Zhu Yuncheng, Ji Haifeng, Tao Lily, Cai Qing, Wang Fang, Ji Weidong, Li Guohai, Fang Yiru
Clinical Research Center & Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Division of Psychiatry, Shanghai Changning Mental Health Center, Affiliated Greenland Hospital of Bio-X Institute, Shanghai Jiao Tong University, Shanghai, China.
Front Psychiatry. 2020 Feb 27;11:65. doi: 10.3389/fpsyt.2020.00065. eCollection 2020.
Neuroendocrine dysfunction is related to the pathogenesis of mental disorders, but conclusions from clinical research lack consistency. We aimed to investigate the neuroendocrinal pathophysiology and its correlation with clinical symptoms in patients with schizophrenia.
The present cross-sectional study included 486 inpatients with schizophrenia admitted at a psychiatric hospital in Shanghai within one year, and 154 healthy controls (HC) matched on age and gender. The serum hemoconcentrations of thyroid-stimulating hormone (TSH), total triiodothyronine (TT3), total thyroxine (TT4), free triiodothyronine (FT3), free thyroxine (FT4), adrenocorticotrophic hormone (ACTH), and cortisol (COR) were measured electrochemical luminescence immunoassay. Pathophysiological conversions of neuroendocrine were then associated with gender, age, age at onset, antipsychotic treatment using hierarchical multiple linear regression.
When compared to HC, the schizophrenia group showed elevated ACTH and COR levels and decreased TT3 and TT4 levels ('s < 0.05). First-episode patients showed lower TSH and higher FT3 and FT4 ('s < 0.05) compared to recurrent patients. Female patients showed higher TSH and lower TT3, FT3, and ACTH levels ('s < 0.05) compared to males. We observed the area under the curve (AUC) of the predictive model to distinguish between schizophrenia and HC to be 0.737 among total samples and between first-episode and recurrent schizophrenia to be 0.890 among subgroups.
Decreased TT3 and TT4 and elevated ACTH and COR levels appear to be associated with schizophrenia symptoms. The chronic recurrent trait of schizophrenia may cause long-term effects on FT3 and FT4 while changes in thyroid, and adrenal function as a result of mental disorder varied with gender. The pathophysiological parameters provide fair to good accuracy of these models.
神经内分泌功能障碍与精神障碍的发病机制相关,但临床研究结论缺乏一致性。我们旨在研究精神分裂症患者的神经内分泌病理生理学及其与临床症状的相关性。
本横断面研究纳入了一年内上海市某精神病院收治的486例精神分裂症住院患者,以及154名年龄和性别匹配的健康对照(HC)。采用电化学发光免疫分析法测定血清促甲状腺激素(TSH)、总三碘甲状腺原氨酸(TT3)、总甲状腺素(TT4)、游离三碘甲状腺原氨酸(FT3)、游离甲状腺素(FT4)、促肾上腺皮质激素(ACTH)和皮质醇(COR)的血液浓度。然后,使用分层多元线性回归分析神经内分泌的病理生理转化与性别、年龄、发病年龄、抗精神病药物治疗之间的关系。
与HC相比,精神分裂症组的ACTH和COR水平升高,TT3和TT4水平降低(P<0.05)。与复发患者相比,首发患者的TSH较低,FT3和FT4较高(P<0.05)。与男性患者相比,女性患者的TSH较高,TT3、FT3和ACTH水平较低(P<0.05)。我们观察到,区分精神分裂症和HC的预测模型在总样本中的曲线下面积(AUC)为0.737,在亚组中首发精神分裂症和复发精神分裂症之间的AUC为0.890。
TT3和TT4降低以及ACTH和COR水平升高似乎与精神分裂症症状相关。精神分裂症的慢性复发特征可能对FT3和FT4产生长期影响,而精神障碍导致的甲状腺和肾上腺功能变化因性别而异。这些病理生理参数为这些模型提供了较好的准确性。