声音作为生物标志物:声带良恶性病变的探索性分析。

IF 3.2 Q1 HEALTH CARE SCIENCES & SERVICES
Frontiers in digital health Pub Date : 2025-08-12 eCollection Date: 2025-01-01 DOI:10.3389/fdgth.2025.1609811
Phillip Jenkins, Rylan Harrison, Steven Bedrick, Lisa Karstens, William Hersh
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引用次数: 0

摘要

良性和恶性声带病变可以改变声音质量,并导致显著的发病率,或在恶性的情况下,死亡。使用语音作为生物标志物,对这些病变进行早期、无创的识别,可能会改善诊断的可及性和结果。在这项研究中,我们分析了最初发布的Bridge2AI-Voice数据集的数据,以评估哪些声学特征最能区分喉癌和良性声带病变与其他声带病变和健康语音功能。七个诊断队列被分为两个分析:第一个包括喉癌、良性病变或无声音障碍的参与者;第二组包括喉癌患者或无其他声音障碍的良性病变患者,以及痉挛性发声障碍或声带麻痹患者。从标准化的语音记录中提取声学特征,包括基频、抖动、闪烁和谐波噪声比(HNR),并使用非参数统计方法进行比较。在整个样本中,良性病变与健康对照和喉癌之间的HNR和基频存在显著差异。在顺性别男性中,也观察到这些差异,特别是在HNR及其变异性中。在顺性别女性中没有观察到统计学上的显著差异,可能是由于样本量有限。这些发现表明,HNR,特别是其可变性,可能有望作为早期发现和监测声带病变的基于声音的标志物。需要对更大、更多样化的人群进行进一步的研究,以完善这些特征并验证其临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Voice as a biomarker: exploratory analysis for benign and malignant vocal fold lesions.

Voice as a biomarker: exploratory analysis for benign and malignant vocal fold lesions.

Benign and malignant vocal fold lesions can alter voice quality and lead to significant morbidity or, in the case of malignancy, mortality. Early, noninvasive identification of these lesions using voice as a biomarker may improve diagnostic access and outcomes. In this study, we analyzed data from the initial release of the Bridge2AI-Voice dataset to evaluate which acoustic features best distinguish laryngeal cancer and benign vocal fold lesions from other vocal pathologies and healthy voice function. Seven diagnostic cohorts were grouped into two analyses: the first included participants with laryngeal cancer, benign lesions, or no voice disorder; the second included those with laryngeal cancer or benign lesions without other voice disorders, as well as individuals with spasmodic dysphonia or vocal fold paralysis. Acoustic features including fundamental frequency, jitter, shimmer, and harmonic-to-noise ratio (HNR) were extracted from standardized speech recordings and compared using nonparametric statistical methods. Among the overall sample, significant differences were identified in HNR and fundamental frequency between benign lesions and both healthy controls and laryngeal cancer. In cisgender men, these distinctions were also observed, particularly in HNR and its variability. No statistically significant differences were observed among cisgender women, likely due to the limited sample size. These findings suggest that HNR, particularly its variability, may hold promise as a voice-based marker for early detection and monitoring of vocal fold lesions. Further research with larger, more diverse populations is needed to refine these features and validate their clinical utility.

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CiteScore
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