Chabroux S, Haffen E, Penfornis A
Service d'endocrinologie-métabolisme et diabétologie-nutrition, pôle PACTE, hôpital Jean-Minjoz, CHU de Besançon, boulevard Fleming, 25030 Besançon cedex, France.
Ann Endocrinol (Paris). 2009 Sep;70(4):202-10. doi: 10.1016/j.ando.2009.07.003. Epub 2009 Aug 22.
Schizophrenia is a common psychiatric illness (1% of the general population), characterized by the association of positive and negative symptoms and cognitive disorders. Antipsychotics, typical or atypical, are known to induce in patients with schizophrenia weight gain and abnormalities in glucose and lipid metabolisms. These modifications, in addition to metabolic risk factors, intrinsic to the psychiatric illness (physical inactivity, smoking, diabetes), increase the risk of cardiovascular complications. Some antipsychotics are associated with a higher risk of metabolic disorders. Before starting such a medication, all risk factors must be taken into account. In case of even effectiveness, one should consider the risk of inducing metabolic disorders, as well as the intrinsic risk factors of the patient, in order to prescribe the medication associated with the lower metabolic risk. Regarding iatrogenic diabetes, the risk of occurrence seems different, depending on the molecules, being more marked for clozapine, olanzapine, risperidone, quietapine then amisulpride, aripiprazole and finally ziprasidone. The physiopathology seems to involve both an increase in insulin resistance and an alteration of insulin secretion. Nevertheless, the benefit/risk often remains largely in favour of treatment, the atypical antipsychotics are at least equally effective and better tolerated on the cognitive and neurological functions than conventional antipsychotics being. They have particularly far fewer extrapyramidal effects. The reversibility of pathologies induced by atypical antipsychotics led to the formulation of guidelines, leading to regular clinical and biological follow-up.
精神分裂症是一种常见的精神疾病(占普通人群的1%),其特征为阳性症状、阴性症状及认知障碍并存。已知典型或非典型抗精神病药物会使精神分裂症患者体重增加,并导致糖脂代谢异常。除了这些代谢危险因素外,精神疾病本身所固有的危险因素(缺乏运动、吸烟、糖尿病)也会增加心血管并发症的风险。一些抗精神病药物与更高的代谢紊乱风险相关。在开始使用此类药物之前,必须考虑所有危险因素。如果疗效相同,应考虑诱发代谢紊乱的风险以及患者的内在危险因素,以便开具代谢风险较低的药物。关于医源性糖尿病,其发生风险似乎因药物分子而异,氯氮平、奥氮平、利培酮、喹硫平的风险更显著,其次是氨磺必利、阿立哌唑,最后是齐拉西酮。其病理生理学似乎涉及胰岛素抵抗增加和胰岛素分泌改变。然而,获益/风险通常仍大多倾向于治疗,非典型抗精神病药物在认知和神经功能方面至少与传统抗精神病药物同样有效且耐受性更好。它们的锥体外系反应尤其少得多。非典型抗精神病药物所致病症的可逆性促使制定了相关指南,从而进行定期的临床和生物学随访。