The neonatal cortical surface is known to be affected by preterm birth, and the subsequent changes to cortical organisation have been associated with poorer neurodevelopmental outcomes. Deep Generative models have the potential to lead to clinically interpretable models of disease, but developing these on the cortical surface is challenging since established techniques for learning convolutional filters are inappropriate on non-flat topologies. To close this gap, we implement a surface-based CycleGAN using mixture model CNNs (MoNet) to translate sphericalised neonatal cortical surface features (curvature and T1w/T2w cortical myelin) between different stages of cortical maturity. Results show our method is able to reliably predict changes in individual patterns of cortical organisation at later stages of gestation, validated by comparison to longitudinal data; and translate appearance between preterm and term gestation (> 37 weeks gestation), validated through comparison with a trained term/preterm classifier. Simulated differences in cortical maturation are consistent with observations in the literature.
翻译:已知新生儿皮质表面会受到早产的影响,随后对皮质组织的变化与神经发育效果较差有关。深基因模型有可能导致临床可解释的疾病模型,但在皮质表面开发这些模型具有挑战性,因为学习进化过滤器的既定技术不适合非负式表层。为了缩小这一差距,我们使用混合物模型CNN(MoNet)实施地表基循环GAN系统,将球状新生儿皮质组织特征(精密和T1w/T2w/T2皮皮质近灵)翻译在不同阶段的成熟期之间。结果显示,我们的方法能够可靠地预测妊娠后期各个皮质组织模式的变化,并通过与长视数据进行比较加以验证;将妊娠期前和学期的外观( > 37周妊娠期)进行翻译,并与经过培训的术语/预变分解器进行比较加以验证。 皮质畸形的模拟差异与文献中的观察结果是一致的。