Department of Geriatric Psychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing, China.
Department of Psychiatry, The Second People's Hospital of Jiangning District, Nanjing, Jiangsu, China.
Schizophr Bull. 2023 May 3;49(3):646-658. doi: 10.1093/schbul/sbac202.
Antipsychotics (APs), the cornerstone of schizophrenia treatment, confer a relatively high risk of constipation. However, the mechanisms underpinning AP-induced constipation are poorly understood. Thus, we hypothesized that (1) schizophrenia patients with AP-induced constipation have distinct metabolic patterns; (2) there is more than one mechanism at play in producing this adverse drug effect; and (3) AP-associated changes in the gut microbiome are related to the altered metabolic profiles.
Eighty-eight schizophrenia patients, including 44 with constipation (C) and 44 matched patients without constipation (NC), were enrolled in this study. Constipation was diagnosed by Rome IV criteria for constipation and colonic transit time using radiopaque markers (ROMs) while severity was evaluated with the Bristol Stool Form Scale (BSS) and Constipation Assessment Scale (CAS). Fasting blood samples were drawn from all participants and were subjected to non-targeted liquid chromatography-mass spectrometry (LC-MS) metabolomic analysis.
Eleven metabolites were significantly altered in AP-induced constipation which primarily disturbed sphingolipid metabolism, choline metabolism, and sphingolipid signaling pathway (P value < .05, FDR < 0.05). In the C group, changes in the gut bacteria showed a certain degree of correlation with 2 of the significantly altered serum metabolites and were associated with alterations in choline metabolism.
Our findings indicated that there were disturbances in distinct metabolic pathways that were associated with AP-induced constipation. In addition, this study presents evidence of a link between alterations in the gut microbiome and host metabolism which provides additional mechanistic insights on AP-induced constipation.
抗精神病药(APs)是精神分裂症治疗的基石,但其会带来较高的便秘风险。然而,AP 导致便秘的机制仍不清楚。因此,我们假设:(1)患有 APs 引起的便秘的精神分裂症患者具有独特的代谢模式;(2)产生这种药物不良反应的机制不止一种;(3)AP 相关的肠道微生物组的变化与代谢特征的改变有关。
本研究纳入了 88 名精神分裂症患者,其中 44 名患有便秘(C 组),44 名匹配的无便秘患者(NC 组)。便秘通过罗马 IV 标准和放射性标记物(ROM)来诊断,结肠转运时间通过来评估,同时采用布里斯托粪便形状量表(BSS)和便秘评估量表(CAS)来评估严重程度。所有参与者均抽取空腹血样,并进行非靶向液相色谱-质谱(LC-MS)代谢组学分析。
在 APs 引起的便秘中,有 11 种代谢物发生了显著改变,主要干扰了神经鞘脂代谢、胆碱代谢和神经鞘脂信号通路(P 值<.05, FDR<.05)。在 C 组中,肠道细菌的变化与 2 种显著改变的血清代谢物具有一定的相关性,并且与胆碱代谢的改变有关。
我们的研究结果表明,存在特定代谢途径的紊乱,这与 APs 引起的便秘有关。此外,本研究还提供了肠道微生物组与宿主代谢之间存在联系的证据,为 APs 引起的便秘提供了额外的机制见解。