental pollution on the quality of mother's milk.Environmental science and pollution research international · 2019
    Pooled it
  2. Trial
  3. Article
  4. Cytokines: From Clinical Significance to Quantification.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  5. Article
  6. Review
  7. Article
  8. Association of circulating inflammation proteins and gallstone disease.Journal of gastroenterology and hepatology · 2018
    Article
  9. Article
  10. The inflammatory inception of gallbladder cancer.Biochimica et biophysica acta · 2016
    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

12 authors at 6 institutions in 2 countries.

Troy J KempHPV Immunology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. Electronic address: kemptj@mail.nih.gov.
Felipe A CastroInfections and Immunoepidemiology Branch, DCEG, NCI, NIH, Bethesda, MD, USA. Electronic address: felipe.castro@nih.gov.
Yu-Tang GaoDepartment of Epidemiology, Shanghai Cancer Institute, Shanghai Cancer Institute, Shanghai, China. Electronic address: ytgao@vip.sina.com.
Allan HildesheimInfections and Immunoepidemiology Branch, DCEG, NCI, NIH, Bethesda, MD, USA. Electronic address: hildesha@exchange.nih.gov.
Leticia NogueiraInfections and Immunoepidemiology Branch, DCEG, NCI, NIH, Bethesda, MD, USA. Electronic address: leticia.nogueira@nih.gov.
Bing-Sheng WangDepartment of General Surgery, Zhongshan Hospital, School of Medicine, Fudan University, Shanghai, China. Electronic address: wang.bingsheng@zs-hospital.sh.cn.
Lu SunDepartment of Epidemiology, Shanghai Cancer Institute, Shanghai, China. Electronic address: sunlush@126.com.
Gloriana SheltonHPV Immunology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. Electronic address: Gloriana.Shelton@nih.gov.
Ruth M PfeifferBiostatistics Branch, DCEG, NCI, NIH, Bethesda, MD, USA. Electronic address: pfeiffer@mail.nih.gov.
Ann W HsingCancer Prevention Institute of California, Fremont, CA, USA; Stanford Cancer Institute, Palo Alto, CA, USA; Department of Health Research and Policy, School of Medicine, Stanford University, Palo Alto, CA, USA. Electronic address: Ann.Hsing@cpic.org.
Ligia A PintoHPV Immunology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. Electronic address: pintol@mail.nih.gov.
Jill KoshiolInfections and Immunoepidemiology Branch, DCEG, NCI, NIH, Bethesda, MD, USA. Electronic address: koshiolj@mail.nih.gov.
National Institutes of Health · USFrederick National Laboratory for Cancer Research · USShanghai Cancer Institute · CNLeidos (United States) · USStanford Cancer InstituteZhongshan Hospital · CN

Funding

Etiology of Biliary Tract CancerZIACP010218 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI KOSHIOL, JILL · 2011 to 2025
$30.4M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS ZIA CP010218NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

backgroundGallbladder disease is highly related to inflammation, but the inflammatory processes are not well understood. Bile provides a direct substrate in assessing the local inflammatory response that develops in the gallbladder. To assess the reproducibility of measuring inflammatory markers in bile, we designed a methods study of 69 multiplexed immune-related markers measured in bile obtained from gallstone patients.

methodsTo evaluate assay performance, a total of 18 bile samples were tested twice within the same plate for each analyte, and the 18 bile samples were tested on two different days for each analyte. We used the following performance parameters: detectability, coefficient of variation (CV), intraclass correlation coefficient (ICC), and percent agreement (concordance among replicate measures above and below detection limit). Furthermore, we examined the association of analyte levels with gallstone characteristics such as type, numbers, and size.

resultsAll but 3 analytes (Stem Cell Factor, SCF; Thrombopoietin, TPO; sIL-1RI) were detectable in bile. 52 of 69 (75.4%) analytes had detectable levels for at least 50% of the subjects tested. The within-plate CVs were ⩽25% for 53 of 66 (80.3%) detectable analytes, and across-plate CVs were ⩽25% for 32 of 66 (48.5%) detectable analytes. Moreover, 64 of 66 (97.0%) analytes had ICC values of at least 0.8. Lastly, the percent agreement was high between replicates for all of the analytes (median; within plate, 97.2%; across plate, 97.2%). In exploratory analyses, we assessed analyte levels by gallstone characteristics and found that levels for several analytes decreased with increasing size of the largest gallstone per patient.

conclusionsOur data suggest that multiplex assays can be used to reliably measure cytokines and chemokines in bile. In addition, gallstone size was inversely related to the levels of select analytes, which may aid in identifying critical pathways and mechanisms associated with the pathogenesis of gallbladder diseases.

Indexed as

AdultAgedBileChemokinesCholelithiasisFemaleHumansMaleMiddle AgedProtein Array AnalysisReproducibility of ResultsChemokinesBileChemokinesCytokinesGallstones

Identifiers

PMID25743242
PMCPMC4382212
OpenAlexW2062924831

What OpenQuestion holds

Textmetadata
LicenceTDM
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.