Department of Psychiatry, McGill University, Montreal, Canada; Douglas Mental Health University Institute, Montreal, Canada; Prevention and Early Intervention Program for Psychosis, Montreal, Canada.
Institut Universitaire en Santé Mentale de Montréal, Canada.
Psychoneuroendocrinology. 2021 Jan;123:104915. doi: 10.1016/j.psyneuen.2020.104915. Epub 2020 Oct 15.
Recent evidence suggests that patients with psychotic disorders have metabolic disturbances (e.g., insulin resistance, dyslipidemia) at the onset of the disease and before antipsychotic exposure. Such disturbances are strongly associated with adipose tissue dysregulation. Measuring adipokines, the molecular mediators of adipose function, could provide a picture of the state of metabolic regulation at the onset of psychosis. The present study explores adipokine changes in a population of first-episode psychosis (FEP) patients with minimal prior exposure to antipsychotics. The effects of social determinants of health (childhood trauma and minority status) associated with both metabolic and psychotic disorders were studied as potential determinants of this phenomenon. Data was collected through the Signature project, a biobank of clinical, socio-demographic, and biological markers. Adipokines (leptin, adiponectin, resistin and chemerin) were measured in serum of FEP patients with minimal exposure to antipsychotics (N = 48) and controls (N = 39). Data were analyzed with univariate (t-tests) and multivariate (linear regression) statistical methods. Patients, compared to controls, had significantly higher levels of adiponectin and resistin, and significantly lower levels of leptin and chemerin. These results persisted after controlling for sex, waist-to-height ratio, childhood trauma, and visible minority status. Adiponectin and chemerin retained their effects after further controlling for tobacco and depression. Resistin increased with childhood trauma scores; chemerin was higher in visible minority patients. Adipose tissue dysfunction is present in FEP patients, before exposure to antipsychotics. Social determinants of health contribute to adipose (and metabolic) dysregulation in FEP, but may not be the main determinants of this relationship.
最近的证据表明,精神病患者在发病前和接触抗精神病药物之前就存在代谢紊乱(如胰岛素抵抗、血脂异常)。这些紊乱与脂肪组织失调密切相关。测量脂肪因子,即脂肪功能的分子介质,可以提供精神病发病时代谢调节状态的情况。本研究探讨了首次发作精神病(FEP)患者中脂肪因子的变化,这些患者接触抗精神病药物的时间极短。与代谢和精神障碍都相关的健康社会决定因素(儿童期创伤和少数族裔地位)被研究为这种现象的潜在决定因素。数据是通过 Signature 项目收集的,该项目是一个临床、社会人口统计学和生物学标志物的生物库。在接触抗精神病药物极少的 FEP 患者(N=48)和对照组(N=39)的血清中测量了脂肪因子(瘦素、脂联素、抵抗素和 chemerin)。使用单变量(t 检验)和多变量(线性回归)统计方法分析数据。与对照组相比,患者的脂联素和抵抗素水平显著升高,瘦素和 chemerin 水平显著降低。这些结果在控制了性别、腰高比、儿童期创伤和可见少数民族地位后仍然存在。在进一步控制了吸烟和抑郁后,脂联素和 chemerin 仍然存在影响。抵抗素随儿童期创伤评分增加;可见少数民族患者的 chemerin 水平较高。在接触抗精神病药物之前,FEP 患者的脂肪组织功能就已经出现异常。健康的社会决定因素导致 FEP 患者的脂肪(和代谢)失调,但可能不是这种关系的主要决定因素。