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<p>Treatment-resistant schizophrenia (TRS) poses a considerable challenge in psychiatric care, with approximately 10–60% of patients exhibiting non-responsiveness to antipsychotic medication. While early treatment could improve clinical outcomes, the absence of objective biomarkers hinders timely intervention. General structural changes have been suggestively associated with TRS. However, there is a lack of clear and robust conclusions due to challenges in obtaining data from TRS cases with large sample sizes. To address this knowledge gap, we collaborated with Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) consortium to investigate brain structural changes associated with TRS. Leveraging data from multiple institutions spanning various continents and ethnic groups, our meta- and mega-analysis revealed a significant reduction in the volume of bilateral putamen and bilateral hippocampus, as well as the left superior frontal gyrus (SFG) surface area in TRS patients compared with non-TRS patients with sufficient statistical power. Further analysis, incorporating data from healthy controls (HCs), unveiled a decreasing trend in bilateral hippocampal volumes and left SFG surface area from HCs to non-TRS patients and further to TRS patients. There were no significant effects of either clozapine dose or cumulative antipsychotic exposure on bilateral hippocampal volumes or left SFG surface area. In contrast, the putamen volume exhibited an increase in non-TRS patients compared with HCs, with no significant difference between TRS patients and HCs. Antipsychotic exposure was significantly correlated with the putamen volume with small effect size. In conclusion, this study underscores the volume of the hippocampus and SFG as potential biomarkers for TRS.</p>

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Brain structural abnormalities in treatment-resistant schizophrenia

  • 期刊论文

  • 发表日期：

    2026年3月28日

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  • Semra Etyemez,
  • Rohit Sivananthan,
  • Andreia V. Faria,
  • Felice Iasevoli,
  • Giuseppe Pontillo,
  • Annabella Di Giorgio,
  • Young-Chul Chung,
  • Woo-Sung Kim,
  • Soyolsaikhan Odkhuu,
  • Jun Soo Kwon,
  • Minah Kim,
  • Minji Ha,
  • Foivos Georgiadis,
  • Beatrice A. Milano,
  • Matthias Kirschner,
  • Stefan Kaiser,
  • Diana Tordesillas-Gutiérrez,
  • Kang Sim,
  • Yunlong Tan,
  • Sherry Kit Wa Chan,
  • Jessica A. Turner,
  • Theo G. M. van Erp,
  • Jimmy Lee,
  • Vince D. Calhoun,
  • Akira Sawa,
  • Kun Yang

摘要

Treatment-resistant schizophrenia (TRS) poses a considerable challenge in psychiatric care, with approximately 10–60% of patients exhibiting non-responsiveness to antipsychotic medication. While early treatment could improve clinical outcomes, the absence of objective biomarkers hinders timely intervention. General structural changes have been suggestively associated with TRS. However, there is a lack of clear and robust conclusions due to challenges in obtaining data from TRS cases with large sample sizes. To address this knowledge gap, we collaborated with Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) consortium to investigate brain structural changes associated with TRS. Leveraging data from multiple institutions spanning various continents and ethnic groups, our meta- and mega-analysis revealed a significant reduction in the volume of bilateral putamen and bilateral hippocampus, as well as the left superior frontal gyrus (SFG) surface area in TRS patients compared with non-TRS patients with sufficient statistical power. Further analysis, incorporating data from healthy controls (HCs), unveiled a decreasing trend in bilateral hippocampal volumes and left SFG surface area from HCs to non-TRS patients and further to TRS patients. There were no significant effects of either clozapine dose or cumulative antipsychotic exposure on bilateral hippocampal volumes or left SFG surface area. In contrast, the putamen volume exhibited an increase in non-TRS patients compared with HCs, with no significant difference between TRS patients and HCs. Antipsychotic exposure was significantly correlated with the putamen volume with small effect size. In conclusion, this study underscores the volume of the hippocampus and SFG as potential biomarkers for TRS.