Weng Jiajun, Zhang Lei, Yu Wenjuan, Zhao Nan, Zhu Binggen, Ye Chengyu, Zhang Zhanxing, Ma Changlin, Li Yan, Yu Yiming, Li Huafang
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Zhongshan Hospital, Shanghai, China.
Front Pharmacol. 2023 Mar 3;14:1077607. doi: 10.3389/fphar.2023.1077607. eCollection 2023.
Drug-induced parkinsonism (DIP) is the most prevalent neurological side effect of antipsychotics in the Chinese population. Early prevention, recognition, and treatment of DIP are important for the improvement of treatment outcomes and medication adherence of schizophrenia patients. However, the risk factors of DIP and the impact on the clinical syndromes of schizophrenia remain unknown. The goal of this study was to explore the risk factors, clinical correlates, and social functions of DIP in Chinese schizophrenia patients. A cross-sectional analysis of a multicenter, observational, real-world, prospective cohort study of the Chinese schizophrenia population with a baseline assessment was conducted from the year 2012 to 2018. Participants were recruited from four mental health centers in Shanghai and totaled 969 subjects. Sociodemographic data, drug treatment, and clinical variables were compared between the DIP group and the non-DIP group. Variables that correlated with the induction of DIP, and with ≤ 0.1, were included in the binary logistic model for analyzing the risk factors of DIP. First generation antipsychotics (FGA)/second generation antipsychotics (SGA) model and high and low/medium D2 receptor antipsychotics were analyzed respectively to control the bias of co-linearity. All risk factors derived from the a forementioned models and clinical variables with ≤ 0.1 were included in the multivariate analysis of clinical correlates and social function of DIP patients. The Positive and Negative Syndrome Scale (PANSS) model and the personal and social performance (PSP) model were analyzed separately to control for co-linearity bias. Age (OR = 1.03, < 0.001), high D2 receptor antagonist antipsychotic dose (OR = 1.08, = 0.032), and valproate dose (OR = 1.01, = 0.001) were the risk factors of DIP. FGA doses were not a significant contributor to the induction of DIP. Psychiatric symptoms, including more severe negative symptoms (OR = 1.09, < 0.001), lower cognition status (OR = 1.08, = 0.033), and lower excited symptoms (OR = 0.91, = 0.002), were significantly correlated with DIP induction. Social dysfunction, including reduction in socially useful activities (OR = 1.27, = 0.004), lower self-care capabilities (OR = 1.53, < 0.001), and milder disturbing and aggressive behavior (OR = 0.65, < 0.001), were significantly correlated with induction of DIP. Valproate dose was significantly correlated with social dysfunction (OR = 1.01, = 0.001) and psychiatric symptoms (OR = 1.01, = 0.004) of DIP patients. Age may be a profound factor that affects not only the induction of DIP but also the severity of psychiatric symptoms (OR = 1.02, < 0.001) and social functions (OR = 1.02, < 0.001) of schizophrenia patients with DIP. Age, high D2 receptor antagonist antipsychotic dose, and valproate dose are risk factors for DIP, and DIP is significantly correlated with psychiatric symptoms and social performance of Chinese schizophrenia patients. The rational application or discontinuation of valproate is necessary. Old age is related to psychotic symptoms and social adaption in Chinese schizophrenic patients, and early intervention and treatment of DIP can improve the prognosis and social performance of schizophrenia patients. Identifier: NCT02640911.
药物性帕金森综合征(DIP)是中国人群中抗精神病药物最常见的神经副作用。早期预防、识别和治疗DIP对于改善精神分裂症患者的治疗效果和药物依从性至关重要。然而,DIP的危险因素以及对精神分裂症临床综合征的影响仍不清楚。本研究的目的是探讨中国精神分裂症患者中DIP的危险因素、临床相关性及社会功能。对2012年至2018年进行基线评估的中国精神分裂症人群的多中心、观察性、真实世界、前瞻性队列研究进行横断面分析。参与者来自上海的四个精神卫生中心,共969名受试者。比较了DIP组和非DIP组的社会人口统计学数据、药物治疗和临床变量。将与DIP诱导相关且P≤0.1的变量纳入二元逻辑模型,以分析DIP的危险因素。分别分析第一代抗精神病药物(FGA)/第二代抗精神病药物(SGA)模型以及高/低/中效D2受体抗精神病药物,以控制共线性偏倚。将上述模型得出的所有危险因素以及P≤0.1的临床变量纳入DIP患者临床相关性和社会功能的多变量分析。分别分析阳性和阴性症状量表(PANSS)模型以及个人和社会表现(PSP)模型,以控制共线性偏倚。年龄(OR = 1.03,P<0.001)、高剂量D2受体拮抗剂抗精神病药物(OR = 1.08,P = 0.032)和丙戊酸盐剂量(OR = 1.01,P = 0.001)是DIP的危险因素。FGA剂量不是DIP诱导的显著因素。精神症状,包括更严重的阴性症状(OR = 1.09,P<0.001)、较低的认知状态(OR = 1.08,P = 0.033)和较低的兴奋症状(OR = 0.91,P = 0.002),与DIP诱导显著相关。社会功能障碍,包括社会有益活动减少(OR = 1.27,P = 0.004)、自我照顾能力较低(OR = 1.53,P<0.001)和较轻的干扰及攻击性行为(OR = 0.65,P<0.001),与DIP诱导显著相关。丙戊酸盐剂量与DIP患者的社会功能障碍(OR = 1.01,P = 0.001)和精神症状(OR = 1.01,P = 0.004)显著相关。年龄可能是一个重要因素,不仅影响DIP的诱导,还影响患有DIP的精神分裂症患者的精神症状严重程度(OR = 1.02,P<0.001)和社会功能(OR = 1.02,P<0.001)。年龄、高剂量D2受体拮抗剂抗精神病药物和丙戊酸盐剂量是DIP 的危险因素,且DIP与中国精神分裂症患者的精神症状和社会表现显著相关。有必要合理应用或停用丙戊酸盐。老年与中国精神分裂症患者的精神症状和社会适应有关,早期干预和治疗DIP可改善精神分裂症患者的预后和社会表现。标识符:NCT02640911。