Evidence map›Paper›PMID 35965830›Full record

ArticleAnnals of translational medicine2022

Mutational characteristics of Chinese Han and ethnic minorities in southwestern China: a propensity score matched analysis.

Yongchun Zhou, Xin Liu, Yinjin Guo, Zhuoying Li, Shunhui Zhu, Quan Li, Xiaoxiong Wang, Ruijiao Yang, Zhenghai Shen, Hongsheng Li and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

15 authors at 1 institution in 1 country.

Yongchun Zhou *Molecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Xin Liu *Molecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Yinjin GuoMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Zhuoying LiMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Shunhui ZhuTumor Molecular and Cell Biology Center, Honghe Prefecture Third People's Hospital, Gejiu, China.
Quan LiMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Xiaoxiong WangMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Ruijiao YangMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Zhenghai ShenMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Hongsheng LiMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Yaxi DuMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Luyao MaMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Shaocong ShenMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Yunyi LanMolecular Diagnostic Center, the Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Yunchao HuangYunnan Key Laboratory of Lung Cancer Research, Kunming, China.
Kunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In China, there has never been a comprehensive analysis of lung cancer-associated genetic mutations focused on ethnic minorities in the southwestern region. Our study aimed to provide valuable information on lung cancer-associated genetic alterations for cancer diagnosis and treatment, especially in ethnic minorities. Methods: Retrospective data acquisition was conducted spanning 3 years (2016.01-2019.06) among all patients who were diagnosed with lung cancer at the Third Affiliated Hospital of Kunming Medical University Hospital. A total of 5,167 patients including 373 ethnic minorities were included in this study. Propensity score matching (PSM) was used to eliminate the bias between Han and other ethnic minorities, including gender, age, smoking history, metastasis status, clinical stage, histological type, sample type, region, and Xuanwei origin. All tests were two-tailed, and significance was defined as P less than 0.05. Results: In terms of the prevalence of Conclusions: This study is the first in-depth large case-control study on genetic mutation profiles among multi-ethnic patients in southwestern China, especially focused on ethnic minorities in this area. Our study may facilitate the understanding of the etiology of this malignant disease and consequently help to reduce the incidence of lung cancer in Yunnan ethnic minority areas.

Indexed as

EGFRlung cancerMulti-ethnic patientspropensity score matching (PSM)Yunnan

Identifiers

PMID35965830
PMCPMC9372700
OpenAlexW4285542268

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.