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Updated: Sep 9, 2025

Investigating the Three-dimensional Flow Separation Induced by a Model Vocal Fold Polyp
Published on: February 3, 2014
Voice as a biomarker: exploratory analysis for benign and malignant vocal fold lesions
Phillip Jenkins1, Rylan Harrison2, Steven Bedrick1
1Division of Informatics, Clinical Epidemiology, Oregon Health and Science University, Portland, OR, United States.
None:
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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