Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Melbourne Health, Melbourne, VIC, Australia.
Department of Biomedical Engineering, The University of Melbourne, Melbourne, VIC, Australia.
Mol Psychiatry. 2021 Jul;26(7):3512-3523. doi: 10.1038/s41380-020-00882-5. Epub 2020 Sep 22.
The heterogeneity of schizophrenia has defied efforts to derive reproducible and definitive anatomical maps of structural brain changes associated with the disorder. We aimed to map deviations from normative ranges of brain structure for individual patients and evaluate whether the loci of individual deviations recapitulated group-average brain maps of schizophrenia pathology. For each of 48 white matter tracts and 68 cortical regions, normative percentiles of variation in fractional anisotropy (FA) and cortical thickness (CT) were established using diffusion-weighted and structural MRI from healthy adults (n = 195). Individuals with schizophrenia (n = 322) were classified as either within the normative range for healthy individuals of the same age and sex (5-95% percentiles), infra-normal (<5% percentile) or supra-normal (>95% percentile). Repeating this classification for each tract and region yielded a deviation map for each individual. Compared to the healthy comparison group, the schizophrenia group showed widespread reductions in FA and CT, involving virtually all white matter tracts and cortical regions. Paradoxically, however, no more than 15-20% of patients deviated from the normative range for any single tract or region. Furthermore, 79% of patients showed infra-normal deviations for at least one locus (healthy individuals: 59 ± 2%, p < 0.001). Thus, while infra-normal deviations were common among patients, their anatomical loci were highly inconsistent between individuals. Higher polygenic risk for schizophrenia associated with a greater number of regions with infra-normal deviations in CT (r = -0.17, p = 0.006). We conclude that anatomical loci of schizophrenia-related changes are highly heterogeneous across individuals to the extent that group-consensus pathological maps are not representative of most individual patients. Normative modeling can aid in parsing schizophrenia heterogeneity and guiding personalized interventions.
精神分裂症的异质性使得人们难以得出与该疾病相关的结构性脑变化的可重复和明确的解剖图谱。我们旨在为个体患者绘制偏离正常脑结构范围的图谱,并评估个体偏差的位置是否能重现精神分裂症病理的群体平均脑图谱。对于 48 条白质束和 68 个皮质区域,我们使用来自健康成年人的弥散加权和结构 MRI 建立了各向异性分数 (FA) 和皮质厚度 (CT) 的正常百分位数变异范围(n=195)。将精神分裂症患者(n=322)分为与同年龄和同性别健康个体的正常范围(5-95%百分位数)内、低于正常(<5%百分位数)或高于正常(>95%百分位数)。对每个束和区域重复此分类,为每个个体生成一个偏差图。与健康对照组相比,精神分裂症组显示出广泛的 FA 和 CT 减少,几乎涉及所有白质束和皮质区域。然而,矛盾的是,只有 15-20%的患者在任何单个束或区域偏离正常范围。此外,79%的患者至少有一个部位的 FA 低于正常(健康个体:59±2%,p<0.001)。因此,虽然在患者中,低于正常的偏差很常见,但它们的解剖位置在个体之间高度不一致。精神分裂症的多基因风险与 CT 中低于正常的区域数量呈正相关(r=-0.17,p=0.006)。我们得出结论,精神分裂症相关变化的解剖位置在个体之间存在高度异质性,以至于群体共识的病理图谱不能代表大多数个体患者。正常模型可以帮助解析精神分裂症的异质性并指导个性化干预。