Li Xue, Fan Xiaoduo, Yuan Xiuxia, Pang Lijuan, Hu Shaohua, Wang Yunpeng, Huang Xufeng, Song Xueqin
Department of Psychiatry, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Biological Psychiatry International Joint Laboratory of Henan, Zhengzhou University, Zhengzhou, China.
Front Psychiatry. 2021 Aug 23;12:724664. doi: 10.3389/fpsyt.2021.724664. eCollection 2021.
Butyric acid, a major short-chain fatty acid (SCFA), has an important role in the microbiota-gut-brain axis and brain function. This study investigated the role of butyric acid in treatment response in drug-naïve first episode schizophrenia. The study recruited 56 Chinese Han schizophrenia inpatients with normal body weight and 35 healthy controls. Serum levels of butyric acid were measured using Gas Chromatography-Mass Spectrometer (GC-MS) analysis at baseline (for all participants) and 24 weeks after risperidone treatment (for patients). Clinical symptoms were measured using the Positive and Negative Syndrome Scale (PANSS) for patients at both time points. At baseline, there was no significant difference in serum levels of butyric acid between patients and healthy controls ( = 0.206). However, there was a significant increase in serum levels of butyric acid in schizophrenia patients after 24-week risperidone treatment ( = 0.030). The PANSS total and subscale scores were decreased significantly after 24-week risperidone treatment ( < 0.001). There were positive associations between baseline serum levels of butyric acid and the reduction ratio of the PANSS total and subscale scores after controlling for age, sex, education, and duration of illness ( < 0.05). Further, there was a positive association between the increase in serum levels of butyric acid and the reduction of the PANSS positive symptoms subscale scores ( = 0.38, = 0.019) after controlling for potential confounding factors. Increased serum levels of butyric acid might be associated with a favorable treatment response in drug-naïve, first episode schizophrenia. The clinical implications of our findings were discussed.
丁酸是一种主要的短链脂肪酸(SCFA),在微生物群-肠-脑轴和脑功能中发挥着重要作用。本研究调查了丁酸在初发未用药的精神分裂症治疗反应中的作用。该研究招募了56名体重正常的中国汉族精神分裂症住院患者和35名健康对照者。在基线时(所有参与者)以及利培酮治疗24周后(患者),使用气相色谱-质谱联用仪(GC-MS)分析测量血清丁酸水平。在两个时间点均使用阳性和阴性症状量表(PANSS)对患者的临床症状进行测量。基线时,患者与健康对照者的血清丁酸水平无显著差异( = 0.206)。然而,利培酮治疗24周后,精神分裂症患者的血清丁酸水平显著升高( = 0.030)。利培酮治疗24周后,PANSS总分及各子量表得分显著降低( < 0.001)。在控制年龄、性别、教育程度和病程后,基线血清丁酸水平与PANSS总分及各子量表得分的降低率之间存在正相关( < 0.05)。此外,在控制潜在混杂因素后,血清丁酸水平的升高与PANSS阳性症状子量表得分的降低之间存在正相关( = 0.38, = 0.019)。血清丁酸水平升高可能与初发未用药的精神分裂症患者良好的治疗反应相关。我们对研究结果的临床意义进行了讨论。