Jixin Hou, Zhengwang Wu, Xianyan Chen, Dajiang Zhu, Tianming Liu, Gang Li, Xianqiao Wang
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These models were subsequently integrated into\ncomputational software to simulate cortical development with anatomically\nrealistic geometric models. We quantified the resulting folding patterns using\nmetrics such as mean curvature, sulcal depth, and gyrification index. Our\nresults demonstrate that regional growth models generate complex brain folding\npatterns that more closely match actual brains structures, both quantitatively\nand qualitatively, compared to uniform growth models. Growth magnitude plays a\ndominant role in shaping folding patterns, while growth trajectory has a minor\ninfluence. Moreover, multi-region models better capture the intricacies of\nbrain folding than single-region models. Our results underscore the necessity\nand importance of incorporating regional growth heterogeneity into brain\nfolding simulations, which could enhance early diagnosis and treatment of\ncortical malformations and neurodevelopmental disorders such as epilepsy and\nautism.","PeriodicalId":501572,"journal":{"name":"arXiv - QuanBio - Tissues and Organs","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Role of Data-driven Regional Growth Model in Shaping Brain Folding Patterns\",\"authors\":\"Jixin Hou, Zhengwang Wu, Xianyan Chen, Dajiang Zhu, Tianming Liu, Gang Li, Xianqiao Wang\",\"doi\":\"arxiv-2408.17334\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The surface morphology of the developing mammalian brain is crucial for\\nunderstanding brain function and dysfunction. 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引用次数: 0
摘要
发育中哺乳动物大脑的表面形态对于了解大脑功能和功能障碍至关重要。计算建模为早期大脑折叠的内在机制提供了宝贵的见解。以往的研究通常假定大脑是均匀生长的,但最近的研究结果表明,大脑组织的生长存在明显的区域性差异。然而,这些变化在大脑皮层发育中的作用仍不清楚。在这项研究中,我们探讨了区域性皮质生长如何影响大脑褶皱模式。我们首先利用 ML 辅助符号回归,基于 1000 多例婴儿核磁共振扫描的纵向数据,建立了典型皮质区域的生长模型,这些数据捕捉了围产期和出生后大脑发育过程中皮质的表面积和厚度。这些模型随后被整合到计算软件中,以解剖学上真实的几何模型模拟大脑皮层的发育过程。我们使用平均曲率、沟深度和回旋指数等指标对由此产生的褶皱模式进行了量化。我们的研究结果表明,与均匀生长模型相比,区域生长模型产生的复杂大脑褶皱模式在数量和质量上都更接近实际大脑结构。生长幅度在塑造褶皱模式中起主要作用,而生长轨迹的影响较小。此外,与单区域模型相比,多区域模型能更好地捕捉大脑折叠的复杂性。我们的研究结果凸显了将区域生长异质性纳入大脑折叠模拟的必要性和重要性,这可以提高对皮层畸形和神经发育疾病(如癫痫和自闭症)的早期诊断和治疗。
Role of Data-driven Regional Growth Model in Shaping Brain Folding Patterns
The surface morphology of the developing mammalian brain is crucial for
understanding brain function and dysfunction. Computational modeling offers
valuable insights into the underlying mechanisms for early brain folding. While
previous studies generally assume uniform growth, recent findings indicate
significant regional variations in brain tissue growth. However, the role of
these variations in cortical development remains unclear. In this study, we
explored how regional cortical growth affects brain folding patterns. We first
developed growth models for typical cortical regions using ML-assisted symbolic
regression, based on longitudinal data from over 1,000 infant MRI scans that
captured cortical surface area and thickness during perinatal and postnatal
brains development. These models were subsequently integrated into
computational software to simulate cortical development with anatomically
realistic geometric models. We quantified the resulting folding patterns using
metrics such as mean curvature, sulcal depth, and gyrification index. Our
results demonstrate that regional growth models generate complex brain folding
patterns that more closely match actual brains structures, both quantitatively
and qualitatively, compared to uniform growth models. Growth magnitude plays a
dominant role in shaping folding patterns, while growth trajectory has a minor
influence. Moreover, multi-region models better capture the intricacies of
brain folding than single-region models. Our results underscore the necessity
and importance of incorporating regional growth heterogeneity into brain
folding simulations, which could enhance early diagnosis and treatment of
cortical malformations and neurodevelopmental disorders such as epilepsy and
autism.