Jin Weifeng, Chen Shuzi, Li Dan, Chen Qing, Zhu Mengyuan, Wang Mengxia, Fu Xiaomei, Lin Ping
Shanghai Mental Health Center, China.
Heliyon. 2024 Nov 20;10(23):e40424. doi: 10.1016/j.heliyon.2024.e40424. eCollection 2024 Dec 15.
To evaluate the metabolic changes of patients with schizophrenia treated with olanzapine and analyze the correlation between the dosage of the drug, the blood concentration and the clinical response, so as to provide a reference for the clinical diagnosis and treatment.
PubMed, web of science, Cochrane Library, MEDLINE databases were used to search for studies on olanzapine treatment in patients with schizophrenia, to extract changes in body weight, BMI, waist circumference, cholesterol, PANSS (The Positive and Negative Syndrome Scale), SAPS (The Positive Syndrome Scale), SANS (The Negative Syndrome Scale), BPRS (Brief Psychiatric Rating Scale), CGI (Clinical Global Impressions Ratings), and so on for meta-analysis, and to analyze the correlation of medication dose, blood concentration, and clinical response.
Twenty clinical trials (1839 participants, 1058 male and 781 female patients) were included in this meta-analysis. The results showed that patients receiving olanzapine had significant weight gain (WMD = 0.25, 95 % CI: 0.06-0.44) and no significant changes in HDL-C, LDL-C, triglycerides, or total cholesterol. They were significantly decreased in PANSS (WMD = -2.05, 95 % CI: -2.83, - 1.26), SAPS (WMD = -1.62, 95 % CI: -2.15, - 1.09), sans (WMD = -0.80, 95 % CI: -0.93, - 0.66), BPRS (WMD = -2.79, 95 % CI: -4.11, - 1.46), and CGI (WMD = -1.81, 95 % CI: -2.25, - 1.36). The dose of medication was positively associated with clinical response, with higher plasma concentrations at the recommended dose associated with better clinical outcomes (or = 2.91, 95 % CI: 1.36-6.27). When the body blood concentration is > 10 μg/L, the clinical response rate reaches about 80 %.
The clinic can make an individualized medication regimen based on adjusting the dosage of drugs based on the results of the detection of blood concentration in the body under the premise of avoiding metabolic side effects to ensure the maximization of efficacy.
评估奥氮平治疗精神分裂症患者的代谢变化,分析药物剂量、血药浓度与临床反应之间的相关性,为临床诊疗提供参考。
通过PubMed、Web of Science、Cochrane图书馆、MEDLINE数据库检索奥氮平治疗精神分裂症患者的研究,提取体重、体重指数、腰围、胆固醇、阳性与阴性症状量表(PANSS)、阳性症状量表(SAPS)、阴性症状量表(SANS)、简明精神病评定量表(BPRS)、临床总体印象量表(CGI)等指标的变化进行荟萃分析,并分析用药剂量、血药浓度与临床反应的相关性。
本荟萃分析纳入20项临床试验(1839名参与者,男性1058例,女性781例)。结果显示,接受奥氮平治疗的患者体重显著增加(加权均数差[WMD]=0.25,95%可信区间[CI]:0.06-0.44),高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、甘油三酯或总胆固醇无显著变化。PANSS(WMD=-2.05,95%CI:-2.83,-1.26)、SAPS(WMD=-1.62,95%CI:-2.15,-1.09)、SANS(WMD=-0.80,95%CI:-0.93,-0.66)、BPRS(WMD=-2.79,95%CI:-4.11,-1.46)和CGI(WMD=-1.81,95%CI:-2.25,-1.36)显著降低。用药剂量与临床反应呈正相关,推荐剂量时较高的血浆浓度与更好的临床结局相关(比值比[OR]=2.91,95%CI:1.36-6.27)。当体内血药浓度>10μg/L时,临床反应率达到约80%。
临床可在避免代谢副作用的前提下,根据体内血药浓度检测结果调整药物剂量,制定个体化用药方案,以确保疗效最大化。