TY - JOUR
T1 - From evidence based medicine to mechanism based medicine
T2 - Reviewing the role of pharmacogenetics
AU - Wilffert, Bob
AU - Swen, Jesse
AU - Mulder, Hans
AU - Touw, Daan
AU - Maitland-Van der Zee, Anke-Hilse
AU - Deneer, Vera
AU - KNMP Working Grp Pharmacogenetics
PY - 2013/6
Y1 - 2013/6
N2 - Aim of the review The translation of evidence based medicine to a specific patient presents a considerable challenge. We present by means of the examples nortriptyline, tramadol, clopidogrel, coumarins, abacavir and antipsychotics the discrepancy between available pharmacogenetic information and its implementation in daily clinical practice. Method Literature review. Results A mechanism based approach may be helpful to personalize medicine for the individual patient to which pharmacogenetics may contribute significantly. The lack of consistency in what we accept in bioequivalence and in pharmacogenetics of drug metabolising enzymes is discussed and illustrated with the example of nortriptyline. The impact of pharmacogenetics on examples like tramadol, clopidogrel, coumarins and abacavir is described. Also the present status of the polymorphisms of 5-HT2A and C receptors in antipsychotic-induced weight gain is presented as a pharmacodynamic example with until now a greater distance to clinical implementation. Conclusion The contribution of pharmacogenetics to tailor-made pharmacotherapy, which especially might be of value for patients deviating from the average, has not yet reached the position it seems to deserve.
AB - Aim of the review The translation of evidence based medicine to a specific patient presents a considerable challenge. We present by means of the examples nortriptyline, tramadol, clopidogrel, coumarins, abacavir and antipsychotics the discrepancy between available pharmacogenetic information and its implementation in daily clinical practice. Method Literature review. Results A mechanism based approach may be helpful to personalize medicine for the individual patient to which pharmacogenetics may contribute significantly. The lack of consistency in what we accept in bioequivalence and in pharmacogenetics of drug metabolising enzymes is discussed and illustrated with the example of nortriptyline. The impact of pharmacogenetics on examples like tramadol, clopidogrel, coumarins and abacavir is described. Also the present status of the polymorphisms of 5-HT2A and C receptors in antipsychotic-induced weight gain is presented as a pharmacodynamic example with until now a greater distance to clinical implementation. Conclusion The contribution of pharmacogenetics to tailor-made pharmacotherapy, which especially might be of value for patients deviating from the average, has not yet reached the position it seems to deserve.
KW - Drug metabolising enzymes
KW - Mechanism based medicine
KW - Pharmacodynamics
KW - Pharmacogenetics
KW - Pharmacokinetics
KW - INDUCED WEIGHT-GAIN
KW - HTR2C GENE POLYMORPHISMS
KW - 5-HT2C RECEPTOR GENE
KW - PHENYTOIN TOXICITY
KW - THE-759C/T POLYMORPHISM
KW - PSYCHIATRIC-PATIENTS
KW - CYP2C POLYMORPHISMS
KW - ANALGESIC TRAMADOL
KW - METABOLIC SYNDROME
KW - CLINICAL-PRACTICE
U2 - 10.1007/s11096-010-9446-1
DO - 10.1007/s11096-010-9446-1
M3 - Article
SN - 2210-7703
VL - 35
SP - 369
EP - 375
JO - International Journal of Clinical Pharmacy
JF - International Journal of Clinical Pharmacy
IS - 3
ER -