Subgroup analysis of genotype guided vs traditional warfarin dosing in Asian patients from an open label randomized trial

Genotype-guided warfarin dosing has shown improved anticoagulation outcomes in individuals of European and Asian ancestry. However, its usefulness in specific subgroups remains uncertain. This open-label, non-inferiority randomized trial (NCT00700895) was conducted across three academic hospitals in Southeast Asia to assess the utility of genotype-guided warfarin dosing in Asian patients, focusing on specific potentially high-risk subgroups. We enrolled 322 newly initiated warfarin patients. The primary endpoint was the number of dose adjustments within the first 14 days of treatment, with a non-inferiority margin of 0.5. Clinical follow-up lasted 90 days. Among 322 randomized patients, 269 (mean age 58.7 years, 59.9% males) were evaluated for the primary endpoint. The pharmacogenetic algorithm significantly reduced dose titrations during the initial 14 days compared to the traditional dosing algorithm, without compromising safety. This benefit was consistent in those with atrial fibrillation (N = 101, mean difference -1.63, 95% CI -2.16 to -1.10), non-atrial fibrillation indications (N = 165, mean difference -0.88, 95% CI -1.26 to -0.49), stroke-only indications (N = 19, mean difference -1.60, 95% CI -2.83 to -0.37), history of acute myocardial infarction (N = 20), congestive heart failure (N = 34), hypertension (N = 152), diabetes mellitus (N = 95), and across races (Chinese, N = 163; Malay, Indian and Others, N = 104), sexes (female, N = 161 and male, N = 108), and age groups (< 65 years, N = 168 and ≥ 65 years, N = 101). However, no significant reduction was observed in patients with a history of stroke. There were no differences in minor or major bleeding complications, recurrent venous thromboembolism, or out-of-range INR measurements across most subgroups. Healthcare providers may consider using pharmacogenetic algorithms to individualize initial warfarin dosages in specific high risk Asian subpopulations. Trial registration: ClinicalTrials.gov NCT00700895 (19/06/2008).

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Journal
Scientific Reports
Published
2026-01-02
DOI
https://doi.org/10.1038/s41598-025-33831-9
Primary Topic
Pharmacogenetics and Drug Metabolism
Type
article
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article

Subgroup analysis of genotype guided vs traditional warfarin dosing in Asian patients from an open label randomized trial

Jen Li Wong, Soo Chin Lee, Nicholas Syn, Ching-Hui Sia et al.
Scientific Reports
Pharmacogenetics and Drug Metabolism
article

Subgroup analysis of genotype guided vs traditional warfarin dosing in Asian patients from an open label randomized trial

Jen Li Wong, Soo Chin Lee, Nicholas Syn, Ching-Hui Sia, Yao Neng Teo, Yao Hao Teo, B. L. Goh, Andrea Li-Ann Wong, Raymond C. S. Seet, Hock-Leun Teoh
article en

Abstract

Genotype-guided warfarin dosing has shown improved anticoagulation outcomes in individuals of European and Asian ancestry. However, its usefulness in specific subgroups remains uncertain. This open-label, non-inferiority randomized trial (NCT00700895) was conducted across three academic hospitals in Southeast Asia to assess the utility of genotype-guided warfarin dosing in Asian patients, focusing on specific potentially high-risk subgroups. We enrolled 322 newly initiated warfarin patients. The primary endpoint was the number of dose adjustments within the first 14 days of treatment, with a non-inferiority margin of 0.5. Clinical follow-up lasted 90 days. Among 322 randomized patients, 269 (mean age 58.7 years, 59.9% males) were evaluated for the primary endpoint. The pharmacogenetic algorithm significantly reduced dose titrations during the initial 14 days compared to the traditional dosing algorithm, without compromising safety. This benefit was consistent in those with atrial fibrillation (N = 101, mean difference -1.63, 95% CI -2.16 to -1.10), non-atrial fibrillation indications (N = 165, mean difference -0.88, 95% CI -1.26 to -0.49), stroke-only indications (N = 19, mean difference -1.60, 95% CI -2.83 to -0.37), history of acute myocardial infarction (N = 20), congestive heart failure (N = 34), hypertension (N = 152), diabetes mellitus (N = 95), and across races (Chinese, N = 163; Malay, Indian and Others, N = 104), sexes (female, N = 161 and male, N = 108), and age groups (< 65 years, N = 168 and ≥ 65 years, N = 101). However, no significant reduction was observed in patients with a history of stroke. There were no differences in minor or major bleeding complications, recurrent venous thromboembolism, or out-of-range INR measurements across most subgroups. Healthcare providers may consider using pharmacogenetic algorithms to individualize initial warfarin dosages in specific high risk Asian subpopulations. Trial registration: ClinicalTrials.gov NCT00700895 (19/06/2008).

Scientific ReportsVol. 16(1)
National University of Singapore (SG), National University Cancer Institute, Singapore (SG), National University Heart Centre Singapore (SG), National University Hospital (SG), National University Health System (SG)
National Research Foundation, Agency for Science, Technology and Research, National Research Foundation Singapore, Medical Research Council, National Medical Research Council, Biomedical Research Council
Good health and well-being
Openalex Percentile: Top 98%
Pharmacogenetics and Drug Metabolism
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