Evidence map›Paper›PMID 30158536›Full record

ArticleScientific reports2018

Genetic polymorphisms of GZMB and vitiligo: A genetic association study based on Chinese Han population.

Meifeng Xu, Yan Liu, Yale Liu, Xiaoli Li, Gang Chen, Wei Dong, Shengxiang Xiao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.1field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Granzyme B Gene Polymorphisms Are Associated With Severe Non-segmental Vitiligo.The Journal of clinical and aesthetic dermatology · 2023
    Article
  7. A common genetic variation inFrontiers in oncology · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Mechanisms of melanocyte death in vitiligo.Medicinal research reviews · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

7 authors at 2 institutions in 1 country.

Meifeng XuDepartment of Dermatology, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China.
Yan LiuDepartment of Dermatology, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China.
Yale LiuDepartment of Dermatology, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China.
Xiaoli LiDepartment of Dermatology, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China.
Gang ChenKey Laboratory of National Ministry of Health for Forensic Sciences, School of Medicine & Forensics, Xi'an Jiaotong University, Xi'an, China.
Wei DongDepartment of Laboratory Medicine, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China.
Shengxiang XiaoDepartment of Dermatology, the Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, Shaanxi, China. shxaxiaoxjtu@163.com.
Second Affiliated Hospital of Xi'an Jiaotong University · CNXi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitiligo is a skin disease that affects 1% of the population worldwide. Both environmental and genetic factors contribute to the risk of vitiligo. GZMB encodes the enzyme Granzyme B, which plays an important role in cytotoxic T cell-induced apoptosis, and it has been considered one of the candidate genes for vitiligo because of its connections with human immune system. Overall, 3,120 study subjects with Chinese Han ancestry were recruited, and 15 pre-selected SNPs of GZMB were genotyped. Genetic association analyses were performed to evaluate the genetic risk of these SNPs to vitiligo. Further bioinformatic analyses were conducted to examine the potential biological function of targeted SNPs. The SNP rs8192917, a non-synonymous coding SNP, was identified to be significantly associated with the disease status of vitiligo, with OR = 1.39 and P = 1.92 × 10

Indexed as

Polymorphism, Single NucleotideAdultAsian PeopleFemaleGenetic Association StudiesGenotypeGranzymesHumansMaleVitiligoYoung AdultGranzymesGZMB protein, human

Identifiers

PMID30158536
PMCPMC6115438
OpenAlexW2888459362

What OpenQuestion holds

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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.