Predicting Range of Initial Warfarin Dose Based on Pharmacometabolomic and Genetic Inputs. Issue 6 (13th September 2021)
- Record Type:
- Journal Article
- Title:
- Predicting Range of Initial Warfarin Dose Based on Pharmacometabolomic and Genetic Inputs. Issue 6 (13th September 2021)
- Main Title:
- Predicting Range of Initial Warfarin Dose Based on Pharmacometabolomic and Genetic Inputs
- Authors:
- Huang, Qing
Cao, Ling
Luo, Nan
Qian, Hanyu
Wei, Meng
Xue, Ling
Zhou, Qiang
Zou, Bingjie
Tan, Li
Chu, Yanan
Ma, Xueping
Wang, Changtian
Wu, Haiwei
Zhang, Lei
Sun, Lei
Li, Demin
Fan, Xialei
Miao, Liyan
Zhou, Guohua - Abstract:
- Abstract : Anticoagulation response to warfarin during the initial stage of therapy varies among individuals. In this study, we aimed to combine pharmacometabolomic and pharmacogenetic data to predict interindividual variation in warfarin response, and, on this basis, suggest an initial daily dose range. The baseline metabolic profiles, genotypes, and clinical information of 160 patients with heart valve disease served as the variables of the function of the last international normalized ratio measured before a patient's discharge (INRday7 ) to screen for potential biomarkers. The partial least‐squares model showed that two baseline metabolites (uridine and guanosine), one single‐nucleotide variation ( VKORC1 ), and four clinical parameters (weight, creatinine level, amiodarone usage, and initial daily dose) had good predictive power for INRday7 ( R 2 = 0.753 for the training set, 0.643 for the test set). With these biomarkers, a machine learning algorithm (two‐dimensional linear discriminant analysis‐multinomial logit model) was used to predict the subgroups with extremely warfarin‐sensitive or less warfarin‐sensitive patients with a prediction accuracy of 91% for the training set and 90% for the test set, indicating that individual responses to warfarin could be effectively predicted. Based on this model, we have successfully designed an algorithm, "IniWarD, " for predicting an effective dose range in the initial 7‐day warfarin therapy. The results indicate that the dailyAbstract : Anticoagulation response to warfarin during the initial stage of therapy varies among individuals. In this study, we aimed to combine pharmacometabolomic and pharmacogenetic data to predict interindividual variation in warfarin response, and, on this basis, suggest an initial daily dose range. The baseline metabolic profiles, genotypes, and clinical information of 160 patients with heart valve disease served as the variables of the function of the last international normalized ratio measured before a patient's discharge (INRday7 ) to screen for potential biomarkers. The partial least‐squares model showed that two baseline metabolites (uridine and guanosine), one single‐nucleotide variation ( VKORC1 ), and four clinical parameters (weight, creatinine level, amiodarone usage, and initial daily dose) had good predictive power for INRday7 ( R 2 = 0.753 for the training set, 0.643 for the test set). With these biomarkers, a machine learning algorithm (two‐dimensional linear discriminant analysis‐multinomial logit model) was used to predict the subgroups with extremely warfarin‐sensitive or less warfarin‐sensitive patients with a prediction accuracy of 91% for the training set and 90% for the test set, indicating that individual responses to warfarin could be effectively predicted. Based on this model, we have successfully designed an algorithm, "IniWarD, " for predicting an effective dose range in the initial 7‐day warfarin therapy. The results indicate that the daily dose range suggested by the IniWarD system is more appropriate than that of the conventional genotype‐based method, and the risk of bleeding or thrombus due to warfarin could thus be avoided. … (more)
- Is Part Of:
- Clinical pharmacology & therapeutics. Volume 110:Issue 6(2021)
- Journal:
- Clinical pharmacology & therapeutics
- Issue:
- Volume 110:Issue 6(2021)
- Issue Display:
- Volume 110, Issue 6 (2021)
- Year:
- 2021
- Volume:
- 110
- Issue:
- 6
- Issue Sort Value:
- 2021-0110-0006-0000
- Page Start:
- 1585
- Page End:
- 1594
- Publication Date:
- 2021-09-13
- Subjects:
- Pharmacology -- Periodicals
Therapeutics -- Periodicals
615.5 - Journal URLs:
- http://www.nature.com/clpt/index.html ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1532-6535 ↗
http://www.nature.com/ ↗
http://firstsearch.oclc.org ↗
http://www.mosby.com/cpt ↗
http://www.sciencedirect.com/science/journal/00099236 ↗
http://www2.us.elsevierhealth.com/scripts/om.dll/serve?action=searchDB&searchdbfor=home&id=cp ↗ - DOI:
- 10.1002/cpt.2407 ↗
- Languages:
- English
- ISSNs:
- 0009-9236
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.330000
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