Reappraising the variability of effects of antipsychotic medication in schizophrenia: a meta-analysis

被引:32
|
作者
McCutcheon, Robert A. [1 ,2 ,3 ]
Pillinger, Toby [1 ,2 ,3 ]
Efthimiou, Orestis [4 ,8 ]
Maslej, Marta [5 ]
Mulsant, Benoit H. [6 ,7 ]
Young, Allan H. [8 ]
Cipriani, Andrea [9 ,10 ]
Howes, Oliver D. [2 ,3 ,8 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, London, England
[2] Imperial Coll London, Hammersmith Hosp, MRC London Inst Med Sci, Psychiat Imaging Grp, London, England
[3] Imperial Coll London, Fac Med, Inst Clin Sci, London, England
[4] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[5] Ctr Addict & Mental Hlth, Krembil Ctr Neuroinformat, Toronto, ON, Canada
[6] Ctr Addict & Mental Hlth, Toronto, ON, Canada
[7] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[8] Kings Coll London, Dept Psychol Med, Inst Psychiat Psychol & Neurosci, London, England
[9] Univ Oxford, Dept Psychiat, Oxford, England
[10] Warneford Hosp, Oxford Hlth NHS Fdn Trust, Oxford, England
基金
美国国家卫生研究院; 瑞士国家科学基金会; 英国医学研究理事会; 加拿大健康研究院; 英国惠康基金;
关键词
Antipsychotic medication; schizophrenia; variability of effects; medication-specific effects; non-specific effects; placebo response; treatment effect heterogeneity; personalization of treatment; precision medicine; CLINICAL CHARACTERIZATION; ADULT PATIENT; PERSONALIZATION; DEPRESSION;
D O I
10.1002/wps.20977
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
It is common experience for practising psychiatrists that individuals with schizophrenia vary markedly in their symptomatic response to antipsychotic medication. What is not clear, however, is whether this variation reflects variability of medication-specific effects (also called "treatment effect heterogeneity"), as opposed to variability of non-specific effects such as natural symptom fluctuation or placebo response. Previous meta-analyses found no evidence of treatment effect heterogeneity, suggesting that a "one size fits all" approach may be appropriate and that efforts at developing personalized treatment strategies for schizophrenia are unlikely to succeed. Recent advances indicate, however, that earlier approaches may have been unable to accurately quantify treatment effect heterogeneity due to their neglect of a key parameter: the correlation between placebo response and medication-specific effects. In the present paper, we address this shortcoming by using individual patient data and study-level data to estimate that correlation and quantitatively characterize antipsychotic treatment effect heterogeneity in schizophrenia. Individual patient data (on 384 individuals who were administered antipsychotic treatment and 88 who received placebo) were obtained from the Yale University Open Data Access (YODA) database. Study-level data were obtained from a meta-analysis of 66 clinical trials including 17,202 patients. Both individual patient and study-level analyses yielded a negative correlation between placebo response and treatment effect for the total score on the Positive and Negative Syndrome Scale (PANSS) (rho=-0.32, p=0.002 and rho=-0.39, p<0.001, respectively). Using the most conservative of these estimates, a meta-analysis of treatment effect heterogeneity provided evidence of a marked variability in antipsychotic-specific effects between individuals with schizophrenia, with the top quartile of patients experiencing beneficial treatment effects of 17.7 points or more on the PANSS total score, while the bottom quartile presented a detrimental effect of treatment relative to placebo. This evidence of clinically meaningful treatment effect heterogeneity suggests that efforts to personalize antipsychotic treatment of schizophrenia have potential for success.
引用
收藏
页码:287 / 294
页数:8
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