Evidence map›Paper›PMID 27182162›Full record

ArticleWorld journal of gastroenterology2016

Elevated serum interleukin-38 level at baseline predicts virological response in telbivudine-treated patients with chronic hepatitis B.

Hong-Juan Wang, Yan-Fang Jiang, Xin-Rui Wang, Man-Li Zhang, Pu-Jun Gao

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
  5. The emerging role of IL-38 in diseases: A comprehensive review.Immunity, inflammation and disease · 2023
    Review
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  15. Interleukin 30 to Interleukin 40.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2018
    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

5 authors.

Hong-Juan WangHong-Juan Wang, Xin-Rui Wang, Pu-Jun Gao, Department of Hepatology, First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
Yan-Fang JiangHong-Juan Wang, Xin-Rui Wang, Pu-Jun Gao, Department of Hepatology, First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
Xin-Rui WangHong-Juan Wang, Xin-Rui Wang, Pu-Jun Gao, Department of Hepatology, First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
Man-Li ZhangHong-Juan Wang, Xin-Rui Wang, Pu-Jun Gao, Department of Hepatology, First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
Pu-Jun GaoHong-Juan Wang, Xin-Rui Wang, Pu-Jun Gao, Department of Hepatology, First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate serum interleukin (IL)-38 level and its clinical role in predicting virological response (VR) to telbivudine (LdT) in patients with chronic hepatitis B (CHB).

methodsThe study participants were divided into two groups; one group consisted of 43 healthy controls (HCs) and the other group consisted of 46 patients with hepatitis B e antigen-positive CHB. All patients were administered 600 mg of oral LdT daily for 52 wk, and they visited physicians every 12 wk for physical examination and laboratory tests. Serum IL-38 levels were determined using ELISA. The concentrations of serum Th1- and Th2-type cytokines were measured using the cytometric bead array (CBA) method.

resultsSerum levels of IL-38 at baseline in all patients were higher than those in HCs [306.97 (123.26-492.79) pg/mL vs 184.50 (135.56-292.16) pg/mL, P = 0.019]; the levels returned to normal after the first 12 wk of treatment with LdT [175.51 (103.90-331.91) pg/mL vs 184.50 (135.56-292.16) pg/mL, P > 0.05]. Serum IL-38 levels at baseline were positively associated with serum aspartate aminotransferase levels in patients with CHB (r = 0.311, P = 0.036). Higher levels of serum IL-38 at baseline were associated with a greater probability of VR to LdT treatment at 24 wk (48.15% vs 15.79%, P = 0.023) and 52 wk (66.67% vs 36.84%, P = 0.044). The levels of serum IL-38 in patients with primary non-response at week 12 after treatment initiation were lower than those in patients with primary response [64.44 (49.85-172.08) pg/mL vs 190.54 (121.35-355.28) pg/mL, P = 0.036]. Serum IL-38 levels were correlated with serum IL-6 and IL-12 levels in patients with CHB during treatment with LdT.

conclusionElevated serum IL-38 levels in untreated CHB patients reflect ongoing liver injury. Higher serum IL-38 levels before treatment indicate a greater probability of VR to LdT treatment.

Indexed as

Sustained Virologic ResponseAdministration, OralAdultAntiviral AgentsBiomarkersCase-Control StudiesDNA, ViralDrug Administration ScheduleEnzyme-Linked Immunosorbent AssayFemaleHepatitis B, ChronicHepatitis B e AntigensHumansInterleukinsMaleTelbivudineAntiviral AgentsBiomarkersDNA, ViralHepatitis B e AntigensIL-38 protein, humanInterleukinsTelbivudineThymidineAlanine aminotransferaseAspartate aminotransferaseChronic hepatitis BInterleukin-12Interleukin-38Interleukin-6Primary non-responseVirological response

Identifiers

PMID27182162
PMCPMC4858634

What OpenQuestion holds

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Registered trials

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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.