Bozikas Vasilis P, Papakosta Maria, Niopas Ioannis, Karavatos Athanasios, Mirtsou-Fidani Vasiliki
1st Department of Psychiatry, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Eur Neuropsychopharmacol. 2004 Jan;14(1):39-44. doi: 10.1016/s0924-977x(03)00061-0.
The purpose of the present study was to assess the impact of smoking on the metabolism of psychotropic drugs in a group of patients with schizophrenia, by measuring CYP1A2 activity. This activity was assessed by the molar ratio (MR) of caffeine metabolites in urine [(AFMU+1U+1X)/17U] and saliva (17X/137X). Participants were 40 patients with schizophrenia: 30 current cigarette smokers and 10 nonsmokers. The two groups (smokers and nonsmokers) differed significantly in their ratio of men to women (83% men and 17% women were among smokers compared with 50% men and 50% women nonsmokers). No other group differences were found regarding age, level of education, PANSS, extrapyramidal symptoms, age of symptoms onset, antipsychotic doses (chloropromazine equivalents), and anticholinergic drug used. Smokers had significant higher MR in urine (P<0.001) as well as in saliva (P=0.001) than nonsmokers, suggesting a higher activity of CYP1A2 dependent on smoking. When gender was used as a covariate, the differences between the two groups remained significant for MR. Cigarette smoking may be a factor influencing the plasma levels of antipsychotics that metabolized through CYP1A2. Clinicians should weight the possibility that smoking and the subsequent modulation of antipsychotic metabolism may be the main reason of treatment resistance. Furthermore, any attempt to reduce or cease smoking in patients with schizophrenia necessitates close monitoring of drug doses, because untoward adverse effects may emerge.
本研究的目的是通过测量CYP1A2活性,评估吸烟对一组精神分裂症患者精神药物代谢的影响。通过尿液[(AFMU + 1U + 1X)/ 17U]和唾液(17X / 137X)中咖啡因代谢物的摩尔比(MR)来评估该活性。研究对象为40例精神分裂症患者:30例当前吸烟者和10例不吸烟者。两组(吸烟者和不吸烟者)的男女比例差异显著(吸烟者中男性占83%,女性占17%,而不吸烟者中男性和女性各占50%)。在年龄、教育水平、阳性和阴性症状量表(PANSS)、锥体外系症状、症状发作年龄、抗精神病药物剂量(氯丙嗪等效剂量)以及所使用的抗胆碱能药物方面,未发现其他组间差异。吸烟者尿液(P<0.001)和唾液(P = 0.001)中的MR显著高于不吸烟者,表明依赖吸烟的CYP1A2活性更高。当将性别作为协变量时,两组之间的MR差异仍然显著。吸烟可能是影响通过CYP1A2代谢的抗精神病药物血浆水平的一个因素。临床医生应考虑吸烟以及随后抗精神病药物代谢的调节可能是治疗抵抗的主要原因。此外,任何试图减少或停止精神分裂症患者吸烟的尝试都需要密切监测药物剂量,因为可能会出现不良副作用。