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利用近红外光谱(NIRS)技术在健康志愿者的肌肉组织中对细胞色素 C 氧化酶模式进行定量评估。

Quantitative assessment of cytochrome C oxidase patterns in muscle tissue by the use of near-infrared spectroscopy (NIRS) in healthy volunteers.

机构信息

Department of Anaesthesia, UZ Ghent, Corneel Heymanslaan 10, 9000, Ghent, Belgium.

Department of Anaesthesia, ASZ Aalst, Aalst, Belgium.

出版信息

J Clin Monit Comput. 2022 Feb;36(1):271-278. doi: 10.1007/s10877-021-00648-6. Epub 2021 Jan 18.

DOI:10.1007/s10877-021-00648-6
PMID:33459945
Abstract

Cytochrome C oxidase (CCO) acts as final electron acceptor in the respiratory chain, possibly providing information concerning cellular oxygenation. CCO is a chromophore with a broad absorption peak in the near-infrared spectrum in its reduced state (835 nm). However, this peak overlaps with deoxygenated haemoglobin (HHb; 755 nm) which is present in much higher concentrations. NIRO-300 measures CCO signals, but did not receive FDA approval for this use due to presumed lack of independency of the measured CCO changes. However, there is no proven evidence for this assumption. We hypothesized that the NIRO-300 provides a HHb independent measurement of CCO concentration changes. In this single-center crossover randomized controlled trial in healthy volunteers, subjects were randomized to receive arterial occlusion to the left arm and venous stasis on the right arm (n = 5) or vice versa (n = 5) during 5 min. After a resting period, the second part of the cross over study was performed. We placed the NIRO-300 optodes bilateral at the level of the brachioradial muscle in order to collect NIRS data continuously. Data was analysed using a generalized additive mixed model. HHb and CCO follow a significant different trend over time during the intervention period for both arterial occlusion (F = 20.645, edf = 3.419, p < 0.001) and venous stasis (F = 9.309, edf = 4.931, p < 0.001). Our data indicate that CCO concentration changes were not affected by HHb changes, thereby proving independency.Clinical trial registration: B670201732023 on June 28, 2017.

摘要

细胞色素 C 氧化酶(CCO)作为呼吸链中的最终电子受体,可能提供有关细胞氧合的信息。CCO 在还原状态下具有近红外光谱中的宽吸收峰(835nm),是一种生色团。然而,该峰与存在浓度高得多的去氧血红蛋白(HHb;755nm)重叠。NIRO-300 可测量 CCO 信号,但由于所测量的 CCO 变化缺乏独立性,未获得 FDA 对此用途的批准。然而,没有证据证明这一假设。我们假设 NIRO-300 提供了一种 HHb 独立的 CCO 浓度变化测量方法。在这项健康志愿者的单中心交叉随机对照试验中,受试者被随机分配在 5 分钟内接受左手臂动脉阻塞和右臂静脉淤滞(n=5)或反之亦然(n=5)。休息一段时间后,进行交叉研究的第二部分。我们将 NIRO-300 光极双侧放置在肱桡肌水平,以便连续收集 NIRS 数据。使用广义加性混合模型分析数据。在干预期间,HHb 和 CCO 随时间呈现出明显不同的趋势,对于动脉阻塞(F=20.645,edf=3.419,p<0.001)和静脉淤滞(F=9.309,edf=4.931,p<0.001)都是如此。我们的数据表明,CCO 浓度变化不受 HHb 变化的影响,从而证明了独立性。临床试验注册:B670201732023 于 2017 年 6 月 28 日。

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