利用鼻腔呼吸气流区分帕金森病患者和健康对照组

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Communications medicine Pub Date : 2024-11-14 DOI:10.1038/s43856-024-00660-2
Michal Andelman-Gur, Kobi Snitz, Danielle Honigstein, Aharon Weissbrod, Timna Soroka, Aharon Ravia, Lior Gorodisky, Liron Pinchover, Adi Ezra, Neomi Hezi, Tanya Gurevich, Noam Sobel
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引用次数: 0

摘要

背景:呼吸模式可为健康提供信息。我们注意到,帕金森病(PD)最早的脑损伤部位是呼吸的神经起搏器。因此,我们假设帕金森病患者呼吸的长期时间动态可能会发生改变:我们在 28 名帕金森氏症患者(多数为 H&Y II 期)和 33 名匹配的健康对照者身上应用了一种可穿戴设备,该设备可精确记录鼻腔气流的时间变化。结果:我们观察到鼻气流的时间模式发生了显著变化:我们观察到,与匹配的对照组相比,帕金森病患者鼻腔气流的时间模式发生了明显改变,吸气时间更长,变化更少(平均帕金森病患者 = -1.22 ± 1.9(呼吸特征综合评分),对照组 = 1.04 ± 2.16,Wilcoxon 秩和检验,z = -4.1,效应大小 Cliff's δ = -0.61,95% 置信区间 = -0.79 - (-0.34),P = 4.3 × 10-5)。这种改变的程度使我们仅用 30 分钟的记录就能以 87% 的准确率(AUC = 0.85,79% 的灵敏度(28 例中的 22 例),94% 的特异性(33 例中的 31 例),z = 5.7,P = 3.5 × 10-9)检测出帕金森病,并预测疾病的严重程度(与 UPDRS-Total 评分的相关性:r = 0.49;P = 0.008):我们的结论是,呼吸模式在疾病级联过程中会因 H&Y II 期而改变,我们的方法将来可能会进一步改进,以提供具有诊断和预后价值的指示。
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Discriminating Parkinson’s disease patients from healthy controls using nasal respiratory airflow
Breathing patterns may inform on health. We note that the sites of earliest brain damage in Parkinson’s disease (PD) house the neural pace-makers of respiration. We therefore hypothesized that ongoing long-term temporal dynamics of respiration may be altered in PD. We applied a wearable device that precisely logs nasal airflow over time in 28 PD patients (mostly H&Y stage-II) and 33 matched healthy controls. Each participant wore the device for 24 h of otherwise routine daily living. We observe significantly altered temporal patterns of nasal airflow in PD, where inhalations are longer and less variable than in matched controls (mean PD = −1.22 ± 1.9 (combined respiratory features score), Control = 1.04 ± 2.16, Wilcoxon rank-sum test, z = −4.1, effect size Cliff’s δ = −0.61, 95% confidence interval = −0.79 – (−0.34), P = 4.3 × 10−5). The extent of alteration is such that using only 30 min of recording we detect PD at 87% accuracy (AUC = 0.85, 79% sensitivity (22 of 28), 94% specificity (31 of 33), z = 5.7, p = 3.5 × 10−9), and also predict disease severity (correlation with UPDRS-Total score: r = 0.49; P = 0.008). We conclude that breathing patterns are altered by H&Y stage-II in the disease cascade, and our methods may be further refined in the future to provide an indication with diagnostic and prognostic value. Andelman-Gur et al. use a nasal airflow monitoring device to detect alterations of respiratory dynamics in patients with Parkinson’s Disease. They reveal longer, but less variable, inhalations and show that changes in airflow dynamics are correlated with disease severity, plus 30 min of data is adequate to discriminate patients from controls. In its earliest stages, Parkinson’s disease damages the parts of the brain that control breathing. We built a small device that measures airflow patterns through the nose over time. People with Parkinson’s disease and healthy individuals wore this device for 24 h. We found that nasal inhalations in Parkinson’s patients were longer and less variable than in healthy individuals. This difference was so pronounced that, using only 30 min of recording, we could accurately determine most people who had Parkinson’s disease and how severe their disease was. Future studies will determine whether this tool can contribute to early diagnosis, and it may be useful to monitor disease progression.
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