Low-Dose Caffeine May Exacerbate Psychotic Symptoms in People With Schizophrenia

Mr. C is a 49-year-old married, jobless man with a history of chronic schizophrenia, paranoid type for more than 10 years. The patient had no history of drug abuse but smoked 20 cigarettes per day for more than 20 years. He was managed with flupenthixol decanoate injections by medical staff at the dose of 40 mg every 2 weeks. Prior to this presentation, the patient started to drink about four cans of coffee daily for 2 weeks and soon developed paranoia, delusion of reference, and agitation. Because of the potential homicidal risk, he was hospitalized, and his consumption of caffeine was halted. Surprisingly, without being prescribed new psychotropic agents, the patient’s symptoms improved gradually. Finally, he was discharged 50 days later and received regular follow-up appointments. He discontinued caffeine intake under the recommendation of the physician, and no apparent delusion or hallucination was noted thereafter.

In contrast to previous case reports that describe the occurrence of psychosis after heavy ingestion of caffeine,^2,3 we reported a case of psychosis consumed relative low dose of caffeine. The patient drank about four cups of coffee a day, and each contained 150 mg of caffeine per cup. The patient weighed 71 kg and, therefore, consumed less than 8.5 mg/kg/day of caffeine, which is slightly higher than average intake between schizophrenia smokers (4.1±4.0 mg/kg/day).⁴ The patient in our case received regular depot injections, therefore, poor adherence to medicine could be ruled out. No known drug-drug interaction was noted between caffeine and flupenthixol. Moreover, no any precipitating factor that could worsen psychotic symptoms was mentioned prior to this admission. Notably, the patient improved upon ceasing caffeine intake, and no apparent positive symptoms was present.

In humans, there are four types of adenosine receptors. Caffeine functions as a competitive antagonist at the adenosine A1 and A2A receptors and increases dopaminergic effects in the striatum.⁵ Through this mechanism, caffeine modulates the mesolimbic dopamine pathway that may be related to its psychotomimetic effect.¹ Caffeine is widely used in our society, but little consideration has been given to its indirect effects on dopamine transmission leading to psychosis exacerbation. Prior case reports mentioned that high-dose caffeine can worsen psychotic symptoms in people with schizophrenia.² Clinicians might consider the effect of caffeine consumption while evaluating psychotic patients, even though the consumption dose is low.