The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×

To the Editor: There have been a number of reports that combination therapy with tramadol and the selective serotonin reuptake inhibitors (SSRIs) fluoxetine (1), paroxetine (2), and sertraline (3) can lead to serotonin syndrome. Citalopram monotherapy has also been described as leading to serotonin syndrome (4), but we believe this has not yet been observed under coadministration with tramadol.

Ms. A was a 70-year-old Caucasian woman with a 30-year history of mild recurrent depressive disorder whose illness had been in remission for 3 years while she was taking 10 mg/day of citalopram. Three days after an abdominal operation, she began taking 50 mg/day of tramadol for pain relief, but she subsequently developed tremors, restlessness, fever, confusion, and visual hallucinations. Her symptoms stopped after termination of tramadol therapy. One year later, she developed identical symptoms upon taking 20 mg/day of tramadol after an abdominal hernia operation. Ms. A had been taking citalopram without interruption.

To assess Ms. A’s drug metabolizing activity, we genotyped her for the functional polymorphisms in cytochrome P450 enzymes CYP2D6 and CYP2C19, revealing her to be heterozygous for alleles causing deficient activity in both enzymes (CYP2D6*1/*4 and CYP2C19*1/*2). Her racemic citalopram clearance was 3.0 ml/kg/min, which is lower than the usual mean of 5.5 ml/kg/min (SD=1.7) (5).

Under combination therapy with citalopram and tramadol, Ms. A showed symptoms typical of serotonin syndrome. Re-exposure to the same drug combination resulted in the same symptoms, leading us to the conclusion that we were indeed dealing with drug-induced serotonin syndrome.

Citalopram is metabolized by CYP2C19, whereas tramadol is O-methylated by CYP2D6(6). The patient was a heterozygous carrier of deficient alleles for both enzymes. Thus, the metabolizing capacity of both pathways was reduced. Furthermore, SSRIs are known to have an inhibitory effect on CYP2D6(7). A decrease in the elimination of citalopram might strengthen this effect, leading to a further reduction in tramadol metabolism. Our patient may exemplify the clinical importance of combined heterozygous genotypes of CYP2D6 and CYP2C19, which occurs in approximately 30% of Caucasians (8).

References

1. Kesavan S, Sobala GM: Serotonin syndrome with fluoxetine plus tramadol. J R Soc Med 1999; 92:474–475Crossref, MedlineGoogle Scholar

2. Egberts AC, ter Borgh J, Brodie-Meijer CC: Serotonin syndrome attributed to tramadol addition to paroxetine therapy. Int Clin Psychopharmacol 1997; 12:181–182Crossref, MedlineGoogle Scholar

3. Mason BJ, Blackburn KH: Possible serotonin syndrome associated with tramadol and sertraline coadministration. Ann Pharmacother 1997; 31:175–177Crossref, MedlineGoogle Scholar

4. Birmes P, Coppin D, Schmitt L, Lauque D: Serotonin syndrome: a brief review. Can Med Assoc J 2003; 168:1439–1442Google Scholar

5. Sidhu J, Priskorn M, Poulsen M, Segonzac A, Grollier G, Larsen F: Steady-state pharmacokinetics of the enantiomers of citalopram and its metabolites in humans. Chirality 1997; 9:686–692Crossref, MedlineGoogle Scholar

6. Paar WD, Poche S, Gerloff J, Dengler HJ: Polymorphic CYP2D6 mediates O-demethylation of the opioid analgesic tramadol. Eur J Clin Pharmacol 1997; 53:235–239Crossref, MedlineGoogle Scholar

7. Jeppesen U, Gram LF, Vistisen K, Loft S, Poulsen HE, Brosen K: Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine. Eur J Clin Pharmacol 1996; 51:73–78Crossref, MedlineGoogle Scholar

8. Sachse C, Brockmoller J, Bauer S, Roots I: Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am J Hum Genet 1997; 60:284–295MedlineGoogle Scholar