Evidence map›Paper›PMID 32052826›Full record

ArticleGenetics and molecular biology2020

Identification of environmental and genetic factors that influence warfarin time in therapeutic range.

Mariana R Botton, Patrícia P Viola, Mariana R Meireles, Estela M Bruxel, Priccila Zuchinali, Eliane Bandinelli, Luis E Rohde, Tiago L L Leiria, Joyce Y Y Salamoni, Arthur P Garbin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genetics and molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 35% 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, 6 citations in OpenAlex.

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  5. Review
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

11 authors at 3 institutions in 1 country.

Mariana R BottonUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.
Patrícia P ViolaUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.
Mariana R MeirelesUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.
Estela M BruxelUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.
Priccila ZuchinaliHospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Eliane BandinelliUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.
Luis E RohdeHospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Tiago L L LeiriaFundação Universitária de Cardiologia, Instituto de Cardiologia do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Joyce Y Y SalamoniHospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Arthur P GarbinHospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Mara H HutzUniversidade Federal do Rio Grande do Sul, Departamento de Genética, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-9146-1229
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BRFundação Universitária de Cardiologia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Warfarin is an oral anticoagulant prescribed to prevent and treat thromboembolic disorders. It has a narrow therapeutic window and must have its effect controlled. Prothrombin test, expressed in INR value, is used for dose management. Time in therapeutic range (TTR) is an important outcome of quality control of anticoagulation therapy and is influenced by several factors. The aim of this study was to identify genetic, demographic, and clinical factors that can potentially influence TTR. In total,422 patients using warfarin were investigated. Glibenclamide co-medication and presence of CYP2C9*2 and/or *3 alleles were associated with higher TTR, while amiodarone, acetaminophen and verapamil co-medication were associated with lower TTR. Our data suggest that TTR is influenced by co-medication and genetic factors. Thus, individuals in use of glibenclamide may need a more careful monitoring and genetic testing (CYP2C9*2 and/or *3 alleles) may improve the anticoagulation management. In addition, in order to reach and maintain the INR in the target for a longer period, it is better to discuss dose adjustment in office instead of by telephone assessment. Other studies are needed to confirm these results and to find more variables that could contribute to this important parameter.

Identifiers

PMID32052826
PMCPMC7198020
OpenAlexW3006013653

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.