Variability in Response to Medicines PDF
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This document discusses the variability in responses to medicines, focusing on the factors that contribute to this variability as well as the complexities of drug metabolism. It explores the influence of aspects like genetics, diet, environmental factors, and ethnic differences. The importance of CYP1A2, caffeine, and warfarin metabolism is also highlighted.
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Variability in response to medicines Ethnic di4erences in drug response Drug response variability. Importance of CYP1A2 - CYP1A2 is an important drug metabolising enzyme (theophylline and olanzapine). - CYP1A2 also plays a role in detoxification and activation of carcinogens. CYP1A2 su...
Variability in response to medicines Ethnic di4erences in drug response Drug response variability. Importance of CYP1A2 - CYP1A2 is an important drug metabolising enzyme (theophylline and olanzapine). - CYP1A2 also plays a role in detoxification and activation of carcinogens. CYP1A2 substrates, inducers and inhibitors à you change intrinsic clearance. It is important for drugs which have a low hepatic extraction ratio. Ca4eine metabolism E4ect of diet CYP1A2 activity is lower in south Asians. - Smoking à inducer - Oral contraceptive pill à inhibitor Ethnic di4erences in CYP1A2 Conclusions - South Asians have a significantly lower CYP1A2 activity than Europeans. - Oral contraceptive use inhibits CYP1A2 activity. - Smoking induces CYP1A2 activity. - Ethnic diIerence in CYP1A2 inducers Warfarin – variability in INR - Warfarin à very narrow safety margin. - Very variable, each line represents individuals. Determinants of warfarin response. - Multifactorial with interactions between PK and PD factors, include: o Age o Organ function o Genetic influences o Dietary influences o Concomitant medicines o Others Metabolism of warfarin Observations in the clinic Warfarin Drug Interactions - why are they clinically significant? - Narrow therapeutic range. - Low extraction ratio in the liver. o Importance of Clint. - Hepatic metabolism (CYP2C9) - (Not because it is) highly protein bound. à not significant. Warfarin drug interactions – multiple mechanisms. - AIect pharmacokinetics of warfarin - AIect pharmacokinetics of vitamin K - AIect blood clotting mechanism. - Drugs that can aIect the integrity of epithelial surfaces of the body. Warfarin drug and food interactions. - Starting or ceasing medicines for patients on warfarin requires careful attention to possible interactions. o Monitor INR and signs of bleeding. - Vitamin K rich foods can reduce the eIects. o Moderation. In summary - Variability in response can be due to pharmacokinetic and pharmacodynamic factors - Genes are important…. but the environmental factors can be very important as well - Understanding the cause of variability in response is essential for individualizing dose regimens. Quiz Studentamine is a new anticoagulant with the following PK/PD characteristics. 0.1 dose excreted unchanged urine à predominantly metabolised in liver. 10% is renally cleared. à rest hepatically cleared. Low extraction ratio à hepatic clearance mainly determined by fraction unbound. Fe 0.1 à change in renal function wouldn’t significantly aIect. Genetic mutation à not important since only 7% of CYP2D6 is metabolised. Genetic variation in CYP3A4 has very little eIect on overall metabolism. But vulnerable to food interaction à grapefruit, pomelo juice. (CYP3A4) Ethnic diIerences à probably not à CYP1A2 à only 5%. Age? à probably eIect it as it is anticoagulant. à have important eIect on clotting cascade.