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A-Textbook-of-Clinical-Pharmacology-and-Therapeutics-5th-edition

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INHERITED DISEASES THAT PREDISPOSE TO DRUG TOXICITY 85<br />

Key points<br />

• Genetic differences contribute substantially to<br />

individual (pharmacokinetic <strong>and</strong> pharmacodynamic)<br />

variability (20–50%) in drug response.<br />

• Mendelian traits that influence drug metabolism<br />

include:<br />

(a) deficient thiopurine methyltransferase (TPMT)<br />

which inactivates 6-MP (excess haematopoietic<br />

suppression);<br />

(b) deficient CYP2D6 activity which hydroxylates<br />

several drug classes, including opioids, β-blockers,<br />

tricyclic antidepressants <strong>and</strong> SSRIs;<br />

(c) deficient CYP2C9 activity which hydroxylates several<br />

drugs including sulphonylureas, S-warfarin,<br />

losartan;<br />

(d) acetylator status (NAT-2), a polymorphism that<br />

affects acetylation <strong>of</strong> drugs, including isoniazid,<br />

hydralazine <strong>and</strong> dapsone;<br />

(e) pseudocholinesterase deficiency; this leads to<br />

prolonged apnoea after suxamethonium, which is<br />

normally inactivated by this enzyme.<br />

• Several inherited diseases predispose to drug toxicity:<br />

(a) glucose-6-phosphate dehydrogenase deficiency<br />

predisposes to haemolysis following many drugs,<br />

including primaquine;<br />

(b) malignant hyperthermia is a Mendelian dominant<br />

affecting the ryanodine receptor in striated muscle,<br />

leading to potentially fatal attacks <strong>of</strong> hyperthermia<br />

<strong>and</strong> muscle spasm after treatment with<br />

suxamethonium <strong>and</strong>/or inhalational anaesthetics;<br />

(c) acute porphyrias, attacks <strong>of</strong> which are particularly<br />

triggered by enzyme-inducing agents, as well as<br />

drugs, e.g. sulphonamides, rifampicin <strong>and</strong> antiseizure<br />

medications.<br />

FURTHER READING<br />

Evans DA, McLeod HL, Pritchard S, Tariq M, Mobarek A. Inter-ethnic<br />

variability in human drug responses. Drug Metabolism <strong>and</strong><br />

Disposition 2001; 29: 606–10.<br />

Evans WE, McLeod HL. Drug therapy: pharmacogenomics – drug<br />

disposition, drug targets, <strong>and</strong> side effects. New Engl<strong>and</strong> Journal <strong>of</strong><br />

Medicine 2003; 348: 538–49.<br />

Wang L, Weinshilboum R. Thiopurine S-methyltransferase pharmacogenetics:<br />

insights, challenges <strong>and</strong> future directions. Oncogene 2006;<br />

25: 1629–38.<br />

Weinshilboum R. Inheritance <strong>and</strong> drug response. New Engl<strong>and</strong> Journal<br />

<strong>of</strong> Medicine 2003; 348: 529–37.<br />

Weinshilboum R, Wang L. Pharmacogenomics: bench to bedside.<br />

Nature Reviews. Drug Discovery 2004; 3: 739–48.<br />

Wilkinson GR. Drug therapy: drug metabolism <strong>and</strong> variability among<br />

patients in drug response. New Engl<strong>and</strong> Journal <strong>of</strong> Medicine 2005;<br />

352: 2211–21.

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