Magnetic resonance imaging–based machine learning classification of schizophrenia spectrum disorders: a meta‐analysis

神经影像学 单变量 精神分裂症(面向对象编程) 多元统计 荟萃分析 功能磁共振成像 多元分析 置信区间 心理学 二元分析 人工智能 医学 机器学习 内科学 计算机科学 精神科 神经科学
作者
Fabio Di Camillo,David Antonio Grimaldi,Giulia Cattarinussi,Annabella Di Giorgio,Clara Locatelli,Adyasha Khuntia,Paolo Enrico,Paolo Brambilla,Nikolaos Koutsouleris,Fabio Sambataro
出处
期刊:Psychiatry and Clinical Neurosciences [Wiley]
被引量:6
标识
DOI:10.1111/pcn.13736
摘要

Background Recent advances in multivariate pattern recognition have fostered the search for reliable neuroimaging‐based biomarkers in psychiatric conditions, including schizophrenia. These approaches consider the complex pattern of alterations in brain function and structure, overcoming the limitations of traditional univariate methods. To assess the reliability of neuroimaging‐based biomarkers and the contribution of study characteristics in distinguishing individuals with schizophrenia spectrum disorder (SSD) from healthy controls (HCs), we conducted a systematic review of the studies that used multivariate pattern recognition for this objective. Methods We systematically searched PubMed, Scopus, and Web of Science for studies on SSD classification using multivariate pattern analysis on magnetic resonance imaging data. We employed a bivariate random‐effects meta‐analytic model to explore the classification of sensitivity (SE) and specificity (SP) across studies while also evaluating the moderator effects of clinical and non‐clinical variables. Results A total of 119 studies (with 12,723 patients with SSD and 13,196 HCs) were identified. The meta‐analysis estimated a SE of 79.1% (95% confidence interval [CI], 77.1%–81.0%) and a SP of 80.0% (95% CI, 77.8%–82.0%). In particular, the Positive and Negative Syndrome Scale and the Global Assessment of Functioning scores, age, age of onset, duration of untreated psychosis, deep learning, algorithm type, features selection, and validation methods had significant effects on classification performance. Conclusions Multivariate pattern analysis reliably identifies neuroimaging‐based biomarkers of SSD, achieving ∼80% SE and SP. Despite clinical heterogeneity, discernible brain modifications effectively differentiate SSD from HCs. Classification performance depends on patient‐related and methodological factors crucial for the development, validation, and application of prospective models in clinical settings.
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