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首页> 外文期刊>The journal of clinical psychiatry >Thyroid function in treatment-resistant schizophrenia patients treated with quetiapine, risperidone, or fluphenazine.
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Thyroid function in treatment-resistant schizophrenia patients treated with quetiapine, risperidone, or fluphenazine.

机译:喹硫平,利培酮或氟奋乃静治疗的难治性精神分裂症患者的甲状腺功能。

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BACKGROUND: Thyroid dysfunction is relatively common in patients with schizophrenia, possibly related to a genetic linkage of the disorders and to antipsychotic treatment. Quetiapine has been implicated as causing some degree of thyroid function changes, yet it remains unclear as to what extent or why these changes may occur. Furthermore, the need for thyroid function monitoring in patients taking this medication is not definitive. METHOD: Thyroid function was assessed in 38 adult DSM-IV-diagnosed schizophrenia patients after 6 weeks of prospective, double-blind, randomized treatment with quetiapine (400 mg/day), risperidone (4 mg/day), or fluphenazine (12.5 mg/day). Data were collected from 1997 to 2002. RESULTS: At baseline, the percentages of randomized patients with abnormal values were 18% (4/22) for serum T(3) resin uptake, 13% (4/30) for thyroid-stimulating hormone (TSH), and 9% (2/22) for total serum thyroxine (TT(4)), representing fairly widespread thyroid abnormalities independent of treatment group. Little change was noted in thyroid function during the 6 weeks of treatment, except for a significant decrease in TT(4) values for those taking quetiapine (p = .01). Clinically, however, no patients demonstrated any signs or symptoms of hypothyroidism during the study, nor were any significant changes in the free thyroxine index or TSH levels noted. CONCLUSIONS: It is expected that TT(4) levels will decrease during quetiapine treatment, and this may possibly be related to competitive metabolism of thyroid hormones and quetiapine by UDP-glucuronosyltransferase. Routine monitoring of thyroid function in quetiapine-treated patients without a history of thyroid disease is not recommended.
机译:背景:甲状腺功能障碍在精神分裂症患者中相对常见,可能与疾病的遗传联系和抗精神病药物治疗有关。喹硫平被认为会引起某种程度的甲状腺功能改变,但尚不清楚这些改变可能发生的程度或原因。此外,服用这种药物的患者对甲状腺功能监测的需求尚不确定。方法:采用喹硫平(400 mg /天),利培酮(4 mg /天)或氟奋乃静(12.5 mg)对前瞻性,双盲,随机治疗6周后,对38名经DSM-IV诊断为成人的精神分裂症患者进行甲状腺功能评估/天)。从1997年至2002年收集了数据。结果:在基线时,随机值异常患者的血清T(3)树脂摄取率为18%(4/22),促甲状腺激素为13%(4/30)。 (TSH)和总血清甲状腺素(TT(4))的9%(2/22),代表了相当广泛的甲状腺异常,与治疗组无关。在治疗的6周中,甲状腺功能几乎未见变化,但喹硫平组的TT(4)值显着下降(p = .01)。然而,在临床上,没有患者在研究期间显示出甲状腺功能减退的任何体征或症状,也未发现游离甲状腺素指数或TSH水平有任何显着变化。结论:在喹硫平治疗期间,预计TT(4)水平会降低,这可能与UDP-葡萄糖醛酸糖基转移酶对甲状腺激素和喹硫平的竞争性代谢有关。不建议对没有喹硫平病史的喹硫平治疗患者进行甲状腺功能的常规监测。

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