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DRD2 启动子区域变异可预测首发精神分裂症患者抗精神病药物引起的体重增加。

DRD2 promoter region variation predicts antipsychotic-induced weight gain in first episode schizophrenia.

机构信息

Division of Psychiatry Research,The Zucker Hillside Hospital, 75-59 263rd Street, Glen Oaks, NY 11004, USA.

出版信息

Pharmacogenet Genomics. 2010 Sep;20(9):569-72. doi: 10.1097/FPC.0b013e32833ca24b.

Abstract

Many antipsychotic medications carry a substantial liability for weight gain, and one mechanism common to all antipsychotics is binding to the dopamine D2 receptor. We therefore examined the relationship between -141C Ins/Del (rs1799732), a functional promoter region polymorphism in DRD2, and antipsychotic-induced weight gain in 58 first episode schizophrenia patients enrolled in a randomized trial of risperidone versus olanzapine. Carriers of the deletion allele (n=29) were compared with Ins/Ins homozygotes (noncarriers, n=29) in a mixed model encompassing 10 weight measurements over 16 weeks. Deletion allele carriers showed significantly more weight gain after 6 weeks of treatment regardless of assigned medication. Although deletion carriers were prescribed higher doses of olanzapine (but not risperidone), dose did not seem to account for the genotype effects on weight gain. Given earlier evidence that deletion carriers show reduced symptom response to medication, additional study of appropriate treatment options for these patients seems warranted.

摘要

许多抗精神病药物会导致体重增加,而所有抗精神病药物的一个共同作用机制是与多巴胺 D2 受体结合。因此,我们研究了 DRD2 基因中的 -141C Ins/Del(rs1799732) 功能性启动子区域多态性与利培酮与奥氮平随机对照试验中 58 例首发精神分裂症患者的抗精神病药引起的体重增加之间的关系。在包含 16 周内 10 次体重测量的混合模型中,我们比较了缺失等位基因携带者(n=29)与 Ins/Ins 纯合子(非携带者,n=29)。无论接受哪种药物治疗,缺失等位基因携带者在治疗 6 周后体重增加明显更多。尽管缺失携带者服用了更高剂量的奥氮平(而非利培酮),但剂量似乎并不能解释基因型对体重增加的影响。鉴于早期有证据表明缺失携带者对药物的症状反应降低,因此似乎需要对这些患者的适当治疗选择进行进一步研究。

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