基于变化点检测的鲁棒信号处理通用方法:了解子痫前期机制的应用。

IF 3.8 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Patricio Cumsille, Felipe Troncoso, Hermes Sandoval, Jesenia Acurio, Carlos Escudero
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引用次数: 0

摘要

在阐明子痫前期潜在机制的激励下,我们开发了一种基于变化点检测的通用和通用方法,可应用于任何实验模型,有效地解决了实验干预产生的高不确定性、内在的高可变性以及灌注信号快速和突然变化的时间动态带来的挑战。该方法为鲁棒灌注信号分析提供了系统可靠的方法。该方法的主要创新是一个由模块化编程组件组成的高效自动数据处理系统。这些组件包括一个信号处理工具,通过分离灌注信号对实验干预的“真实”血管反应来优化灌注信号的分割,以及一个新的和合适的归一化工具,以评估实验参考状态(通常是基础或干预前)的反应。通过这种方式,我们可以通过分解实验干预后过渡期间的噪声来识别实验组与对照组的异常情况。我们已经成功地将我们的一般方法应用于我们研究组开发的子痫前期样综合征模型的灌注信号测量。我们的研究结果显示子痫前期后代的脑灌注受损,特别是脑灌注信号功能障碍,对热物理刺激的灌注信号血管反应性不足。这种通用的方法是朝着系统、准确和可靠的方法迈出的重要一步,可以跨不同的实验设置和不同的干预方案进行鲁棒灌注信号分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Changepoint Detection-Based General Methodology for Robust Signal Processing: An Application to Understand Preeclampsia's Mechanisms.

Motivated by illuminating the underlying mechanisms of preeclampsia, we develop a changepoint detection-based general and versatile methodology that can be applied to any experimental model, effectively addressing the challenges of high uncertainty produced by experimental interventions, intrinsic high variability, and rapidly and abruptly varying time dynamics in perfusion signals. This methodology provides a systematic and reliable approach for robust perfusion signal analysis. The main innovation of our methodology is a highly efficient automatic data processing system consisting of modular programming components. These components include a signal processing tool for optimal segmentation of perfusion signals by isolating their "genuine" vascular response to experimental interventions, and a novel and suitable normalization to evaluate this response concerning an experimental reference state, typically basal or pre-intervention. In this way, we can identify anomalies in an experimental group compared to a control group by disaggregating noise during the transitions just after experimental interventions. We have successfully applied our general methodology to perfusion signals measured from a preeclampsia-like syndrome model developed by our research group. Our findings revealed impaired brain perfusion in offspring from preeclampsia, particularly dysfunctional brain perfusion signals with inadequate perfusion signal vasoreactivity to thermal physical stimuli. This general methodology represents a significant step towards a systematic, accurate, and reliable approach to robust perfusion signals analysis across various experimental settings with diverse intervention protocols.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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