Evidence map›Paper›PMID 24966969›Full record

ArticleInternational journal of clinical and experimental pathology2014

High resolution melting method to detect single nucleotide polymorphism of VKORC1 and CYP2C9.

Chunxia Chen, Siyue Li, Xiaojun Lu, Bin Tan, Chunyan Huang, Li Qin

Open access · greenAbstract readValidation Study
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Rapid screening ofExperimental and therapeutic medicine · 2021
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  3. Review
  4. Hereditary cancer in clinical practice · 2017
    Review
  5. Prothrombin C20209T mutation in deep vein thrombosis: a case report.International journal of clinical and experimental medicine · 2015
    Article
  6. 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.

Chunxia ChenDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Siyue LiDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Xiaojun LuDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Bin TanDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Chunyan HuangDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Li QinDepartment of Laboratory Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) of VKORC (1173T/C, rs9934438) and CYP2C9 (1075A/C, rs1057910) are major contributory factors on the sensitivity of warfarin in Chinese. Analysis of the two genomic loci could help warfarin treatment individual from bleeding or thrombosis events. An assay with the advantages of simplicity, speed, high sensitivity and low cost for genotyping is calling for clinical laboratories. High resolution method (HRM) meets these callings, but no study with large sample tested its performance in genotyping of rs9934438 and rs1057910. In this study, we identified polymorphisms of rs9934438 and rs1057910 in 255 unrelated Chinese heart valve replacement patients of Han ethnic group from West China Hospital. The two genomic loci were genotyped by HRM using LightCycler® 480 High Resolution Melting Master on LightCycler® 480 Real-Time PCR instruments (Roche Diagnostics), and all amplified PCR products were sent for direct DNA sequencing. The genotyping of rs1057910 between HRM and sequencing showed perfect 100% concordance. While the concordance of rs9934438 between HRM and sequencing was 99.2%. Unexpected mutation interfered genotyping results of HRM when genotyping rs9934438. HRM is a valuable technique for genotype detection of rs9934438 and rs1057910 to assess individual sensitivity to warfarin, where DNA sequencing is added inevitably sometimes.

Indexed as

Polymorphism, Single NucleotideAdultAgedAnticoagulantsAsian PeopleChinaCytochrome P-450 CYP2C9FemaleGene FrequencyGenotypeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedPharmacogeneticsPhenotypeAnticoagulantsCYP2C9 protein, humanCytochrome P-450 CYP2C9Vitamin K Epoxide ReductasesVKORC1 protein, humanWarfarinCYP2C9genotypingHRMVKORCwarfarin

Identifiers

PMID24966969
PMCPMC4069951
OpenAlexW2172682103

What OpenQuestion holds

Textmetadata
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.