Evidence map›Paper›PMID 31689880›Full record

ArticleMedicine2019

The role of IL22 polymorphisms on liver cirrhosis in patients with hepatitis B virus: A case control study.

Yan-Hang Gao, Qing-Quan Li, Chun-Guang Wang, Jing Sun, Xiao-Mei Wang, Ya-Jun Li, Xiu-Ting He, Hong-Qin Xu, Jun-Qi Niu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yan-Hang GaoDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Qing-Quan LiDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Chun-Guang WangDepartment of Surgery, The Second Hospital of Jilin University, Changchun, Jilin.
Jing SunDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Xiao-Mei WangDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Ya-Jun LiDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Xiu-Ting HeDepartment of Geriatrics, The First Hospital of Jilin University.
Hong-Qin XuDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Jun-Qi NiuDepartment of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun.
Jilin University · CNFirst Hospital of Jilin University · CNSecond Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsInterleukin(IL)-22 plays an important role in promoting liver regeneration and repair, but its role in chronic HBV-related liver diseasesis not clear. The goal of this study was to evaluate associations between eight IL22 single nucleotide polymorphisms (SNPs) and the development of chronic HBV cirrhosis and HBV-related HCC within a Chinese Han population.

methodsWe investigated associations between single nucleotide polymorphisms (SNPs) in the IL22 gene (rs1026788, rs2227472, rs2227491, rs2227485, rs1179249, rs2046068,rs2227473, and rs7314777) and the risk of HBV-related chronic liver diseases within a Han population in Northeast China. A total of 649 participants were included in the study, including 103 patients with CHB, 264 patients with LC, and 282 patients with HCC. The odds ratios (OR) and corresponding 95% confidence intervals (CI) were calculated using chi-square test. Haplotype analysis was conducted by haploview software.

resultsGenotype and allele distributions of SNPs rs1179249 and rs2227472 differed between LC and CHB groups (both P < 0.05).The G alleles of SNP rs2227491 and rs1026788 were more frequent in the LC group than in the CHB group (P = 0.046, P = 0.041 respectively). A IL22 haplotype consisting of the minor alleles of SNP rs1179249 and the major alleles of seven other SNPs occurred less frequently in the LC and HCC groups than in the CHB group (28.2%, 33.94%, and 37.86%, respectively, P < 0.05). Moreover, there were no significant associations between smoking or drinking and IL22 SNPs on the risk of HCC (P > 0.05).

conclusionIL22 genetic variations were associated with chronic HBV infection progression, especially in the HBV-LC group. The IL22 genetic variations may help clinicians initiate the correct treatment strategy at the CHB stage.

Indexed as

Polymorphism, Single NucleotideAdultAlcohol DrinkingAsian PeopleCarcinoma, HepatocellularCase-Control StudiesDisease ProgressionFemaleHepatitis B, ChronicHumansInterleukin-22InterleukinsLiver CirrhosisLiver NeoplasmsMaleMiddle AgedInterleukin-22Interleukins

Identifiers

PMID31689880
PMCPMC6946515
OpenAlexW2988364284

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.