Indian Council of Medical Research - Centre for Ageing and Mental Health, Kolkata, India.
Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
BMC Psychiatry. 2024 Oct 8;24(1):663. doi: 10.1186/s12888-024-06104-4.
Pharmacogenomic (PGx) factors significantly influence how patients respond to antipsychotic medications This systematic review was performed to synthesize the clinical utility of PGx-assisted treatment versus standard of care in schizophrenia.
PubMed, Embase, and Cochrane CENTRAL databases were searched for randomized controlled trials (RCTs) from inception till June 2024 that had compared the clinical utility of PGx-assisted intervention as compared to the standard of care in schizophrenia. The primary outcome was safety, and the secondary outcomes were efficacy and medication adherence. Pooled standardized mean differences (SMD) along with a 95% confidence interval (CI) were calculated (random-effects model) wherever feasible.
A total of 18,821 studies were screened, and five were included for review. All the RCTs had a high risk of bias. Four studies included the commonly used antipsychotics. Three studies reported negative outcomes (safety, efficacy, and medication adherence) and two reported positive outcomes (safety) using different scales. In the meta-analysis, there were significant differences in the total Udvalg for Kliniske Undersogelser Side-Effect Rating scale score [SMD 0.95 (95% CI: 0.76-1.13), p < 0.001); I = 0%] and the total Positive and Negative Syndrome Scale score [SMD 10.65 (95% CI: 2.37-18.93), p = 0.01); I = 100%] between the PGx-assisted treatment and standard of care arms. However, the results were inconsistent, and the certainty of evidence (GRADE criteria) was very low.
Current evidence on the clinical utility of PGx-assisted treatment in schizophrenia is limited and inconsistent and further evidence is required in this regard.
药物基因组学(PGx)因素显著影响患者对抗精神病药物的反应。本系统评价旨在综合比较精神分裂症患者接受 PGx 辅助治疗与标准治疗的临床效果。
检索 PubMed、Embase 和 Cochrane CENTRAL 数据库,纳入截至 2024 年 6 月比较 PGx 辅助干预与精神分裂症标准治疗临床效果的随机对照试验(RCT)。主要结局为安全性,次要结局为疗效和药物依从性。若可行,采用随机效应模型计算标准化均数差值(SMD)及其 95%置信区间。
共筛选出 18821 项研究,纳入 5 项研究进行综述。所有 RCT 均存在高偏倚风险。四项研究纳入了常用的抗精神病药物。三项研究报告了阴性结局(安全性、疗效和药物依从性),两项研究使用不同的量表报告了阳性结局(安全性)。Meta 分析结果显示,总 Udvalg for Kliniske Undersogelser 副作用评定量表评分[SMD 0.95(95%CI:0.76-1.13),p<0.001);I²=0%]和阳性与阴性综合征量表总分[SMD 10.65(95%CI:2.37-18.93),p=0.01);I²=100%]在 PGx 辅助治疗与标准治疗组之间存在显著差异。然而,结果不一致,证据确定性(GRADE 标准)非常低。
目前关于精神分裂症患者接受 PGx 辅助治疗的临床效果的证据有限且不一致,需要进一步研究。