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下采样模板曲线以加速LDDMM曲线并应用于胼胝体形状分析。

Down-sampling template curve to accelerate LDDMM-curve with application to shape analysis of the corpus callosum.

作者信息

Huang Weikai, Tang Xiaoying

机构信息

Department of Electrical and Electronic Engineering Southern University of Science and Technology Shenzhen Guangdong China.

出版信息

Healthc Technol Lett. 2021 May 2;8(3):78-83. doi: 10.1049/htl2.12011. eCollection 2021 Jun.

DOI:10.1049/htl2.12011
PMID:34035928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8136766/
Abstract

Large deformation diffeomorphic metric mapping for curve (LDDMM-curve) has been widely used in deformation based statistical shape analysis of the mid-sagittal corpus callosum. A main limitation of LDDMM-curve is that it is time-consuming and computationally complex. In this study, down-sampling strategies for accelerating LDDMM-curve are investigated and tested on two large datasets, one on Alzheimer's disease (155 Alzheimer's disease, 325 mild cognitive impairment and 185 healthy controls) and the other on first-episode schizophrenia (92 first-episode schizophrenia and 106 healthy controls). For both datasets a variety of down-sampling factors are tested in terms of registration accuracy, registration speed, and most importantly disease-related patterns. Experimental results revealed that down-sampling template curve by a factor of 2 can significantly reduce the running time of LDDMM-curve without sacrificing the registration accuracy. Also, the disease-induced patterns, or more specifically the group comparison results, were almost identical before and after down-sampling. It is also shown that there was no need to down-sample the target population curves but only the single template curve of the study of interest. Comprehensive analyses were conducted.

摘要

用于曲线的大变形微分同胚度量映射(LDDMM - 曲线)已广泛应用于基于变形的正中矢状胼胝体统计形状分析。LDDMM - 曲线的一个主要局限性在于它耗时且计算复杂。在本研究中,对加速LDDMM - 曲线的下采样策略进行了研究,并在两个大型数据集上进行了测试,一个数据集用于阿尔茨海默病(155例阿尔茨海默病患者、325例轻度认知障碍患者和185例健康对照),另一个数据集用于首发精神分裂症(92例首发精神分裂症患者和106例健康对照)。对于这两个数据集,在配准精度、配准速度以及最重要的疾病相关模式方面测试了多种下采样因子。实验结果表明,将模板曲线下采样2倍可显著减少LDDMM - 曲线的运行时间,同时不牺牲配准精度。此外,下采样前后疾病诱导模式,或者更具体地说,组间比较结果几乎相同。研究还表明,无需对目标人群曲线进行下采样,只需对感兴趣研究的单个模板曲线进行下采样即可。进行了综合分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/6e53e83ab9ff/HTL2-8-78-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/5b020111e28f/HTL2-8-78-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/f77fdb573858/HTL2-8-78-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/6e53e83ab9ff/HTL2-8-78-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/5b020111e28f/HTL2-8-78-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/f77fdb573858/HTL2-8-78-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/8136766/6e53e83ab9ff/HTL2-8-78-g003.jpg

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