Olanzapine-Associated Rhabdomyolysis: A Case Report

被引:2
作者
Skryabin, Valentin Y. [1 ]
Zastrozhin, Michael [2 ]
Sychev, Dmitry A. [3 ]
机构
[1] Moscow Res & Pract Ctr Addict, Dept 2, Moscow, Russia
[2] Moscow Res & Pract Ctr Addict, Lab Genet & Fundamental Studies, Moscow, Russia
[3] Russian Med Acad Continuous Profess Educ, Minist Hlth Russian Federat, Clin Pharmacol & Therapy Dept, Moscow, Russia
关键词
pharmacogenetics; olanzapine; creatine kinase; rhabdomyolysis; personalized medicine; pgx2; PHARMACOGENETICS; ANTIPSYCHOTICS; EFFICACY;
D O I
10.7759/cureus.12568
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This paper presents the case of a 20-year-old patient with a suspected diagnosis of paranoid schizophrenia. He was prescribed oral olanzapine at a dose of 10 mg per day, and the treatment was associated with rhabdomyolysis (serum creatine kinase = 9,725 U/L on day four of the therapy). On suspicion of its contribution to rhabdomyolysis, olanzapine was immediately withdrawn. Pharmacogenetic testing demonstrated that the patient's CYP2D6 genotype was *4/*4 (1846G>A, rs3892097). Based on these results, the patient was switched to trifluoperazine, a medication that is not metabolized by the CYP2D6 isoenzyme. Subsequently, the patient recovered well and was discharged without any nephrological sequelae. The presented case demonstrates that pharmacogenetic-guided personalization of treatment may allow selecting the best medication and determining the right dosage, resulting in the reduced risk of adverse drug reactions and pharmacoresistance.
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页数:4
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