TARGETED PRINCIPLE COMPONENT ANALYSIS: A NEW MOTION ARTIFACT CORRECTION APPROACH FOR NEAR-INFRARED SPECTROSCOPY.

IF 2.3 3区 医学 Q2 OPTICS
Meryem A Yücel, Juliette Selb, Robert J Cooper, David A Boas
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引用次数: 96

Abstract

As near-infrared spectroscopy (NIRS) broadens its application area to different age and disease groups, motion artifacts in the NIRS signal due to subject movement is becoming an important challenge. Motion artifacts generally produce signal fluctuations that are larger than physiological NIRS signals, thus it is crucial to correct for them before obtaining an estimate of stimulus evoked hemodynamic responses. There are various methods for correction such as principle component analysis (PCA), wavelet-based filtering and spline interpolation. Here, we introduce a new approach to motion artifact correction, targeted principle component analysis (tPCA), which incorporates a PCA filter only on the segments of data identified as motion artifacts. It is expected that this will overcome the issues of filtering desired signals that plagues standard PCA filtering of entire data sets. We compared the new approach with the most effective motion artifact correction algorithms on a set of data acquired simultaneously with a collodion-fixed probe (low motion artifact content) and a standard Velcro probe (high motion artifact content). Our results show that tPCA gives statistically better results in recovering hemodynamic response function (HRF) as compared to wavelet-based filtering and spline interpolation for the Velcro probe. It results in a significant reduction in mean-squared error (MSE) and significant enhancement in Pearson's correlation coefficient to the true HRF. The collodion-fixed fiber probe with no motion correction performed better than the Velcro probe corrected for motion artifacts in terms of MSE and Pearson's correlation coefficient. Thus, if the experimental study permits, the use of a collodion-fixed fiber probe may be desirable. If the use of a collodion-fixed probe is not feasible, then we suggest the use of tPCA in the processing of motion artifact contaminated data.

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目标主成分分析:一种新的近红外光谱运动伪影校正方法。
随着近红外光谱(NIRS)的应用范围越来越广,涉及到不同年龄和疾病人群,近红外光谱信号中由于受试者运动而产生的运动伪影成为一个重要的挑战。运动伪影通常会产生比生理近红外光谱信号更大的信号波动,因此在获得刺激引起的血流动力学反应的估计之前对它们进行校正是至关重要的。校正方法有主成分分析(PCA)、小波滤波和样条插值等。在这里,我们引入了一种新的运动伪影校正方法,即目标主成分分析(tPCA),该方法仅在识别为运动伪影的数据段上集成PCA滤波器。预计这将克服过滤期望信号的问题,这些问题困扰着整个数据集的标准PCA过滤。我们将新方法与最有效的运动伪影校正算法进行了比较,这些算法同时获得了一组数据,这些数据是由胶定探针(低运动伪影含量)和标准尼龙搭扣探针(高运动伪影含量)获得的。我们的研究结果表明,与基于小波滤波和样条插值的Velcro探针相比,tPCA在恢复血流动力学响应函数(HRF)方面具有统计学上更好的结果。它导致均方误差(MSE)的显著降低和Pearson相关系数对真实HRF的显著增强。在MSE和Pearson相关系数方面,没有运动校正的胶体固定纤维探针比运动伪影校正的尼龙搭扣探针表现更好。因此,如果实验研究允许,使用胶固纤维探针可能是可取的。如果使用胶体固定探针是不可行的,那么我们建议使用tPCA来处理运动伪影污染的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Innovative Optical Health Sciences
Journal of Innovative Optical Health Sciences OPTICS-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
4.50
自引率
20.00%
发文量
69
审稿时长
>12 weeks
期刊介绍: JIOHS serves as an international forum for the publication of the latest developments in all areas of photonics in biology and medicine. JIOHS will consider for publication original papers in all disciplines of photonics in biology and medicine, including but not limited to: -Photonic therapeutics and diagnostics- Optical clinical technologies and systems- Tissue optics- Laser-tissue interaction and tissue engineering- Biomedical spectroscopy- Advanced microscopy and imaging- Nanobiophotonics and optical molecular imaging- Multimodal and hybrid biomedical imaging- Micro/nanofabrication- Medical microsystems- Optical coherence tomography- Photodynamic therapy. JIOHS provides a vehicle to help professionals, graduates, engineers, academics and researchers working in the field of intelligent photonics in biology and medicine to disseminate information on the state-of-the-art technique.
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