Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital of Sichuan University, Chengdu, China.
Hope Recovery and Rehabilitation Center, West China Hospital of Sichuan University, Chengdu, China.
Schizophr Bull. 2023 May 3;49(3):697-705. doi: 10.1093/schbul/sbad043.
Early prediction of treatment response to antipsychotics in schizophrenia remains a challenge in clinical practice. This study aimed to investigate if brain morphometries including gray matter volume and cortical thickness could serve as potential predictive biomarkers in first-episode schizophrenia.
Sixty-eight drug-naïve first-episode patients underwent baseline structural MRI scans and were subsequently randomized to receive a single antipsychotic throughout the first 12 weeks. Assessments for symptoms and social functioning were conducted by eight "core symptoms" selected from the Positive and Negative Syndrome Scale (PANSS-8) and the Personal and Social performance scale (PSP) multiple times during follow-ups. Treatment outcome was evaluated as subject-specific slope coefficients for PANSS-8 and PSP scores using linear mixed model. LASSO regression model were conducted to examine the performance of baseline gray matter volume and cortical thickness in prediction of individualized treatment outcome.
The study showed that individual brain morphometries at baseline, especially the orbitofrontal, temporal and parietal cortex, pallidum and amygdala, significantly predicted 12-week treatment outcome of PANSS-8 (r[predicted vs observed] = 0.49, P = .001) and PSP (r[predicted vs observed] = 0.40, P = .003) in first-episode schizophrenia. Moreover, the gray matter volume performed better than cortical thickness in the prediction the symptom changes (P = .034), while cortical thickness outperformed gray matter volume in the prediction of outcome of social functioning (P = .029).
These findings provide initial evidence that brain morphometry have potential to be used as prognostic predictors for antipsychotic response in patients, encouraging the future investigation of the translational value of these measures in precision psychiatry.
精神分裂症患者对抗精神病药物治疗反应的早期预测在临床实践中仍然是一个挑战。本研究旨在探讨首发精神分裂症患者的脑形态是否可以作为潜在的预测生物标志物。
68 名未经药物治疗的首发精神分裂症患者接受基线结构 MRI 扫描,随后随机分为在头 12 周内接受单一抗精神病药物治疗。通过从阳性和阴性症状量表(PANSS-8)和个人和社会表现量表(PSP)中选择的 8 个“核心症状”,在随访期间多次对症状和社会功能进行评估。使用线性混合模型,通过 PANSS-8 和 PSP 评分的个体斜率系数评估治疗效果。使用 LASSO 回归模型来检验基线灰质体积和皮质厚度在预测个体化治疗效果中的表现。
研究表明,基线时的个体脑形态,尤其是眶额、颞叶和顶叶皮层、苍白球和杏仁核,显著预测了首发精神分裂症患者 12 周时的 PANSS-8(r[预测值与观察值之比] = 0.49,P =.001)和 PSP(r[预测值与观察值之比] = 0.40,P =.003)的治疗效果。此外,灰质体积在预测症状变化方面优于皮质厚度(P =.034),而皮质厚度在预测社会功能结局方面优于灰质体积(P =.029)。
这些发现初步表明,脑形态学具有作为预测抗精神病药物反应的预后生物标志物的潜力,鼓励未来研究这些措施在精准精神病学中的转化价值。