Evidence map›Paper›PMID 32347657›Full record

ArticleMolecular genetics & genomic medicine2020

Genetic polymorphisms of pharmacogenomic VIP variants in the Dai population from Yunnan province.

Yujing Cheng, Run Dai, Wanlu Chen, Qi Li, Chan Zhang, Tonghua Yang

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

6 authors at 1 institution in 1 country.

Yujing ChengDepartment of Blood Transfusion, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
Run DaiDepartment of Blood Transfusion, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
Wanlu ChenDepartment of Blood Transfusion, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
Qi LiDepartment of Blood Transfusion, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
Chan ZhangDepartment of Blood Transfusion, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
Tonghua YangDepartment of Hematology, The First People's Hospital of Yunnan Province, Yunnan Province, Kunming, China.
First People's Hospital of Yunnan Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPharmacogenomics plays a crucial role in individualized therapy, but the variant information of pharmacogenomics in the Dai population is limited. We therefore aimed to screen very important pharmacogenetic (VIP) in the Dai population and compared differences between Dai and other 25 populations.

methodsIn this study, we genotyped 73 VIP variants from the PharmGKB and compared genotype distribution of variants in Dai with other 25 populations by χ2 test. To assess the genetic relationship among 26 populations, we performed the structure analysis. In addition, pair-wise F-statistics (Fst) was calculated to measure the population differentiation.

resultsWe found 12, 10, 13, 17, 11, 39, 46, 46, 45, 43, 49, 46, 46, 46, 49, 45, 41, 42, 48, 53, 45, 50, 50, 51, 47, and 50 significantly different variants in Dai compared with other 25 populations. Genetic structure analysis showed Dai had close relationships with CDX (Chinese Dai in Xishuangbanna), CHB (Han Chinese in Beijing), JPT (Japanese in Tokyo), and KHV (Kinh in Ho Chi Minh City, Vietnam). Moreover, Dai is the most similar to KHV according to Fst analysis.

conclusionsOur study complement the pharmacogenomics information of Dai population from Yunnan province and provide a theoretical basis for personalized medicine.

Indexed as

Pharmacogenomic VariantsPolymorphism, Single NucleotideChinaHumansPopulationDaigenetic polymorphismspopulationsvery important pharmacogenetic

Identifiers

PMID32347657
PMCPMC7336744
OpenAlexW3017694586

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.