Institute of Mental Health, Peking University Sixth Hospital, Beijing, China.
National Clinical Research Center for Mental Disorders, Peking University Sixth Hospital, Beijing, China.
JAMA Netw Open. 2023 Oct 2;6(10):e2335518. doi: 10.1001/jamanetworkopen.2023.35518.
Limited evidence supports multigenetic pharmacogenomics-guided treatment (MPGT) in schizophrenia.
To evaluate the clinical effectiveness of MPGT in schizophrenia in a randomized clinical trial (RCT).
DESIGN, SETTING, AND PARTICIPANTS: This RCT was conducted from March 2020 to March 2022. Male Chinese Han inpatients aged 18 to 60 years diagnosed with schizophrenia with a Positive and Negative Symptom Scale (PANSS) score of 60 or more from 2 selected study hospitals were included. Patients and raters were masked to MPGT or treatment as usual (TAU) randomization.
Participants were randomly assigned in a 1:1 ratio to receive either MPGT or TAU for 12 weeks.
The primary efficacy outcome was the percentage change in PANSS total scores (range, 30 to 210) from baseline to week 6 analyzed by a modified intention-to-treat mixed model for repeated measures. The secondary outcome included response and symptomatic remission rates.
A total of 210 participants (mean [SD] age, 29.2 [8.8] years) were enrolled and analyzed, with 113 assigned to MPGT and 97 to TAU. Compared with those randomized to TAU, participants randomized to MPGT demonstrated a significantly higher percentage change in PANSS score (74.2% vs 64.9%; adjusted mean difference, 9.2 percentage points; 95% CI, 4.4-14.1 percentage points; P < .001) and a higher response rate (93 of 113 [82.3%] vs 63 of 97 [64.9%]; adjusted odds ratio, 2.48; 95% CI, 1.28-4.80; P = .01) at the end of week 6.
In this RCT of MPGT, MPGT was more effective than TAU in treating patients with schizophrenia. These findings suggest that multigenetic pharmacogenomic testing could serve as an effective tool to guide the treatment of schizophrenia.
Chinese Clinical Trial Registry Identifier: ChiCTR2000029671.
有限的证据支持精神分裂症的多基因药物基因组学指导治疗(MPGT)。
在一项随机临床试验(RCT)中评估 MPGT 在精神分裂症中的临床疗效。
设计、地点和参与者:这项 RCT 于 2020 年 3 月至 2022 年 3 月进行。入选的是来自 2 家选定研究医院的、年龄在 18 至 60 岁之间的、被诊断为精神分裂症且阳性和阴性症状量表(PANSS)评分大于等于 60 分的男性汉族住院患者。患者和评估者对 MPGT 或常规治疗(TAU)随机化情况均不知情。
参与者以 1:1 的比例随机分配,接受 MPGT 或 TAU 治疗 12 周。
主要疗效结局是由重复测量混合模型的意向治疗改良分析得到的,从基线到第 6 周时 PANSS 总分(范围,30 至 210)的变化百分比。次要结局包括反应率和症状缓解率。
共有 210 名(平均[SD]年龄,29.2[8.8]岁)参与者入组并进行了分析,其中 113 名被分配至 MPGT 组,97 名被分配至 TAU 组。与接受 TAU 治疗的参与者相比,接受 MPGT 治疗的参与者的 PANSS 评分变化百分比显著更高(74.2%比 64.9%;调整后的平均差值,9.2 个百分点;95%CI,4.4-14.1 个百分点;P<0.001),第 6 周末的反应率也更高(113 名中的 93 名[82.3%]比 97 名中的 63 名[64.9%];调整后的优势比,2.48;95%CI,1.28-4.80;P=0.01)。
在这项 MPGT 的 RCT 中,MPGT 比 TAU 更有效地治疗精神分裂症患者。这些发现表明,多基因药物基因组学检测可以作为一种有效的工具,用于指导精神分裂症的治疗。
中国临床试验注册中心标识符:ChiCTR2000029671。