Progress in Neuro-Psychopharmacology and Biological PsychiatryNeurosciencePeer-reviewed journal article
Neurodevelopmental deviations in schizophrenia: Evidences from multimodal connectome-based brain ages
Yun‐Shuang FaniD, Pengfei YangiD, Yucheng ZhuiD, Wenfeng Jing, Yuting XuiD, Yong Xu, Jing GuoiD, Fengmei LuiD, Mi YangiD, Wei HuangiD, Huafu CheniD
Abstract
BackgroundPathologic schizophrenia process originate early in brain development, leading to detectable brain alterations via structural and functional magnetic resonance imaging (MRI). Recent MRI studies have sought to characterize disease effects from a brain age perspective, but developmental deviations from the typical brain age trajectory in youths with schizophrenia remain unestablished. AimThis study investigated brain development deviations in early-onset schizophrenia (EOS) patients by applying machine learning algorithms to structural and functional MRI data. MethodsMultimodal MRI data, including T1-weighted MRI (T1w-MRI), diffusion MRI, and resting-state functional MRI (rs-fMRI) data, were collected from 80 antipsychotic-naive first-episode EOS patients and 91 typically developing (TD) controls. The morphometric similarity connectome (MSC), structural connectome (SC), and functional connectome (FC) were separately constructed by using these three modalities. According to these connectivity features, eight brain age estimation models were first trained with the TD group, the best of which was then used to predict brain ages in patients. Individual brain age gaps (BAGs) were assessed as brain ages minus chronological ages. ResultsBoth the SC and MSC features performed well in brain age estimation, whereas the FC features did not. Compared with the TD controls, the EOS patients presented widened structural BAGs, with opposite trends between childhood and adolescence. These increased absolute BAG scores for EOS patients were positively correlated with the severity of their clinical symptoms. ConclusionThese findings from a multimodal brain age perspective suggest that advanced BAGs exist early in youths with schizophrenia.
- organism: human
- assay: bulk RNA-seq
- assay: multiome
- research focus: benchmarking
- approach: machine learning (classical)
- Citations
- 2
- FWCI
- 1.13
- Field percentile
- top 22%
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