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食欲素-A 水平与服用抗精神病药物的精神分裂症患者代谢综合征风险的关系。

Orexin-A Levels in Relation to the Risk of Metabolic Syndrome in Patients with Schizophrenia Taking Antipsychotics.

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.

Department of Psychiatry, Taipei City Psychiatric Center, Taipei City Hospital, Taipei, Taiwan.

出版信息

Int J Neuropsychopharmacol. 2019 Jan 1;22(1):28-36. doi: 10.1093/ijnp/pyy075.

Abstract

BACKGROUND

The role of orexin-A in regulating metabolic homeostasis has been recognized, but its association with antipsychotic-induced metabolic abnormalities remains unclear. We investigated the association between orexin-A levels and metabolic syndrome in patients with schizophrenia treated with clozapine or less obesogenic antipsychotics compared with nonpsychiatric controls.

METHODS

Plasma orexin-A levels and metabolic parameters were determined in 159 patients with schizophrenia: 109 taking clozapine; 50 taking aripiprazole, amisulpride, ziprasidone, or haloperidol; and 60 nonpsychiatric controls.

RESULTS

Orexin-A levels were significantly higher in the group taking less obesogenic antipsychotics, followed by the clozapine group and the controls (F=104.6, P<.01). Higher orexin-A levels were correlated with better metabolic profiles in the patient groups but not in the controls. Regression analyses revealed that the patients with higher orexin-A levels had significantly lower risk of metabolic syndrome (adjusted odds ratio [OR]=0.04, 95% CI: 0.01-0.38 for the 2nd tertile; OR=0.04, 95% CI: 0.01-0.36 for the 3rd tertile, compared with the first tertile), after adjustment for age, sex, smoking history, types of antipsychotics (clozapine vs less obesogenic antipsychotics), duration of antipsychotic treatment, and disease severity.

CONCLUSIONS

Our results revealed that the orexin-A level was upregulated in patients with schizophrenia treated with antipsychotics, especially for the group taking less obesogenic antipsychotics. Furthermore, higher orexin-A levels were independently associated with better metabolic profiles. These observations suggest that an upregulation of orexin-A has a protective effect against the development of metabolic abnormalities in patients with schizophrenia receiving antipsychotic treatment.

摘要

背景

已认识到食欲素-A 在调节代谢稳态中的作用,但它与抗精神病药引起的代谢异常的关系尚不清楚。我们研究了与精神分裂症患者相比,接受氯氮平或较少致肥胖的抗精神病药治疗与非精神科对照者的代谢综合征相关的食欲素-A 水平。

方法

测定了 159 例精神分裂症患者的血浆食欲素-A 水平和代谢参数:109 例服用氯氮平;50 例服用阿立哌唑、氨磺必利、齐拉西酮或氟哌啶醇;60 例非精神科对照者。

结果

食欲素-A 水平在服用较少致肥胖的抗精神病药的组中显著升高,其次是氯氮平组和对照组(F=104.6,P<.01)。较高的食欲素-A 水平与患者组的代谢谱更好相关,但与对照组无关。回归分析显示,较高的食欲素-A 水平的患者患代谢综合征的风险显著降低(调整后的优势比[OR]=0.04,95%可信区间:第 2 tertile 为 0.01-0.38;第 3 tertile 为 0.04,95% CI:0.01-0.36,与第 1 tertile 相比),调整年龄、性别、吸烟史、抗精神病药类型(氯氮平与较少致肥胖的抗精神病药)、抗精神病药治疗持续时间和疾病严重程度后。

结论

我们的结果表明,接受抗精神病药治疗的精神分裂症患者的食欲素-A 水平上调,特别是服用较少致肥胖的抗精神病药的患者。此外,较高的食欲素-A 水平与更好的代谢谱独立相关。这些观察结果表明,食欲素-A 的上调对抗精神病药治疗的精神分裂症患者代谢异常的发展具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9074/6313111/b6f7bcddcba6/pyy07501.jpg

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