Tsuchimine Shoko, Hattori Kotaro, Ota Miho, Hidese Shinsuke, Teraishi Toshiya, Sasayama Daimei, Hori Hiroaki, Noda Takamasa, Yoshida Sumiko, Yoshida Fuyuko, Kunugi Hiroshi
Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo 187-8502, Japan.
Department of Psychiatry, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo 187-8551, Japan.
Neuropsychiatr Dis Treat. 2019 Aug 6;15:2221-2230. doi: 10.2147/NDT.S209023. eCollection 2019.
Orexins are hypothalamic neuropeptides involved in the regulation of sleep, appetite and arousal. An altered orexin system has been implicated in the pathophysiology of psychiatric disorders. This study aimed to examine whether plasma orexin-A levels differ in patients with schizophrenia, major depressive disorder (MDD), or bipolar disorder (BD) compared to in healthy controls. We also examined the possible correlations between plasma orexin-A levels and clinical variables.
All participants were Japanese. The sample consisted of 80 patients with schizophrenia (42 women, 52.5%; mean age 36.8 years), 80 patients with MDD (43 women, 53.8%; 43.7 years), and 40 patients with BD (24 women, 60%; 41.1 years), as well as 80 healthy controls (48 women, 60%; 47.0 years). Plasma orexin-A levels were quantified by an enzyme-linked immunosorbent assay.
Mean orexin-A levels were significantly different across the four diagnostic groups (F=4.09; df=3; =0.007, =0.06). In particular, the patients with BD showed significantly lower orexin-A levels than did the controls. When the median value of the control group (109.8 pg/ml) was set as a cut-off value, subjects whose orexin-A levels were below the cut-off were more common in all psychiatric groups (schizophrenia: 73.8%, =9.56, df=1, =0.003, OR=2.81, 95% CI: 1.45 to 5.45, =0.57; MDD: 78.5%, =14.02, df=1, <0.001, OR=3.65, 95% CI: 1.82 to 7.29, =0.72; BD: 87.5%, =16.0, df=1, <0.001, OR=7.00, 95% CI: 2.49 to 19.70, =1.07). We found no association between plasma orexin-A levels and any clinical symptoms, depression severity, or medication doses.
Our results suggest that plasma orexin-A levels are reduced in patients with BD.
食欲素是下丘脑神经肽,参与睡眠、食欲和觉醒的调节。食欲素系统改变与精神疾病的病理生理学有关。本研究旨在探讨精神分裂症、重度抑郁症(MDD)或双相情感障碍(BD)患者的血浆食欲素-A水平与健康对照者相比是否存在差异。我们还研究了血浆食欲素-A水平与临床变量之间的可能相关性。
所有参与者均为日本人。样本包括80例精神分裂症患者(42名女性,占52.5%;平均年龄36.8岁)、80例MDD患者(43名女性,占53.8%;43.7岁)、40例BD患者(24名女性,占60%;41.1岁)以及80名健康对照者(48名女性,占60%;47.0岁)。采用酶联免疫吸附测定法对血浆食欲素-A水平进行定量。
四个诊断组的食欲素-A平均水平存在显著差异(F = 4.09;自由度 = 3;P = 0.007,η² = 0.06)。特别是,BD患者的食欲素-A水平显著低于对照组。以对照组的中位数(109.8 pg/ml)作为临界值,在所有精神疾病组中,食欲素-A水平低于临界值的受试者更为常见(精神分裂症:73.8%,χ² = 9.56,自由度 = 1,P = 0.003,OR = 2.81,95%可信区间:1.45至5.45,Cramer's V = 0.57;MDD:78.5%,χ² = 14.02,自由度 = 1,P < 0.001,OR = 3.65,95%可信区间:1.82至7.29,Cramer's V = 0.72;BD:87.5%,χ² = 16.0,自由度 = 1,P < 0.001,OR = 7.00,95%可信区间:2.49至19.70,Cramer's V = 1.07)。我们未发现血浆食欲素-A水平与任何临床症状、抑郁严重程度或药物剂量之间存在关联。
我们的结果表明,BD患者的血浆食欲素-A水平降低。