Evidence map›Paper›PMID 36708395›Full record

ArticleEuropean journal of clinical pharmacology2023

Pharmacogenetics of warfarin dosing in Chinese adults with nonvalvular atrial fibrillation.

Ye Zhu, Jia You, Xiang Gu, Hua Zhu, Jia Liu

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Article in European journal of clinical pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Ye ZhuClinical Medical College, Yangzhou University, Nantong West Road No. 98, Yangzhou, 225001, Jiangsu, China.
Jia YouDepartment of Internal Medicine, Yangzhou Maternal and Child Health Care Hospital, Yangzhou, 225001, Jiangsu, China.
Xiang GuClinical Medical College, Yangzhou University, Nantong West Road No. 98, Yangzhou, 225001, Jiangsu, China.
Hua ZhuClinical Medical College, Yangzhou University, Nantong West Road No. 98, Yangzhou, 225001, Jiangsu, China.
Jia LiuClinical Medical College, Yangzhou University, Nantong West Road No. 98, Yangzhou, 225001, Jiangsu, China. liujia85912@163.com.
Yangzhou University · CNNorthern Jiangsu People's Hospital · CN

Funding

China National Natural Science Foundation 81800250Jiangsu Research Hospital Association for Precision Medication JY202121Yangzhou Science and Technology bureau for social development YZ2020074Yangzhou thirteen five Plan Special Funding for Strengthening Health through Science and Education ZDRC20181
6 · The paper itself

Abstract

backgroundThe guide for the use of genotype-guided warfarin dosing in patients for the treatment of non-valvular atrial fibrillation (AF) is still lacking.

aimWe aimed to evaluate whether genotype-guided warfarin dosing is superior to conventional clinical dosing for the outcomes of interest in Chinese patients.

methodOur study consisted of 508 newly recruited and 471 existing Chinese AF patients. Among the total 979 patients, 585 patients received their dose of warfarin determined by a genetic and clinical factor (gene group), while the remaining 394 patients whose dosing was determined empirically in control group. We incorporated CYP2C9 and VKORC1 genotypes into the gene group. The international normalized ratio (INR) measurement and standard protocols were used for further dose adjustment in both groups. The primary outcomes were the percentage of time in the therapeutic range (%TTR) and INR during 12-month follow-up. Secondary safety outcome included bleeding and thrombotic events.

resultsCompared with the control group, the average TTR of the gene group was higher [68.4 ± 20.6% vs 48.5 ± 21.6%, P < 0.001]. The average INR monitoring times to reach the therapeutic time in the gene group was lower (P < 0.001). The risk ratios (RR) for cumulative incidence of total bleeding events, minor bleeding events, gastrointestinal bleeding, and intracerebral bleeding events were not significantly different between the two groups (P > 0.05). Comparing to the analysis using existing 471 patients, the analysis using total 979 patients showed that the gene group experienced a lower (RR 0.4 (95% CI 0.2 to 0.8), P = 0.008) incidence of cumulative ischemic stroke.

conclusionGenotype-guided warfarin administration increases the average TTR, reaches higher TTR levels in the early anticoagulant phase, and significantly reduces the risk of ischemic stroke events.

Indexed as

Atrial FibrillationPharmacogeneticsWarfarinAdultAnticoagulantsCytochrome P-450 CYP2C9East Asian PeopleGastrointestinal HemorrhageHumansInternational Normalized RatioIschemic StrokeTreatment OutcomeVitamin K Epoxide ReductasesAnticoagulantsCytochrome P-450 CYP2C9Vitamin K Epoxide ReductasesVKORC1 protein, humanWarfarinAtrial fibrillationCYP2C9Time in therapeutic rangeVKORC1Warfarin

Identifiers

PMID36708395
OpenAlexW4318336413

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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.