Evidence map›Paper›PMID 28928388›Full record

Trial reportScientific reports2017

Differential Serum Cytokine Profiles in Patients with Chronic Hepatitis B, C, and Hepatocellular Carcinoma.

Jacqueline Estevez, Vincent L Chen, Ondrej Podlaha, Biao Li, An Le, Philip Vutien, Ellen T Chang, Yael Rosenberg-Hasson, Zhaoshi Jiang, Stefan Pflanz and 3 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 58 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

13 authors at 3 institutions in 1 country.

Jacqueline EstevezStanford University Medical Center, Division of Gastroenterology and Hepatology, Stanford, CA, 94305, USA.
Vincent L ChenStanford University Medical Center, Department of Medicine, Stanford, CA, 94305, USA.
Ondrej PodlahaGilead Sciences, Foster City, CA, 94404, USA.
Biao LiGilead Sciences, Foster City, CA, 94404, USA.
An LeStanford University Medical Center, Division of Gastroenterology and Hepatology, Stanford, CA, 94305, USA.
Philip VutienStanford University Medical Center, Division of Gastroenterology and Hepatology, Stanford, CA, 94305, USA.
Ellen T ChangStanford University School of Medicine, Department of Health Research and Policy (Epidemiology), Stanford, CA, 94305, USA.
Yael Rosenberg-HassonStanford University Medical Center, The Human Immune Monitoring Center, Stanford, CA, 94305, USA.
Zhaoshi JiangGilead Sciences, Foster City, CA, 94404, USA.
Stefan PflanzGilead Sciences, Foster City, CA, 94404, USA.
Dongliang GeGilead Sciences, Foster City, CA, 94404, USA.
Anuj GaggarGilead Sciences, Foster City, CA, 94404, USA.
Mindie H NguyenStanford University Medical Center, Division of Gastroenterology and Hepatology, Stanford, CA, 94305, USA. mindiehn@stanford.edu.
Gilead Sciences (United States) · USStanford University · USStanford Medicine · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

Cytokines play an important role in the pathogenesis of cirrhosis and hepatocellular carcinoma (HCC), most cases of which are related to either hepatitis B virus (HBV) or hepatitis C virus (HCV). Prior studies have examined differences in individual cytokine levels in patients with chronic liver disease, but comprehensive cytokine profiling data across different clinical characteristics are lacking. We examined serum cytokine profiles of 411 patients with HCC (n = 102: 32% HBV, 54% HCV, 14% non-viral) and without HCC (n = 309: 39% HBV, 39% HCV, 22% non-viral). Multiplex analysis (Luminex 200 IS) was used to measure serum levels of 51 common cytokines. Random forest machine learning was used to obtain receiver operator characteristic curves and to determine individual cytokine importance using Z scores of mean fluorescence intensity for individual cytokines. Among HCC and non-HCC patients, cytokine profiles differed between HBV and HCV patients (area under curve (AUC) 0.82 for HCC, 0.90 for non-HCC). Cytokine profiles did not distinguish cirrhotic HBV patients with and without HCC (AUC 0.503) or HCV patients with and without HCC (AUC 0.63). In conclusion, patients with HBV or HCV infection, with or without HCC, have distinctly different cytokine profiles, suggesting potential differences in disease pathogenesis and/or disease characteristics.

Indexed as

AdultCarcinoma, HepatocellularCytokinesFemaleHepatitis B, ChronicHepatitis C, ChronicHumansLiver NeoplasmsMaleMiddle AgedNeoplasm ProteinsProspective StudiesCytokinesNeoplasm Proteins

Identifiers

PMID28928388
PMCPMC5605527
OpenAlexW2755753638

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.